Natalie Loundon - Otorhinolaryngol & Head & Neck Surg Dept, AP HP

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论文共 102 篇作者统计合作学者相似作者

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HDR syndrome: Large cohort and systematic review

Nicolas Rive Le Gouard, Valentin Lafond-Rive, Laurence Jonard,Natalie Loundon, Sophie Achard,Laurence Heidet, Isabelle Mosnier, Stanislas Lyonnet, Frederic Brioude, Margaux Serey Gaut,Sandrine Marlin

Clinical genetics (2024)

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A 22q13.1 duplication in mosaicism including SOX10

William Bertani‐Torres,Margaux Serey‐Gaut,Judite de Oliveira,Christine Bole,Mélanie Parisot, Patrick Nistschké,Marie‐Laure Maurin,Jean‐Michel Lapierre,Natalie Loundon,Kahina Belhous,Nadége Bondurand,Sandrine Marlin,

American Journal of Medical Genetics - Part Ano. 12 (2023): 2813-2818

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ACTG1: a spectrum ranging from non-syndromic hearing impairment to polymalfomative fetal presentations

Margaux Serey-Gaut,Isabelle Rouillon,Natalie Loundon, Genevieve Lina Granade,Souad Gherbi Halem,Anne-Marie Guerrot,Yline Capri, Arnaud Molin, Christine Poncet Wallet,Ghizlene Lahlou, Tania Attie-Bitach,Luke Mansard,

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 111-111

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A 22q13.1 duplication in mosaicism including SOX10

William Bertani-Torres,Margaux Serey-Gaut,Judite de Oliveira,Christine Bole,Mélanie Parisot, Patrick Nistschké,Marie-Laure Maurin,Jean-Michel Lapierre,Natalie Loundon,Kahina Belhous,Nadège Bondurand,Sandrine Marlin,

American journal of medical genetics. Part A (2023)

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RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models

Godelieve Morel,Sylvain Ernest,Margaux Serey-Gaut,Laurence Jonard, Abeke Ralyath Balogoun,Marine Parodi,Natalie Loundon,Sophie Achard,Sandrine Marlin

Clinical geneticsno. 6 (2023): 669-673

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Preclinical Development of an Adeno Associated Vector-Based Gene Therapy (SENS-501) for the Autosomal Recessive Non-Syndromic Deafness 9 (DFNB9)

Guillaume Olivier,Christophe Tran Van Ba, Lise Barrot,Rafik Boudra,Julie Duron Dos Reis,Pierre Rambeau, Charlene Vaux,Sandra Pierredon,Anais Riviere,Pauline Liaudet,Audrey Broussy, Anne-Gabrielle Harrus,

MOLECULAR THERAPYno. 4 (2023): 459-460

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Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment

Laurence Jonard,Davide Brotto,Miguel A Moreno-Pelayo,Ignacio Del Castillo,Hannie Kremer,Ronald Pennings,Helena Caria,Graça Fialho,An Boudewyns,Guy Van Camp,Monika Ołdak,Dominika Oziębło,

Audiology researchno. 3 (2023): 341-346

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Robot-Assisted Transcanal Endoscopic Ear Surgery for Congenital Cholesteatoma

Francois Simon, Yann Nguyen,Natalie Loundon,Francoise Denoyelle

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS（2023）

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Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions

Sophie Achard,Margaux Campion,Marine Parodi, Melissa Macaskill,Baptiste Hochet,Francois Simon,Isabelle Rouillon,Laurence Jonard,Margaux Serey-Gaut,Francoise Denoyelle,Natalie Loundon,Sandrine Marlin

OTOLOGY & NEUROTOLOGY（2023）

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The recognition of human voice in deaf and hearing infants

Arnaud Coez,Natalie Loundon,Isabelle Rouillon,Marine Parodi,Marion Blanchard,Sophie Achard,Erea-Noel Garabedian,Eric Bizaguet, Tabassome Simon, Natacha Tessier,Francoise Denoyelle,Judit Gervain

HEARING BALANCE AND COMMUNICATION（2022）

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