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22. The intelligence of patients with Friedreich's ataxia. DAVIES DL J Neurol Neurosurg Psychiatry; 1949 Feb; 12(1):34-8. PubMed ID: 18124004 [No Abstract] [Full Text] [Related]
23. Friedreich's ataxia (a familial herditary study of three cases). LIPSON HA; DeNARDI JM Dis Nerv Syst; 1946 Sep; 7():261-7. PubMed ID: 20995544 [No Abstract] [Full Text] [Related]
24. Clinical and genetic aspects of spinocerebellar degeneration. Durr A; Brice A Curr Opin Neurol; 2000 Aug; 13(4):407-13. PubMed ID: 10970057 [TBL] [Abstract][Full Text] [Related]
25. [Friedreich's ataxia with optic atrophy & imbecility involving selectively the boys in a family]. NAYRAC P; GRAUX P; FRANCOIS P; RABACHE R Rev Neurol (Paris); 1957 Oct; 97(4):295-307. PubMed ID: 13528368 [No Abstract] [Full Text] [Related]
26. [HEREDITARY CEREBELLAR ATAXIA IN 2 OUT OF 6 SIBLINGS]. SUGA M; KONO Y; NAGOSHI T; KUSUMOTO M Naika; 1963 Nov; 12():961-6. PubMed ID: 14096047 [No Abstract] [Full Text] [Related]
27. [Spinocerebellar hereditary degeneration (SCHD) associated with the Klinefelter syndrome]. INDEMINI M; AMMANN F Confin Neurol; 1963; 23():155-64. PubMed ID: 13956475 [No Abstract] [Full Text] [Related]
28. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia. Kumar D; Blank CE Indian Pediatr; 1989 Oct; 26(10):1014-9. PubMed ID: 2630444 [TBL] [Abstract][Full Text] [Related]
30. [A CASE OF FAMILIAL HEREDITARY CEREBELLAR ATAXIA WITH DYSTONIC HYPERKINESIA]. Neurol Neurochir Psychiatr Pol; 1963; 13():633-5. PubMed ID: 14091509 [No Abstract] [Full Text] [Related]
31. A Milestone in the Treatment of Ataxias: Approval of Omaveloxolone for Friedreich Ataxia. Subramony SH; Lynch DL Cerebellum; 2024 Apr; 23(2):775-777. PubMed ID: 37219716 [TBL] [Abstract][Full Text] [Related]
35. [Magnetic resonance imaging in spinocerebellar degenerative diseases (apropos of 8 cases)]. Nicolau A; Diard F; Fontan D; Chateil JF; Kien P Pediatrie; 1987; 42(5):359-65. PubMed ID: 3481070 [TBL] [Abstract][Full Text] [Related]
36. [Study of taurine levels in the blood and urine of patients with hereditary spinocerebellar degeneration]. Magalov ShI; Arzumanova KG Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):16-20. PubMed ID: 2163160 [TBL] [Abstract][Full Text] [Related]
37. [Clinical and genetic study of a new family of hereditary Friedreich ataxia]. PFAENDLER U Schweiz Med Wochenschr; 1947 Mar; 77(12):350. PubMed ID: 20296850 [No Abstract] [Full Text] [Related]
38. [New insights in the molecular genetics and pathophysiology of hereditary ataxias]. Bürk K; Klockgether T; Dichgans J Nervenarzt; 1999 Jun; 70(6):491-5. PubMed ID: 10412692 [TBL] [Abstract][Full Text] [Related]
39. [Hereditary ataxia-problems in the classification, genetics and genetic counseling]. Bachmann H; Lössner J Z Gesamte Inn Med; 1981 Jun; 36(11):387-93. PubMed ID: 7303765 [TBL] [Abstract][Full Text] [Related]
40. Tabes of Friedreich with degeneration of the substantia nigra, a special type of hereditary parkinsonism. BIEMOND A; SINNEGE JL Confin Neurol; 1955; 15(3):129-42. PubMed ID: 13261552 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]