References
- Spiro A. J., Shy G. M., Gonatas N. K. Myotubular myopathy. Persistence of fetal muscle in an adolescent boy. Arch Neurol 1966; 14: 1–14
- Heckmatt J. Z., Sewry C. A., Hodes D., Dubowitz V. Congenital centronuclear (myotubular) myopathy: A clinical pathological and genetic study in eight children. Brain 1985; 108: 941–64
- Dubowitz V. Muscle Biopsy. A Practical Approach.2nd ed. Bailliere Tindall, London 1985; 443–59
- Edstrom L., Wroblewski R., Mair W. G. Genuine myotubular myopathy. Muscle Nerve 1982; 5: 604–13
- Ambler M. W., Neave C., Singer D. B. X-linked recessive myotubular myopathy. II. Muscle morphology and human myogenesis. Hum Pathol 1984; 15: 1107–20
- Sarnat H. B., Roth S. I., Jimenez J. F. Neonatal myotubular myopathy: Neuropathy and failure of postnatal maturation of fetal muscle. Can J Neurol Sci 1981; 8: 313–20
- Pongratz D., Heuser M., Mittelbach F., Struppler A. So-called congenital centronuclear myopathy—a primary neuropathy?. (In German) Acta Neuropathol (Berl) 1975; 32: 9–19
- Elder G. B., Dean D., McComas A. J., Paes B., DeSa D. Infantile centronuclear myopathy. Evidence suggesting incomplete innervation. J Neurol Sci 1983; 60: 79–88
- Kinoshita M., Satoyoshi E., Matsuo N. Myotubular myopathy and type [fiber atrophy in a family. J Neurol Sci 1975; 26: 575–82
- Reske-Nielsen E., Hein-Sorensen O., Vorre P. Familial centronuclear myopathy: A clinical and pathological study. Acta Neurol Scand 1987; 76: 115–22
- Textbook of Fetal and Perinatal Pathology, J. S. Wigglesworth, D. B. Singer. Blackwell Scientific Publications, Boston 1991; 35
- Reitter B., Mortier W., Wille L. Neonatal respiratory insufficiency due to centronuclear myopathy. Acta Paediatr Scand 1979; 68: 773–8
- Campbell M. J., Rebeiz J. J., Walton J. N. Myotubular, centronuclear, or peri-centronuclear myopathy?. J Neurol Sci 1969; 8: 425–43
- Ricoy J. R., Cabello A. Dysmaturative myopathy. Evolution of the morphological picture in three cases. Acta Neuropathol (Berl) 1981; Suppl VII: 313–6
- Bucher H. U., Boltshauser E., Briner J., Gnehm H. E., Janzer R. C. Severe neonatal centronuclear (myotubular) myopathy: An X-linked recessive disorder. Helv Paediatr Acta 1986; 14: 291–300
- Radu H., Killyen I., Vlonescu, Radu A. Myotubular (centronuclear) (neuro-) myopathy. I. Clinical genetical and morphological studies. Eur Neurol 1977; 15: 285–300
- Barth P. G., Van Wijngaarden G. K., Bethlem J. X-linked myotubular myopathy with fatal neonatal asphyxia. Neurology (Minneap) 1975; 25: 531–6
- Giacoia G. P., Hale J. E. X-linked neonatal myotubular myopathy. South Med J 1984; 77: 1182–5
- Ambler M. W., Neave C., Tutschka B. G., Pueschel S. M., Orson J. M., Singer D. B. X-linked recessive myotubular myopathy. I. Clinical and pathologic findings in a family. Hum Pathol 1984; 15: 566–74
- Donders G., Moerman P., Devlieger H., Spitz B., Van Assche F. A. X-linked centronuclear myopathy as a cause of floppy baby. Eur J Obstet Gynecol Reprod Biol 1987; 24: 33–8
- Otsuji Y., Osame M., Tei C., et al. Cardiac involvement in congenital myopathy. Int J Cardiol 1985; 9: 311–22
- Verhiest W., Brucher J. M., Goddeeris P., Lauwoyns J., De Geest H. Familial centronuclear myopathy associated with cardiomyopathy. Br Heart J 1996; 38: 504–9
- Carpenter S., Karpati G. Pathology of Skeletal Muscle. Churchill Livingstone, New York 1984; 429–34
- Duran M., Mitchell G., De Klerk J. B., et al. Octanoic acidemia and octanoylcanitine excretion with dicarboxylic aciduria due to defective oxidation of medium chain fatty acids. J Pediatr 1985; 107: 397–404
- Bougneres P. F., Rocchiccioli F., Kolvraa S., et al. Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome. J Pediatr 1985; 106: 918–21
- Sugiyama S., Miyazaki Y., Kotaka K., Kato T., Suzuki S., Ozawa T. Mechanism of free fatty acid-induced arrhythmias. J Electrocardiol 1982; 15: 227–32
- Keppen L. D., Husain M. M., Woody R. C. X-linked myotubular myopathy: Intrafamilial variability and normal muscle biopsy in a heterozygous female. Clin Genet 1987; 32: 95–9