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27. [Intermediate forms of infantile spinal amyotrophy. Apropos of 20 personal observations]. Pou-Serradell A; Montserrat L; Ugarte A Rev Neurol (Paris); 1978 Jan; 134(1):35-44. PubMed ID: 674984 [TBL] [Abstract][Full Text] [Related]
28. A study of infantile motor neuron disease with neurofilament and ubiquitin immunocytochemistry. Lee S; Park YD; Yen SH; Ksiezak-Reding H; Goldman JE; Dickson DW Neuropediatrics; 1989 May; 20(2):107-11. PubMed ID: 2544822 [TBL] [Abstract][Full Text] [Related]
29. [Amyotonia and amyotrophy with severe retardation. Diagnostic uncertainties]. Kohler C; Nivelon JL; Planson C; Chalamel MJ Rev Neuropsychiatr Infant; 1970; 18(4):393-9. PubMed ID: 5421582 [No Abstract] [Full Text] [Related]
31. [Usefulness of ECG in the early diagnosis of infantile spinal muscular dystrophy]. Carboni P; Porro G Minerva Pediatr; 1988 Jun; 40(6):321-5. PubMed ID: 3185431 [No Abstract] [Full Text] [Related]
32. [Findings on a case of progressive muscular atrophy of spinal origin]. TEIXEIRA O; BLASI R Pediatr Prat; 1958 Mar; 29(3):65-76. PubMed ID: 13566897 [No Abstract] [Full Text] [Related]
33. Compound heterozygous mutation in two unrelated cases of Chinese spinal muscular atrophy patients. Qu YJ; Song F; Yang YL; Jin YW; Bai JL Chin Med J (Engl); 2011 Feb; 124(3):385-9. PubMed ID: 21362338 [TBL] [Abstract][Full Text] [Related]
34. [Torticollis ex amyotonia congenita]. DEZYNA M Chir Narzadow Ruchu Ortop Pol; 1957; 22(1):49-51. PubMed ID: 13473007 [No Abstract] [Full Text] [Related]
36. Value of immunohistochemical investigation in the diagnosis of neuromuscular diseases in children. Matei D; Gherghina I; Cinteză E; Matei A; Alexianu M Rom J Morphol Embryol; 2011; 52(1):111-5. PubMed ID: 21424041 [TBL] [Abstract][Full Text] [Related]
37. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease]. Priora U; Quaglia P; Vivalda M; Giachino-Amistà MT; Domeneghetti G; Sardi R Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861 [No Abstract] [Full Text] [Related]
38. Spinal muscular atrophy with respiratory distress type 1 (SMARD1). Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757 [TBL] [Abstract][Full Text] [Related]
39. [Clinical and genetic study of a family with progressive neuropathic muscular atrophy (Charcot-Marie amyotrophy)]. STARK P J Genet Hum; 1958 Jul; 7(1-2):1-32. PubMed ID: 13575796 [No Abstract] [Full Text] [Related]
40. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]