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Azza Al Shidhani

Showing results (11-20 of 14) with videos related to

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Frontiers in Pediatrics|March 17, 2022
Patients' Perception of the Use of the EasyPod™ Growth Hormone Injector Device and Impact on Injection Adherence: A Multi-Center Regional StudyAsma Deeb, Saif Al Yaarubi, Bassam Bin Abbas, et al.
Orphanet Journal of Rare Diseases|March 14, 2024
Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North AfricaSaif Al Yaarubi, Afaf Alsagheir, Azza Al Shidhani, et al.
American Journal of Medical Genetics. Part A|January 18, 2024
Metabolic and other morbid complications in congenital generalized lipodystrophy type 4Gulcin Akinci, Saif Alyaarubi, Nivedita Patni, et al.
American Journal of Human Genetics|April 11, 2025
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signatureNavin B Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Frontiers in Pediatrics|March 17, 2022
Patients' Perception of the Use of the EasyPod™ Growth Hormone Injector Device and Impact on Injection Adherence: A Multi-Center Regional StudyAsma Deeb, Saif Al Yaarubi, Bassam Bin Abbas, et al.
Orphanet Journal of Rare Diseases|March 14, 2024
Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North AfricaSaif Al Yaarubi, Afaf Alsagheir, Azza Al Shidhani, et al.
American Journal of Medical Genetics. Part A|January 18, 2024
Metabolic and other morbid complications in congenital generalized lipodystrophy type 4Gulcin Akinci, Saif Alyaarubi, Nivedita Patni, et al.
American Journal of Human Genetics|April 11, 2025
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signatureNavin B Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, et al.
Pageof 2