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Meshael Alswailem

Showing results (11-20 of 24) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|July 27, 2022
A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked HypophosphatemiaKheloud M Alhamoudi, Balgees Alghamdi, Meshael Alswailem, et al.
Frontiers in Endocrinology|December 28, 2023
An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline <i>SDHB</i> pathogenic variant in the absence of paraganglioma or pheochromocytomaAli S Alzahrani, Abdulghani Bin Nafisah, Meshael Alswailem, et al.
Frontiers in Endocrinology|October 20, 2023
How do <i>BRAF</i><sup>V600E</sup> and <i>TERT</i> promoter mutations interact with the ATA and TNM staging systems in thyroid cancer?Noha Mukhtar, Kheloud Alhamoudi, Meshael Alswailem, et al.
Endocrine-Related Cancer|September 11, 2015
TERT promoter mutations in thyroid cancer: a report from a Middle Eastern populationEbtesam Qasem, Avaniyapuram Kannan Murugan, Hindi Al-Hindi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2020
Genetic Alterations in Pediatric Thyroid Cancer Using a Comprehensive Childhood Cancer Gene PanelAli S Alzahrani, Meshael Alswailem, Anwar Ali Alswailem, et al.
Endocrine-Related Cancer|May 20, 2024
EPAS1-related pheochromocytoma/paragangliomaAli S Alzahrani, Meshael Alswailem, Alexandre Buffet, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2023
Molecular Genetics of Diffuse Sclerosing Papillary Thyroid CancerMeshael Alswailem, Balgees Alghamdi, Anwar Alotaibi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2018
Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and OutcomeAli S Alzahrani, Meshael Alswailem, Yosra Moria, et al.
Oncotarget|November 1, 2019
Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paragangliomaShatha Albattal, Meshael Alswailem, Yosra Moria, et al.
Kidney International|March 6, 2021
A novel claudin-10 mutation with a unique mechanism in two unrelated families with HELIX syndromeAli S Alzahrani, Maged Hussein, Meshael Alswailem, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Endocrinology and Metabolism|July 27, 2022
A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked HypophosphatemiaKheloud M Alhamoudi, Balgees Alghamdi, Meshael Alswailem, et al.
Frontiers in Endocrinology|December 28, 2023
An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline <i>SDHB</i> pathogenic variant in the absence of paraganglioma or pheochromocytomaAli S Alzahrani, Abdulghani Bin Nafisah, Meshael Alswailem, et al.
Frontiers in Endocrinology|October 20, 2023
How do <i>BRAF</i><sup>V600E</sup> and <i>TERT</i> promoter mutations interact with the ATA and TNM staging systems in thyroid cancer?Noha Mukhtar, Kheloud Alhamoudi, Meshael Alswailem, et al.
Endocrine-Related Cancer|September 11, 2015
TERT promoter mutations in thyroid cancer: a report from a Middle Eastern populationEbtesam Qasem, Avaniyapuram Kannan Murugan, Hindi Al-Hindi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2020
Genetic Alterations in Pediatric Thyroid Cancer Using a Comprehensive Childhood Cancer Gene PanelAli S Alzahrani, Meshael Alswailem, Anwar Ali Alswailem, et al.
Endocrine-Related Cancer|May 20, 2024
EPAS1-related pheochromocytoma/paragangliomaAli S Alzahrani, Meshael Alswailem, Alexandre Buffet, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2023
Molecular Genetics of Diffuse Sclerosing Papillary Thyroid CancerMeshael Alswailem, Balgees Alghamdi, Anwar Alotaibi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2018
Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and OutcomeAli S Alzahrani, Meshael Alswailem, Yosra Moria, et al.
Oncotarget|November 1, 2019
Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paragangliomaShatha Albattal, Meshael Alswailem, Yosra Moria, et al.
Kidney International|March 6, 2021
A novel claudin-10 mutation with a unique mechanism in two unrelated families with HELIX syndromeAli S Alzahrani, Maged Hussein, Meshael Alswailem, et al.
Pageof 3