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7. Spinal muscular atrophy with progressive myoclonic epilepsy linked to mutations in ASAH1. Yildiz EP; Yesil G; Bektas G; Caliskan M; Tatlı B; Aydinli N; Ozmen M Clin Neurol Neurosurg; 2018 Jan; 164():47-49. PubMed ID: 29169047 [TBL] [Abstract][Full Text] [Related]
8. Prospective analysis of strength in spinal muscular atrophy. DCN/Spinal Muscular Atrophy Group. Iannaccone ST; Russman BS; Browne RH; Buncher CR; White M; Samaha FJ J Child Neurol; 2000 Feb; 15(2):97-101. PubMed ID: 10695894 [TBL] [Abstract][Full Text] [Related]
9. [A congenital form of progressive spinal muscular atrophy of the Werdnig-Hoffman type]. HOFMAN H; KOWALCZYK Z; ZELMAN I Pol Tyg Lek; 1962 Nov; 17():1761-3. PubMed ID: 13963967 [No Abstract] [Full Text] [Related]
10. Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells. Oates EC; Reddel S; Rodriguez ML; Gandolfo LC; Bahlo M; Hawke SH; Lamandé SR; Clarke NF; North KN Brain; 2012 Jun; 135(Pt 6):1714-23. PubMed ID: 22628388 [TBL] [Abstract][Full Text] [Related]
11. [Spinal muscular atrophy with open bite: A case report]. Zheng W; Lin J Hua Xi Kou Qiang Yi Xue Za Zhi; 2013 Jun; 31(3):315-6. PubMed ID: 23841309 [TBL] [Abstract][Full Text] [Related]
12. [Study of the clinical aspects of infantile spinal progressive muscular atrophy of the Werdnig-Hoffman type]. SCHMID PC Z Kinderheilkd; 1958; 81(1):13-25. PubMed ID: 13604538 [No Abstract] [Full Text] [Related]
13. Neurofibromatosis 1 associated with spinal muscular atrophy. Coutinho Dos Santos LH; Scola RH; Rosário NA; Munhoz da Rocha LE; Bruck I Pediatr Neurol; 2009 Feb; 40(2):117-9. PubMed ID: 19135626 [TBL] [Abstract][Full Text] [Related]
15. [A case of progressive bulbar paralysis in a child (Fazio-Londe disease)]. Drozdowski W; Czerwińska-Ciechan K; Jankowicz E; Smigielska J Neurol Neurochir Pol; 1992; 26(5):723-8. PubMed ID: 1291912 [TBL] [Abstract][Full Text] [Related]
16. [Acute respiratory insufficiency as the initial clinical manifestation of spinal muscular atrophy]. Poets C; Heyer R; von der Hardt H; Walter GF Monatsschr Kinderheilkd; 1990 Mar; 138(3):157-9. PubMed ID: 2352537 [TBL] [Abstract][Full Text] [Related]
17. A sporadic case of bulbospinal muscular atrophy of late onset. Takayama H; Ichiki K; Oishi T; Suga Y; Kuroda S; Ogawa N J Med; 1991; 22(2):123-30. PubMed ID: 1895014 [TBL] [Abstract][Full Text] [Related]
18. [Heart involvement in progressive spinal muscular atrophy. A review of the literature and case histories in childhood]. Distefano G; Sciacca P; Parisi MG; Parano E; Smilari P; Marletta M; Fiumara A Pediatr Med Chir; 1994; 16(2):125-8. PubMed ID: 8078785 [TBL] [Abstract][Full Text] [Related]
19. Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsy. Gan JJ; Garcia V; Tian J; Tagliati M; Parisi JE; Chung JM; Lewis R; Baloh R; Levade T; Pierson TM Neuromuscul Disord; 2015 Dec; 25(12):959-63. PubMed ID: 26526000 [TBL] [Abstract][Full Text] [Related]
20. Consensus statement for standard of care in spinal muscular atrophy. Wang CH; Finkel RS; Bertini ES; Schroth M; Simonds A; Wong B; Aloysius A; Morrison L; Main M; Crawford TO; Trela A; J Child Neurol; 2007 Aug; 22(8):1027-49. PubMed ID: 17761659 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]