J. Cuisset and F. Rivier, Manifestations centrales des dystrophinopathies, vol.22, pp.12-58, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01756201

B. Chabrol and I. Desguerre, Dystrophies musculaires (DM) de Duchenne (DMD) et de Becker (DMB), Arch Pédiatrie, vol.22, pp.12-13, 2015.

F. Leturcq and S. Tuffery-giraud, Aspects génétiques et moléculaires des dystrophinopathies, Arch Pédiatrie, vol.22, pp.12-15, 2015.

Y. Péréon, S. Mercier, and A. Magot, Physiopathologie de la dystrophie musculaire de Duchenne, Arch Pédiatrie, vol.22, pp.12-18, 2015.

D. M. Connuck, L. A. Sleeper, and S. D. Colan, Characteristics and Outcomes of Cardiomyopathy in Children with Duchenne or Becker Muscular Dystrophy: A Comparative Study from The Pediatric Cardiomyopathy Registry, Am Heart J, vol.155, pp.998-1005, 2008.

I. Desguerre and V. Laugel, Diagnostic et histoire naturelle de la dystrophie musculaire de Duchenne, Arch Pédiatrie, vol.22, pp.12-24, 2015.

, Perret j (2001) avant-propos, Ann Réadapt Médecine Phys, vol.44, pp.5-6

C. Boulay and G. Finidori, Aspects fonctionnels et orthopédiques des dystrophinopathies, Arch Pédiatrie, vol.22, pp.12-42, 2015.

Y. Xhardez, VADE-MECUM de KINESITHERAPIE 4ème édition, 1996.

F. Shapiro, D. Zurakowski, T. Bui, and B. T. Darras, Progression of spinal deformity in wheelchairdependent patients with Duchenne muscular dystrophy who are not treated with steroids: coronal plane (scoliosis) and sagittal plane (kyphosis, lordosis) deformity, Bone Jt J 96-B, pp.100-105, 2014.

L. E. Gayet, Traitement chirurgical des scolioses de la dystrophie musculaire de Duchenne, Chirurgie, vol.124, pp.423-431, 1999.

T. Nedelcu and I. Georgescu, Evaluation of the Unit Rod surgical instrumentation in Duchenne scoliosis. A retrospective study, J Med Life, vol.9, pp.437-443, 2016.

M. Takaso, T. Nakazawa, and T. Imura, Surgical management of severe scoliosis with high risk pulmonary dysfunction in Duchenne muscular dystrophy: patient function, quality of life and satisfaction, Int Orthop, vol.34, pp.695-702, 2010.

I. Desguerre, Subphénotypes de la maladie de Duchenne et caractérisation de la myofibrose dystrophique humaine et expérimentale, 2008.

K. Patte, J. Pélissier, C. Bénaim, E. M. Laassel, C. Guibal et al., Analyse de la marche au cours de la dystrophie musculaire de Duchenne, Ann Réadaptation Méd Phys, vol.43, pp.57-68, 2000.

C. Vuillerot, F. Girardot, C. Payan, J. Fermanian, J. Iwaz et al., Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure, Dev Med Child Neurol, vol.52, pp.60-65, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00539251

P. Jeannet, K. Aminian, C. Bloetzer, B. Najafi, and A. Paraschiv-ionescu, Continuous monitoring and quantification of multiple parameters of daily physical activity in ambulatory Duchenne muscular dystrophy patients, Eur J Paediatr Neurol EJPN Off J Eur Paediatr Neurol Soc, vol.15, pp.40-47, 2011.

G. S. Paleg, B. A. Smith, and L. B. Glickman, Systematic review and evidence-based clinical recommendations for dosing of pediatric supported standing programs, Pediatr Phys Ther Off Publ Sect Pediatr Am Phys Ther Assoc, vol.25, pp.232-247, 2013.

L. Claire and L. Guiet, Technique de verticalisation et maladie neuromusculaire, pp.37-40, 1997.

A. Afm, Modalités, indications, limites de la rééducation dans les pathologies neuromusculaires non acquises, 2001.

. Y. Cornu-j, Ann Réadapt Médecine Phys, vol.44, pp.176-184, 2001.

E. L. Townsend, C. Bibeau, and T. M. Holmes, Supported Standing in Boys With Duchenne Muscular Dystrophy, Pediatr Phys Ther Off Publ Sect Pediatr Am Phys Ther Assoc, vol.28, pp.320-329, 2016.

K. Wahbi, Aspects cardiologiques des dystrophinopathies, Arch Pédiatrie, vol.22, pp.12-37, 2015.

D. Duboc, C. Meune, G. Lerebours, J. Devaux, G. Vaksmann et al., Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy, J Am Coll Cardiol, vol.45, pp.855-857, 2005.

D. Duboc, C. Meune, B. Pierre, K. Wahbi, B. Eymard et al., Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up, Am Heart J, vol.154, pp.596-602, 2007.

Y. Rideau, L. W. Jankowski, and J. Grellet, Respiratory function in the muscular dystrophies, Muscle Nerve, vol.4, pp.155-164, 1981.

M. Kohler, C. F. Clarenbach, C. Bahler, T. Brack, E. W. Russi et al., Disability and survival in Duchenne muscular dystrophy, J Neurol Neurosurg Psychiatry, vol.80, pp.320-325, 2009.

N. Almenrader and D. Patel, Spinal fusion surgery in children with non-idiopathic scoliosis: is there a need for routine postoperative ventilation?, Br J Anaesth, vol.97, pp.851-857, 2006.

X. Ambrosi, L. Lamothe, N. Heming, and D. Orlikowski, Aspects respiratoires et réanimatoires des dystrophies musculaires, Arch Pédiatrie, vol.22, pp.12-51, 2015.

B. Lanini, G. Misuri, F. Gigliotti, I. Iandelli, A. Pizzi et al., Perception of dyspnea in patients with neuromuscular disease, Chest, vol.120, pp.402-408, 2001.

S. K. Archer, R. Garrod, N. Hart, and S. Miller, Dysphagia in Duchenne muscular dystrophy assessed objectively by surface electromyography, Dysphagia, vol.28, pp.188-198, 2013.

S. Ward, M. Chatwin, S. Heather, and A. Simonds, Randomised controlled trial of non-invasive ventilation (NIV) for nocturnal hypoventilation in neuromuscular and chest wall disease patients with daytime normocapnia, Thorax, vol.60, pp.1019-1024, 2005.

S. Lyager, B. Steffensen, and B. Juhl, Indicators of Need for Mechanical Ventilation in Duchenne Muscular Dystrophy and Spinal Muscular Atrophy, Chest, vol.108, pp.779-785, 1995.

, Modalités pratiques de la ventilation non invasive en pression positive, au long cours, à domicile, dans les maladies neuromusculaires, 2006.

J. Y. Wu, K. Kuban, E. Allred, F. Shapiro, and B. T. Darras, Association of Duchenne muscular dystrophy with autism spectrum disorder, J Child Neurol, vol.20, pp.790-795, 2005.

Y. Ishikawa, T. Miura, Y. Ishikawa, T. Aoyagi, H. Ogata et al., Duchenne muscular dystrophy: survival by cardio-respiratory interventions, Neuromuscul Disord NMD, vol.21, pp.47-51, 2011.

M. Eagle, J. Bourke, R. Bullock, M. Gibson, J. Mehta et al., Managing Duchenne muscular dystrophy--the additive effect of spinal surgery and home nocturnal ventilation in improving survival, Neuromuscul Disord NMD, vol.17, pp.470-475, 2007.

H. Amthor, Principes des approches thérapeutiques des DMD, vol.22, pp.12-63, 2015.

D. J. Birnkrant, K. Bushby, and C. M. Bann, Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management, Lancet Neurol, vol.17, pp.251-267, 2018.

D. J. Birnkrant, K. Bushby, and C. M. Bann, Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management, Lancet Neurol, vol.17, pp.347-361, 2018.

H. Autorité-de-santé, TRANSLARNA (ataluren), ARN interférant, 2015.

K. Bushby, F. Muntoni, A. Urtizberea, R. Hughes, and R. Griggs, Report on the 124th ENMC International Workshop. Treatment of Duchenne muscular dystrophy; defining the gold standards of management in the use of corticosteroids, Neuromuscul Disord NMD, vol.14, pp.526-534, 2004.

I. Sanzarello, L. Merlini, F. Traina, M. A. Rosa, and C. Faldini, Corticosteroid Treatment Impact on Spinal Deformity in Duchenne Muscular Dystrophy, 2014.

H. T. Harcke, H. H. Kecskemethy, D. Conklin, M. Scavina, W. G. Mackenzie et al., Assessment of Bone Mineral Density in Duchenne Muscular Dystrophy Using the Lateral Distal Femur, J Clin Neuromuscul Dis, vol.8, p.1, 2006.

R. C. Henderson, L. M. Berglund, and R. May, The Relationship Between Fractures and DXA Measures of BMD in the Distal Femur of Children and Adolescents With Cerebral Palsy or Muscular Dystrophy, J Bone Miner Res, vol.25, pp.520-526, 2010.

C. Tian, B. L. Wong, L. Hornung, J. C. Khoury, L. Miller et al., Bone health measures in glucocorticoid-treated ambulatory boys with Duchenne muscular dystrophy, Neuromuscul Disord NMD, vol.26, pp.760-767, 2016.

D. Souza, M. A. Figueiredo, M. De-baptista-cr-de, J. A. Aldaves, R. D. Mattiello-sverzut et al., Beneficial effects of ankle-foot orthosis daytime use on the gait of Duchenne muscular dystrophy patients, Clin Biomech Bristol Avon, vol.35, pp.102-110, 2016.

V. Humbertclaude, D. Hamroun, and K. Bezzou, Motor and respiratory heterogeneity in Duchenne patients: implication for clinical trials, Eur J Paediatr Neurol EJPN Off J Eur Paediatr Neurol Soc, vol.16, pp.149-160, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01681808

B. Chabrol and M. Mayer, Principes de prise en charge multidisciplinaire des dystrophies musculaires de Duchenne, Arch Pédiatrie, vol.22, pp.12-69, 2015.