Centronuclear myopathy: clinical, morphological and genetic characters. A review of 288 cases.

[1]  I. Nonaka,et al.  Muscle histochemistry in myotubular (centronuclear) myopathy , 1989, Brain and Development.

[2]  P. Girlanda,et al.  Adult‐onset centronuclear myopathy: evidence against a neurogenic pathology , 1989, Acta neurologica Scandinavica.

[3]  A. Oldfors,et al.  X‐linked myotubular myopathy: clinical and pathological findings in a family , 1989, Clinical genetics.

[4]  G. Danieli,et al.  Problems in genetic counseling in a family with an "atypical" centronuclear myopathy. , 1989, American journal of medical genetics.

[5]  J. Lamarche,et al.  High Stature in Neonatal Myotubular Myopathy , 1988, Acta paediatrica Scandinavica.

[6]  A. Moosa,et al.  Centronuclear Myopathy in Black African Children - Report of 4 Cases , 1987, Neuropediatrics.

[7]  L. Keppen,et al.  X‐linked myotubular myopathy: intrafamilial variability and normal muscle biopsy in a heterozygous female , 1987, Clinical genetics.

[8]  E. Reske‐Nielsen,et al.  Familial centronuclear myopathy: a clinical and pathological study , 1987, Acta neurologica Scandinavica.

[9]  C. Angelini,et al.  Quantitative histopathology in congenital myopathies. , 1987, Rivista di neurologia.

[10]  G. Ferrari,et al.  Centronuclear myopathy with unusual clinical picture. , 1987, European neurology.

[11]  P. Moerman,et al.  X-linked centronuclear myopathy as a cause of floppy baby. , 1987, European journal of obstetrics, gynecology, and reproductive biology.

[12]  G. Serratrice,et al.  [A case of centronuclear myopathy in adults with facio-scapulo-peroneal topography]. , 1987, Revue neurologique.

[13]  J. Gilbert,et al.  Morphologic and morphometric analysis of muscle in X-linked myotubular myopathy. , 1986, Human pathology.

[14]  D. Leys,et al.  [Myocardiopathy disclosing a centronuclear myopathy in an adult]. , 1986, Annales de cardiologie et d'angeiologie.

[15]  R. Janzer,et al.  Severe neonatal centronuclear (myotubular) myopathy: an X-linked recessive disorder. , 1986, Helvetica paediatrica acta.

[16]  Strøm Eh,et al.  Craniopharyngioma in a boy with centronuclear (myotubular) myopathy: clinical and postmortem findings , 1986 .

[17]  V. Dubowitz,et al.  Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children. , 1985, Brain : a journal of neurology.

[18]  R. Griggs,et al.  Severe neonatal centronuclear myopathy with autosomal dominant inheritance. , 1985, Archives of neurology.

[19]  T. Pavia,et al.  Centronuclear myopathy. Report of a sporadic case. , 1985, Acta neurologica.

[20]  A. Cabello,et al.  Hypotrophy of type I fibres with central nuclei: recovery 4 years after diagnosis. , 1985, Journal of neurology, neurosurgery, and psychiatry.

[21]  G. Comi,et al.  Centronuclear myopathy with unusual mitochondrial abnormalities. , 1985, Clinical neuropathology.

[22]  M. Ambler,et al.  X-linked recessive myotubular myopathy: II. Muscle morphology and human myogenesis. , 1984, Human pathology.

[23]  Giacoia Gp,et al.  X-linked neonatal myotubular myopathy. , 1984 .

[24]  M. Ambler,et al.  X-linked recessive myotubular myopathy: I. Clinical and pathologic findings in a family. , 1984, Human pathology.

[25]  H. Goebel,et al.  Centronuclear myopathy with special consideration of the adult form. , 1984, European neurology.

[26]  L. Santoro,et al.  A case of "centronuclear myopathy" with late clinical onset. Clinical electrophysiological, histochemical study. , 1983, Acta neurologica.

[27]  I. Siegel Foot deformity in myotubular myopathy. Pathology of intrinsic foot musculature. , 1983, Archives of neurology.

[28]  A. McComas,et al.  Infantile centronuclear myopathy Evidence suggesting incomplete innervation , 1983, Journal of the Neurological Sciences.

[29]  A. Collins,et al.  Perinatal diagnosis of myotubular (centronuclear) myopathy: a case report. , 1983, Clinical neuropathology.

[30]  R. Fitzsimons,et al.  Myopathy with pathological features of both centronuclear myopathy and multicore disease , 1982, Journal of the Neurological Sciences.

[31]  L. Edström,et al.  Genuine myotubular myopathy , 1982, Muscle & nerve.

[32]  J. Peyronnard,et al.  Type I fiber atrophy and internal nuclei. A form of centronuclear myopathy? , 1982, Archives of neurology.

[33]  M. Pagès,et al.  [Centronuclear myopathy. Complete review of the literature apropos of a case]. , 1982, Annales de pathologie.

[34]  H. Sarnat,et al.  Neonatal Myotubular Myopathy: Neuropathy and Failure of Postnatal Maturation of Fetal Muscle , 1981, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[35]  N. Hülsmann,et al.  Cytopathology of an unusual case of centronuclear myopathy Light- and electron-microscopic investigations , 1981, Journal of the Neurological Sciences.

[36]  D. Jadro-Šantel,et al.  Centronuclear myopathy with type I fibre hypotrophy and “Fingerprint” inclusions associated with Marfan's syndrome , 1980, Journal of the Neurological Sciences.

[37]  L. Pavone,et al.  Familial centronuclear myopathy , 1980, Acta neurologica Scandinavica.

[38]  Y. Yoshino,et al.  [A case of myotubular myopathy with autosomal dominant inheritance (author's transl)]. , 1980, No to shinkei = Brain and nerve.

[39]  B. J. Shaw,et al.  41 CENTRONUCLEAR MYOPATHY - A UNIFYING CONCEPT , 1980 .

[40]  W. Wilson,et al.  Centronuclear myopathy: Extraocular‐ and limb‐muscle findings in an adult , 1980, Muscle & nerve.

[41]  J. Martín,et al.  Centronuclear myopathy: follow-up study of a case reported as an early onset myopathy (1966): muscle biopsies in parents and sibs. , 1980, Acta neurologica Belgica.

[42]  W. Engel,et al.  X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue cultures. , 1979, Archives of neurology.

[43]  B. Reitter,et al.  NEONATAL RESPIRATORY INSUFFICIENCY DUE TO CENTRONUCLEAR MYOPATHY , 1979, Acta paediatrica Scandinavica.

[44]  P. Bill,et al.  Crural hypertrophy associated with centronuclear myopathy , 1979, Journal of neurology, neurosurgery, and psychiatry.

[45]  I. Na,et al.  [X-linked myotubular myopathy]. , 1979 .

[46]  I. Kanazawa,et al.  [Centronuclear (myotubular) myopathy in a middle-aged woman--histochemical and biochemical study of the muscle biopsy (author's transl)]. , 1979, Rinsho shinkeigaku = Clinical neurology.

[47]  W. Markesbery,et al.  Metabolic implications of distal atrophy Carbohydrate metabolism in centronuclear myopathy , 1978, Journal of the Neurological Sciences.

[48]  A. Gil-Peralta,et al.  Myotonia in centronuclear myopathy , 1978, Journal of neurology, neurosurgery, and psychiatry.

[49]  D. Schiffer,et al.  Histochemical and ultrastructural findings in a case of centronuclear myopathy. , 1978, European neurology.

[50]  J. Cracco,et al.  Centronuclear Myopathy: Clinical and Pathologic Features , 1978, Clinical pediatrics.

[51]  G. Serratrice,et al.  Centronuclear myopathy: Possible central nervous system origin , 1978, Muscle & nerve.

[52]  J. Martín,et al.  [Centronuclear myopathy (author's transl)]. , 1977, Acta neurologica Belgica.

[53]  M. B. Bender,et al.  Muscle fiber hypotrophy with intact neuromuscular junctions , 1977, Neurology.

[54]  S. Chokroverty,et al.  Centronuclear myopathy in the newborn period causing severe respiratory distress. , 1977, Pediatrics.

[55]  A. Radu,et al.  Myotubular (Centronuclear) (Neuro-)Myopathy , 1977 .

[56]  J. Mikol,et al.  [Familial form of centronuclear myopathy in the adult]. , 1976, Revue neurologique.

[57]  H. Szliwowski,et al.  Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathies , 1976, Neurology.

[58]  M. Fukase,et al.  [3 cases of Wilson's disease in adults, with special reference to copper metabolism screening with 64Cu]. , 1976, Rinsho shinkeigaku = Clinical neurology.

[59]  A. Weindl,et al.  [Congenital centronuclear myopathy. Two morphological variants in one family (author's transl)]. , 1976, Klinische Wochenschrift.

[60]  J. Brucher,et al.  Familial centronuclear myopathy associated with 'cardiomyopathy'. , 1976, British heart journal.

[61]  A. Emery Methodology in medical genetics: An introduction to statistical methods , 1976 .

[62]  E. Satoyoshi,et al.  “Myotubular myopathy” and “type I fiber atrophy” in a family , 1975, Journal of the Neurological Sciences.

[63]  C. Hawkes,et al.  Myotubular myopathy associated with cataract and electrical myotonia. , 1975, Journal of neurology, neurosurgery, and psychiatry.

[64]  P. Barth,et al.  X‐linked myotubular myopathy with fatal neonatal asphyxia , 1975, Neurology.

[65]  T. Santa,et al.  A case of type 1 muscle fibre hypotrophy and internal nuclei. , 1975, Journal of neurology, neurosurgery, and psychiatry.

[66]  J. McNamara,et al.  Centronuclear myopathy: histochemistry and electron microscopy. Report of two cases. , 1975, Archives of pathology.

[67]  K. R. Meyers,et al.  Familial neuromuscular disease with “myotubes“ , 1974, Clinical genetics.

[68]  A. Marian,et al.  Hypotrophic type I muscle fibres with central nuclei, and central myofibrillar lysis preferentially involving type II fibres. , 1974, European neurology.

[69]  S. Araki,et al.  Centronuclear Myopathy: A Light and Electron Microscopic Study and a Review of the Literature , 1973, Folia psychiatrica et neurologica japonica.

[70]  V. Dubowitz,et al.  Muscle biopsy: A modern approach , 1973 .

[71]  D. Harriman,et al.  Centronuclear myopathy in old age , 1972, The Journal of pathology.

[72]  V. Ionasescu,et al.  Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature. , 1972, Journal of the neurological sciences.

[73]  J. Mcleod,et al.  Centronuclear myopathy with autosomal dominant inheritance. , 1972, Journal of the neurological sciences.

[74]  D. Price,et al.  Familial centronuclear myopathy , 1970, Journal of neurology, neurosurgery, and psychiatry.

[75]  J. Vallat,et al.  [Clinical and ultrastructural study of a case of centronuclear myopathy (myotubular myopathy) in an adult]. , 1970, Revue neurologique (Paris).

[76]  A. Meijer,et al.  Centronuclear myopathy with type I fiber atrophy and "myotubes". , 1970, Archives of neurology.

[77]  S. Carpenter,et al.  Type I muscle fibre atrophy and central nuclei. A rare familial neuromuscular disease. , 1970, Journal of the neurological sciences.

[78]  J. Ortiz de Zárate,et al.  The descending ocular myopathy of early childhood; myotubular or centronuclear myopathy. , 1970, European Neurology.

[79]  J. Bethlem,et al.  Familial “myotubular” myopathy , 1969, Neurology.

[80]  W. C. Hülsmann,et al.  Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube‐like structures , 1969, Neurology.

[81]  M. J. Campbell,et al.  Myotubular, centronuclear or Peri-Centronuclear myopathy? , 1969, Journal of the neurological sciences.

[82]  T. Munsat,et al.  Centronuclear ("myotubular") myopathy. , 1969, Archives of neurology.

[83]  W. Engel,et al.  Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model. , 1968, Archives of neurology.

[84]  S. Aronson,et al.  Familial centronuclear myopathy , 1967, Neurology.

[85]  N. Gonatas,et al.  Myotubular myopathy. Persistence of fetal muscle in an adolescent boy. , 1966, Archives of neurology.