These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
97 related articles for article (PubMed ID: 3770735)
1. Morphologic and morphometric analysis of muscle in X-linked myotubular myopathy. Silver MM; Gilbert JJ; Stewart S; Brabyn D; Jung J Hum Pathol; 1986 Nov; 17(11):1167-78. PubMed ID: 3770735 [TBL] [Abstract][Full Text] [Related]
2. X-linked neonatal myotubular myopathy. Giacoia GP; Hale JE South Med J; 1984 Sep; 77(9):1182-5. PubMed ID: 6484690 [TBL] [Abstract][Full Text] [Related]
3. "Myotubular Myopathy" and "type I fiber atrophy" in a family. Kinoshita M; Satoyoshi E; Matsuo N J Neurol Sci; 1975 Dec; 26(4):575-82. PubMed ID: 1206433 [TBL] [Abstract][Full Text] [Related]
5. Familial centronuclear myopathy: a clinical and pathological study. Reske-Nielsen E; Hein-Sørensen O; Vorre P Acta Neurol Scand; 1987 Aug; 76(2):115-22. PubMed ID: 3673497 [TBL] [Abstract][Full Text] [Related]
6. Neonatal myotubular myopathy with respiratory distress: report of a case. Hung FC; Huang SC; Jong YJ J Formos Med Assoc; 1991 Sep; 90(9):844-7. PubMed ID: 1683384 [TBL] [Abstract][Full Text] [Related]
7. X-linked myotubular myopathy: intrafamilial variability and normal muscle biopsy in a heterozygous female. Keppen LD; Husain MM; Woody RC Clin Genet; 1987 Aug; 32(2):95-9. PubMed ID: 3652496 [TBL] [Abstract][Full Text] [Related]
8. Myotubular (centronuclear) (neuro-)myopathy. I. Clinical, genetical and morphological studies. Radu H; Killyen I; Ionescu V; Radu A Eur Neurol; 1977; 15(5):285-300. PubMed ID: 913442 [TBL] [Abstract][Full Text] [Related]
9. X-linked myotubular myopathy: clinical and pathological findings in a family. Oldfors A; Kyllerman M; Wahlström J; Darnfors C; Henriksson KG Clin Genet; 1989 Jul; 36(1):5-14. PubMed ID: 2670345 [TBL] [Abstract][Full Text] [Related]
10. [3 examples of fetal genetic neuromuscular disorders which lead to hydramnion]. Teeuw AH; Barth PG; van Sonderen L; Zondervan HA Ned Tijdschr Geneeskd; 1993 May; 137(18):908-13. PubMed ID: 8492834 [TBL] [Abstract][Full Text] [Related]
11. Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothers. Marbini A; Gemignani F; Saccardi F; Rimoldi M J Neurol; 1989 Oct; 236(7):418-20. PubMed ID: 2809644 [TBL] [Abstract][Full Text] [Related]
12. Diagnostic value of the muscle biopsy in the neonatal period. Sarnat HB Am J Dis Child; 1978 Aug; 132(8):782-5. PubMed ID: 685892 [TBL] [Abstract][Full Text] [Related]
13. [Perinatal form of myotubular myopathy in the differential diagnosis of early childhood neuromuscular diseases]. Reitter B; Stolzis L; Schmitt HP; Scheffner D Monatsschr Kinderheilkd (1902); 1977 May; 125(5):498-500. PubMed ID: 876218 [No Abstract] [Full Text] [Related]
14. X-linked recessive myotubular myopathy: I. Clinical and pathologic findings in a family. Ambler MW; Neave C; Tutschka BG; Pueschel SM; Orson JM; Singer DB Hum Pathol; 1984 Jun; 15(6):566-74. PubMed ID: 6539297 [TBL] [Abstract][Full Text] [Related]
15. Abundant minute myotubes in a patient who later developed centronuclear myopathy. Wöckel L; Ketelsen UP; Stötter M; Laule S; Meyermann R; Bornemann A Acta Neuropathol; 1998 May; 95(5):547-51. PubMed ID: 9600602 [TBL] [Abstract][Full Text] [Related]
17. Perinatal diagnosis of myotubular (centronuclear) myopathy: a case report. Collins JE; Collins A; Radford MR; Weller RO Clin Neuropathol; 1983; 2(2):79-82. PubMed ID: 6851300 [TBL] [Abstract][Full Text] [Related]
18. X-linked myotubular myopathy: a case report of prenatal and perinatal aspects. Tyson RW; Ringel SP; Manchester DK; Shikes RH; Goodman SI Pediatr Pathol; 1992; 12(4):535-43. PubMed ID: 1409152 [TBL] [Abstract][Full Text] [Related]
19. Muscle fiber hypotrophy with intact neuromuscular junctions. A study of a patient with congenital neuromuscular disease and ophthalmoplegia. Bender AN; Bender MB Neurology; 1977 Mar; 27(3):206-12. PubMed ID: 557754 [TBL] [Abstract][Full Text] [Related]