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International Journal of Pediatric Otorhinolaryngology
|
September 4, 2018
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome
Soukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Molecular Biology Reports
|
March 18, 2022
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco
Imane AitRaise, Ghita Amalou, Amale Bousfiha, et al.
Biochemical Genetics
|
October 1, 2023
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families
Imane AitRaise, Ghita Amalou, Amina Bakhchane, et al.
Molecular Vision
|
July 22, 2016
Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis
Imen Ben-Rebeh, Mhamed Grati, Crystel Bonnet, et al.
Orphanet Journal of Rare Diseases
|
August 19, 2015
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
Malika Dahmani, Fatima Ammar-Khodja, Crystel Bonnet, et al.
Rejuvenation Research
|
May 24, 2007
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits
Crystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, et al.
American Journal of Human Genetics
|
September 6, 2008
Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction
Sami Ellouze, Sébastien Augustin, Aicha Bouaita, et al.
Human Heredity
|
January 24, 2021
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
Soukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Genes
|
November 27, 2019
Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy
Ana Fakin, Maja Šuštar, Jelka Brecelj, et al.
International Journal of Pediatric Otorhinolaryngology
|
November 25, 2020
A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
Ghita Amalou, Crystel Bonnet, Zied Riahi, et al.
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of 8
Search research articles
Search
Showing results (21-30 of 72) with videos related to
Sort By:
Page
of 8
International Journal of Pediatric Otorhinolaryngology
|
September 4, 2018
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome
Soukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Molecular Biology Reports
|
March 18, 2022
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco
Imane AitRaise, Ghita Amalou, Amale Bousfiha, et al.
Biochemical Genetics
|
October 1, 2023
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families
Imane AitRaise, Ghita Amalou, Amina Bakhchane, et al.
Molecular Vision
|
July 22, 2016
Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis
Imen Ben-Rebeh, Mhamed Grati, Crystel Bonnet, et al.
Orphanet Journal of Rare Diseases
|
August 19, 2015
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
Malika Dahmani, Fatima Ammar-Khodja, Crystel Bonnet, et al.
Rejuvenation Research
|
May 24, 2007
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits
Crystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, et al.
American Journal of Human Genetics
|
September 6, 2008
Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction
Sami Ellouze, Sébastien Augustin, Aicha Bouaita, et al.
Human Heredity
|
January 24, 2021
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
Soukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Genes
|
November 27, 2019
Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy
Ana Fakin, Maja Šuštar, Jelka Brecelj, et al.
International Journal of Pediatric Otorhinolaryngology
|
November 25, 2020
A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
Ghita Amalou, Crystel Bonnet, Zied Riahi, et al.
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of 8