S F Ahmed
Overview
Explore the profile of S F Ahmed including associated specialties, affiliations and a list of published articles.
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137
Citations
2678
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Recent Articles
21.
Yamout B, Khoury S, Ayyoubi N, Doumiati H, Fakhreddine M, Ahmed S, et al.
Mult Scler Relat Disord
. 2017 Nov;
18:85-89.
PMID: 29141828
Objectives: The aim of this study is to explore the frequency, type, and predictors of alternative diagnoses among patients referred with a recent diagnosis of multiple sclerosis (MS) to two...
22.
Nixon R, Cerqueira V, Kyriakou A, Lucas-Herald A, McNeilly J, McMillan M, et al.
Hum Reprod
. 2017 Sep;
32(10):2130-2137.
PMID: 28938747
Study Question: What is the likelihood of identifying genetic or endocrine abnormalities in a group of boys with 46, XY who present to a specialist clinic with a suspected disorder...
23.
Rodie M, Mudaliar M, Herzyk P, McMillan M, Boroujerdi M, Chudleigh S, et al.
Eur J Endocrinol
. 2017 Jul;
177(4):339-346.
PMID: 28733293
Background: It is unclear whether a short-term change in circulating androgens is associated with changes in the transcriptome of the peripheral blood mononuclear cells (PBMC). Aims And Methods: To explore...
24.
Abdalrahaman N, Mccomb C, Foster J, Lindsay R, Drummond R, McKay G, et al.
Clin Endocrinol (Oxf)
. 2017 Jun;
87(4):327-335.
PMID: 28656591
Background: The relationship between bone health and adiposity and how it may be affected in people with chronic metabolic conditions is complex. Methods: Seventeen women with type 1 diabetes mellitus...
25.
Kourime M, Bryce J, Jiang J, Nixon R, Rodie M, Ahmed S
Orphanet J Rare Dis
. 2017 Mar;
12(1):56.
PMID: 28320446
Background: With the proliferation of rare disease registries, there is a need for registries to undergo an assessment of their quality against agreed standards to ensure their long-term sustainability and...
26.
Chen S, Brooks R, Houskeeper J, Bremner S, Dunlop J, Viollet B, et al.
Mol Cell Endocrinol
. 2017 Feb;
443:176.
PMID: 28183460
No abstract available.
27.
Alhomaidah D, McGowan R, Ahmed S
Clin Genet
. 2017 Jan;
91(2):157-162.
PMID: 28127758
Disorders of sex development (DSD), are a group of rare congenital conditions. Unlike 46, XX DSD where the cause is usually clear, identification of a cause of XY DSD is...
28.
Cox K, Kyriakou A, Amjad B, OToole S, Flett M, Welsh M, et al.
J Pediatr Urol
. 2016 Sep;
13(1):57.e1-57.e5.
PMID: 27670783
Introduction: Anogenital distance (AGD) is a recognised marker of in utero androgen action. Objective: This study aimed to evaluate the relationship between severity of hypospadias and AGD. Study Design: Boys...
29.
Hornig N, Ukat M, Schweikert H, Hiort O, Werner R, Drop S, et al.
J Clin Endocrinol Metab
. 2016 Sep;
101(11):4468-4477.
PMID: 27583472
Context: Only approximately 85% of patients with a clinical diagnosis complete androgen insensitivity syndrome and less than 30% with partial androgen insensitivity syndrome can be explained by inactivating mutations in...
30.
Lucas-Herald A, Bertelloni S, Juul A, Bryce J, Jiang J, Rodie M, et al.
J Clin Endocrinol Metab
. 2016 Jul;
101(11):3959-3967.
PMID: 27403927
Background: In boys with suspected partial androgen insensitivity syndrome (PAIS), systematic evidence that supports the long-term prognostic value of identifying a mutation in the androgen receptor gene (AR) is lacking....