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43. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family. Camu W; Billiard M Muscle Nerve; 1993 May; 16(5):569-70. PubMed ID: 8515770 [No Abstract] [Full Text] [Related]
44. [Spinal amyotonia-amyotrophy (Werdnig-Hoffman disease) on the basis of observation of 40 cases]. Lesný I; Kocura P; Jirásek A; Krahulec B Cesk Neurol Neurochir; 1980 Jan; 43(1):26-31. PubMed ID: 7357655 [No Abstract] [Full Text] [Related]
45. [Werdnig-Hoffmann amyotrophy in a 7-month-old child]. Kutafin IuF; Osipov SM Pediatriia; 1990; (4):91-3. PubMed ID: 2371136 [No Abstract] [Full Text] [Related]
46. Morphological and morphometrical study of human muscle spindles in Werdnig-Hoffmann disease (infantile spinal muscular atrophy type I). Kararizou E; Manta P; Kalfakis N; Gkiatas K; Vassilopoulos D Acta Histochem; 2006; 108(4):265-9. PubMed ID: 16730053 [TBL] [Abstract][Full Text] [Related]
47. [Werdnig-Hoffmann's congenital spinal atrophy in nursing infants]. Kutafin IuF; Osipov SM; Osipov ES Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):15-8. PubMed ID: 1646528 [TBL] [Abstract][Full Text] [Related]
48. CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE. NORMAN RM; KAY JM Arch Dis Child; 1965 Jun; 40(211):302-8. PubMed ID: 14294750 [No Abstract] [Full Text] [Related]
49. [Changes in the motor apparatus of the bronchial cilia. Comparative study of two types of myopathies: nemaline myopathy and the Werdnig-Hoffmann syndrome]. Calì A; Berni Canani M; De Luca L; Terraciano L; Foggia L; Corradino G; Berni Canani R; Chiummariello S Pediatr Med Chir; 1991; 13(4):345-8. PubMed ID: 1754465 [TBL] [Abstract][Full Text] [Related]
51. Amyotonia congenita with pyloric stenosis. (A case report). VYAS KJ Indian J Child Health; 1962 Nov; 11():585-6. PubMed ID: 13998079 [No Abstract] [Full Text] [Related]
52. [Urinary amino acids in progressive muscular dystrophy and amyotonia congenita]. BAUZA C Arch Pediatr Urug; 1959 Dec; 30():749-55. PubMed ID: 13797772 [No Abstract] [Full Text] [Related]
53. Total intravenous anesthesia (TIVA) in an infant with Werdnig-Hoffmann disease. Case report. de Resende MA; da Silva EV; Nascimento OJ; Gemal AE; Quintanilha G; Vasconcelos EM Rev Bras Anestesiol; 2010; 60(2):170-5, 98-101. PubMed ID: 20485962 [TBL] [Abstract][Full Text] [Related]
54. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes. Stipoljev F; Sertić J; Latin V; Rukavina-Stavljenić A; Kurjak A Croat Med J; 1999 Sep; 40(3):433-7. PubMed ID: 10411975 [TBL] [Abstract][Full Text] [Related]
55. Epidemiological data on Werdnig-Hoffmann disease in Germany (West-Thüringen). Thieme A; Mitulla B; Schulze F; Spiegler AW Hum Genet; 1993 Apr; 91(3):295-7. PubMed ID: 8478016 [TBL] [Abstract][Full Text] [Related]
56. [Werdnig-Hoffmann disease type I with progressive ophthalmoplegia and ptosis]. Ohkura M; Mitsudome A; Yasumoto S; Ogawa A No To Hattatsu; 1996 Jul; 28(4):332-5. PubMed ID: 8753133 [TBL] [Abstract][Full Text] [Related]
57. [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]
58. Human leg neuromuscular diseases: P-31 MR spectroscopy. Bárány M; Siegel IM; Venkatasubramanian PN; Mok E; Wilbur AC Radiology; 1989 Aug; 172(2):503-8. PubMed ID: 2748832 [TBL] [Abstract][Full Text] [Related]
59. [Case of amyotonia congenita]. MARTINELLI P Lattante; 1953 Jan; 24(1):26-45. PubMed ID: 13053799 [No Abstract] [Full Text] [Related]
60. Early diaphragmatic paralysis. In infants with genetic disorders. Sivan Y; Galvis A Clin Pediatr (Phila); 1990 Mar; 29(3):169-71. PubMed ID: 2407409 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]