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Mapping the Fine-Scale Organization and Plasticity of the Brain Vasculature
Christoph Kirst
,
Sophie Skriabine
,
Alba Vieites-Prado
,
Thomas Topilko
,
Paul Bertin
,
et al.
Journal articles
pasteur-02874557v1
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Hair Cell Afferent Synapses: Function and Dysfunction
Stuart Johnson
,
Saaid Safieddine
,
Mirna Mustapha
,
Walter Marcotti
Journal articles
hal-02365401v1
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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
Ghita Amalou
,
Crystel Bonnet
,
Zied Riahi
,
Aymane Bouzidi
,
Soukaina Elrharchi
,
et al.
Journal articles
pasteur-03215242v1
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SpiCee: A Genetic Tool for Subcellular and Cell-Specific Calcium Manipulation
Oriol Ros
,
Yvrick Zagar
,
Sandrine Couvet
,
Alain Aghaie
,
Fiona Roche
,
et al.
2019
Preprints, Working Papers, ...
hal-02361424v1
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Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage
Jean Defourny
,
Alain Aghaie
,
Isabelle Perfettini
,
Paul Avan
,
Sedigheh Delmaghani
,
et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019, 116 (16), pp.8010-8017. ⟨10.1073/pnas.1821844116⟩
Journal articles
hal-02318679v1
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ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis
Malika Dahmani
,
Sonia Talbi
,
Fatima Ammar-Khodja
,
Sofiane Ouhab
,
Farid Boudjenah
,
et al.
Journal articles
pasteur-03219608v1
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Hearing Protection, Restoration, and Regeneration
Anne Schilder
,
Matthew Su
,
Helen Blackshaw
,
Lawrence Lustig
,
Hinrich Staecker
,
et al.
Journal articles
hal-02365389v1
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Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study
Katarina Stingl
,
Anne Kurtenbach
,
Gesa Hahn
,
Christoph Kernstock
,
Stephanie Hipp
,
et al.
Journal articles
pasteur-03219625v1
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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
Soukaina Elrharchi
,
Zied Riahi
,
Sara Salime
,
Hicham Charoute
,
Lamiae Elkhattabi
,
et al.
Journal articles
pasteur-03219602v1
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GABA A receptors contribute more to rate than temporal coding in the IC of awake mice
Boris Gourévitch
,
Elena Mahrt
,
Warren Bakay
,
Cameron Elde
,
Christine Portfors
Journal articles
hal-03080522v1
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Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene
Olaia Subirà
,
Jaume Català-Mora
,
Jesús Díaz-Cascajosa
,
Noel Padrón-Pérez
,
M. Claveria
,
et al.
Journal articles
pasteur-03219607v1
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A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene
Marwa Sayeb
,
Zied Riahi
,
Nadia Laroussi
,
Crystel Bonnet
,
Lilia Romdhane
,
et al.
Journal articles
pasteur-03219630v1
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Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
Amale Bousfiha
,
Zied Riahi
,
Lamiae Elkhattabi
,
Amina Bakhchane
,
Hicham Charoute
,
et al.
Journal articles
pasteur-03219615v1
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PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
Samer Khateb
,
Saddek Mohand-Saïd
,
Marco Nassisi
,
Crystel Bonnet
,
Anne-Françoise Roux
,
et al.
Journal articles
pasteur-03215234v1
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Telemedicine in Audiology. Best practice recommendations from the French Society of Audiology (SFA) and the French Society of Otorhinolaryngology-Head and Neck Surgery (SFORL)
H. Thai-Van
,
D. Bakhos
,
D. Bouccara
,
N. Loundon
,
M. Marx
,
et al.
Journal articles
hal-03234124v1
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Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis
Sophie Boucher
,
Fabienne Wong Jun Tai
,
Sedigheh Delmaghani
,
Andrea Lelli
,
Amrit Singh-Estivalet
,
et al.
Proceedings of the National Academy of Sciences of the United States of America, 2020, 117 (49), pp.31278-31289. ⟨10.1073/pnas.2010782117⟩
Journal articles
pasteur-03215054v1
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