نتائج البحث - Isabelle Desguerre
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Expert recommendations and clinical considerations in the use of onasemnogene abeparvovec gene therapy for spinal muscular atrophy حسب Elizabeth Kichula, Crystal M. Proud, Michelle A. Farrar, Jennifer M. Kwon, Kayoko Saito, Isabelle Desguerre, Hugh J. McMillan
منشور في 2021Revisão -
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Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis حسب Christine Barnérias, Jean‐Marie Saudubray, Guy Touati, Pascale de Lonlay, Olivier Dulac, G Ponsot, C. Marsac, M. Brivet, Isabelle Desguerre
منشور في 2009Artigo -
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Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36 حسب Behzad Moghadaszadeh, Isabelle Desguerre, Haluk Topaloğlu, Francesco Muntoni, Sylvana Pavek, Caroline A. Sewry, M. Mayer, Michel Fardeau, F.M.S. Tomé, Pascale Guicheney
منشور في 1998Artigo -
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Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotype حسب Lisa Ouss, Dorothée Leunen, Jacques Laschet, Nicole Chémaly, Giulia Barcia, Emma Losito, Aveline Aouidad, Zoe Barrault, Isabelle Desguerre, Delphine Breuillard, Rima Nabbout
منشور في 2018Artigo -
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Very Low Residual Dystrophin Quantity Is Associated with Milder Dystrophinopathy حسب Yvan de Féraudy, Rabah Ben Yaou, Karim Wahbi, Caroline Stalens, Amalia Stantzou, Vincent Laugel, Isabelle Desguerre, Laurent Servais, France Leturcq, Helge Amthor
منشور في 2020Artigo -
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Clinical Heterogeneity of Duchenne Muscular Dystrophy (DMD): Definition of Sub-Phenotypes and Predictive Criteria by Long-Term Follow-Up حسب Isabelle Desguerre, Christo Christov, M. Mayer, Reinhard Zeller, Henri-Marc Becane, Sylvie Bastuji‐Garin, France Leturcq, Catherine Chiron, Jamel Chelly, Romain K. Gherardi
منشور في 2009Artigo -
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Epileptic phenotypes in children with respiratory chain disorders حسب Sandra Sabbagh, Anne-Sophie Lèbre, Nadia Bahi‐Buisson, Pascale Delonlay, Christine Soufflet, Nathalie Boddaert, Marlène Rio, Agnès Rötig, Olivier Dulac, Arnold Münnich, Isabelle Desguerre
منشور في 2010Artigo -
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Regional Pediatric Acute Stroke Protocol حسب Laurence Tabone, Nicolas Médiamolle, Céline Bellesme, Fabrice Lesage, D. Grévent, Augustin Ozanne, Olivier Naggara, B. Husson, Isabelle Desguerre, Catherine Lamy, Christian Denier, Manoëlle Kossorotoff
منشور في 2017Artigo -
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Severe paediatric conditions linked with EV-A71 and EV-D68, France, May to October 2016 حسب Denise Antona, Manoëlle Kossorotoff, Isabelle Schuffenecker, Audrey Mirand, Marianne Leruez‐Ville, Clément Bassi, Mélodie Aubart, Florence Moulin, D Lévy-Brühl, Cécile Henquell, Bruno Lina, Isabelle Desguerre
منشور في 2016Artigo -
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CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures حسب Julie Mollet, Agnès Delahodde, Valérie Serre, Dominique Chrétien, Dimitri Schlemmer, Anne Lombès, Nathalie Boddaert, Isabelle Desguerre, Pascale de Lonlay, Hélène Ogier de Baulny, Arnold Münnich, Agnès Rötig
منشور في 2008Artigo -
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Fatal thrombotic microangiopathy case following adeno-associated viral <i>SMN</i> gene therapy حسب Julia Guillou, Alice de Pellegars, Florence Porcheret, Véronique Frémeaux‐Bacchi, Emma Allain‐Launay, Camille Debord, M. Denis, Yann Péréon, Christine Barnérias, Isabelle Desguerre, G. Roussey, Sandra Mercier
منشور في 2022Artigo -
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A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy حسب Lam Son Nguyen, Taiane Schneider, Marlène Rio, Sébastien Moutton, Karine Siquier-Pernet, Florine Verny, Nathalie Boddaert, Isabelle Desguerre, Arnold Munich, José Luís Rosa, Valérie Cormier‐Daire, Laurence Colleaux
منشور في 2015Artigo -
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Cellular micro-environments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors حسب A. Bertrand, Simindokht Ziaei, Camille Ehret, Hélène Duchemin, Kamel Mamchaoui, Anne Bigot, M. Mayer, Susana Quijano-Roy, Isabelle Desguerre, Jeanne Lainé, Rabah Ben Yaou, Gisèle Bonne, Catherine Coirault
منشور في 2014Artigo -
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Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network حسب Guilhem Solé, Emmanuelle Salort‐Campana, Yann Péréon, Tanya Stojkovic, Karim Wahbi, Pascal Cintas, David H. Adams, Pascal Laforêt, V. Tiffreau, Isabelle Desguerre, Lucie I. Pisella, Annamaria Molon, Shahram Attarian
منشور في 2020Artigo
أدوات البحث:
موضوعات ذات صلة
Medicine
Biology
Internal medicine
Gene
Genetics
Pediatrics
Disease
Pathology
Phenotype
Mutation
Neuroscience
Duchenne muscular dystrophy
Biochemistry
Missense mutation
Muscular dystrophy
Psychiatry
Epilepsy
Immunology
Physical therapy
Cell biology
Clinical trial
Bioinformatics
Physical medicine and rehabilitation
Biopsy
Dystrophin
Atrophy
Cancer research
Cohort
Computer science
Endocrinology