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Afaf Alsagheir

Showing results (1-10 of 51) with videos related to

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Journal of Medical Case Reports|April 6, 2024
Graves' disease thyroid dermopathy: a case reportLoay Tashkandi, Afaf Alsagheir, Saud Alobaida, et al.
International Journal of Pediatrics & Adolescent Medicine|February 27, 2019
Coexistence of endocrinopathies in children with rheumatic diseasesDoha Alhomaidah, Afaf Alsagheir, Sulaiman M Al-Mayouf
Journal of Medical Case Reports|July 12, 2025
Hyperinsulinism-hyperammonemia syndrome associated with GLUD1 gene mutation: a case seriesMiral M Abdulghfar, Afaf Alsagheir, Ismail A Abdullah, et al.
Frontiers in Pediatrics|September 8, 2025
Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (<i>SECISBP2</i>) gene mutation in a pediatric patientLina Almohammadi, Lama Alsayel, Mohammad Aljumaa, et al.
Frontiers in Endocrinology|February 23, 2026
Clinical tools for evaluating congenital adrenal hyperplasia in resource-limited hospitals: a study at a tertiary hospital in Saudi ArabiaDaniah Alhazmi, Azzam Alabdulqader, Shahad Almeqbel, 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.
Journal of the Endocrine Society|December 11, 2024
Use of Whole-Exome Sequencing and Pedigree Analysis to Identify X-linked Hypophosphatemia in Saudi Arabian FamiliesMohamed H Al-Hamed, Sarah Bakhamis, Sara I Abdelfattah, et al.
Journal of Medical Case Reports|April 4, 2023
Munchausen syndrome by proxy: a case reportFadiah Alkhattabi, Israa Bamogaddam, Afaf Alsagheir, et al.
Cureus|December 29, 2021
A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and RhabdomyolysisWaheeb AlDhalaan, Faaezuddin Syed, Haroon A Javaid, et al.
Bone Reports|September 4, 2023
Hajdu-Cheney syndrome with a novel variant in NOTCH2 gene: A case reportMariam Abdelkarim, Dalal Alageel, Faridul Ahsan, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Journal of Medical Case Reports|April 6, 2024
Graves' disease thyroid dermopathy: a case reportLoay Tashkandi, Afaf Alsagheir, Saud Alobaida, et al.
International Journal of Pediatrics & Adolescent Medicine|February 27, 2019
Coexistence of endocrinopathies in children with rheumatic diseasesDoha Alhomaidah, Afaf Alsagheir, Sulaiman M Al-Mayouf
Journal of Medical Case Reports|July 12, 2025
Hyperinsulinism-hyperammonemia syndrome associated with GLUD1 gene mutation: a case seriesMiral M Abdulghfar, Afaf Alsagheir, Ismail A Abdullah, et al.
Frontiers in Pediatrics|September 8, 2025
Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (<i>SECISBP2</i>) gene mutation in a pediatric patientLina Almohammadi, Lama Alsayel, Mohammad Aljumaa, et al.
Frontiers in Endocrinology|February 23, 2026
Clinical tools for evaluating congenital adrenal hyperplasia in resource-limited hospitals: a study at a tertiary hospital in Saudi ArabiaDaniah Alhazmi, Azzam Alabdulqader, Shahad Almeqbel, 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.
Journal of the Endocrine Society|December 11, 2024
Use of Whole-Exome Sequencing and Pedigree Analysis to Identify X-linked Hypophosphatemia in Saudi Arabian FamiliesMohamed H Al-Hamed, Sarah Bakhamis, Sara I Abdelfattah, et al.
Journal of Medical Case Reports|April 4, 2023
Munchausen syndrome by proxy: a case reportFadiah Alkhattabi, Israa Bamogaddam, Afaf Alsagheir, et al.
Cureus|December 29, 2021
A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and RhabdomyolysisWaheeb AlDhalaan, Faaezuddin Syed, Haroon A Javaid, et al.
Bone Reports|September 4, 2023
Hajdu-Cheney syndrome with a novel variant in NOTCH2 gene: A case reportMariam Abdelkarim, Dalal Alageel, Faridul Ahsan, et al.
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