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Meshael Alswailem

Showing results (1-10 of 24) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 25, 2022
Fumarate Hydratase is a Novel Gene for Familial Non-Medullary Thyroid CancerAli S Alzahrani, Meshael Alswailem, Balgees Alghamdi, et al.
Medicina (Kaunas, Lithuania)|February 25, 2022
A Novel Mutation in a Gene Causes Sclerosteosis in a Family of Mediterranean OriginAishah A Ekhzaimy, Ebtihal Y Alyusuf, Meshael Alswailem, et al.
Frontiers in Endocrinology|October 22, 2024
Case report: Familial hypoparathyroidism with elevated parathyroid hormone due to an inactivating <i>PTH</i> mutationNoha Mukhtar, Balgees Alghamdi, Meshael Alswailem, et al.
Endocrine|August 18, 2020
One genotype, many phenotypes: SDHB p.R90X mutation-associated paragangliomasAli S Alzahrani, Meshael Alswailem, Yosra Moria, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 14, 2020
Molecular genetics of disorders of sex development in a highly consanguineous populationMeshael Alswailem, Afaf Alsagheir, Bassam Ben Abbas, et al.
Heliyon|August 19, 2024
A <i>CYP11A1</i> homozygous exonic variant inducing an alternative splicing, frameshift and truncation in a family with congenital adrenal hyperplasiaKheloud M Alhamoudi, Meshael Alswailem, Balgees Alghamdi, et al.
Journal of the Endocrine Society|June 8, 2022
Papillary Thyroid Cancer and a <i>TERT</i> Promotor Mutation-positive Paraganglioma in a Patient With a Germline <i>SDHB</i> MutationAli S Alzahrani, Meshael Alswailem, Avaniyapuram Kannan Murugan, et al.
Endocrine|October 12, 2021
Controversy on the management of patients carrying RET p.V804M mutationAli S Alzahrani, Meshael Alswailem, Balgees Alghamdi, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel <i>NR5A1</i> VariantKheloud M Alhamoudi, Balgees Alghamdi, Abeer Aljomaiah, et al.
Thyroid : Official Journal of the American Thyroid Association|November 9, 2016
Single Point Mutations in Pediatric Differentiated Thyroid CancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Endocrinology and Metabolism|June 25, 2022
Fumarate Hydratase is a Novel Gene for Familial Non-Medullary Thyroid CancerAli S Alzahrani, Meshael Alswailem, Balgees Alghamdi, et al.
Medicina (Kaunas, Lithuania)|February 25, 2022
A Novel Mutation in a Gene Causes Sclerosteosis in a Family of Mediterranean OriginAishah A Ekhzaimy, Ebtihal Y Alyusuf, Meshael Alswailem, et al.
Frontiers in Endocrinology|October 22, 2024
Case report: Familial hypoparathyroidism with elevated parathyroid hormone due to an inactivating <i>PTH</i> mutationNoha Mukhtar, Balgees Alghamdi, Meshael Alswailem, et al.
Endocrine|August 18, 2020
One genotype, many phenotypes: SDHB p.R90X mutation-associated paragangliomasAli S Alzahrani, Meshael Alswailem, Yosra Moria, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 14, 2020
Molecular genetics of disorders of sex development in a highly consanguineous populationMeshael Alswailem, Afaf Alsagheir, Bassam Ben Abbas, et al.
Heliyon|August 19, 2024
A <i>CYP11A1</i> homozygous exonic variant inducing an alternative splicing, frameshift and truncation in a family with congenital adrenal hyperplasiaKheloud M Alhamoudi, Meshael Alswailem, Balgees Alghamdi, et al.
Journal of the Endocrine Society|June 8, 2022
Papillary Thyroid Cancer and a <i>TERT</i> Promotor Mutation-positive Paraganglioma in a Patient With a Germline <i>SDHB</i> MutationAli S Alzahrani, Meshael Alswailem, Avaniyapuram Kannan Murugan, et al.
Endocrine|October 12, 2021
Controversy on the management of patients carrying RET p.V804M mutationAli S Alzahrani, Meshael Alswailem, Balgees Alghamdi, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel <i>NR5A1</i> VariantKheloud M Alhamoudi, Balgees Alghamdi, Abeer Aljomaiah, et al.
Thyroid : Official Journal of the American Thyroid Association|November 9, 2016
Single Point Mutations in Pediatric Differentiated Thyroid CancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Pageof 3