Muhammad S. Arslan

Bahawalpur, PB 63100, Pakistan

Last Updated: 09/26/2026

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Found 13 publications

Finite element analysis of cervicomedullary stress and strain in atlas orthogonal correction using radiographic rotational inputs: A multi-case study.

Finite element analysis of cervicomedullary stress and strain in atlas orthogonal correction using radiographic rotational inputs: A multi-case study.

Journal: Journal of bodywork and movement therapies

Published: January 31, 2026

Weight-bearing MRI of the cervical spine: A scoping review of clinical utility and emerging applications.

Weight-bearing MRI of the cervical spine: A scoping review of clinical utility and emerging applications.

Journal: European journal of radiology open

Published: August 19, 2025

Biallelic variants in SREK1 downregulating SNORD115 and SNORD116 cause a Prader-Willi-like syndrome.

Biallelic variants in SREK1 downregulating SNORD115 and SNORD116 cause a Prader-Willi-like syndrome.

Journal: The Journal of clinical investigation

Published: June 23, 2025

Inversed impaired osteogenic activity in children with severe obesity due to MC4R deficiency compared to LEP and LEPR deficiency.

Inversed impaired osteogenic activity in children with severe obesity due to MC4R deficiency compared to LEP and LEPR deficiency.

Journal: International journal of obesity (2005)

Published: May 05, 2025

Development and Optimization of Stimuli-Responsive Fenugreek/Carrageenan-Co-poly (Methacrylate) Hydrogel Matrices for Controlled Delivery of 5-Fluorouracil.

Development and Optimization of Stimuli-Responsive Fenugreek/Carrageenan-Co-poly (Methacrylate) Hydrogel Matrices for Controlled Delivery of 5-Fluorouracil.

Journal: AAPS PharmSciTech

Published: January 28, 2025

High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor.

High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor.

Journal: Cell reports. Medicine

Published: March 21, 2023

Biallelic Mutations in P4HTM Cause Syndromic Obesity.

Biallelic Mutations in P4HTM Cause Syndromic Obesity.

Journal: Diabetes

Published: December 12, 2022

Rare Variant Analysis of Obesity-Associated Genes in Young Adults With Severe Obesity From a Consanguineous Population of Pakistan.

Rare Variant Analysis of Obesity-Associated Genes in Young Adults With Severe Obesity From a Consanguineous Population of Pakistan.

Journal: Diabetes

Published: April 29, 2021

Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan.

Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan.

Journal: Diabetes

Published: December 16, 2019

Loss-of-function mutations in ADCY3 cause monogenic severe obesity.

Loss-of-function mutations in ADCY3 cause monogenic severe obesity.

Journal: Nature genetics

Published: April 30, 2017

Genetics of Obesity in Consanguineous Populations: Toward Precision Medicine and the Discovery of Novel Obesity Genes.

Genetics of Obesity in Consanguineous Populations: Toward Precision Medicine and the Discovery of Novel Obesity Genes.

Journal: Obesity (Silver Spring, Md.)

Published: January 24, 2016

Evidence of male hypogonadism at an early age as a familial risk of type 2 diabetes.

Evidence of male hypogonadism at an early age as a familial risk of type 2 diabetes.

Journal: Annales d'endocrinologie

Published: April 06, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026