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.
121 related articles for article (PubMed ID: 872842)
1. A progressive congenital myopathy. Initial involvement of the diaphragm with type I muscle fiber atrophy. De Reuck J; Hooft C; De Coster W; van den Bossche H; Cuvelier C Eur Neurol; 1977; 15(4):217-56. PubMed ID: 872842 [TBL] [Abstract][Full Text] [Related]
2. Diaphragm paralysis and ventilatory failure in chronic proximal spinal muscular atrophy. Haas H; Johnson LR; Gill TH; Armentrout TS Am Rev Respir Dis; 1981 Apr; 123(4 Pt 1):465-7. PubMed ID: 7224359 [TBL] [Abstract][Full Text] [Related]
3. Congenital non-progressive myopathy with type II fibre atrophy and internal nuclei. Scelsi R; Lanzi G; Nespoli L; Poggi P Eur Neurol; 1976; 14(4):285-93. PubMed ID: 954775 [TBL] [Abstract][Full Text] [Related]
4. Congenital myopathy with type II muscle fiber hypoplasia. Yoshioka M; Kuroki S; Ohkura K; Itagaki Y; Saida K Neurology; 1987 May; 37(5):860-3. PubMed ID: 3574691 [TBL] [Abstract][Full Text] [Related]
5. Pathologic quiz case: Male infant with generalized hypotonia and absence of respirations at birth, Kelly NA; Thomas C Arch Pathol Lab Med; 2001 Apr; 125(4):575-6. PubMed ID: 11260644 [No Abstract] [Full Text] [Related]
6. Diaphragmatic paralysis due to spinal muscular atrophy. An unrecognised cause of respiratory failure in infancy? McWilliam RC; Gardner-Medwin D; Doyle D; Stephenson JB Arch Dis Child; 1985 Feb; 60(2):145-9. PubMed ID: 3977387 [TBL] [Abstract][Full Text] [Related]
7. Diaphragmatic paralysis due to partial diaphragmatic hypoplasia mimicking a localized muscular dystrophy: a case report. Bosman C; Bachelet V; Boldrini R; Bertini E Clin Neuropathol; 1988; 7(1):33-8. PubMed ID: 3286072 [TBL] [Abstract][Full Text] [Related]
9. Isolated myopathic involvement of the diaphragmatic musculature in a neonate. Bergen BJ; Sangalang VE; Aterman K Ann Neurol; 1977 Apr; 1(4):403-7. PubMed ID: 617257 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Neonatal hypotonias with congenital disproportion of various types of muscular fiber, especially type I fibers. Demonstration of the familial character of this new entity]. Fardeau M; Harpey JP; Caille B; Lafourcade J Arch Fr Pediatr; 1975 Dec; 32(10):901-13. PubMed ID: 1231675 [TBL] [Abstract][Full Text] [Related]
12. [A case of congenital myopathy with type 2 fiber hypotrophy]. Touge T; Nasu Y; Yamada A; Miki H; Takeuchi H Rinsho Shinkeigaku; 1988 Feb; 28(2):147-50. PubMed ID: 3409612 [No Abstract] [Full Text] [Related]
13. Neonatal spinal muscular atrophy presenting as respiratory distress: a clinical variant. Schapira D; Swash M Muscle Nerve; 1985 Oct; 8(8):661-3. PubMed ID: 4058474 [TBL] [Abstract][Full Text] [Related]
14. A fatal congenital myopathy with severe type I fibre atrophy, central nuclei and multicores. Lee YS; Yip WC J Neurol Sci; 1981 May; 50(2):277-90. PubMed ID: 7229670 [TBL] [Abstract][Full Text] [Related]
15. Nemaline (rod) myopathy: a possible cause of rapidly fatal infantile hypotonia. Gillies C; Raye J; Vasan U; Hart WE; Goldblatt PJ Arch Pathol Lab Med; 1979 Jan; 103(1):1-5. PubMed ID: 581546 [TBL] [Abstract][Full Text] [Related]
16. Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration. Sugie H; Hanson R; Rasmussen G; Verity MA J Neurol Neurosurg Psychiatry; 1982 Jun; 45(6):507-12. PubMed ID: 7119813 [TBL] [Abstract][Full Text] [Related]