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Journal Abstract Search
85 related items for PubMed ID: 4102462
41. Ataxia-telangiectasia, an evolving phenotype. Chun HH, Gatti RA. DNA Repair (Amst); 2004; 3(8-9):1187-96. PubMed ID: 15279807 [Abstract] [Full Text] [Related]
43. [Friedreich ataxia--diagnosis after a decade. Differential diagnosis of inherited spinocerebellar ataxias]. Vitaszil E, Jelencsik I, Szirmai I. Ideggyogy Sz; 2002 Nov 20; 55(11-12):382-93. PubMed ID: 12632799 [Abstract] [Full Text] [Related]
45. [Hereditary spino-cerebellar degeneration and cardiopathy]. GIRAUD G, LATOUR H, PUECH P, LEVY A, ROUJON J, DERMENGHEM. Montp Med; 1956 Dec 20; 50(4):552-9. PubMed ID: 13418683 [No Abstract] [Full Text] [Related]
46. [On a case of polyneuritic ataxic hereditary disease. Refsum disease]. VELTEMA AN, VERJAAL A. Rev Prat; 1961 Jan 20; 104():15-23. PubMed ID: 13780681 [No Abstract] [Full Text] [Related]
47. Hartnup disease. BORRIE PF, LEWIS CA. Proc R Soc Med; 1962 Mar 20; 55(3):231-2. PubMed ID: 13871450 [No Abstract] [Full Text] [Related]
52. Heredopathia atactica polyneuritiformis. REFSUM S. J Nerv Ment Dis; 1952 Dec 20; 116(6):1046-50. PubMed ID: 13045168 [No Abstract] [Full Text] [Related]
53. [Forms of heredo-ataxia of children and adolescents with severe involvement of the spinobulbomesencephalic motor nuclei]. van BOGAERT L. Rev Neurol (Paris); 1951 Feb 20; 84(2):121-30. PubMed ID: 14845378 [No Abstract] [Full Text] [Related]
54. A Rare Case of Ophthalmoplegia with Ataxia in Genetically Proven Abetalipoproteinemia. Gurram S, Holla VV, Sriram N, Phulpagar P, Jha S, Sharma P, Mallithavana S, Kamble N, Netravathi M, Yadav R, Muthusamy B, Pal PK. Mov Disord Clin Pract; 2023 Mar 20; 10(3):514-517. PubMed ID: 36949797 [No Abstract] [Full Text] [Related]
59. The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias. Di Donato S, Gellera C, Mariotti C. Neurol Sci; 2001 Jun 08; 22(3):219-28. PubMed ID: 11731874 [Abstract] [Full Text] [Related]