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From diagnosis to prognosis: Revisiting the meaning of muscle ISG15 overexpression in juvenile inflammatory myopathies
Hou C, Durrleman C, Periou B, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2020
Assessment of respiratory muscles and motor function in children with SMA treated by nusinersen
Gomez-Garcia de la Banda M, Amaddeo A, Khirani S, et al.
Pediatric pulmonology, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies
Guimaraes-Costa R, Fernandez-Eulate G, Wahbi K, et al.
European journal of neurology, 2020
Effects of nusinersen after one year of treatment in 123 children with SMA type 1 or 2: a French real-life observational study
Audic F, De la Banda MGG, Bernoux D, et al.
Orphanet journal of rare diseases, 2020, 15, 1, p 148
Palliative Care in SMA Type 1: A Prospective Multicenter French Study Based on Parents' Reports
Hully M, Barnerias C, Chabalier D, et al.
Frontiers in pediatrics, 2020, 8, 4
Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies
Wahbi K, Ben Yaou R, Gandjbakhch E, et al.
Circulation, 2019
Thoracic circumference: A new outcome measure in spinal muscular atrophy type 1?
Ropars J, Barnerias C, Hully M, et al.
Neuromuscular disorders : NMD, 2019
A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management
Lagrue E, Dogan C, De Antonio M, et al.
Neurology, 2019, 92, 8, p 852
Clinical features and evolution of juvenile myasthenia gravis in a French cohort
Barraud C, Desguerre I, Barnerias C, et al.
Muscle & Nerve, 2018, 57, 4, p 603
Respiratory insight to congenital muscular dystrophies and congenital myopathies and its relation to clinical trial
Fauroux B, Fauroux B, Amaddeo A, et al.
Neuromuscular disorders : NMD, 2018, 28, 9, p 731
Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis
Aouizerate J, De Antonio M, Bader-Meunier B, et al.
Rheumatology (Oxford, England), 2018, 57, 5, p 873
Sleep in infants with congenital myasthenic syndromes
Caggiano S, Khirani S, Verrillo E, et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2017, 21, 6, p 842
A novel neuromuscular form of glycogen storage disease type IV with arthrogryposis, spinal stiffness and rare polyglucosan bodies in muscle
Malfatti E, Barnerias C, Hedberg-Oldfors C, et al.
Neuromuscular disorders : NMD, 2016, 26, 10, p 681
Vasculopathy-related clinical and pathological features are associated with severe juvenile dermatomyositis
Gitiaux C, De Antonio M, Aouizerate J, et al.
Rheumatology (Oxford), 2016, 55, 3, p 470
Syndrome de Chanarin-Dorfman - Quand la myopathie et l’atteinte cutanée ne font qu’un : Chanarin-Dorfman syndrome in a 7-year-old child: when myophathy and skin involvement are all but one
Barnerias C, Bassez G, Schischmanoff O
médecine/sciences, 2015, 31, HS3, p 11
Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable pattern
Hankiewicz K, Carlier RY, Lazaro L, et al.
Muscle & Nerve, 2015, 52, 5, p. 728-35
Myasthénie auto-immune de l'enfant : A propos d'une cohorte de 40 cas
Barraud C, Desguerre I, Barnerias C, et al.
Archives de pédiatrie, 2015, 22, 5, suppl 1, p. 225
Actualités thérapeutiques dans la myopathie de Duchenne
Desguerre I, Barnerias C
MTP. Médecine thérapeutique pédiatrie, 2014, 17, 3, p. 179-184
Myasthénie auto-immune de l'enfant : nouvelles approches thérapeutiques ?
Barnerias C, Desguerre I
MTP. Médecine thérapeutique pédiatrie, 2014, 17, 3, p. 197-201
Les soins palliatifs dans les maladies neuromusculaires de l'enfant sont-ils un sujet de recherche ?
Desguerre I, Barnerias C, Ledivenah A, et al.
MTP. Médecine thérapeutique pédiatrie, 2014, 17, 3, p. 202-206
Amyotrophie spinale type 1 : enquête multicentrique des pratiques de soins et d'accompagnement palliatif sur deux périodes successives de 10 ans : Multicentric study of medical care and practices in spinal muscular atrophy type 1 over two 10-year periods
Barnerias C, Quijano S, Mayer M, et al.
Archives de pédiatrie, 2014, 21, 4, p 347
Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies
Marttila M, Lehtokari VL, Marston S, et al.
Human mutation, 2014, 35, 7, p 779
Traitements des déformations rachidiennes des maladies neuromusculaires
Finidori G, Barnerias C, Topouchian V, et al.
MTP. Médecine thérapeutique pédiatrie, 2014, 17, 3, p. 185-196
Les principaux changements apportés par la trachéotomie chez des enfants atteints de maladies neuromusculaires
Rul B, Quijano-Roy S, Golse A, et al.
Recherche en soins infirmiers, 2013, 114, p. 46-57
Maladies neuromusculaires de l'enfant et soins palliatifs
Desguerre I, Barnerias C, Le Divenah A, et al.
Les Cahiers de Myologie, 2013, 8, p. 11-14
