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ArticlesPeer ReviewedFull Text
Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
Author / Creator:Depienne, Christel ; Bouteiller, Delphine ; Keren, Boris ; Cheuret, Emmanuel ; Poirier, Karine ; Trouillard, Oriane ; Benyahia, Baya ; Quelin, Chloé ; Carpentier, Wassila ; Julia, Sophie ; Afenjar, Alexandra ; Gautier, Agnès ; Rivier, François ; Meyer, Sophie ; Berquin, Patrick ; Hélias, Marie ; Py, Isabelle ; Rivera, Serge ; Bahi-Buisson, Nadia ; Gourfinkel-An, Isabelle ; Cazeneuve, Cécile ; Ruberg, Merle ; Brice, Alexis ; Nabbout, Rima ; LeGuern, Eric
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2009-02, Vol.5 (2), p.e1000381-e1000381
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ArticlesPeer ReviewedFull Text
Heterozygous and homozygous JAK2(V617F) states modeled by induced pluripotent stem cells from myeloproliferative neoplasm patients
Author / Creator:Saliba, Joseph ; Hamidi, Sofiane ; Lenglet, Gaëlle ; Langlois, Thierry ; Yin, Jingkui ; Cabagnols, Xénia ; Secardin, Lise ; Legrand, Céline ; Galy, Anne ; Opolon, Paule ; Benyahia, Baya ; Solary, Eric ; Bernard, Olivier A ; Chen, Longyun ; Debili, Najet ; Raslova, Hana ; Norol, Françoise ; Vainchenker, William ; Plo, Isabelle ; Di Stefano, Antonio
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013, Vol.8 (9), p.e74257-e74257
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ArticlesPeer ReviewedFull Text
Immunohistochemical analysis of anti-Hu-associated paraneoplastic encephalomyelitis
Author / Creator:Bernal, Fabián ; Graus, Francesc ; Pifarré, Àlex ; Saiz, Albert ; Benyahia, Baya ; Ribalta, Teresa
Publisher:Berlin: Springer
Journal title:Acta neuropathologica, 2002-05, Vol.103 (5), p.509-515
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ArticlesPeer ReviewedFull Text
Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
Author / Creator:Depienne, Christel ; Bouteiller, Delphine ; Keren, Boris ; Cheuret, Emmanuel ; Poirier, Karine ; Trouillard, Oriane ; Benyahia, Baya ; Quelin, Chloé ; Carpentier, Wassila ; Julia, Sophie ; Afenjar, Alexandra ; Gautier, Agnès ; Rivier, François ; Meyer, Sophie ; Berquin, Patrick ; Hélias, Marie ; Py, Isabelle ; Rivera, Serge ; Bahi-Buisson, Nadia ; Gourfinkel-An, Isabelle ; Cazeneuve, Cécile ; Ruberg, Merle ; Brice, Alexis ; Nabbout, Rima ; LeGuern, Eric
Publisher:San Francisco, USA: Public Library of Science
Journal title:PLoS genetics, 2009-04, Vol.5 (4)
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ArticlesPeer ReviewedFull Text
Heterozygous and Homozygous JAK2V617F States Modeled by Induced Pluripotent Stem Cells from Myeloproliferative Neoplasm Patients
Author / Creator:Saliba, Joseph ; Hamidi, Sofiane ; Lenglet, Gaëlle ; Langlois, Thierry ; Yin, Jingkui ; Cabagnols, Xénia ; Secardin, Lise ; Legrand, Céline ; Galy, Anne ; Opolon, Paule ; Benyahia, Baya ; Solary, Eric ; Bernard, Olivier A. ; Chen, Longyun ; Debili, Najet ; Raslova, Hana ; Norol, Françoise ; Vainchenker, William ; Plo, Isabelle ; Di Stefano, Antonio
Journal title:PloS one, 2013-09, Vol.8 (9), p.e74257
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ArticlesPeer ReviewedFull Text
Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10
Author / Creator:Keren, Boris ; Jacquette, Aurélia ; Depienne, Christel ; Leite, Patricia ; Durr, Alexandra ; Carpentier, Wassila ; Benyahia, Baya ; Ponsot, Gerard ; Soubrier, Florent ; Brice, Alexis ; Héron, Delphine
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Neurogenetics, 2010-05, Vol.11 (2), p.273-274
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ArticlesPeer ReviewedFull Text
Autism, language delay and mental retardation in a patient with 7q11 duplication: Autism and 7q11 duplication
Author / Creator:Depienne, Christel ; Héron, Delphine ; Betancur, Catalina ; Benyahia, Baya ; Trouillard, Oriane ; Bouteiller, Delphine ; Verloes, Alain ; Leguern, Eric ; Leboyer, Marion ; Brice, Alexis
Publisher:BMJ Publishing Group
Journal title:Journal of medical genetics, 2007-07, Vol.44 (7), p.452-8
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ArticlesPeer ReviewedFull Text
Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in Resembles Dravet Syndrome but Mainly Affects Females
Author / Creator:Christel Depienne ; Delphine Bouteiller ; Boris Keren ; Emmanuel Cheuret ; Karine Poirier ; Oriane Trouillard ; Baya Benyahia ; Chloé Quelin ; Wassila Carpentier ; Sophie Julia ; Alexandra Afenjar ; Agnès Gautier ; François Rivier ; Sophie Meyer ; Patrick Berquin ; Marie Hélias ; Isabelle Py ; Serge Rivera ; Nadia Bahi-Buisson ; Isabelle Gourfinkel-An ; Cécile Cazeneuve ; Merle Ruberg ; Alexis Brice ; Rima Nabbout ; Eric LeGuern
Publisher:Public Library of Science (PLoS)
Journal title:PLoS genetics, 2009-04, Vol.5 (4)
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ArticlesPeer ReviewedFull Text
Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females: e1000381
Author / Creator:Depienne, Christel ; Bouteiller, Delphine ; Keren, Boris ; Cheuret, Emmanuel ; Poirier, Karine ; Trouillard, Oriane ; Benyahia, Baya ; Quelin, Chloé ; Carpentier, Wassila ; Julia, Sophie ; Afenjar, Alexandra ; Gautier, Agnès ; Rivier, François ; Meyer, Sophie ; Berquin, Patrick ; Hélias, Marie ; Py, Isabelle ; Rivera, Serge ; Bahi-Buisson, Nadia ; Gourfinkel-An, Isabelle ; Cazeneuve, Cécile ; Ruberg, Merle ; Brice, Alexis ; Nabbout, Rima ; LeGuern, Eric
Publisher:San Francisco: Public Library of Science
Journal title:PLoS genetics, 2009-02, Vol.5 (2)
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ArticlesPeer ReviewedFull Text
Heterozygous and Homozygous JAK2V617F States Modeled by Induced Pluripotent Stem Cells from Myeloproliferative Neoplasm Patients
Author / Creator:Saliba, Joseph ; Hamidi, Sofiane ; Lenglet, Gaëlle ; Langlois, Thierry ; Yin, Jingkui ; Cabagnols, Xénia ; Secardin, Lise ; Legrand, Céline ; Galy, Anne ; Opolon, Paule ; Benyahia, Baya ; Solary, Eric ; Bernard, Olivier A ; Chen, Longyun ; Debili, Najet ; Raslova, Hana ; Norol, Françoise ; Vainchenker, William ; Plo, Isabelle ; Antonio Di Stefano
Publisher:San Francisco: Public Library of Science
Journal title:PloS one, 2013-09, Vol.8 (9), p.e74257
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ArticlesPeer ReviewedFull Text
Clinical relevance of non-neuronal auto-antibodies in patients with anti-Hu or anti-Yo paraneoplastic diseases
Author / Creator:Aguirre-Cruz, Lucinda ; Charuel, Jean-Luc ; Carpentier, Antoine F. ; Benyahia, Baya ; Delattre, Jean-Yves ; Musset, Lucile
Publisher:Dordrecht: Springer
Journal title:Journal of neuro-oncology, 2005-01, Vol.71 (1), p.39-41
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Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

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Heterozygous and homozygous JAK2(V617F) states modeled by induced pluripotent stem cells from myeloproliferative neoplasm patients

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Immunohistochemical analysis of anti-Hu-associated paraneoplastic encephalomyelitis

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Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

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Heterozygous and Homozygous JAK2V617F States Modeled by Induced Pluripotent Stem Cells from Myeloproliferative Neoplasm Patients

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Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10

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Autism, language delay and mental retardation in a patient with 7q11 duplication: Autism and 7q11 duplication

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Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in Resembles Dravet Syndrome but Mainly Affects Females

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Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females: e1000381

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Heterozygous and Homozygous JAK2V617F States Modeled by Induced Pluripotent Stem Cells from Myeloproliferative Neoplasm Patients

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Clinical relevance of non-neuronal auto-antibodies in patients with anti-Hu or anti-Yo paraneoplastic diseases

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