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Journal Abstract Search
144 related items for PubMed ID: 3556183
21. [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]
23. The heart in Friedreich ataxia: definition of cardiomyopathy, disease severity, and correlation with neurological symptoms. Weidemann F, Rummey C, Bijnens B, Störk S, Jasaityte R, Dhooge J, Baltabaeva A, Sutherland G, Schulz JB, Meier T, Mitochondrial Protection with Idebenone in Cardiac or Neurological Outcome (MICONOS) study group. Circulation; 2012 Apr 03; 125(13):1626-34. PubMed ID: 22379112 [Abstract] [Full Text] [Related]
24. SKIN REACTION IN CHILDREN AND ADULTS WITH CENTRAL NERVOUS SYSTEM DISEASE AFTER INTRACUTANEOUS ADMINISTRATION OF MYELIN PREPARATIONS DERIVED FROM HUMAN BRAIN. BOEHME D, PAAL G, KERSTEN W, KERSTEN H. Nature; 1963 Jul 06; 199():84-5. PubMed ID: 14054526 [No Abstract] [Full Text] [Related]
25. [Paraneoplastic polyneuromyopathy]. Rasenack U. Med Klin; 1975 Dec 19; 70(51-52):2066-8. PubMed ID: 178986 [No Abstract] [Full Text] [Related]
26. Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome. Brust JC, Lovelace RE, Devi S. Acta Neurol Scand Suppl; 1978 Dec 19; 68():1-142. PubMed ID: 212921 [No Abstract] [Full Text] [Related]
27. Cardiac rhabdomyomata as a marker for the antenatal detection of tuberous sclerosis. Crawford DC, Garrett C, Tynan M, Neville BG, Allan LD. J Med Genet; 1983 Aug 19; 20(4):303-4. PubMed ID: 6620331 [Abstract] [Full Text] [Related]
28. Animal model of human disease: Werdnig-Hoffmann disease (infantile spinal muscular atrophy). Leestma JE. Am J Pathol; 1980 Sep 19; 100(3):821-4. PubMed ID: 7416238 [No Abstract] [Full Text] [Related]
30. Patterns of neurologic diseases on guam. Chen KM, Brody JA, Kurland LT. Arch Neurol; 1968 Dec 19; 19(6):573-8. PubMed ID: 4973215 [No Abstract] [Full Text] [Related]
31. An overview of neurological and neuromuscular signs in mitochondrial diseases. Chaussenot A, Paquis-Flucklinger V. Rev Neurol (Paris); 2014 May 19; 170(5):323-38. PubMed ID: 24792434 [Abstract] [Full Text] [Related]
32. A syndrome resembling Friedreich's ataxia with relapsing polyneuropathy and hyperalaninemia. Dunn HG, Perry TL, Dolman CL. Neurology; 1968 Mar 19; 18(3):301. PubMed ID: 5690400 [No Abstract] [Full Text] [Related]
33. Vitamin E deficiency in Werdnig-Hoffmann disease. Shapira Y, Amit R, Rachmilewitz E. Ann Neurol; 1981 Sep 19; 10(3):266-8. PubMed ID: 7294734 [Abstract] [Full Text] [Related]
34. Radiological patterns of obstructive cardiomyopathy of the left ventricle in childhood. Pernot C, Hoeffel JC, Henry M, Worms AM, Rothhahn G. Am Heart J; 1973 Oct 19; 86(4):462-6. PubMed ID: 4125568 [No Abstract] [Full Text] [Related]
35. [Syndrome of myatrophic ataxia]. Lange E, Kulawik H, Kunath B. Psychiatr Neurol Med Psychol (Leipz); 1972 Apr 19; 24(4):177-88. PubMed ID: 5050809 [No Abstract] [Full Text] [Related]
36. [Hydrocephalus and hypsarhythmia]. Canubi A, Taccone F. Clin Pediatr (Bologna); 1966 Jun 19; 48(6):237-47. PubMed ID: 4865919 [No Abstract] [Full Text] [Related]
37. The neurocutaneous syndromes: diagnosis and management for the primary care pediatrician. McIntosh C, Dehkharghani F. J Ark Med Soc; 1984 Dec 19; 81(7):354-60. PubMed ID: 6240482 [No Abstract] [Full Text] [Related]
38. [Clinical study of muscular atrophy]. Shinoda M. Hokkaido Igaku Zasshi; 1974 Jan 19; 49(1):23-31. PubMed ID: 4376121 [No Abstract] [Full Text] [Related]
39. Pediatric neurology. Erenberg G, Golden GS, Rapin I, French JH, Spiro AJ, Rose AL. Prog Neurol Psychiatry; 1971 Jan 19; 26():239-59. PubMed ID: 5164240 [No Abstract] [Full Text] [Related]
40. Clinical and genetic patterns of neurological diseases other than amyotrophic lateral sclerosis on Guam. Chen K, Brody JA, Kurland KT, Elizan TS. Neurology; 1970 Oct 19; 20(10):954-64. PubMed ID: 5273171 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]