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 | 2251 | 2006 |
Consensus statement on management of intersex disorders PA Lee, CP Houk, SF Ahmed, IA Hughes, ... Pediatrics 118 (2), e488-e500, 2006 | 1448 | 2006 |
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 | 782 | 2016 |
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 | 680 | 1999 |
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 | 452 | 2000 |
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 | 398 | 2003 |
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 | 344 | 2022 |
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 | 288 | 2000 |
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 | 286 | 2018 |
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 | 257 | 2016 |
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 | 227 | 2008 |
The impact of corticosteroids on growth and bone health T Mushtaq, SF Ahmed Archives of Disease in Childhood 87 (2), 93-96, 2002 | 216 | 2002 |
Summary of consensus statement on intersex disorders and their management CP Houk, IA Hughes, SF Ahmed, PA Lee, ... Pediatrics 118 (2), 753-757, 2006 | 211 | 2006 |
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 | 210 | 2013 |
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 | 187 | 2006 |
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 | 186 | 2011 |
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 | 172 | 1998 |
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 | 163 | 2018 |
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 | 154 | 2018 |
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 | 154 | 2007 |