Update on neuromuscular diseases: Pathology and molecular pathogenesis, Biochim Biophys Acta. avr, vol.1852, issue.4, pp.561-563, 2015. ,
, Maladies neuromusculaires
, , 2016.
,
Pregnancy course and outcome in women with hereditary neuromuscular disorders: comparison of obstetric risks in 178 patients, Eur J Obstet Gynecol Reprod Biol. juin, vol.162, issue.2, pp.153-162, 2012. ,
Clinical commentary: obstetric and respiratory management of pregnancy with severe spinal muscular atrophy, Obstet Gynecol Int, p.942301, 2009. ,
Amyotrophie spinale proximale: Spinal muscular atrophy, Prise en charge des maladies rares en anesthésie et analgésie obstétricales, pp.33-36, 2015. ,
Spinal muscular atrophy: a clinical and research update, Pediatr Neurol. janv, vol.46, issue.1, pp.1-12, 2012. ,
Charcot-Marie-Tooth disease, Neurology, vol.81, issue.18, pp.1617-1642, 2013. ,
Syndrome/maladie de Charcot-Marie-Tooth: CharcotMarie-Tooth disease, Prise en charge des maladies rares en anesthésie et analgésie obstétricales, vol.118, 2015. ,
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population, Brain J Neurol, vol.132, pp.3175-86, 2009. ,
Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms, Biochim Biophys Acta. avr, vol.1852, issue.4, pp.594-606, 2015. ,
Dystrophies myotoniques: Myotonic dystrophy, Prise en charge des maladies rares en anesthésie et analgésie obstétricales, pp.227-232, 2015. ,
The myotonic dystrophies: molecular, clinical, and therapeutic challenges, Lancet Neurol, vol.11, issue.10, pp.891-905, 2012. ,
Epigenetic mechanisms in amyotrophic lateral sclerosis: A short review, Mech Ageing Dev. 12 mars, 2018. ,
Sclérose latérale amyotrophique: Amyotrophic lateral sclerosis, Prise en charge des maladies rares en anesthésie et analgésie obstétricales, pp.646-649, 2015. ,
Neurologic disease with pregnancy and considerations for the obstetric anesthesiologist, Semin Perinatol. oct, vol.38, issue.6, pp.359-69, 2014. ,
Interprétation et utilisation des explorations fonctionnelles respiratoires de routine de l'adulte : spirométrie, volumes non mobilisables, diffusion, hématose, test de provocation bronchique à la métacholine et test de marche, Rev Médecine Interne. févr, vol.37, issue.2, pp.100-110, 2016. ,
Pregnancy outcomes in women with spinal muscular atrophy: A review, J Neurol Sci. 15 mai, vol.388, pp.50-60, 2018. ,
Management of a pregnancy complicated by type III spinal muscular atrophy, BMJ Case, vol.18, issue.2011, 2011. ,
Normal vaginal delivery in a patient with autosomal recessive limb-girdle muscular dystrophy, Obstet Med. juin, vol.3, issue.2, pp.81-83, 2010. ,
Pregnancy course and outcome in women with hereditary neuromuscular disorders: comparison of obstetric risks in 178 patients, Eur J Obstet Gynecol Reprod Biol. juin, vol.162, issue.2, pp.153-162, 2012. ,
Clinical Commentary: Obstetric and Respiratory Management of Pregnancy with Severe Spinal Muscular Atrophy, Obstet Gynecol Int, 2009. ,
The Impact of Pregnancy on Myotonic Dystrophy: A Registry-Based Study, J Neuromuscul Dis, vol.2, issue.4, pp.447-52, 2015. ,
Access and quality of maternity care for disabled women during pregnancy, birth and the postnatal period in England: data from a national survey, BMJ Open, vol.20, issue.7, p.16757, 2017. ,
The ambiguity of disabled women's experiences of pregnancy, childbirth and motherhood: a phenomenological understanding, Midwifery. avr, vol.28, issue.2, pp.156-62, 2012. ,
, Haute Autorité de Santé-Sortie de maternité après accouchement : conditions et organisation du retour à domicile des mères et de leurs nouveau-nés, p.15