B. Q. Banker, Discussion of the presentation by Sher JH, Rimalovski AB, Athanassiades TJ, Aronson SM Familial myotubular myopathy, a clinical, pathological, histochemical and ultrastructural study, J Neuro Pathol Exp Neurol, vol.26, p.133, 1967.

M. Bitoun, S. Maugenre, P. Y. Jeannet, E. Lacene, X. Ferrer et al., Mutations in dynamin 2 cause dominant centronuclear myopathy, Nat Genet, vol.37, pp.1207-1216, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00187451

M. J. Campbell, J. J. Rebeiz, and J. N. Walton, Myotubular, centronuclear or peri-centronuclear myopathy?, J Neurol Sci, vol.8, pp.425-468, 1969.

W. K. Engel, G. N. Gold, and G. Karpati, Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model, Arch Neurol, vol.18, pp.435-479, 1968.

M. Fardeau and F. Tomé, Congenital myopathies, pp.1500-1504, 1994.

K. J. Felice and M. L. Grunnet, Autosomal dominant centronuclear myopathy: report of a new family with clinical features simulating facioscapulohumeral syndrome, Muscle Nerve, vol.20, pp.1194-1200, 1997.

X. Ferrer, C. Vital, M. Coquet, B. Deleplanque, E. E. Lagueny et al., Autosomal dominant centronuclear myopathy, Rev Neurol, vol.148, pp.622-652, 1992.

D. Fischer, M. C. Walter, K. Kesper, J. A. Petersen, S. Aurino et al., Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs, J Neurol, vol.252, pp.538-585, 2005.

M. Goulon, M. Fardeau, L. Got, P. Babinet, and E. Manko, Centronuclear myopathy with late clinical manifestations. Clinical, histological and ultrastructural study of a new case, Rev Neurol, vol.132, pp.275-90, 1976.

A. E. Harding and P. K. Thomas, The clinical features of hereditary motor and sensory neuropathy types I and II, Brain, vol.103, pp.259-80, 1980.

P. Y. Jeannet, G. Bassez, B. Eymard, P. Laforet, J. A. Urtizberea et al., Clinical and histologic findings in autosomal centronuclear myopathy, Neurology, vol.62, pp.1484-90, 2004.

H. Jungbluth, M. R. Davis, C. Muller, S. Counsell, J. Allsop et al., Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations, Neuromuscul Disord, vol.14, pp.785-90, 2004.

H. Jungbluth, C. A. Sewry, S. Counsell, J. Allsop, A. Chattopadhyay et al., Magnetic resonance imaging of muscle in nemaline myopathy, Neuromuscul Disord, vol.14, pp.779-84, 2004.

A. E. Lamminen, Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement, Br J Radiol, vol.63, pp.946-50, 1990.

J. G. Mcleod, W. Baker, and A. K. Lethlean, Centronuclear myopathy with autosomal dominant inheritance, J Neurol Sci, vol.15, pp.375-87, 1972.

J. G. Mcleod, C. Baker-wde, A. K. Lethlean, and C. D. Shorey, Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype, Neuromuscul Disord, vol.13, pp.554-562, 2003.

E. Mercuri, A. Pichiecchio, and S. Counsell, A short protocol for muscle MRI in children with muscular dystrophies, Eur J Paediatr Neurol, vol.6, pp.305-312, 2002.

E. Mercuri, B. Talim, and B. Moghadaszadeh, Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1), Neuromuscul Disord, vol.12, pp.631-639, 2002.

E. Mercuri, C. Cini, A. Pichiecchio, J. Allsop, S. Counsell et al., Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and ulrich phenotype, Neuromuscul Discord, vol.13, pp.554-58, 2003.

E. Mercuri, H. Jungbluth, and F. Muntoni, Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders, Curr Opin Neurol, vol.18, pp.526-563, 2005.

E. Mercuri, A. Lampe, J. Allsop, R. Knight, M. Pane et al., Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy, Neuromuscul Disord, vol.15, pp.303-313, 2005.

K. R. Meyers, H. M. Golomb, J. L. Hansen, and V. A. Mckusick, Familial neuromuscular disease with 'myotubes', Clin Genet, vol.5, pp.327-364, 1974.

M. Mora, L. Morandi, L. Merlini, G. Vita, A. Baradello et al., Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathies, Muscle Nerve, vol.17, pp.1176-84, 1994.

L. Pavone, F. Mollica, A. Grasso, and G. Pero, Familial centronuclear myopathy, Act Neurol Scand, vol.62, pp.33-40, 1980.

B. Pepin, J. Mikol, B. Goldstein, M. Haguenau, and S. Godlewski, Familial form of centronuclear myopathy in the adult, Rev Neurol, vol.132, pp.845-57, 1976.

J. H. Sher, A. B. Rimalovski, T. J. Athanassiades, and S. M. Aronson, Familial centronuclear myopathy: a clinical and pathological study, Neurol, vol.17, pp.727-769, 1967.

J. H. Sher, A. B. Rimalovski, T. J. Athanassiades, and S. M. Aronson, Familial myotubular myopathy: a clinical, pathological, histochemical, and ultrastructural study, J Neuropath Exp Neurol, vol.26, pp.132-135, 1967.

A. J. Spiro, G. M. Shy, and N. K. Gonatas, Myotubular myopathy. Persistence of fetal muscle in an adolescent boy, Arch Neurol, vol.14, pp.1-14, 1966.

G. K. Van-wijngaarden, P. Fleury, J. Bethlem, and A. E. Meijer, Familial 'myotubular' myopathy, Neurol, vol.19, pp.901-909, 1969.

S. Zuchner, M. Noureddine, M. Kennerson, K. Verhoeven, K. Claeys et al., Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease, Nat Genet, vol.37, pp.1463-1469, 2005.