Mehmood Z. Mughal

Oxford Road
Manchester, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 85 publications

Perspective on unmet need for effective treatment in fibrous dysplasia and rare paediatric bone disease.

Perspective on unmet need for effective treatment in fibrous dysplasia and rare paediatric bone disease.

Journal: Bone

Published: July 22, 2026

Second interim analysis of the post-authorisation safety study (PASS) of burosumab in paediatric patients with X-linked hypophosphataemia.

Second interim analysis of the post-authorisation safety study (PASS) of burosumab in paediatric patients with X-linked hypophosphataemia.

Journal: European journal of endocrinology

Published: January 20, 2026

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

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

Journal: Clinical medicine insights. Endocrinology and diabetes

Published: December 19, 2025

Reference data for peripheral quantitative computed tomography for assessment of bone geometry and strength in Indian children and youth.

Reference data for peripheral quantitative computed tomography for assessment of bone geometry and strength in Indian children and youth.

Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry

Published: July 17, 2025

Phenotypic diversity in autosomal recessive hypophosphatemic rickets type 2.

Phenotypic diversity in autosomal recessive hypophosphatemic rickets type 2.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: June 30, 2025

Pediatric ABCC6 deficiency: a genotypic and phenotypic analysis.

Pediatric ABCC6 deficiency: a genotypic and phenotypic analysis.

Journal: Orphanet journal of rare diseases

Published: June 06, 2025

Delayed diagnosis of X-linked hypophosphatemia in the absence of family history: a global unmet need.

Delayed diagnosis of X-linked hypophosphatemia in the absence of family history: a global unmet need.

Journal: JBMR plus

Published: May 07, 2025

Correction to: Base of Skull & Spinal Canal Narrowing in an Adolescent with Autosomal Recessive Hypophosphatemic Rickets Type 2.

Correction to: Base of Skull & Spinal Canal Narrowing in an Adolescent with Autosomal Recessive Hypophosphatemic Rickets Type 2.

Journal: Calcified tissue international

Published: March 03, 2025

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

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

Journal: Advances in therapy

Published: January 27, 2025

Quality of life of 26 family members from four generations with X-linked hypophosphatemia: a cross-sectional study.

Quality of life of 26 family members from four generations with X-linked hypophosphatemia: a cross-sectional study.

Journal: Frontiers in endocrinology

Published: December 12, 2024

Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2.

Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2.

Journal: JBMR plus

Published: November 07, 2024

Base of Skull & Spinal Canal Narrowing in an Adolescent with Autosomal Recessive Hypophosphatemic Rickets Type 2.

Base of Skull & Spinal Canal Narrowing in an Adolescent with Autosomal Recessive Hypophosphatemic Rickets Type 2.

Journal: Calcified tissue international

Published: May 18, 2024

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Last Updated: 09/26/2026