يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Vasselon Raina, Maryline"', وقت الاستعلام: 0.36s تنقيح النتائج
  1. 1
    Academic Journal
    DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy

    المؤلفون: Picard, Fabienne, Makrythanasis, Periklis, Navarro, Vincent, Ishida, Saeko, de Bellescize, Julitta, Ville, Dorothée, Weckhuysen, Sarah, Fosselle, Erwin, Suls, Arvid, De Jonghe, Peter, Vasselon Raina, Maryline, Lesca, Gaetan, Depienne, Christel, An-Gourfinkel, Isabelle, Vlaicu, Mihaela, Baulac, Michel, Mundwiller, Emeline, Couarch, Philippe, Combi, Romina, Ferini-Strambi, Luigi, Gambardella, Antonio, Antonarakis, Stylianos, Leguern, Eric, Steinlein, Ortrud, Baulac, Stéphanie

    المصدر: ISSN: 0028-3878 ; Neurology, vol. 82, no. 23 (2014) p. 2101-2106.

    مصطلحات موضوعية: info:eu-repo/classification/ddc/616.8, info:eu-repo/classification/ddc/576.5, Adolescent, Adult, Aged, Child, Preschool, Chromosomes, Human, Pair 22 / genetics, Drug Resistance / genetics, Epilepsy, Frontal Lobe / genetics, Europe, Exome / genetics, Female, GTPase-Activating Proteins, Humans, Male, Middle Aged, Mutation / genetics, Pedigree, Phenotype, Repressor Proteins / genetics

    Relation: info:eu-repo/semantics/altIdentifier/pmid/24814846; https://archive-ouverte.unige.ch/unige:37943; unige:37943

    الاتاحة: https://archive-ouverte.unige.ch/unige:37943

    View record in BASE

    أضف إلى المفضلة
  2. 2
    Academic Journal
    EARLY DIAGNOSIS OF STAPHYLOCOCCAL TOXIC SHOCK SYNDROME BY DETECTION OF THE TSST-1 VBETA SIGNATURE IN PERIPHERAL BLOOD OF A 12-YEAR-OLD BOY

    المؤلفون: Ferry, Tristan, Thomas, Damien, Bouchut, Jean-Christophe, Lina, Gerard, Vasselon-Raina, Maryline, Dauwalder, Olivier, Gillet, Yves, Vandenesch, François, Floret, Daniel, Etienne, Jerome

    المصدر: Pediatric Infectious Disease Journal ; volume 27, issue 3, page 274-277 ; ISSN 0891-3668

    الاتاحة: http://dx.doi.org/10.1097/inf.0b013e31815c93a3
    http://journals.lww.com/00006454-200803000-00018

    View record in BASE

    أضف إلى المفضلة
  3. 3
    Periodical
    DEPDC5mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy

    المؤلفون: Picard, Fabienne, Makrythanasis, Periklis, Navarro, Vincent, Ishida, Saeko, de Bellescize, Julitta, Ville, Dorothée, Weckhuysen, Sarah, Fosselle, Erwin, Suls, Arvid, De Jonghe, Peter, Vasselon Raina, Maryline, Lesca, Gaetan, Depienne, Christel, An-Gourfinkel, Isabelle, Vlaicu, Mihaela, Baulac, Michel, Mundwiller, Emeline, Couarch, Philippe, Combi, Romina, Ferini-Strambi, Luigi, Gambardella, Antonio, Antonarakis, Stylianos E., Leguern, Eric, Steinlein, Ortrud, Baulac, Stéphanie

    المصدر: Neurology (Ovid); June 2014, Vol. 82 Issue: 23 p2101-2106, 6p


    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS – أرسل هذا البحث بالبريد الإلكتروني – حفظ البحث – جدول التنبيهات: لا شيء