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Muhammad Mahajnah

Showing results (21-30 of 52) with videos related to

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Biomed Research International|May 19, 2015
Clinical characteristics of autism spectrum disorder in Israel: impact of ethnic and social diversitiesMuhammad Mahajnah, Rajech Sharkia, Haitham Shalabe, et al.
Ultrastructural Pathology|July 7, 2007
The liver in congenital disorders of glycosylation: ultrastructural featuresTheodore C Iancu, Muhammad Mahajnah, Irena Manov, et al.
European Journal of Medical Genetics|April 23, 2013
Comparative screening of FMF mutations in various communities of the Israeli societyRajech Sharkia, Muhammad Mahajnah, Abdelnaser Zalan, et al.
Frontiers in Genetics|November 16, 2020
Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR MutationNatalia Borovok, Celeste Weiss, Rajech Sharkia, et al.
Genes|August 26, 2022
<i>CLN8</i> Gene Compound Heterozygous Variants: A New Case and Protein Bioinformatics AnalysesRajech Sharkia, Abdelnaser Zalan, Hazar Zahalka, et al.
Genes|May 27, 2023
<i>PTRH2</i> Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics AnalysisRajech Sharkia, Sahil Jain, Muhammad Mahajnah, et al.
The Israel Medical Association Journal : IMAJ|May 11, 2010
The prevalence of Parkinson's disease in an Arab population, Wadi Ara, IsraelRafik Masalha, Ella Kordysh, Gershon Alpert, et al.
American Journal of Medical Genetics. Part A|May 19, 2019
A novel biallelic loss-of-function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro-facio-thoracic dysplasiaRajech Sharkia, Abdelnaser Zalan, Azhar Jabareen-Masri, et al.
Pediatric Neurology|July 14, 2007
Pediatric-onset gelastic seizures: clinical data and outcomeEli Shahar, Uri Kramer, Muhammad Mahajnah, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|January 9, 2022
Multidomain Cognitive Impairment in Children With Pseudotumor Cerebri SyndromeMuhammad Mahajnah, Ariel T Suchi, Hazar Zahakah, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Biomed Research International|May 19, 2015
Clinical characteristics of autism spectrum disorder in Israel: impact of ethnic and social diversitiesMuhammad Mahajnah, Rajech Sharkia, Haitham Shalabe, et al.
Ultrastructural Pathology|July 7, 2007
The liver in congenital disorders of glycosylation: ultrastructural featuresTheodore C Iancu, Muhammad Mahajnah, Irena Manov, et al.
European Journal of Medical Genetics|April 23, 2013
Comparative screening of FMF mutations in various communities of the Israeli societyRajech Sharkia, Muhammad Mahajnah, Abdelnaser Zalan, et al.
Frontiers in Genetics|November 16, 2020
Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR MutationNatalia Borovok, Celeste Weiss, Rajech Sharkia, et al.
Genes|August 26, 2022
<i>CLN8</i> Gene Compound Heterozygous Variants: A New Case and Protein Bioinformatics AnalysesRajech Sharkia, Abdelnaser Zalan, Hazar Zahalka, et al.
Genes|May 27, 2023
<i>PTRH2</i> Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics AnalysisRajech Sharkia, Sahil Jain, Muhammad Mahajnah, et al.
The Israel Medical Association Journal : IMAJ|May 11, 2010
The prevalence of Parkinson's disease in an Arab population, Wadi Ara, IsraelRafik Masalha, Ella Kordysh, Gershon Alpert, et al.
American Journal of Medical Genetics. Part A|May 19, 2019
A novel biallelic loss-of-function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro-facio-thoracic dysplasiaRajech Sharkia, Abdelnaser Zalan, Azhar Jabareen-Masri, et al.
Pediatric Neurology|July 14, 2007
Pediatric-onset gelastic seizures: clinical data and outcomeEli Shahar, Uri Kramer, Muhammad Mahajnah, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|January 9, 2022
Multidomain Cognitive Impairment in Children With Pseudotumor Cerebri SyndromeMuhammad Mahajnah, Ariel T Suchi, Hazar Zahakah, et al.
Pageof 6