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Author/Creator Baudou, Eloise

1. Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy. Issue 9 (29th September 2020)

Authors:
Géraud, Justine; Dieterich, Klaus; Rendu, John; Uro Coste, Emmanuelle; Dobrzynski, Murielle; Marcorelle, Pascale; Ioos, Christine; Romero, Norma Beatriz; Baudou, Eloise; Brocard, Julie; Coville, Anne-Cécile; Fauré, Julien; Koenig, Michel; Juntas Morales, Raul; Lacène, Emmanuelle; Madelaine, Angél...
Journal:
Journal of medical genetics
Issue:
Volume 58:Issue 9(2021)
Page Start:
602
Record Type:
Journal Article
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2. Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress. (March 2021)

Authors:
François-Heude, Marie-Céline; Walther-Louvier, Ulrike; Espil-Taris, Caroline; Beze-Beyrie, Pierre; Rivier, François; Baudou, Eloise; Uro-Coste, Emmanuelle; Rigau, Valérie; Martin Negrier, Marie Laure; Rendu, John; Morales, Raul Juntas; Pégeot, Henri; Thèze, Corinne; Lacourt, Delphine; Coville, An...
Journal:
European journal of paediatric neurology
Issue:
Volume 31(2021)
Page Start:
78
Record Type:
Journal Article
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4. Reading Comprehension Impairment in Children With Neurofibromatosis Type 1 (NF1): The Need of Multimodal Assessment of Attention. (July 2021)

Authors:
Biotteau, Maëlle; Tournay, Elodie; Baudou, Eloise; Destarac, Sandrine; Iannuzzi, Stéphanie; Faure-Marie, Nathalie; Castelnau, Pierre; Schweitzer, Elisabeth; Rodriguez, Diana; Kemlin, Isabelle; Dorison, Nathalie; Rivier, François; Carneiro, Maryline; Preclaire, Elodie; Barbarot, Sebastien; Lauwers...
Journal:
Journal of child neurology
Issue:
Volume 36:Number 8(2021)
Page Start:
625
Record Type:
Journal Article
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