Renaud Touraine

Affiliations
  • Department of Genetics, CHU-Hôpital Nord, Saint Etienne, France.

Publications (33)

TuberOus SClerosis registry to increAse disease awareness (TOSCA) Post-Authorisation Safety Study of Everolimus in Patients With Tuberous Sclerosis Complex.

Frontiers in neurology
Avec: J Chris Kingswood , Elena Belousova , Mirjana P Benedik , Klemens Budde , Tom Carter , Vincent Cottin , Paolo Curatolo , Maria Dahlin , Lisa D'Amato , Guillaume B d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Ruben Marques , Rima Nabbout , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Matthias Sauter , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , Anna C Jansen , Auteur inconnu

Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?

Prenatal diagnosis
Avec: Kamran Moradkhani , Laurence Cuisset , Pierre Boisseau , Olivier Pichon , Marine Lebrun , Houda Hamdi-Rozé , Marie-Laure Maurin , Nicolas Gruchy , Marie-Christine Manca-Pellissier , Perrine Malzac , Frédéric Bilan , Marie-Pierre Audrezet , Pascale Saugier-Veber , Anne-Laure Fauret-Amsellem , Chantal Missirian , Paul Kuentz , Gregory Egea , Agnès Guichet , Isabelle Creveaux , Caroline Janel , Ines Harzallah , Carole Goumy , Nicole Joyé , Jacques Puechberty , Emmanuelle Haquet , Sandra Chantot-Bastaraud , Sébastien Schmitt , Philippe Gosset , Bénédicte Duban-Bedu , Bruno Delobel , Philippe Vago , François Vialard , Denise Molina Gomes , Jean-Pierre Siffroi , Jean-Paul Bonnefont , Jean-Michel Dupont , Philippe Jonveaux , Martine Doco-Fenzy , Damien Sanlaville , Cédric Le Caignec

Care management in a French cohort with Down syndrome from the AnDDI-Rares/CNSA study.

European journal of medical genetics
Avec: Pierre-Henri Roux-Levy , Damien Sanlaville , Bénédicte De Freminville , Alice Masurel , Isabelle Gueneau , Audrey Cotinaud-Ricou , Sophie Chancenotte , Frédérique Debomy , Delphine Minot , Marie Bournez , Isabelle Rousseau , Sandrine Daniel , Elodie Gautier , Didier Lacombe , Emmanuelle Taupiac , Sylvie Odent , Myriam Mikaty , Sylvie Manouvrier , Jamal Ghoumid , David Geneviève , Natacha Lehman , Tiffany Busa , Charles-Patrick Edery , Jenny Cornaton , Jennifer Gallard , Delphine Héron , Coralie Rastel , Christel Thauvin-Robinet , Alain Verloes , Christine Binquet , Laurence Faivre , Catherine Lejeune

Clinical heterogeneity of NADSYN1-associated VCRL syndrome.

Clinical genetics
Avec: Marion Aubert-Mucca , Caroline Janel , Valérie Porquet-Bordes , Olivier Patat , Thomas Edouard , Caroline Michot , Aude Tessier , Valérie Cormier-Daire , Tania Attie-Bitach , Geneviève Baujat

Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literature.

Clinical genetics
Avec: Virginie Carmignac , Sophie Nambot , Daphné Lehalle , Patrick Callier , Stephanie Moortgat , Valérie Benoit , Jamal Ghoumid , Bruno Delobel , Thomas Smol , Caroline Thuillier , Cécile Zordan , Sophie Naudion , Thierry Bienvenu , Francis Ramond , Christiane Zweier , André Reis , Cornelia Kraus , Mathilde Nizon , Benjamin Cogné , Alain Verloes , Frédéric Tran Mau-Them , Arthur Sorlin , Thibaud Jouan , Yannis Duffourd , Emilie Tisserant , Christophe Philippe , Antonio Vitobello , Julien Thevenon , Laurence Faivre , Christel Thauvin-Robinet

Renal angiomyolipoma in patients with tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increase disease Awareness.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Avec: J Chris Kingswood , Elena Belousova , Mirjana P Benedik , Tom Carter , Vincent Cottin , Paolo Curatolo , Maria Dahlin , Lisa D' Amato , Guillaume Beaure d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Ruben Marques , Rima Nabbout , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Matthias Sauter , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , Anna C Jansen

Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis.

American journal of medical genetics. Part A
Avec: Brice Poreau , Francis Ramond , Radu Harbuz , Véronique Satre , Claire Barro , Claire Vettier , Véronique Adouard , Julien Thevenon , Pierre-Simon Jouk , Charles Coutton , Klaus Dieterich

Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study.

Epilepsia open
Avec: Rima Nabbout , Elena Belousova , Mirjana P Benedik , Tom Carter , Vincent Cottin , Paolo Curatolo , Maria Dahlin , Lisa D Amato , Guillaume Beaure d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Ruben Marques , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Matthias Sauter , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , Anna Jansen , John C Kingswood , Auteur inconnu

Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications.

American journal of human genetics
Avec: Erik Rosenhahn , Thomas J O'Brien , Maha S Zaki , Ina Sorge , Dagmar Wieczorek , Kevin Rostasy , Antonio Vitobello , Sophie Nambot , Fowzan S Alkuraya , Mais O Hashem , Amal Alhashem , Brahim Tabarki , Abdullah S Alamri , Ayat H Al Safar , Dalal K Bubshait , Nada F Alahmady , Joseph G Gleeson , Mohamed S Abdel-Hamid , Nicole Lesko , Sofia Ygberg , Sandrina P Correia , Anna Wredenberg , Shahryar Alavi , Seyed M Seyedhassani , Mahya Ebrahimi Nasab , Haytham Hussien , Tarek E I Omar , Ines Harzallah , Homa Tajsharghi , Heba Morsy , Henry Houlden , Mohammad Shahrooei , Maryam Ghavideldarestani , Ghada M H Abdel-Salam , Annalaura Torella , Mariateresa Zanobio , Gaetano Terrone , Nicola Brunetti-Pierri , Abdolmajid Omrani , Julia Hentschel , Johannes R Lemke , Heinrich Sticht , Rami Abou Jamra , Andre E X Brown , Reza Maroofian , Konrad Platzer

Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases.

Journal of medical genetics
Avec: Quentin Testard , Xavier Vanhoye , Kevin Yauy , Marie-Emmanuelle Naud , Gaelle Vieville , Francis Rousseau , Benjamin Dauriat , Valentine Marquet , Sylvie Bourthoumieu , David Geneviève , Vincent Gatinois , Constance Wells , Marjolaine Willems , Christine Coubes , Lucile Pinson , Rodolphe Dard , Aude Tessier , Bérénice Hervé , François Vialard , Ines Harzallah , Benjamin Cogné , Wallid Deb , Thomas Besnard , Olivier Pichon , Béatrice Laudier , Laurent Mesnard , Alice Doreille , Tiffany Busa , Chantal Missirian , Véronique Satre , Charles Coutton , Tristan Celse , Radu Harbuz , Laure Raymond , Jean-François Taly , Julien Thevenon

Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.

Clinical genetics
Avec: Laurence Faivre , Jean-Charles Crépin , Manon Réda , Sophie Nambot , Virginie Carmignac , Caroline Abadie , Tristan Mirault , Cécile Faure-Conter , Juliette Mazereeuw-Hautier , Aude Maza , Eve Puzenat , Marie-Agnès Collonge-Rame , Anne-Claire Bursztejn , Christophe Philippe , Christel Thauvin-Robinet , Martin Chevarin , Claire Abasq-Thomas , Jeanne Amiel , Stéphanie Arpin , Sébastien Barbarot , Geneviève Baujat , Didier Bessis , Emmanuelle Bourrat , Odile Boute , Nicolas Chassaing , Christine Coubes , Bénédicte Demeer , Patrick Edery , Salima El Chehadeh , Alice Goldenberg , Smail Hadj-Rabia , Damien Haye , Bertrand Isidor , Marie-Line Jacquemont , Philippe Khau Van Kien , Didier Lacombe , Daphné Lehalle , Laetitia Lambert , Ludovic Martin , Annabel Maruani , Fanny Morice-Picard , Florence Petit , Alice Phan , Lucile Pinson , Massimiliano Rossi , Clémence Vanlerberghe , Marie Vincent , Catherine Vincent-Delorme , Sandra Whalen , Marjolaine Willems , Nathalie Marle , Virginie Verkarre , Christine Devalland , Mojgan Devouassoux-Shisheboran , Marine Abad , Nathalie Rioux-Leclercq , Bertille Bonniaud , Yannis Duffourd , Jehanne Martel , Christine Binquet , Paul Kuentz , Pierre Vabres

Tuberous Sclerosis Complex: Genetic counselling and perinatal follow-up.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Avec: R Touraine , Q Hauet , I Harzallah , A-E Baruteau

AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case.

Journal of inherited metabolic disease
Avec: Francis Ramond , Marlène Rio , Bénédicte Héron , Apolline Imbard , Sandrine Marie , Kareen Billiemaz , Anne-Sophie Denommé-Pichon , Paul Kuentz , Irène Ceballos , Monique Piraud , Marie-Françoise Vincent ,

Epileptogenicity in tuberous sclerosis complex: A stereoelectroencephalographic study.

Epilepsia
Avec: Andrew Neal , Karine Ostrowsky-Coste , Julien Jung , Stanislas Lagarde , Louis Maillard , Philippe Kahane , Helene Catenoix , Alexandra Montavont , Jean Isnard , Alexis Arzimanoglou , Fabrice Bartolomei , Marc Guenot , Sylvain Rheims

Phenotypic and genetic spectrum of alveolar capillary dysplasia: a retrospective cohort study.

Archives of disease in childhood. Fetal and neonatal edition
Avec: Laurélia Jourdan-Voyen , Jean-Pierre Masutti , Tiffany Busa , Catherine Vincent-Delorme , Lelia Dreyfus , Arnaud Molin , Baptiste Savey , Abraham Mounzer , Ziad Assaf , Veronique Atallah , Vanessa da Cruz , Dominique Gaillard , Elise Leroy-Terquem , Jean-Baptiste Mouton , Jamal Ghoumid , Jean-Charles Picaud , Frederique Dijoud , Sonia Bouquillon , Cédric Baumann , Laetitia Lambert

Treatment Patterns and Use of Resources in Patients With Tuberous Sclerosis Complex: Insights From the TOSCA Registry.

Frontiers in neurology
Avec: Ruben Marques , Elena Belousova , Mirjana P Benedik , Tom Carter , Vincent Cottin , Paolo Curatolo , Maria Dahlin , Lisa D'Amato , Guillaume Beaure d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Rima Nabbout , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Matthias Sauter , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , John C Kingswood , Anna C Jansen

Experience of follow-up, quality of life, and transition from pediatric to adult healthcare of patients with tuberous sclerosis complex.

Epilepsy & behavior : E&B
Avec: Claire Bar , Rouba Ghobeira , Rita Azzi , Dorothée Ville , Audrey Riquet , Nicole Chemaly , Rima Nabbout

Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy.

Human mutation
Avec: Hui Liu , Anna-Gaëlle Giguet-Valard , Thomas Simonet , Emmanuelle Szenker-Ravi , Laetitia Lambert , Catherine Vincent-Delorme , Sophie Scheidecker , Mélanie Fradin , Fanny Morice-Picard , Sophie Naudion , Viorica Ciorna-Monferrato , Estelle Colin , Florence Fellmann , Sophie Blesson , Pierre-Simon Jouk , Christine Francannet , Florence Petit , Sébastien Moutton , Daphné Lehalle , Nicolas Chassaing , Loubna El Zein , Anne Bazin , Claire Bénéteau , Tania Attié-Bitach , Sylvie M Hanu , Marie-Pierre Brechard , Jean Chiesa , Laurent Pasquier , Caroline Rooryck-Thambo , Lionel Van Maldergem , Christelle Cabrol , Salima El Chehadeh , Alexandre Vasiljevic , Bertrand Isidor , Carine Abel , Julien Thevenon , Sylvie Di Filippo , Adeline Vigouroux-Castera , Jocelyne Attia , Chloé Quelin , Sylvie Odent , Juliette Piard , Fabienne Giuliano , Audrey Putoux , Philippe Khau Van Kien , Catherine Yardin , Bruno Reversade , Patrice Bouvagnet

Renal Manifestations of Tuberous Sclerosis Complex: Key Findings From the Final Analysis of the TOSCA Study Focussing Mainly on Renal Angiomyolipomas.

Frontiers in neurology
Avec: J Chris Kingswood , Elena Belousova , Mirjana P Benedik , Tom Carter , Vincent Cottin , Paolo Curatolo , Maria Dahlin , Lisa D'Amato , Guillaume Beaure d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Ruben Marques , Rima Nabbout , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , Anna C Jansen , Matthias Sauter

X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variant.

Neurogenetics
Avec: Idriss Bousquet , Muriel Bozon , Valérie Castellani , Amélie Piton , Bénédicte Gérard , Laurent Guibaud , Damien Sanlaville , Patrick Edery , Pascale Saugier-Veber , Audrey Putoux

Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA).

Orphanet journal of rare diseases
Avec: Matthias Sauter , Elena Belousova , Mirjana P Benedik , Tom Carter , Vincent Cottin , Paolo Curatolo , Maria Dahlin , Lisa D'Amato , Guillaume B d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Ruben Marques , Rima Nabbout , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , Anna Jansen , J Chris Kingswood , Auteur inconnu

Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance.

Human genomics
Avec: Valerie Jacquemin , Nassim Versbraegen , Sarah Duerinckx , Annick Massart , Julie Soblet , Camille Perazzolo , Nicolas Deconinck , Elise Brischoux-Boucher , Anne De Leener , Nicole Revencu , Sandra Janssens , Stèphanie Moorgat , Bettina Blaumeiser , Kristiina Avela , Imad Abou Jaoude , Kathelijn Keymolen , Pascale Saugier-Veber , Tom Lenaerts , Marc Abramowicz , Isabelle Pirson

Expanding the clinical spectrum of Coffin-Siris syndrome with Anorectal Malformations: case report and review of the literature.

European journal of medical genetics
Avec: Ralah Alharbi , Anna Suchet-Dechaud , Inès Harzallah , Francis Ramond

Protein-extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation.

Annals of clinical and translational neurology
Avec: Johanna Ranta-Aho , Kevin J Felice , Per Harald Jonson , Jaakko Sarparanta , Cédric Yvorel , Ines Harzallah , Lynn Pais , Christina A Austin-Tse , Vijay S Ganesh , Melanie C O'Leary , Heidi L Rehm , Michael K Hehir , Sub Subramony , Qian Wu , Bjarne Udd , Marco Savarese

Newly Diagnosed and Growing Subependymal Giant Cell Astrocytoma in Adults With Tuberous Sclerosis Complex: Results From the International TOSCA Study.

Frontiers in neurology
Avec: Anna C Jansen , Elena Belousova , Mirjana P Benedik , Tom Carter , Vincent Cottin , Paolo Curatolo , Lisa D'Amato , Guillaume Beaure d'Augères , Petrus J de Vries , José C Ferreira , Martha Feucht , Carla Fladrowski , Christoph Hertzberg , Sergiusz Jozwiak , John A Lawson , Alfons Macaya , Ruben Marques , Rima Nabbout , Finbar O'Callaghan , Jiong Qin , Valentin Sander , Matthias Sauter , Seema Shah , Yukitoshi Takahashi , Sotiris Youroukos , Bernard Zonnenberg , John C Kingswood

Screening of the duplication 24 pb of ARX gene in Moroccan patients with X-linked Intellectual Disability.

BMC research notes
Avec: Yousra Benmakhlouf , Ines Harzallah , Zeineb Zian , Kaoutar Ben Makhlouf , Amina Barakat , Naima Ghailani Nourouti , Mohcine Bennani Mechita

Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS.

Annals of neurology
Avec: Laure Mazzola , Karen L Oliver , Audrey Labalme , Betül Baykan , Mikko Muona , Tarja H Joensuu , Carolina Courage , Nicolas Chatron , Giuseppe Borsani , Eudeline Alix , Francis Ramond , Melanie Bahlo , Nerses Bebek , Samuel F Berkovic , Anna-Elina Lehesjoki , Gaetan Lesca

Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum.

American journal of medical genetics. Part A
Avec: Yanick J Crow , Heather Marshall , Gillian I Rice , Luis Seabra , Emma M Jenkinson , Kristin Baranano , Roberta Battini , Andrea Berger , Edward Blair , Thomas Blauwblomme , Francois Bolduc , Natalie Boddaert , Johannes Buckard , Heather Burnett , Sophie Calvert , Roseline Caumes , Andy Cheuk-Him Ng , Diana Chiang , David B Clifford , Duccio M Cordelli , Anna de Burca , Natasha Demic , Isabelle Desguerre , Liesbeth De Waele , Alessio Di Fonzo , S Richard Dunham , Sarah Dyack , Frances Elmslie , Mickaël Ferrand , Gemma Fisher , Ehsan Ghayoor Karimiani , Jamal Ghoumid , Frances Gibbon , Himanshu Goel , Hilde T Hilmarsen , Imelda Hughes , Anu Jacob , Elizabeth A Jones , Ram Kumar , Richard J Leventer , Shelley MacDonald , Reza Maroofian , Sarju G Mehta , Imke Metz , Edoardo Monfrini , Daniela Neumann , Michael Noetzel , Mary O'Driscoll , Katrin Õunap , Axel Panzer , Sumit Parikh , Prab Prabhakar , Francis Ramond , Richard Sandford , Russell Saneto , Calvin Soh , Chloe A Stutterd , Gopinath M Subramanian , Kevin Talbot , Rhys H Thomas , Camilo Toro , Emma Wakeling , Evangeline Wassmer , Andrea Whitney , John H Livingston , Raymond T O'Keefe , Andrew P Badrock

A second individual with rhizomelic spondyloepimetaphyseal dysplasia and homozygous variant in GNPNAT1.

European journal of medical genetics
Avec: Quentin Sabbagh , Fanny Alkar , Karine Patte , Olivier Prodhomme , Caroline Janel , Claire Jeandel , David Geneviève

Rare

medRxiv : the preprint server for health sciences
Avec: Johanna Ranta-Aho , Kevin J Felice , Per Harald Jonson , Jaakko Sarparanta , Johanna Palmio , Giorgio Tasca , Mario Sabatelli , Cédric Yvorel , Ines Harzallah , Lynn Pais , Christina A Austin-Tse , Vijay Ganesh , Melanie C O'Leary , Heidi L Rehm , Michael K Hehir , Sub Subramony , Qian Wu , Bjarne Udd , Marco Savarese

Epileptic spasms are associated with increased stereo-electroencephalography derived functional connectivity in tuberous sclerosis complex.

Epilepsia
Avec: Andrew Neal , Romain Bouet , Stanislas Lagarde , Karine Ostrowsky-Coste , Louis Maillard , Philippe Kahane , Helene Catenoix , Alexandra Montavont , Jean Isnard , Alexis Arzimanoglou , Marc Hermier , Marc Guenot , Fabrice Bartolomei , Sylvain Rheims , Julien Jung

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

European journal of human genetics : EJHG
Avec: Thomas Husson , François Lecoquierre , Gaël Nicolas , Anne-Claire Richard , Alexandra Afenjar , Séverine Audebert-Bellanger , Catherine Badens , Frédéric Bilan , Varoona Bizaoui , Anne Boland , Marie-Noëlle Bonnet-Dupeyron , Elise Brischoux-Boucher , Céline Bonnet , Marie Bournez , Odile Boute , Perrine Brunelle , Roseline Caumes , Perrine Charles , Nicolas Chassaing , Nicolas Chatron , Benjamin Cogné , Estelle Colin , Valérie Cormier-Daire , Rodolphe Dard , Benjamin Dauriat , Julian Delanne , Jean-François Deleuze , Florence Demurger , Anne-Sophie Denommé-Pichon , Christel Depienne , Anne Dieux , Christèle Dubourg , Patrick Edery , Salima El Chehadeh , Laurence Faivre , Patricia Fergelot , Mélanie Fradin , Aurore Garde , David Geneviève , Brigitte Gilbert-Dussardier , Cyril Goizet , Alice Goldenberg , Evan Gouy , Anne-Marie Guerrot , Anne Guimier , Inès Harzalla , Delphine Héron , Bertrand Isidor , Didier Lacombe , Xavier Le Guillou Horn , Boris Keren , Alma Kuechler , Elodie Lacaze , Alinoë Lavillaureix , Daphné Lehalle , Gaëtan Lesca , James Lespinasse , Jonathan Levy , Stanislas Lyonnet , Godeliève Morel , Nolwenn Jean-Marçais , Sandrine Marlin , Luisa Marsili , Cyril Mignot , Sophie Nambot , Mathilde Nizon , Robert Olaso , Laurent Pasquier , Laurine Perrin , Florence Petit , Veronique Pingault , Amélie Piton , Fabienne Prieur , Audrey Putoux , Marc Planes , Sylvie Odent , Chloé Quélin , Sylvia Quemener-Redon , Mélanie Rama , Marlène Rio , Massimiliano Rossi , Elise Schaefer , Sophie Rondeau , Pascale Saugier-Veber , Thomas Smol , Sabine Sigaudy , Frederic Tran Mau-Them , Aurélien Trimouille , Julien Van Gils , Clémence Vanlerberghe , Valérie Vantalon , Gabriella Vera , Marie Vincent , Alban Ziegler , Olivier Guillin , Dominique Campion , Camille Charbonnier

[Genetic diffuse cystic lung disease in adults].

Revue des maladies respiratoires
Avec: R Diesler , K Ahmad , L Chalabreysse , J-C Glérant , I Harzallah , R Touraine , S Si-Mohamed , V Cottin

Réseau de co-auteurs

Rima Nabbout 8 collaborations
Elena Belousova 7 collaborations
Mirjana P Benedik 7 collaborations
Tom Carter 7 collaborations
Vincent Cottin 7 collaborations
Paolo Curatolo 7 collaborations
Petrus J de Vries 7 collaborations
José C Ferreira 7 collaborations
Martha Feucht 7 collaborations
Carla Fladrowski 7 collaborations
Christoph Hertzberg 7 collaborations
Sergiusz Jozwiak 7 collaborations
John A Lawson 7 collaborations
Alfons Macaya 7 collaborations
Ruben Marques 7 collaborations
Finbar O'Callaghan 7 collaborations
Jiong Qin 7 collaborations
Valentin Sander 7 collaborations
Matthias Sauter 7 collaborations
Seema Shah 7 collaborations
Yukitoshi Takahashi 7 collaborations
Sotiris Youroukos 7 collaborations
Bernard Zonnenberg 7 collaborations
Maria Dahlin 6 collaborations
Ines Harzallah 6 collaborations
Francis Ramond 6 collaborations
Lisa D'Amato 5 collaborations
Anna C Jansen 5 collaborations
Guillaume Beaure d'Augères 5 collaborations
J Chris Kingswood 4 collaborations
Pascale Saugier-Veber 4 collaborations
Jamal Ghoumid 4 collaborations
David Geneviève 4 collaborations
Laurence Faivre 4 collaborations
Sophie Nambot 4 collaborations
Daphné Lehalle 4 collaborations
Julien Thevenon 4 collaborations
None None 3 collaborations
Paul Kuentz 3 collaborations
Caroline Janel 3 collaborations
Damien Sanlaville 3 collaborations
Didier Lacombe 3 collaborations
Sylvie Odent 3 collaborations
Tiffany Busa 3 collaborations
Christel Thauvin-Robinet 3 collaborations
Benjamin Cogné 3 collaborations
John C Kingswood 3 collaborations
Nicolas Chassaing 3 collaborations
Patrick Edery 3 collaborations
Salima El Chehadeh 3 collaborations
Bertrand Isidor 3 collaborations
Laetitia Lambert 3 collaborations
Florence Petit 3 collaborations
Catherine Vincent-Delorme 3 collaborations
Audrey Putoux 3 collaborations
Guillaume B d'Augères 2 collaborations
Olivier Pichon 2 collaborations
Frédéric Bilan 2 collaborations
Chantal Missirian 2 collaborations
Bruno Delobel 2 collaborations
François Vialard 2 collaborations
Marie Bournez 2 collaborations
Delphine Héron 2 collaborations
Alain Verloes 2 collaborations
Christine Binquet 2 collaborations
Aude Tessier 2 collaborations
Valérie Cormier-Daire 2 collaborations
Geneviève Baujat 2 collaborations
Virginie Carmignac 2 collaborations
Thomas Smol 2 collaborations
Sophie Naudion 2 collaborations
Mathilde Nizon 2 collaborations
Yannis Duffourd 2 collaborations
Christophe Philippe 2 collaborations
Antonio Vitobello 2 collaborations
Radu Harbuz 2 collaborations
Véronique Satre 2 collaborations
Pierre-Simon Jouk 2 collaborations
Charles Coutton 2 collaborations
Anna Jansen 2 collaborations
Reza Maroofian 2 collaborations
Benjamin Dauriat 2 collaborations
Marjolaine Willems 2 collaborations
Christine Coubes 2 collaborations
Lucile Pinson 2 collaborations
Rodolphe Dard 2 collaborations
Odile Boute 2 collaborations
Alice Goldenberg 2 collaborations
Philippe Khau Van Kien 2 collaborations
Fanny Morice-Picard 2 collaborations
Massimiliano Rossi 2 collaborations
Clémence Vanlerberghe 2 collaborations
Marie Vincent 2 collaborations
R Touraine 2 collaborations
I Harzallah 2 collaborations
Marlène Rio 2 collaborations
Anne-Sophie Denommé-Pichon 2 collaborations
Andrew Neal 2 collaborations
Karine Ostrowsky-Coste 2 collaborations
Julien Jung 2 collaborations
Stanislas Lagarde 2 collaborations
Louis Maillard 2 collaborations
Philippe Kahane 2 collaborations
Helene Catenoix 2 collaborations
Alexandra Montavont 2 collaborations
Jean Isnard 2 collaborations
Alexis Arzimanoglou 2 collaborations
Fabrice Bartolomei 2 collaborations
Marc Guenot 2 collaborations
Sylvain Rheims 2 collaborations
Mélanie Fradin 2 collaborations
Estelle Colin 2 collaborations
Laurent Pasquier 2 collaborations
Amélie Piton 2 collaborations
Elise Brischoux-Boucher 2 collaborations
Johanna Ranta-Aho 2 collaborations
Kevin J Felice 2 collaborations
Per Harald Jonson 2 collaborations
Jaakko Sarparanta 2 collaborations
Cédric Yvorel 2 collaborations
Lynn Pais 2 collaborations
Christina A Austin-Tse 2 collaborations
Melanie C O'Leary 2 collaborations
Heidi L Rehm 2 collaborations
Michael K Hehir 2 collaborations
Sub Subramony 2 collaborations
Qian Wu 2 collaborations
Bjarne Udd 2 collaborations
Marco Savarese 2 collaborations
Nicolas Chatron 2 collaborations
Roseline Caumes 2 collaborations
Klemens Budde 1 collaboration
Kamran Moradkhani 1 collaboration
Laurence Cuisset 1 collaboration
Pierre Boisseau 1 collaboration
Marine Lebrun 1 collaboration
Houda Hamdi-Rozé 1 collaboration
Marie-Laure Maurin 1 collaboration
Nicolas Gruchy 1 collaboration
Marie-Christine Manca-Pellissier 1 collaboration
Perrine Malzac 1 collaboration
Marie-Pierre Audrezet 1 collaboration
Anne-Laure Fauret-Amsellem 1 collaboration
Gregory Egea 1 collaboration
Agnès Guichet 1 collaboration
Isabelle Creveaux 1 collaboration
Carole Goumy 1 collaboration
Nicole Joyé 1 collaboration
Jacques Puechberty 1 collaboration
Emmanuelle Haquet 1 collaboration
Sandra Chantot-Bastaraud 1 collaboration
Sébastien Schmitt 1 collaboration
Philippe Gosset 1 collaboration
Bénédicte Duban-Bedu 1 collaboration
Philippe Vago 1 collaboration
Denise Molina Gomes 1 collaboration
Jean-Pierre Siffroi 1 collaboration
Jean-Paul Bonnefont 1 collaboration
Jean-Michel Dupont 1 collaboration
Philippe Jonveaux 1 collaboration
Martine Doco-Fenzy 1 collaboration
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