S. Faisal Ahmed

University of Glasgow

United Kingdom

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Articles (14)

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (12)

Alice Moroni

Istituto Ortopedico Rizzoli

ITALY

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Anna Nordenström

Karolinska Institutet

SWEDEN

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Marco Bonomi

Associate Professor

University of Milan

ITALY

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David Unuane

Vrije Universiteit Brussel

BELGIUM

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Gen Yamada

Wakayama Medical University

JAPAN

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Martine Cools

Ghent University

BELGIUM

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Cécile Brachet

Université libre de Bruxelles

BELGIUM

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Mehul Dattani

University College London

UNITED KINGDOM

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XANTHIPPI TSERETOPOULOU

University of Glasgow

UNITED KINGDOM

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Alexander Gheldof

Vrije Universiteit Brussel

BELGIUM

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Neil Lawrence

University of Sheffield

UNITED KINGDOM

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Svetlana Lajic

Karolinska Institutet

SWEDEN

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S. Faisal Ahmed

Research Interests

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Articles (14)

The Role of the European Reference Network for Rare Bone Diseases (ERN BOND) and European Registries for Rare Bone and Mineral Conditions (EuRR-Bone) in the Governance of the Management of Rare Bone and Mineral Diseases

Health-Related Quality of Life in Children and Adolescents With Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis

Service evaluation suggests variation in clinical care provision in adults with congenital adrenal hyperplasia in the UK and Ireland

The I‐CAH Registry: A platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasia

Starting point for benchmarking outcomes and reporting of pituitary adenoma surgery within the European Reference Network on Rare Endocrine Conditions (Endo-ERN): results from a meta-analysis and survey study

I-DSD: The First 10 Years

Salivary androgens in adolescence and their value as a marker of puberty: results from the SCAMP cohort

Pubertal induction and transition to adult sex hormone replacement in patients with congenital pituitary or gonadal reproductive hormone deficiency: an Endo-ERN clinical practice guideline

The genetic diagnosis of rare endocrine disorders of sex development and maturation

Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

A critical evaluation of the EU-virtual consultation platform (CPMS) within the European Reference Network on Rare Endocrine Conditions

3T-MRI-based age, sex and site-specific markers of musculoskeletal health in healthy children and young adults

Congenital Micropenis: Etiology And Management

A Nationwide Study of the Prevalence and Initial Management of Atypical Genitalia in the Newborn in Scotland

Collaborators (12)

Alice Moroni

Anna Nordenström

Marco Bonomi

David Unuane

Gen Yamada

Martine Cools

Cécile Brachet

Mehul Dattani

XANTHIPPI TSERETOPOULOU

Alexander Gheldof

Neil Lawrence

Svetlana Lajic

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