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Afif Ben-Mahmoud

Showing results (1-10 of 35) with videos related to

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Microorganisms|September 28, 2023
<i>Bacillus amyloliquefaciens</i>: Harnessing Its Potential for Industrial, Medical, and Agricultural Applications-A Comprehensive ReviewImen Zalila-Kolsi, Afif Ben-Mahmoud, Ray Al-Barazie
Journal of Molecular Neuroscience : MN|November 14, 2019
Evaluating the Role of MAST1 as an Intellectual Disability Disease Gene: Identification of a Novel De Novo Variant in a Patient with Developmental DisabilitiesAfif Ben-Mahmoud, Aisha M Al-Shamsi, Bassam R Ali, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|February 1, 2026
Overestimation of Pathogenic Variants in Idiopathic Hypogonadotropic Hypogonadism and Kallmann SyndromeLindsey Grater, Zoe Hawkins, Afif Ben Mahmoud, et al.
Seminars in Reproductive Medicine|March 11, 2026
Clinical Testing for Genetic ConditionsHyung-Goo Kim, Sumia Brakta, Afif Ben-Mahmoud, et al.
Microbiological Research|September 25, 2016
Antagonist effects of Bacillus spp. strains against Fusarium graminearum for protection of durum wheat (Triticum turgidum L. subsp. durum)Imen Zalila-Kolsi, Afif Ben Mahmoud, Hacina Ali, et al.
Mitochondrial DNA|July 12, 2013
A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathyEmna Mkaouar-Rebai, Afif Ben Mahmoud, Imen Chamkha, et al.
Journal of Cellular and Molecular Medicine|March 27, 2024
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decadesMadiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz, et al.
Molecular and Cellular Endocrinology|June 1, 2021
Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counselingErica D Louden, Alexandra Poch, Hyung-Goo Kim, et al.
Computational Biology and Chemistry|January 16, 2015
Evaluation of the effect of c.2946+1G>T mutation on splicing in the SCN1A geneAfif Ben Mahmoud, Riadh Ben Mansour, Fatma Driss, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing lossNesrin Gariballa, Afif Ben-Mahmoud, Makanko Komara, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Microorganisms|September 28, 2023
<i>Bacillus amyloliquefaciens</i>: Harnessing Its Potential for Industrial, Medical, and Agricultural Applications-A Comprehensive ReviewImen Zalila-Kolsi, Afif Ben-Mahmoud, Ray Al-Barazie
Journal of Molecular Neuroscience : MN|November 14, 2019
Evaluating the Role of MAST1 as an Intellectual Disability Disease Gene: Identification of a Novel De Novo Variant in a Patient with Developmental DisabilitiesAfif Ben-Mahmoud, Aisha M Al-Shamsi, Bassam R Ali, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|February 1, 2026
Overestimation of Pathogenic Variants in Idiopathic Hypogonadotropic Hypogonadism and Kallmann SyndromeLindsey Grater, Zoe Hawkins, Afif Ben Mahmoud, et al.
Seminars in Reproductive Medicine|March 11, 2026
Clinical Testing for Genetic ConditionsHyung-Goo Kim, Sumia Brakta, Afif Ben-Mahmoud, et al.
Microbiological Research|September 25, 2016
Antagonist effects of Bacillus spp. strains against Fusarium graminearum for protection of durum wheat (Triticum turgidum L. subsp. durum)Imen Zalila-Kolsi, Afif Ben Mahmoud, Hacina Ali, et al.
Mitochondrial DNA|July 12, 2013
A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathyEmna Mkaouar-Rebai, Afif Ben Mahmoud, Imen Chamkha, et al.
Journal of Cellular and Molecular Medicine|March 27, 2024
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decadesMadiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz, et al.
Molecular and Cellular Endocrinology|June 1, 2021
Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counselingErica D Louden, Alexandra Poch, Hyung-Goo Kim, et al.
Computational Biology and Chemistry|January 16, 2015
Evaluation of the effect of c.2946+1G>T mutation on splicing in the SCN1A geneAfif Ben Mahmoud, Riadh Ben Mansour, Fatma Driss, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing lossNesrin Gariballa, Afif Ben-Mahmoud, Makanko Komara, et al.
Pageof 4