Dr Mohammed Guftar Shaikh

  • Honorary Clinical Associate Professor (School of Medicine, Dentistry & Nursing)

email: Guftar.Shaikh@glasgow.ac.uk

Dept of Endocrinology, Royal Hospital for Children, 1345 Govan Road, Glasgow G51 4TF

Import to contacts

Publications

List by: Type | Date

Jump to: 2024 | 2023 | 2022 | 2021 | 2020 | 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2012 | 2011 | 2008 | 2007 | 2006 | 2005 | 2004 | 2003 | 1993
Number of items: 71.

2024

Miller, J. L. et al. (2024) Diazoxide choline extended‐release tablet in people with Prader‐Willi syndrome: results from long‐term open‐label study. Obesity, 32(2), pp. 252-261. (doi: 10.1002/oby.23928) (PMID:37919617)

Kuah, X. Y. C. et al. (2024) Presentation and outcomes of paediatric craniopharyngioma in the west of Scotland: a 25 year experience. Journal of Neuro-Oncology, 166(1), pp. 51-57. (doi: 10.1007/s11060-023-04490-5) (PMID:38224403)

Rashid, A. et al. (2024) Advancing the understanding of clinical sepsis using gene expression-driven machine learning to improve patient outcomes. Shock: Injury, Inflammation and Sepsis, 61(1), pp. 4-18. (doi: 10.1097/shk.0000000000002227) (PMID:37752080)

2023

Shaikh, M. G. et al. (2023) Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus. Frontiers in Endocrinology, 14, 1231043. (doi: 10.3389/fendo.2023.1231043) (PMID:38027197) (PMCID:PMC10646160)

2022

Ahmed Zaki, S., Shaikh, M. G. and Rashid, A. (2022) Severe hypertension in pediatric diabetic ketoacidosis – a case report and review of literature. Malaysian Family Physician, 17(3), pp. 149-152. (doi: 10.51866/cr.93) (PMID:36606170) (PMCID:PMC9809442)

McCowan, R., Wild, E., Lucas-Herald, A. K. , Mcneilly, J., Mason, A., Wong, S. C. , Ahmed, S. F. and Shaikh, M. G. (2022) The effect of COVID-19 on the presentation of thyroid disease in children. Frontiers in Endocrinology, 13, 1014533. (doi: 10.3389/fendo.2022.1014533) (PMID:36325445) (PMCID:PMC9618596)

Upners, E. N. et al. (2022) Timing of puberty, pubertal growth, and adult height in short children born small for gestational age treated with growth hormone. Journal of Clinical Endocrinology and Metabolism, 107(8), pp. 2286-2295. (doi: 10.1210/clinem/dgac282) (PMID:35521800)

Brady, C. and Shaikh, M. G. (2022) Liraglutide does not provide sustainable results for weight improvement in adolescents with obesity. Archives of Disease in Childhood: Education and Practice, 107, 232. (doi: 10.1136/archdischild-2020-319807) (PMID:32988963)

García-Miñaúr, S. et al. (2022) European Medical Education Initiative on Noonan Syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe. European Journal of Medical Genetics, 65(1), 104371. (doi: 10.1016/j.ejmg.2021.104371) (PMID:34757053)

Wolf, C. M., Zenker, M., Burkitt-Wright, E., Edouard, T., García-Miñaúr, S., Lebl, J., Shaikh, G., Tartaglia, M., Verloes, A. and Östman-Smith, I. (2022) Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists. European Journal of Medical Genetics, 65(1), 104372. (doi: 10.1016/j.ejmg.2021.104372) (PMID:34757052)

2021

Kherra, S., Forsyth Paterson, W., Cizmecioğlu, F. M., Jones, J. H., Kourime, M., Elsedfy, H. H., Amer, S. T., Kyriakou, A., Shaikh, M. G. and Donaldson, M. D. C. (2021) Hypogonadism in the Prader-Willi syndrome from birth to adulthood: a 28-year experience in a single centre. Endocrine Connections, 10(9), pp. 1134-1146. (doi: 10.1530/ec-21-0277) (PMID:34382580) (PMCID:PMC8494419)

McCallion, S., Smith, S., Kyle, H., Shaikh, M. G., Wilkinson, G. and Kyriakou, A. (2021) An appraisal of current service delivery and future models of care for young people with gender dysphoria. European Journal of Pediatrics, 180, pp. 2969-2976. (doi: 10.1007/s00431-021-04075-2) (PMID:33855617)

Buonocore, F. et al. (2021) Genetic analysis of pediatric primary adrenal insufficiency of unknown etiology: 25 years’ experience in the UK. Journal of the Endocrine Society, 5(8), bvab086. (doi: 10.1210/jendso/bvab086) (PMID:34258490) (PMCID:PMC8266051)

McNally, R., Jones, J. H., Shaikh, M. G., Donaldson, M., Blakey, K. and Cheetham, T. (2021) Congenital hypothyroidism: Space-time clustering of thyroid dysgenesis indicates a role for environmental factors in disease etiology. Thyroid, 31(6), pp. 876-883. (doi: 10.1089/thy.2020.0005) (PMID:33183175) (PMCID:PMC8215409)

Carroll, J., Johnston, A., Ahmed, S. F., O’Toole, S., Mason, A., Shaikh, M.G. and Sabharwal, A. (2021) Paediatric surgical management of primary pigmented nodular adrenocortical disease: a single tertiary centre experience and review of literature. Journal of Pediatric Endoscopic Surgery, 3(2), pp. 73-79. (doi: 10.1007/s42804-021-00091-z)

Frixou, M., Vlek, D., Lucas-Herald, A. K. , Keir, L., Kyriakou, A. and Shaikh, M. G. (2021) The use of growth hormone therapy in adults with Prader Willi Syndrome: a systematic review. Clinical Endocrinology, 94(4), pp. 645-655. (doi: 10.1111/cen.14372) (PMID:33296095)

Farouq, M. W. et al. (2021) A novel coupled reaction-diffusion system for explainable gene expression profiling. Sensors, 21(6), 2190. (doi: 10.3390/s21062190) (PMID:33801002) (PMCID:PMC8003942)

2020

El Tonbary, K., Robinson, P., Banerjee, I. and Shaikh, M.G. (2020) Congenital hyperinsulinism: management and outcome, a single tertiary centre experience. European Journal of Pediatrics, 179, pp. 947-952. (doi: 10.1007/s00431-020-03581-z) (PMID:32002613)

Wegmann, M. G. et al. (2020) Increases in bioactive IGF do not parallel increases in total IGF-I during growth hormone treatment of children born SGA. Journal of Clinical Endocrinology and Metabolism, 105(4), e1291-e1298. (doi: 10.1210/clinem/dgz118) (PMID:31665326)

Ali, S. R., Macqueen, Z., Gardner, M., Xin, Y. , Kyriakou, A., Mason, A., Shaikh, M. G., Wong, S. C. , Sandberg, D. E. and Ahmed, S. F. (2020) Parent-reported outcomes in young children with disorders/differences of sex development. International Journal of Pediatric Endocrinology, 2020, 3. (doi: 10.1186/s13633-020-0073-x) (PMID:32082389) (PMCID:PMC7020572)

Brusgaard, K. et al. (2020) Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389. PLoS ONE, 15(2), e0228417. (doi: 10.1371/journal.pone.0228417) (PMID:32027664) (PMCID:PMC7004321)

Gregoriou, K., Craigie, I., Gibson, B., Mason, A. and Shaikh, M. G. (2020) Risk factors and management of corticosteroid‐induced hyperglycaemia in paediatric acute lymphoblastic leukaemia. Pediatric Blood and Cancer, 67(2), e28085. (doi: 10.1002/pbc.28085) (PMID:31736211)

Houghton, J. A. et al. (2020) Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinism. Journal of Pathology: Clinical Research, 6(1), pp. 12-16. (doi: 10.1002/cjp2.144) (PMID:31577849) (PMCID:PMC6966704)

2019

Chen, S. C. et al. (2019) Diazoxide‐induced pulmonary hypertension in hyperinsulinaemic hypoglycaemia: Recommendations from a multicentre study in the United Kingdom. Clinical Endocrinology, 91(6), pp. 770-775. (doi: 10.1111/cen.14096) (PMID:31520536)

Milner, T. D., Ronghe, M., Shaikh, M. G., MacGregor, F. B. and Reed, N. (2019) Vandetanib tumor shrinkage in metastatic medullary thyroid cancer allowing surgical resection of the primary site: A case report. Journal of Pediatric Hematology/Oncology, 41(5), e329-e332. (doi: 10.1097/MPH.0000000000001330) (PMID:30334899)

2018

Ahmid, M., Ahmed, S. F. and Shaikh, M. G. (2018) Childhood-onset growth hormone deficiency and the transition to adulthood: current perspective. Therapeutics and Clinical Risk Management, 14, pp. 2283-2291. (doi: 10.2147/TCRM.S136576) (PMID:30538484) (PMCID:PMC6260189)

Lucas-Herald, A. K. , Mason, E., Beaumont, P., Mason, A., Shaikh, M. G., Wong, S. C. and Ahmed, S. F. (2018) Single-centre experience of testosterone therapy for boys with hypogonadism. Hormone Research in Paediatrics, 90(2), pp. 123-127. (doi: 10.1159/000490738) (PMID:30021202)

Çizmecioğlu, F. M., Jones, J. H., Forsyth Paterson, W., Kherra, S., Kourime, M., McGowan, R., Shaikh, M. G. and Donaldson, M. (2018) Neonatal features of the Prader-Willi syndrome; the case for making the diagnosis during the first week of life. Journal of Clinical Research in Pediatric Endocrinology, 10(3), pp. 264-273. (doi: 10.4274/jcrpe.0029) (PMID:29553044) (PMCID:PMC6083474)

Shepherd, S., Kyriakou, A., Shaikh, M. G., McDevitt, H., Oakley, C., Thrower, M., Ahmed, S. F. and Mason, A. (2018) Longitudinal changes in bone parameters in young girls with anorexia nervosa. Bone, (doi: 10.1016/j.bone.2018.03.022) (PMID:29601899)

Ali, S.R., Shaheen, I., Young, D., Ramage, I., Maxwell, H., Hughes, D.A., Athavale, D. and Shaikh, M.G. (2018) Fludrocortisone-a treatment for tubulopathy post-paediatric renal transplantation: A national paediatric nephrology unit experience. Pediatric Transplantation, 22(2), e13134. (doi: 10.1111/petr.13134) (PMID:29345400)

Khan, M. J., Gerasimidis, K. , Edwards, C. A. and Shaikh, M. G. (2018) Mechanisms of obesity in Prader-Willi syndrome. Pediatric Obesity, 13(1), pp. 3-13. (doi: 10.1111/ijpo.12177) (PMID:27863129)

2017

Jones, J. H., Smith, S., Dorrian, C., Mason, A. and Shaikh, M. G. (2017) Permanent congenital hypothyroidism with blood spot thyroid stimulating hormone <10 mU/L. Archives of Disease in Childhood, 103, pp. 65-67. (doi: 10.1136/archdischild-2015-309564) (PMID:27016213)

Wegmann, M. G. et al. (2017) The exon3-deleted growth hormone receptor gene polymorphism (d3-GHR) is associated with insulin and spontaneous growth in short SGA children (NESGAS). Growth Hormone and IGF Research, 35, pp. 45-51. (doi: 10.1016/j.ghir.2017.07.001) (PMID:28719834)

2016

Lucaccioni, L., Mcneilly, J., Mason, A., Giacomozzi, C., Kyriakou, A., Shaikh, M. G., Iughetti, L. and Ahmed, S. F. (2016) The measurement of urinary gonadotropins for assessment and management of pubertal disorder. Hormones, 15(3), pp. 377-384. (doi: 10.14310/horm.2002.1690) (PMID:27838606)

Pokrovska, T., Jones, J., Shaikh, M. G., Smith, S. and Donaldson, M. D.C. (2016) How well does the capillary thyroid-stimulating hormone test for newborn thyroid screening predict the venous free thyroxine level. Archives of Disease in Childhood, 101(6), pp. 539-545. (doi: 10.1136/archdischild-2015-309529) (PMID:26966265) (PMCID:PMC4893081)

Ahmid, M., Perry, C.G., Ahmed, S.F. and Shaikh, M.G. (2016) Growth hormone deficiency during young adulthood and the benefits of growth hormone replacement. Endocrine Connections, 5(3), R1-R11. (doi: 10.1530/ec-16-0024) (PMID:27129699) (PMCID:PMC5002964)

Mcneilly, J.D., Boal, R., Shaikh, M.G. and Ahmed, S.F. (2016) Frequency and aetiology of hypercalcaemia. Archives of Disease in Childhood, 101(4), pp. 344-347. (doi: 10.1136/archdischild-2015-309029) (PMID:26903499)

Ahmid, M. et al. (2016) An audit of the management of childhood-onset growth hormone deficiency during young adulthood in Scotland. International Journal of Pediatric Endocrinology, 2016, 6. (doi: 10.1186/s13633-016-0024-8) (PMID:6985190) (PMCID:PMC479349)

Edgar, O. S., Lucas-Herald, A. K. and Shaikh, M. G. (2016) Pituitary-adrenal axis in Prader Willi syndrome. Diseases, 4(1), 5. (doi: 10.3390/diseases4010005) (PMID:28933385) (PMCID:PMC5456314)

Narayanan, V. K., Ronghe, M., MacGregor, F. B., Bradshaw, N., Davidson, R., Welbury, R., Reed, N. and Shaikh, M. G. (2016) Use of vandetanib in metastatic medullary carcinoma of thyroid in a pediatric patient with multiple endocrine neoplasia 2B. Journal of Pediatric Hematology/Oncology, 38(2), pp. 155-157. (doi: 10.1097/MPH.0000000000000432) (PMID:26479990)

Khan, M. J., Gerasimidis, K. , Edwards, C. A. and Shaikh, M. G. (2016) Role of gut microbiota in the aetiology of obesity: proposed mechanisms and review of the literature. Journal of Obesity, 2016, 7353642. (doi: 10.1155/2016/7353642) (PMID:7703805) (PMCID:PMC5040794)

2015

Abdalrahaman, N. et al. (2015) Deficits in trabecular bone microarchitecture in young women with Type 1 diabetes mellitus. Journal of Bone and Mineral Research, 30(8), pp. 1386-1393. (doi: 10.1002/jbmr.2465) (PMID:25627460)

Chen, S. C., Murphy, D., Sastry, J. and Shaikh, M. G. (2015) Predicting, monitoring, and managing hypercalcemia secondary to 13-cis-retinoic acid therapy in children with high-risk neuroblastoma. Journal of Pediatric Hematology/Oncology, 37(6), pp. 477-481. (doi: 10.1097/MPH.0000000000000362) (PMID:26056798)

Giacomozzi, C., Deodati, A., Shaikh, M. G., Ahmed, S. F. and Cianfarani, S. (2015) The impact of growth hormone therapy on adult height in noonan syndrome: a systematic review. Hormone Research in Paediatrics, 83(3), pp. 167-176. (doi: 10.1159/000371635) (PMID:25721697)

Lucas-Herald, A. K. , Rodie, M., Lucaccioni, L., Shapiro, D., McNeilly, J., Shaikh, M. G. and Ahmed, S. F. (2015) The pitfalls associated with urinary steroid metabolite ratios in children undergoing investigations for suspected disorders of steroid synthesis. International Journal of Pediatric Endocrinology, 2015, 10. (doi: 10.1186/s13633-015-0007-1)

Khan, M. J. et al. (2015) A Detailed Analysis of the Gut Microbial Diversity and Metabolic Activity in Children with Obesity of Different Aetiology and Lean Controls. The Nutrition Society Summer Meeting: Carbohydrates in Health: Friends or Foes?, Glasgow, UK, 14-17 Jul 2014. (doi: 10.1017/S0029665115000907)

Khan, M. J., Humayun, K. N., Donaldson, M., Ahmed, S. F. and Shaikh, M. G. (2015) Longitudinal changes in body mass index in children with craniopharyngioma. Hormone Research in Paediatrics, 82(6), pp. 372-379. (doi: 10.1159/000368798) (PMID:25359623)

Chen, S. C., McDevitt, H., Clement, W. A., Wynne, D. M., Mason, A., Donaldson, M. D.C., Ahmed, S. F. and Shaikh, M. G. (2015) Early identification of pituitary dysfunction in congenital nasal pyriform aperture stenosis: recommendations based on experience in a single centre. Hormone Research in Paediatrics, 83(5), pp. 302-310. (doi: 10.1159/000369805) (PMID:25791686)

Lucas-Herald, A. K., Perry, C. G. and Shaikh, M. G. (2015) Review of growth hormone therapy in adolescents and young adults with Prader–Willi syndrome. Expert Review of Endocrinology and Metabolism, 10(2), pp. 259-267. (doi: 10.1586/17446651.2015.1007126) (PMID:30293507)

2014

Stevens, A. et al. (2014) Insights into the pathophysiology of catch-up compared with non-catch-up growth in children born small for gestational age: An integrated analysis of metabolic and transcriptomic data. Pharmacogenomics Journal, 14, pp. 376-384. (doi: 10.1038/tpj.2014.4) (PMID:24614687)

McComb, C., Harpur, A., Yacoubian, C., Leddy, C., Anderson, G., Shepherd, S., Perry, C., Shaikh, M.G., Foster, J. and Ahmed, S.F. (2014) MRI-based abnormalities in young adults at risk of adverse bone health due to childhood-onset metabolic & endocrine conditions. Clinical Endocrinology, 80(6), pp. 811-817. (doi: 10.1111/cen.12367)

Shaikh, M. G., Crabtree, N., Kirk, J. M.W. and Shaw, N. J. (2014) The relationship between bone mass and body composition in children with hypothalamic and simple obesity. Clinical Endocrinology, 80(1), pp. 85-91. (doi: 10.1111/cen.12263) (PMID:23745601)

El-Fakhri, N., McDevitt, H., Shaikh, M.G., Halsey, C. and Ahmed, S.F. (2014) Vitamin D and its effects on glucose homeostasis, cardiovascular function and immune function. Hormone Research in Paediatrics, 81(6), pp. 363-378. (doi: 10.1159/000357731)

2012

Viner, R. M. et al. (2012) Assessment of childhood obesity in secondary care: OSCA consensus statement. Archives of Disease in Childhood: Education and Practice, 97, pp. 98-105. (doi: 10.1136/edpract-2011-301426) (PMID:22611124)

2011

Ahmed, S. F. , Franey, C., McDevitt, H., Somerville, L., Butler, S., Galloway, P., Reynolds, L., Shaikh, M. G. and Wallace, A. M. (2011) Recent trends and clinical features of childhood vitamin D deficiency presenting to a children's hospital in Glasgow. Archives of Disease in Childhood, 96(7), pp. 694-696. (doi: 10.1136/adc.2009.173195) (PMID:20584848)

2008

Shaikh, M. G., Grundy, R. G. and Kirk, J. M.W. (2008) Hyperleptinaemia rather than fasting hyperinsulinaemia is associated with obesity following hypothalamic damage in children. European Journal of Endocrinology, 159(6), pp. 791-797. (doi: 10.1530/EJE-08-0533) (PMID:18819946)

Shaikh, M. G. et al. (2008) Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita. Journal of Medical Genetics, 45(9), e1. (doi: 10.1136/jmg.2007.055129) (PMID:18762570) (PMCID:PMC2602739)

Rajab, A. et al. (2008) Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. Human Molecular Genetics, 17(14), pp. 2150-2159. (doi: 10.1093/hmg/ddn114) (PMID:18407919)

Shaikh, M. G., Grundy, R. G. and Kirk, J. M. W. (2008) Reductions in basal metabolic rate and physical activity contribute to hypothalamic obesity. Journal of Clinical Endocrinology and Metabolism, 93(7), pp. 2588-2593. (doi: 10.1210/jc.2007-2672) (PMID:18413428)

Welzel, M., Wüstemann, N., Ŝimić-Schleicher, G., Dörr, H. G., Schulze, E., Shaikh, G., Clayton, P., Grötzinger, J., Holterhus, P.-M. and Riepe, F. G. (2008) Carboxyl-terminal mutations in 3β-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenital adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 93(4), pp. 1418-1425. (doi: 10.1210/jc.2007-1874) (PMID:18252794)

2007

Shaikh, M.G., Crabtree, N.J., Shaw, N.J. and Kirk, J.M.W. (2007) Body fat estimation using bioelectrical impedance. Hormone Research in Paediatrics, 68(1), pp. 8-10. (doi: 10.1159/000098481) (PMID:17213729)

Shaikh, M.G., McLachlan, K. and Stirling, H. (2007) Renal and hepatic dysfunction in hypothyroid children. Acta Paediatrica, 96(4), pp. 605-606. (doi: 10.1111/j.1651-2227.2006.00160.x) (PMID:17274804)

Amin, R., Smit, E., Shaikh, G., Rawling, P. and Alexander, E. (2007) Mycoplasma respiratory tract infection complicated by Stevens-Johnson syndrome and surgical emphysema. Acta Paediatrica, 96(3), p. 472. (doi: 10.1111/j.1651-2227.2007.00088.x) (PMID:17407485)

2006

Minton, J.A.L. et al. (2006) Syndromic obesity and diabetes: Changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alström syndrome. Journal of Clinical Endocrinology and Metabolism, 91(8), pp. 3110-3116. (doi: 10.1210/jc.2005-2633) (PMID:16720663)

Shaikh, M. G., Wickramasuriya, N., McLachlan, K., Stirling, H. and Kirk, J. M.W. (2006) Thyroxine: Cause and cure for headache. Acta Paediatrica, 95(5), pp. 632-633. (doi: 10.1111/j.1651-2227.2006.tb02303.x) (PMID:16825155)

2005

Rainbow, L.A., Rees, S.A., Shaikh, M.G., Shaw, N.J., Cole, T., Barrett, T.G. and Kirk, J.M.W. (2005) Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia. Clinical Endocrinology, 62(2), pp. 163-168. (doi: 10.1111/j.1365-2265.2004.02189.x) (PMID:15670191)

2004

Shaikh, M.G., Lewis, P. and Kirk, J.M.W. (2004) Thyroxine unmasks Addison's disease. Acta Paediatrica, 93(12), pp. 1663-1665. (doi: 10.1111/j.1651-2227.2004.tb00860.x) (PMID:15918231)

Evans, H. M., Shaikh, M. G., McKiernan, P. J., Hockley, A. D., Crowne, E. C., Kirk, J. M.W. and Kelly, D. A. (2004) Acute fatty liver disease after suprasellar tumor resection. Journal of Pediatric Gastroenterology and Nutrition, 39(3), pp. 288-291. (doi: 10.1097/00005176-200409000-00012) (PMID:15319631)

Shaikh, M.G. and Anderson, J.M. (2004) Omeprazole may delay the diagnosis of pyloric stenosis. Acta Paediatrica, 93(2), p. 283. (doi: 10.1111/j.1651-2227.2004.tb00724.x) (PMID:15046292)

2003

Shaikh, M. G., Anderson, J.M., Hall, S.K. and Jackson, M.A. (2003) Transient neonatal hypothyroidism due to a maternal vegan diet. Journal of Pediatric Endocrinology and Metabolism, 16, pp. 111-113. (doi: 10.1515/JPEM.2003.16.1.111) (PMID:12585349)

1993

Shaikh, M.G., Heys, S.D., Brown, P.A. and Whiting, P.H. (1993) Chronic cyclosporin A (CsA) nephrotoxicity in the rat: the effect of calcium blockade with verapamil. International Journal of Experimental Pathology, 74(4), pp. 389-396. (PMID:8398812) (PMCID:PMC2001848)

This list was generated on Sun Apr 21 19:22:52 2024 BST.
Number of items: 71.

Articles

Miller, J. L. et al. (2024) Diazoxide choline extended‐release tablet in people with Prader‐Willi syndrome: results from long‐term open‐label study. Obesity, 32(2), pp. 252-261. (doi: 10.1002/oby.23928) (PMID:37919617)

Kuah, X. Y. C. et al. (2024) Presentation and outcomes of paediatric craniopharyngioma in the west of Scotland: a 25 year experience. Journal of Neuro-Oncology, 166(1), pp. 51-57. (doi: 10.1007/s11060-023-04490-5) (PMID:38224403)

Rashid, A. et al. (2024) Advancing the understanding of clinical sepsis using gene expression-driven machine learning to improve patient outcomes. Shock: Injury, Inflammation and Sepsis, 61(1), pp. 4-18. (doi: 10.1097/shk.0000000000002227) (PMID:37752080)

Shaikh, M. G. et al. (2023) Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus. Frontiers in Endocrinology, 14, 1231043. (doi: 10.3389/fendo.2023.1231043) (PMID:38027197) (PMCID:PMC10646160)

Ahmed Zaki, S., Shaikh, M. G. and Rashid, A. (2022) Severe hypertension in pediatric diabetic ketoacidosis – a case report and review of literature. Malaysian Family Physician, 17(3), pp. 149-152. (doi: 10.51866/cr.93) (PMID:36606170) (PMCID:PMC9809442)

McCowan, R., Wild, E., Lucas-Herald, A. K. , Mcneilly, J., Mason, A., Wong, S. C. , Ahmed, S. F. and Shaikh, M. G. (2022) The effect of COVID-19 on the presentation of thyroid disease in children. Frontiers in Endocrinology, 13, 1014533. (doi: 10.3389/fendo.2022.1014533) (PMID:36325445) (PMCID:PMC9618596)

Upners, E. N. et al. (2022) Timing of puberty, pubertal growth, and adult height in short children born small for gestational age treated with growth hormone. Journal of Clinical Endocrinology and Metabolism, 107(8), pp. 2286-2295. (doi: 10.1210/clinem/dgac282) (PMID:35521800)

Brady, C. and Shaikh, M. G. (2022) Liraglutide does not provide sustainable results for weight improvement in adolescents with obesity. Archives of Disease in Childhood: Education and Practice, 107, 232. (doi: 10.1136/archdischild-2020-319807) (PMID:32988963)

García-Miñaúr, S. et al. (2022) European Medical Education Initiative on Noonan Syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe. European Journal of Medical Genetics, 65(1), 104371. (doi: 10.1016/j.ejmg.2021.104371) (PMID:34757053)

Wolf, C. M., Zenker, M., Burkitt-Wright, E., Edouard, T., García-Miñaúr, S., Lebl, J., Shaikh, G., Tartaglia, M., Verloes, A. and Östman-Smith, I. (2022) Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists. European Journal of Medical Genetics, 65(1), 104372. (doi: 10.1016/j.ejmg.2021.104372) (PMID:34757052)

Kherra, S., Forsyth Paterson, W., Cizmecioğlu, F. M., Jones, J. H., Kourime, M., Elsedfy, H. H., Amer, S. T., Kyriakou, A., Shaikh, M. G. and Donaldson, M. D. C. (2021) Hypogonadism in the Prader-Willi syndrome from birth to adulthood: a 28-year experience in a single centre. Endocrine Connections, 10(9), pp. 1134-1146. (doi: 10.1530/ec-21-0277) (PMID:34382580) (PMCID:PMC8494419)

McCallion, S., Smith, S., Kyle, H., Shaikh, M. G., Wilkinson, G. and Kyriakou, A. (2021) An appraisal of current service delivery and future models of care for young people with gender dysphoria. European Journal of Pediatrics, 180, pp. 2969-2976. (doi: 10.1007/s00431-021-04075-2) (PMID:33855617)

Buonocore, F. et al. (2021) Genetic analysis of pediatric primary adrenal insufficiency of unknown etiology: 25 years’ experience in the UK. Journal of the Endocrine Society, 5(8), bvab086. (doi: 10.1210/jendso/bvab086) (PMID:34258490) (PMCID:PMC8266051)

McNally, R., Jones, J. H., Shaikh, M. G., Donaldson, M., Blakey, K. and Cheetham, T. (2021) Congenital hypothyroidism: Space-time clustering of thyroid dysgenesis indicates a role for environmental factors in disease etiology. Thyroid, 31(6), pp. 876-883. (doi: 10.1089/thy.2020.0005) (PMID:33183175) (PMCID:PMC8215409)

Carroll, J., Johnston, A., Ahmed, S. F., O’Toole, S., Mason, A., Shaikh, M.G. and Sabharwal, A. (2021) Paediatric surgical management of primary pigmented nodular adrenocortical disease: a single tertiary centre experience and review of literature. Journal of Pediatric Endoscopic Surgery, 3(2), pp. 73-79. (doi: 10.1007/s42804-021-00091-z)

Frixou, M., Vlek, D., Lucas-Herald, A. K. , Keir, L., Kyriakou, A. and Shaikh, M. G. (2021) The use of growth hormone therapy in adults with Prader Willi Syndrome: a systematic review. Clinical Endocrinology, 94(4), pp. 645-655. (doi: 10.1111/cen.14372) (PMID:33296095)

Farouq, M. W. et al. (2021) A novel coupled reaction-diffusion system for explainable gene expression profiling. Sensors, 21(6), 2190. (doi: 10.3390/s21062190) (PMID:33801002) (PMCID:PMC8003942)

El Tonbary, K., Robinson, P., Banerjee, I. and Shaikh, M.G. (2020) Congenital hyperinsulinism: management and outcome, a single tertiary centre experience. European Journal of Pediatrics, 179, pp. 947-952. (doi: 10.1007/s00431-020-03581-z) (PMID:32002613)

Wegmann, M. G. et al. (2020) Increases in bioactive IGF do not parallel increases in total IGF-I during growth hormone treatment of children born SGA. Journal of Clinical Endocrinology and Metabolism, 105(4), e1291-e1298. (doi: 10.1210/clinem/dgz118) (PMID:31665326)

Ali, S. R., Macqueen, Z., Gardner, M., Xin, Y. , Kyriakou, A., Mason, A., Shaikh, M. G., Wong, S. C. , Sandberg, D. E. and Ahmed, S. F. (2020) Parent-reported outcomes in young children with disorders/differences of sex development. International Journal of Pediatric Endocrinology, 2020, 3. (doi: 10.1186/s13633-020-0073-x) (PMID:32082389) (PMCID:PMC7020572)

Brusgaard, K. et al. (2020) Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389. PLoS ONE, 15(2), e0228417. (doi: 10.1371/journal.pone.0228417) (PMID:32027664) (PMCID:PMC7004321)

Gregoriou, K., Craigie, I., Gibson, B., Mason, A. and Shaikh, M. G. (2020) Risk factors and management of corticosteroid‐induced hyperglycaemia in paediatric acute lymphoblastic leukaemia. Pediatric Blood and Cancer, 67(2), e28085. (doi: 10.1002/pbc.28085) (PMID:31736211)

Houghton, J. A. et al. (2020) Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinism. Journal of Pathology: Clinical Research, 6(1), pp. 12-16. (doi: 10.1002/cjp2.144) (PMID:31577849) (PMCID:PMC6966704)

Chen, S. C. et al. (2019) Diazoxide‐induced pulmonary hypertension in hyperinsulinaemic hypoglycaemia: Recommendations from a multicentre study in the United Kingdom. Clinical Endocrinology, 91(6), pp. 770-775. (doi: 10.1111/cen.14096) (PMID:31520536)

Milner, T. D., Ronghe, M., Shaikh, M. G., MacGregor, F. B. and Reed, N. (2019) Vandetanib tumor shrinkage in metastatic medullary thyroid cancer allowing surgical resection of the primary site: A case report. Journal of Pediatric Hematology/Oncology, 41(5), e329-e332. (doi: 10.1097/MPH.0000000000001330) (PMID:30334899)

Ahmid, M., Ahmed, S. F. and Shaikh, M. G. (2018) Childhood-onset growth hormone deficiency and the transition to adulthood: current perspective. Therapeutics and Clinical Risk Management, 14, pp. 2283-2291. (doi: 10.2147/TCRM.S136576) (PMID:30538484) (PMCID:PMC6260189)

Lucas-Herald, A. K. , Mason, E., Beaumont, P., Mason, A., Shaikh, M. G., Wong, S. C. and Ahmed, S. F. (2018) Single-centre experience of testosterone therapy for boys with hypogonadism. Hormone Research in Paediatrics, 90(2), pp. 123-127. (doi: 10.1159/000490738) (PMID:30021202)

Çizmecioğlu, F. M., Jones, J. H., Forsyth Paterson, W., Kherra, S., Kourime, M., McGowan, R., Shaikh, M. G. and Donaldson, M. (2018) Neonatal features of the Prader-Willi syndrome; the case for making the diagnosis during the first week of life. Journal of Clinical Research in Pediatric Endocrinology, 10(3), pp. 264-273. (doi: 10.4274/jcrpe.0029) (PMID:29553044) (PMCID:PMC6083474)

Shepherd, S., Kyriakou, A., Shaikh, M. G., McDevitt, H., Oakley, C., Thrower, M., Ahmed, S. F. and Mason, A. (2018) Longitudinal changes in bone parameters in young girls with anorexia nervosa. Bone, (doi: 10.1016/j.bone.2018.03.022) (PMID:29601899)

Ali, S.R., Shaheen, I., Young, D., Ramage, I., Maxwell, H., Hughes, D.A., Athavale, D. and Shaikh, M.G. (2018) Fludrocortisone-a treatment for tubulopathy post-paediatric renal transplantation: A national paediatric nephrology unit experience. Pediatric Transplantation, 22(2), e13134. (doi: 10.1111/petr.13134) (PMID:29345400)

Khan, M. J., Gerasimidis, K. , Edwards, C. A. and Shaikh, M. G. (2018) Mechanisms of obesity in Prader-Willi syndrome. Pediatric Obesity, 13(1), pp. 3-13. (doi: 10.1111/ijpo.12177) (PMID:27863129)

Jones, J. H., Smith, S., Dorrian, C., Mason, A. and Shaikh, M. G. (2017) Permanent congenital hypothyroidism with blood spot thyroid stimulating hormone <10 mU/L. Archives of Disease in Childhood, 103, pp. 65-67. (doi: 10.1136/archdischild-2015-309564) (PMID:27016213)

Wegmann, M. G. et al. (2017) The exon3-deleted growth hormone receptor gene polymorphism (d3-GHR) is associated with insulin and spontaneous growth in short SGA children (NESGAS). Growth Hormone and IGF Research, 35, pp. 45-51. (doi: 10.1016/j.ghir.2017.07.001) (PMID:28719834)

Lucaccioni, L., Mcneilly, J., Mason, A., Giacomozzi, C., Kyriakou, A., Shaikh, M. G., Iughetti, L. and Ahmed, S. F. (2016) The measurement of urinary gonadotropins for assessment and management of pubertal disorder. Hormones, 15(3), pp. 377-384. (doi: 10.14310/horm.2002.1690) (PMID:27838606)

Pokrovska, T., Jones, J., Shaikh, M. G., Smith, S. and Donaldson, M. D.C. (2016) How well does the capillary thyroid-stimulating hormone test for newborn thyroid screening predict the venous free thyroxine level. Archives of Disease in Childhood, 101(6), pp. 539-545. (doi: 10.1136/archdischild-2015-309529) (PMID:26966265) (PMCID:PMC4893081)

Ahmid, M., Perry, C.G., Ahmed, S.F. and Shaikh, M.G. (2016) Growth hormone deficiency during young adulthood and the benefits of growth hormone replacement. Endocrine Connections, 5(3), R1-R11. (doi: 10.1530/ec-16-0024) (PMID:27129699) (PMCID:PMC5002964)

Mcneilly, J.D., Boal, R., Shaikh, M.G. and Ahmed, S.F. (2016) Frequency and aetiology of hypercalcaemia. Archives of Disease in Childhood, 101(4), pp. 344-347. (doi: 10.1136/archdischild-2015-309029) (PMID:26903499)

Ahmid, M. et al. (2016) An audit of the management of childhood-onset growth hormone deficiency during young adulthood in Scotland. International Journal of Pediatric Endocrinology, 2016, 6. (doi: 10.1186/s13633-016-0024-8) (PMID:6985190) (PMCID:PMC479349)

Edgar, O. S., Lucas-Herald, A. K. and Shaikh, M. G. (2016) Pituitary-adrenal axis in Prader Willi syndrome. Diseases, 4(1), 5. (doi: 10.3390/diseases4010005) (PMID:28933385) (PMCID:PMC5456314)

Narayanan, V. K., Ronghe, M., MacGregor, F. B., Bradshaw, N., Davidson, R., Welbury, R., Reed, N. and Shaikh, M. G. (2016) Use of vandetanib in metastatic medullary carcinoma of thyroid in a pediatric patient with multiple endocrine neoplasia 2B. Journal of Pediatric Hematology/Oncology, 38(2), pp. 155-157. (doi: 10.1097/MPH.0000000000000432) (PMID:26479990)

Khan, M. J., Gerasimidis, K. , Edwards, C. A. and Shaikh, M. G. (2016) Role of gut microbiota in the aetiology of obesity: proposed mechanisms and review of the literature. Journal of Obesity, 2016, 7353642. (doi: 10.1155/2016/7353642) (PMID:7703805) (PMCID:PMC5040794)

Abdalrahaman, N. et al. (2015) Deficits in trabecular bone microarchitecture in young women with Type 1 diabetes mellitus. Journal of Bone and Mineral Research, 30(8), pp. 1386-1393. (doi: 10.1002/jbmr.2465) (PMID:25627460)

Chen, S. C., Murphy, D., Sastry, J. and Shaikh, M. G. (2015) Predicting, monitoring, and managing hypercalcemia secondary to 13-cis-retinoic acid therapy in children with high-risk neuroblastoma. Journal of Pediatric Hematology/Oncology, 37(6), pp. 477-481. (doi: 10.1097/MPH.0000000000000362) (PMID:26056798)

Giacomozzi, C., Deodati, A., Shaikh, M. G., Ahmed, S. F. and Cianfarani, S. (2015) The impact of growth hormone therapy on adult height in noonan syndrome: a systematic review. Hormone Research in Paediatrics, 83(3), pp. 167-176. (doi: 10.1159/000371635) (PMID:25721697)

Lucas-Herald, A. K. , Rodie, M., Lucaccioni, L., Shapiro, D., McNeilly, J., Shaikh, M. G. and Ahmed, S. F. (2015) The pitfalls associated with urinary steroid metabolite ratios in children undergoing investigations for suspected disorders of steroid synthesis. International Journal of Pediatric Endocrinology, 2015, 10. (doi: 10.1186/s13633-015-0007-1)

Khan, M. J., Humayun, K. N., Donaldson, M., Ahmed, S. F. and Shaikh, M. G. (2015) Longitudinal changes in body mass index in children with craniopharyngioma. Hormone Research in Paediatrics, 82(6), pp. 372-379. (doi: 10.1159/000368798) (PMID:25359623)

Chen, S. C., McDevitt, H., Clement, W. A., Wynne, D. M., Mason, A., Donaldson, M. D.C., Ahmed, S. F. and Shaikh, M. G. (2015) Early identification of pituitary dysfunction in congenital nasal pyriform aperture stenosis: recommendations based on experience in a single centre. Hormone Research in Paediatrics, 83(5), pp. 302-310. (doi: 10.1159/000369805) (PMID:25791686)

Lucas-Herald, A. K., Perry, C. G. and Shaikh, M. G. (2015) Review of growth hormone therapy in adolescents and young adults with Prader–Willi syndrome. Expert Review of Endocrinology and Metabolism, 10(2), pp. 259-267. (doi: 10.1586/17446651.2015.1007126) (PMID:30293507)

Stevens, A. et al. (2014) Insights into the pathophysiology of catch-up compared with non-catch-up growth in children born small for gestational age: An integrated analysis of metabolic and transcriptomic data. Pharmacogenomics Journal, 14, pp. 376-384. (doi: 10.1038/tpj.2014.4) (PMID:24614687)

McComb, C., Harpur, A., Yacoubian, C., Leddy, C., Anderson, G., Shepherd, S., Perry, C., Shaikh, M.G., Foster, J. and Ahmed, S.F. (2014) MRI-based abnormalities in young adults at risk of adverse bone health due to childhood-onset metabolic & endocrine conditions. Clinical Endocrinology, 80(6), pp. 811-817. (doi: 10.1111/cen.12367)

Shaikh, M. G., Crabtree, N., Kirk, J. M.W. and Shaw, N. J. (2014) The relationship between bone mass and body composition in children with hypothalamic and simple obesity. Clinical Endocrinology, 80(1), pp. 85-91. (doi: 10.1111/cen.12263) (PMID:23745601)

El-Fakhri, N., McDevitt, H., Shaikh, M.G., Halsey, C. and Ahmed, S.F. (2014) Vitamin D and its effects on glucose homeostasis, cardiovascular function and immune function. Hormone Research in Paediatrics, 81(6), pp. 363-378. (doi: 10.1159/000357731)

Viner, R. M. et al. (2012) Assessment of childhood obesity in secondary care: OSCA consensus statement. Archives of Disease in Childhood: Education and Practice, 97, pp. 98-105. (doi: 10.1136/edpract-2011-301426) (PMID:22611124)

Ahmed, S. F. , Franey, C., McDevitt, H., Somerville, L., Butler, S., Galloway, P., Reynolds, L., Shaikh, M. G. and Wallace, A. M. (2011) Recent trends and clinical features of childhood vitamin D deficiency presenting to a children's hospital in Glasgow. Archives of Disease in Childhood, 96(7), pp. 694-696. (doi: 10.1136/adc.2009.173195) (PMID:20584848)

Shaikh, M. G., Grundy, R. G. and Kirk, J. M.W. (2008) Hyperleptinaemia rather than fasting hyperinsulinaemia is associated with obesity following hypothalamic damage in children. European Journal of Endocrinology, 159(6), pp. 791-797. (doi: 10.1530/EJE-08-0533) (PMID:18819946)

Shaikh, M. G. et al. (2008) Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita. Journal of Medical Genetics, 45(9), e1. (doi: 10.1136/jmg.2007.055129) (PMID:18762570) (PMCID:PMC2602739)

Rajab, A. et al. (2008) Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. Human Molecular Genetics, 17(14), pp. 2150-2159. (doi: 10.1093/hmg/ddn114) (PMID:18407919)

Shaikh, M. G., Grundy, R. G. and Kirk, J. M. W. (2008) Reductions in basal metabolic rate and physical activity contribute to hypothalamic obesity. Journal of Clinical Endocrinology and Metabolism, 93(7), pp. 2588-2593. (doi: 10.1210/jc.2007-2672) (PMID:18413428)

Welzel, M., Wüstemann, N., Ŝimić-Schleicher, G., Dörr, H. G., Schulze, E., Shaikh, G., Clayton, P., Grötzinger, J., Holterhus, P.-M. and Riepe, F. G. (2008) Carboxyl-terminal mutations in 3β-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenital adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 93(4), pp. 1418-1425. (doi: 10.1210/jc.2007-1874) (PMID:18252794)

Shaikh, M.G., Crabtree, N.J., Shaw, N.J. and Kirk, J.M.W. (2007) Body fat estimation using bioelectrical impedance. Hormone Research in Paediatrics, 68(1), pp. 8-10. (doi: 10.1159/000098481) (PMID:17213729)

Shaikh, M.G., McLachlan, K. and Stirling, H. (2007) Renal and hepatic dysfunction in hypothyroid children. Acta Paediatrica, 96(4), pp. 605-606. (doi: 10.1111/j.1651-2227.2006.00160.x) (PMID:17274804)

Amin, R., Smit, E., Shaikh, G., Rawling, P. and Alexander, E. (2007) Mycoplasma respiratory tract infection complicated by Stevens-Johnson syndrome and surgical emphysema. Acta Paediatrica, 96(3), p. 472. (doi: 10.1111/j.1651-2227.2007.00088.x) (PMID:17407485)

Minton, J.A.L. et al. (2006) Syndromic obesity and diabetes: Changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alström syndrome. Journal of Clinical Endocrinology and Metabolism, 91(8), pp. 3110-3116. (doi: 10.1210/jc.2005-2633) (PMID:16720663)

Shaikh, M. G., Wickramasuriya, N., McLachlan, K., Stirling, H. and Kirk, J. M.W. (2006) Thyroxine: Cause and cure for headache. Acta Paediatrica, 95(5), pp. 632-633. (doi: 10.1111/j.1651-2227.2006.tb02303.x) (PMID:16825155)

Rainbow, L.A., Rees, S.A., Shaikh, M.G., Shaw, N.J., Cole, T., Barrett, T.G. and Kirk, J.M.W. (2005) Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia. Clinical Endocrinology, 62(2), pp. 163-168. (doi: 10.1111/j.1365-2265.2004.02189.x) (PMID:15670191)

Shaikh, M.G., Lewis, P. and Kirk, J.M.W. (2004) Thyroxine unmasks Addison's disease. Acta Paediatrica, 93(12), pp. 1663-1665. (doi: 10.1111/j.1651-2227.2004.tb00860.x) (PMID:15918231)

Evans, H. M., Shaikh, M. G., McKiernan, P. J., Hockley, A. D., Crowne, E. C., Kirk, J. M.W. and Kelly, D. A. (2004) Acute fatty liver disease after suprasellar tumor resection. Journal of Pediatric Gastroenterology and Nutrition, 39(3), pp. 288-291. (doi: 10.1097/00005176-200409000-00012) (PMID:15319631)

Shaikh, M.G. and Anderson, J.M. (2004) Omeprazole may delay the diagnosis of pyloric stenosis. Acta Paediatrica, 93(2), p. 283. (doi: 10.1111/j.1651-2227.2004.tb00724.x) (PMID:15046292)

Shaikh, M. G., Anderson, J.M., Hall, S.K. and Jackson, M.A. (2003) Transient neonatal hypothyroidism due to a maternal vegan diet. Journal of Pediatric Endocrinology and Metabolism, 16, pp. 111-113. (doi: 10.1515/JPEM.2003.16.1.111) (PMID:12585349)

Shaikh, M.G., Heys, S.D., Brown, P.A. and Whiting, P.H. (1993) Chronic cyclosporin A (CsA) nephrotoxicity in the rat: the effect of calcium blockade with verapamil. International Journal of Experimental Pathology, 74(4), pp. 389-396. (PMID:8398812) (PMCID:PMC2001848)

Conference or Workshop Item

Khan, M. J. et al. (2015) A Detailed Analysis of the Gut Microbial Diversity and Metabolic Activity in Children with Obesity of Different Aetiology and Lean Controls. The Nutrition Society Summer Meeting: Carbohydrates in Health: Friends or Foes?, Glasgow, UK, 14-17 Jul 2014. (doi: 10.1017/S0029665115000907)

This list was generated on Sun Apr 21 19:22:52 2024 BST.