Zulf Mughal

8PUBLICATIONS
37CO-AUTHORS
Adolescent healthPacific Peoples biomedical and clinical scienceMedical genetics (excl. cancer genetics)Infant and child healthGene and molecular therapy
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Publications (8)

|Sep 15, 2026
Phenotypic spectrum and quality of life in pediatric Bruck syndrome due to FKBP10 and PLOD2 variants: a 2-center United Arab Emirates experience.

|Jun 15, 2026
XLH Matters 2024 GCC Edition: Insights and Recommendations to Improve Outcomes for People Living With XLH in the Gulf Region.

|Feb 10, 2026
Phenotypic diversity in autosomal recessive hypophosphatemic rickets type 2.

Maimoona Al Qanoobi, Maryam Al Badi, Aisha Al Sinani

|May 29, 2025
Mobility and Quality of Life in Children with Paediatric-Onset Hypophosphatasia Treated with Asfotase Alfa: Results from UK Managed Access Agreement.

Raja Padidela, Nick Bishop, Paul Arundel

|May 31, 2024
Severity of acute phase reaction in children receiving the first dose of zoledronic acid and the impact of the underlying condition: a cross-sectional study.

Sapna Nayak, Lauren Rayner, Zulf Mughal

|Nov 05, 2023
A rare homozygous variant in TERT gene causing variable bone marrow failure, fragility fractures, rib anomalies and extremely short telomere lengths with high serum IgE.

Mahmoud I Elbadry, Ahmed Tawfeek, Tomonori Hirano

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Frequent Collaborators

2 joint publications

Mohamed Kenawey

2 joint publications

Raja Padidela

1 joint publications

Ibrahim Al Alwan

1 joint publications

Nouf Al Issa