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Faisal Ahmed
Faisal Ahmed
Samson Gemmell Chair of Child Health, University of Glasgow
Verified email at glasgow.ac.uk - Homepage
Title
Cited by
Cited by
Year
Consensus statement on management of intersex disorders
IA Hughes, C Houk, SF Ahmed, PA Lee, LWPE Society
Journal of pediatric urology 2 (3), 148-162, 2006
22512006
Consensus statement on management of intersex disorders
PA Lee, CP Houk, SF Ahmed, IA Hughes, ...
Pediatrics 118 (2), e488-e500, 2006
14482006
Global disorders of sex development update since 2006: perceptions, approach and care
PA Lee, A Nordenström, CP Houk, SF Ahmed, R Auchus, A Baratz, ...
Hormone research in paediatrics 85 (3), 158-180, 2016
7822016
PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome
DJ Marsh, JB Kum, KL Lunetta, MJ Bennett, RJ Gorlin, SF Ahmed, ...
Human molecular genetics 8 (8), 1461-1472, 1999
6801999
Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome
SF Ahmed, A Cheng, L Dovey, JR Hawkins, H Martin, J Rowland, ...
The Journal of Clinical Endocrinology & Metabolism 85 (2), 658-665, 2000
4522000
Psychological outcomes and gender-related development in complete androgen insensitivity syndrome
M Hines, SF Ahmed, IA Hughes
Archives of sexual behavior 32, 93-101, 2003
3982003
Congenital adrenal hyperplasia—current insights in pathophysiology, diagnostics, and management
HL Claahsen-van der Grinten, PW Speiser, SF Ahmed, W Arlt, RJ Auchus, ...
Endocrine reviews 43 (1), 91-159, 2022
3442022
The role of a clinical score in the assessment of ambiguous genitalia
SF Ahmed, O Khwaja, IA Hughes
BJU international 85 (1), 120-124, 2000
2882000
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
G Mantovani, M Bastepe, D Monk, L De Sanctis, S Thiele, A Usardi, ...
Nature Reviews Endocrinology 14 (8), 476-500, 2018
2862018
Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015)
SF Ahmed, JC Achermann, W Arlt, A Balen, G Conway, Z Edwards, ...
Clinical endocrinology 84 (5), 771-788, 2016
2572016
Randomized, controlled trial of a best-practice individualized behavioral program for treatment of childhood overweight: Scottish Childhood Overweight Treatment Trial (SCOTT)
AR Hughes, L Stewart, J Chapple, JH McColl, MDC Donaldson, ...
Pediatrics 121 (3), e539-e546, 2008
2272008
The impact of corticosteroids on growth and bone health
T Mushtaq, SF Ahmed
Archives of Disease in Childhood 87 (2), 93-96, 2002
2162002
Summary of consensus statement on intersex disorders and their management
CP Houk, IA Hughes, SF Ahmed, PA Lee, ...
Pediatrics 118 (2), 753-757, 2006
2112006
Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial
N Bishop, S Adami, SF Ahmed, J Antón, P Arundel, CP Burren, ...
The Lancet 382 (9902), 1424-1432, 2013
2102013
Lawson Wilkins Pediatric Endocrine Society/European Society for Paediatric Endocrinology Consensus Group Consensus statement on management of intersex disorders
IA Hughes, C Houk, SF Ahmed, PA Lee
J Pediatr Urol 2 (3), 148-162, 2006
1872006
UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development
SF Ahmed, JC Achermann, W Arlt, AH Balen, G Conway, ZL Edwards, ...
Clinical Endocrinology 75 (1), 12-26, 2011
1862011
Effects of intensive chemotherapy on bone and collagen turnover and the growth hormone axis in children with acute lymphoblastic leukemia
PM Crofton, SF Ahmed, JC Wade, R Stephen, MW Elmlinger, MB Ranke, ...
The Journal of Clinical Endocrinology & Metabolism 83 (9), 3121-3129, 1998
1721998
Recommendations for improving the quality of rare disease registries
Y Kodra, J Weinbach, M Posada-De-La-Paz, A Coi, SL Lemonnier, ...
International journal of environmental research and public health 15 (8), 1644, 2018
1632018
Genetics in endocrinology: approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM …
L Audi, SF Ahmed, N Krone, M Cools, K McElreavey, PM Holterhus, ...
European Journal of Endocrinology 179 (4), R197-R206, 2018
1542018
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 …
A Ali, PT Christie, IV Grigorieva, B Harding, H Van Esch, SF Ahmed, ...
Human molecular genetics 16 (3), 265-275, 2007
1542007
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