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Hepatology Communications
|
October 22, 2021
Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1
Tassos Grammatikopoulos, Nedim Hadzic, Pierre Foskett, et al.
F1000Research
|
April 28, 2026
An Improved Deep Learning Algorithm for Breast Cancer Survival Prediction Based on Multi-Omics Data
Nurul Athirah Nasarudin, Fatma Al-Jasmi, Nor Hidayati Abdul Aziz, et al.
Therapeutics and Clinical Risk Management
|
April 22, 2016
Guidelines for acute management of hyperammonemia in the Middle East region
Majid Alfadhel, Fuad Al Mutairi, Nawal Makhseed, et al.
Journal of Molecular Neuroscience : MN
|
August 31, 2019
A Novel Homozygous Missense Variant in the NAGA Gene with Extreme Intrafamilial Phenotypic Heterogeneity
Fedah E Mohamed, Mohammad Al Sorkhy, Mohammad A Ghattas, et al.
Scientific Reports
|
August 28, 2019
Assessment of methylcitrate and methylcitrate to citrate ratio in dried blood spots as biomarkers for inborn errors of propionate metabolism
Osama Y Al-Dirbashi, Majid Alfadhel, Khalid Al-Thihli, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2016
Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophy
Linyan Meng, Taraka Donti, Fan Xia, et al.
Molecular Genetics and Metabolism
|
May 9, 2018
Clinical and molecular spectrum of thymidine kinase 2-related mtDNA maintenance defect
Julia Wang, Emily Kim, Honzheng Dai, et al.
Genes
|
September 28, 2021
Clinical, Biochemical, and Genetic Heterogeneity in Glutaric Aciduria Type II Patients
Amanat Ali, Fatmah Saeed Ali Almesmari, Nahid Al Dhahouri, et al.
International Journal of Molecular Sciences
|
April 17, 2025
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin Reductase
Feda E Mohamed, Lara Alzyoud, Mohammad A Ghattas, et al.
International Journal of Molecular Sciences
|
June 10, 2023
Introducing and Implementing Genetic Assessment in Cardio-Obstetrics Clinical Practice: Clinical and Genetic Workup of Patients with Cardiomyopathy
Ghadeera Al Mansoori, Wael Al Mahmeed, Saleema Wani, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Hepatology Communications
|
October 22, 2021
Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1
Tassos Grammatikopoulos, Nedim Hadzic, Pierre Foskett, et al.
F1000Research
|
April 28, 2026
An Improved Deep Learning Algorithm for Breast Cancer Survival Prediction Based on Multi-Omics Data
Nurul Athirah Nasarudin, Fatma Al-Jasmi, Nor Hidayati Abdul Aziz, et al.
Therapeutics and Clinical Risk Management
|
April 22, 2016
Guidelines for acute management of hyperammonemia in the Middle East region
Majid Alfadhel, Fuad Al Mutairi, Nawal Makhseed, et al.
Journal of Molecular Neuroscience : MN
|
August 31, 2019
A Novel Homozygous Missense Variant in the NAGA Gene with Extreme Intrafamilial Phenotypic Heterogeneity
Fedah E Mohamed, Mohammad Al Sorkhy, Mohammad A Ghattas, et al.
Scientific Reports
|
August 28, 2019
Assessment of methylcitrate and methylcitrate to citrate ratio in dried blood spots as biomarkers for inborn errors of propionate metabolism
Osama Y Al-Dirbashi, Majid Alfadhel, Khalid Al-Thihli, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2016
Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophy
Linyan Meng, Taraka Donti, Fan Xia, et al.
Molecular Genetics and Metabolism
|
May 9, 2018
Clinical and molecular spectrum of thymidine kinase 2-related mtDNA maintenance defect
Julia Wang, Emily Kim, Honzheng Dai, et al.
Genes
|
September 28, 2021
Clinical, Biochemical, and Genetic Heterogeneity in Glutaric Aciduria Type II Patients
Amanat Ali, Fatmah Saeed Ali Almesmari, Nahid Al Dhahouri, et al.
International Journal of Molecular Sciences
|
April 17, 2025
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin Reductase
Feda E Mohamed, Lara Alzyoud, Mohammad A Ghattas, et al.
International Journal of Molecular Sciences
|
June 10, 2023
Introducing and Implementing Genetic Assessment in Cardio-Obstetrics Clinical Practice: Clinical and Genetic Workup of Patients with Cardiomyopathy
Ghadeera Al Mansoori, Wael Al Mahmeed, Saleema Wani, et al.
Page
of 6