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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Ahmed Al Rumayyan

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Nature Genetics|August 24, 2004

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromeRussell J Ferland, Wafaa Eyaid, Randall V Collura, et al.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 11, 2017

Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new casesMajid Alfadhel, Marwan Nashabat, Muhammad Talal Alrifai, et al.

Annals of Clinical and Translational Neurology|September 27, 2019

Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screeningMajid Alfadhel, Muhammad Umair, Bader Almuzzaini, et al.

Neurodegenerative Disease Management|June 6, 2019

Current management of Duchenne muscular dystrophy in the Middle East: expert reportMohammed Al Jumah, Mohammad Al Muhaizea, Ahmed Al Rumayyan, et al.

European Journal of Human Genetics : EJHG|November 17, 2016

Clinical exome sequencing: results from 2819 samples reflecting 1000 familiesDaniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, et al.

Frontiers in Pediatrics|May 31, 2021

The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic DataMajid Alfadhel, Mohammed Almuqbil, Fuad Al Mutairi, et al.

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Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

Nature Genetics|August 24, 2004

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromeRussell J Ferland, Wafaa Eyaid, Randall V Collura, et al.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 11, 2017

Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new casesMajid Alfadhel, Marwan Nashabat, Muhammad Talal Alrifai, et al.

Annals of Clinical and Translational Neurology|September 27, 2019

Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screeningMajid Alfadhel, Muhammad Umair, Bader Almuzzaini, et al.

Neurodegenerative Disease Management|June 6, 2019

Current management of Duchenne muscular dystrophy in the Middle East: expert reportMohammed Al Jumah, Mohammad Al Muhaizea, Ahmed Al Rumayyan, et al.

European Journal of Human Genetics : EJHG|November 17, 2016

Clinical exome sequencing: results from 2819 samples reflecting 1000 familiesDaniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, et al.

Frontiers in Pediatrics|May 31, 2021

The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic DataMajid Alfadhel, Mohammed Almuqbil, Fuad Al Mutairi, et al.

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