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Mohammed Almannai

Showing results (11-20 of 56) with videos related to

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Clinical Genetics|June 26, 2026
Further Support of Autosomal Recessive CSF3-Related Severe Congenital NeutropeniaMohammed Almannai, Ahmed A Alhanshani, Khadijah Bakur, et al.
Molecular Genetics and Metabolism|October 27, 2018
Mitochondrial dynamics: Biological roles, molecular machinery, and related diseasesAyman W El-Hattab, Jehan Suleiman, Mohammed Almannai, et al.
Molecular Genetics and Metabolism|September 26, 2017
Therapies for mitochondrial diseases and current clinical trialsAyman W El-Hattab, Ana Maria Zarante, Mohammed Almannai, et al.
Molecular Genetics and Metabolism|November 1, 2020
Clinical trials in mitochondrial disorders, an updateMohammed Almannai, Ayman W El-Hattab, May Ali, et al.
Molecular Genetics and Metabolism|August 1, 2022
Mitochondrial DNA maintenance defects: potential therapeutic strategiesMohammed Almannai, Ayman W El-Hattab, Mahshid S Azamian, et al.
Circulation. Genomic and Precision Medicine|April 2, 2021
Homozygous <i>SPEG</i> Mutation Is Associated With Isolated Dilated CardiomyopathyMohammed Almannai, Shiyu Luo, Eissa Faqeih, et al.
Frontiers in Neurology|July 23, 2021
Metabolic SeizuresMohammed Almannai, Rabah A Al Mahmoud, Mohammed Mekki, et al.
Molecular Genetics and Metabolism|September 11, 2017
Quantitation of phenylbutyrate metabolites by UPLC-MS/MS demonstrates inverse correlation of phenylacetate:phenylacetylglutamine ratio with plasma glutamine levelsYi Jiang, Mohammed Almannai, V Reid Sutton, et al.
Clinical Chemistry|January 8, 2021
Hyperammonemia, Lactic Acidosis, and Arrhythmia in a NewbornMohammed Almannai, Abdulwahed Aldehaimi, Roy W A Peake, et al.
Clinical Genetics|June 17, 2022
Disorders of histone methylation: Molecular basis and clinical syndromesMode Al Ojaimi, Bashar J Banimortada, Amna Othman, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Clinical Genetics|June 26, 2026
Further Support of Autosomal Recessive CSF3-Related Severe Congenital NeutropeniaMohammed Almannai, Ahmed A Alhanshani, Khadijah Bakur, et al.
Molecular Genetics and Metabolism|October 27, 2018
Mitochondrial dynamics: Biological roles, molecular machinery, and related diseasesAyman W El-Hattab, Jehan Suleiman, Mohammed Almannai, et al.
Molecular Genetics and Metabolism|September 26, 2017
Therapies for mitochondrial diseases and current clinical trialsAyman W El-Hattab, Ana Maria Zarante, Mohammed Almannai, et al.
Molecular Genetics and Metabolism|November 1, 2020
Clinical trials in mitochondrial disorders, an updateMohammed Almannai, Ayman W El-Hattab, May Ali, et al.
Molecular Genetics and Metabolism|August 1, 2022
Mitochondrial DNA maintenance defects: potential therapeutic strategiesMohammed Almannai, Ayman W El-Hattab, Mahshid S Azamian, et al.
Circulation. Genomic and Precision Medicine|April 2, 2021
Homozygous <i>SPEG</i> Mutation Is Associated With Isolated Dilated CardiomyopathyMohammed Almannai, Shiyu Luo, Eissa Faqeih, et al.
Frontiers in Neurology|July 23, 2021
Metabolic SeizuresMohammed Almannai, Rabah A Al Mahmoud, Mohammed Mekki, et al.
Molecular Genetics and Metabolism|September 11, 2017
Quantitation of phenylbutyrate metabolites by UPLC-MS/MS demonstrates inverse correlation of phenylacetate:phenylacetylglutamine ratio with plasma glutamine levelsYi Jiang, Mohammed Almannai, V Reid Sutton, et al.
Clinical Chemistry|January 8, 2021
Hyperammonemia, Lactic Acidosis, and Arrhythmia in a NewbornMohammed Almannai, Abdulwahed Aldehaimi, Roy W A Peake, et al.
Clinical Genetics|June 17, 2022
Disorders of histone methylation: Molecular basis and clinical syndromesMode Al Ojaimi, Bashar J Banimortada, Amna Othman, et al.
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