Publications by authors named "Shatha Alharazy"

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Effects of magnesium and potassium on insulin resistance and blood sugar level among insomniac patients with diabetes mellitus-A randomized controlled trial.
Sidra Khalid, Shahid Bashir, Riffat Mehboob, Humaira Waseem, Imran Shahid, Shatha Alharazy

J Investig Med· September 2025

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Genetic Variants in Vitamin-D Metabolism Genes (rs1155563, rs12785878 and rs10500804) among Females with Type-2 Diabetes Mellitus in Saudi Arabia.
Shatha Alharazy

Pak J Med Sci· September 2024

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Pretreatment with troxerutin protects/improves neurological deficits in a mouse model of traumatic brain injury.
Ashfaq Ahmed Khan Malik, Waqas Ahmad, Farhan Younas, Haroon Badshah, Shatha Alharazy

Heliyon· July 2023

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Occurrence of axillary web syndrome without surgical intervention: a case report.
Shatha Matoug Alharazy

J Int Med Res· January 2023

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Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study.
Shatha Alharazy, Muhammad Imran Naseer

Pak J Med Sci· January 2023

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Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia.
Shatha Alharazy, M Denise Robertson, Susan Lanham-New, Muhammad Imran Naseer, Adeel G Chaudhary

Endocr Connect· December 2021

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Association of SNPs in GC and CYP2R1 with total and directly measured free 25-hydroxyvitamin D in multi-ethnic postmenopausal women in Saudi Arabia.
Shatha Alharazy, Muhammad Imran Naseer, Eman Alissa, M Denise Robertson, Susan Lanham-New

Saudi J Biol Sci· August 2021

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Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia.
Shatha Alharazy, Eman Alissa, Susan Lanham-New, Muhammad Imran Naseer, Adeel G Chaudhary

BMC Endocr Disord· August 2021

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Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia.
Shatha Alharazy, Muhammad Imran Naseer, Eman Alissa, Margaret Denise Robertson, Susan Lanham-New

Front Genet· June 2021

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Next generation sequencing reveals novel homozygous frameshift in and splice acceptor variants in gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly.
Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Mohammed M Jan, Adeel G Chaudhary, Shatha Alharazy

Saudi J Biol Sci· November 2020

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