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Annie Barois

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Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.
Chest|September 15, 2004
Respiratory capacity course in patients with infantile spinal muscular atrophyChristine Ioos, Danièle Leclair-Richard, Slah Mrad, et al.
Bulletin De L'Academie Nationale De Medecine|May 2, 2008
[Jeune'disease (asphyxiating thoracic dystrophy) and respiratory failure: importance of early respiratory management with periodic hyperinsufflation]Claire Do Ngoc Thanh, Annie Barois, Brigitte Estournet-Mathiaud, et al.
British Journal of Clinical Pharmacology|February 3, 2011
Riluzole pharmacokinetics in young patients with spinal muscular atrophyChadi Abbara, Brigitte Estournet, Lucette Lacomblez, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiencySusana Quijano-Roy, Lucía Galan, Ana Ferreiro, et al.
Bulletin De L'Academie Nationale De Medecine|January 26, 2006
[Spinal muscular atrophy. A 4-year prospective, multicenter, longitudinal study (168 cases)]Annie Barois, Michèle Mayer, Isabelle Desguerre, et al.
Journal of Neuromuscular Diseases|December 5, 2019
Muscular, Ocular and Brain Involvement Associated with a De Novo 11q13.2q14.1 Duplication: Contribution to the Differential Diagnosis of Muscle-Eye-Brain Congenital Muscular DystrophyRocío N Villar-Quiles, Marta Gomez-Garcia de la Banda, Annie Barois, et al.
Neuromuscular Disorders : NMD|September 18, 2012
Whole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutationsMohamed Jarraya, Susana Quijano-Roy, Nicole Monnier, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutationRabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, et al.
Annals of Neurology|July 12, 2002
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13Louis Viollet, Annie Barois, Jean G Rebeiz, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.
Chest|September 15, 2004
Respiratory capacity course in patients with infantile spinal muscular atrophyChristine Ioos, Danièle Leclair-Richard, Slah Mrad, et al.
Bulletin De L'Academie Nationale De Medecine|May 2, 2008
[Jeune'disease (asphyxiating thoracic dystrophy) and respiratory failure: importance of early respiratory management with periodic hyperinsufflation]Claire Do Ngoc Thanh, Annie Barois, Brigitte Estournet-Mathiaud, et al.
British Journal of Clinical Pharmacology|February 3, 2011
Riluzole pharmacokinetics in young patients with spinal muscular atrophyChadi Abbara, Brigitte Estournet, Lucette Lacomblez, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiencySusana Quijano-Roy, Lucía Galan, Ana Ferreiro, et al.
Bulletin De L'Academie Nationale De Medecine|January 26, 2006
[Spinal muscular atrophy. A 4-year prospective, multicenter, longitudinal study (168 cases)]Annie Barois, Michèle Mayer, Isabelle Desguerre, et al.
Journal of Neuromuscular Diseases|December 5, 2019
Muscular, Ocular and Brain Involvement Associated with a De Novo 11q13.2q14.1 Duplication: Contribution to the Differential Diagnosis of Muscle-Eye-Brain Congenital Muscular DystrophyRocío N Villar-Quiles, Marta Gomez-Garcia de la Banda, Annie Barois, et al.
Neuromuscular Disorders : NMD|September 18, 2012
Whole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutationsMohamed Jarraya, Susana Quijano-Roy, Nicole Monnier, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutationRabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, et al.
Annals of Neurology|July 12, 2002
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13Louis Viollet, Annie Barois, Jean G Rebeiz, et al.
Pageof 2