143 related articles for article (PubMed ID: 4434656)
1. Adult-onset hereditary cerebellar ataxia and neurosensory deafness.
Schimke RN
Clin Genet; 1974; 6(5):416-21. PubMed ID: 4434656
[No Abstract] [Full Text] [Related]
2. Cataract, deafness, cerebellar ataxia, psychosis and dementia--a new syndrome.
Strömgren E; Dalby A; Dalby MA; Ranheim B
Acta Neurol Scand; 1970; 46(S43):261-2. PubMed ID: 5457846
[No Abstract] [Full Text] [Related]
3. Clinical presentation of rapidly progressive familial Danish dementia.
Zhou Z; Ainger TJ; Han DY
Neurocase; 2018; 24(5-6):287-289. PubMed ID: 30843473
[TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.
Baraitser M; Gooddy W; Halliday AM; Harding AE; Rudge P; Scaravilli F
J Neurol Neurosurg Psychiatry; 1984 Jan; 47(1):21-5. PubMed ID: 6319613
[TBL] [Abstract][Full Text] [Related]
5. [Recessive hereditary ataxia with early onset. Clinical study of 27 cases].
Serlenga L; Trizio M; Pozio G; Oteri G; Caldarazzo M
Riv Neurol; 1987; 57(5):285-9. PubMed ID: 3445070
[TBL] [Abstract][Full Text] [Related]
6. Spino-cerebellar ataxia in Western Norway.
Skre H
Clin Genet; 1974; 6(4):265-88. PubMed ID: 4442232
[No Abstract] [Full Text] [Related]
7. First case of autosomal dominant cerebellar ataxia with deafness and narcolepsy (ADCA-DN) with confirmed DMNT1 gene mutation in Spain. Review of the DMNT1 mutation syndromes.
de Miguel-Sanchez CJ; Gomez-Roldós A; Leal-Hidalgo R; Lafuente-Gómez G; Estrada-Huesa D; Bravo-Quelle N; González-Sánchez M
Neurol Sci; 2024 Feb; 45(2):791-793. PubMed ID: 37828385
[No Abstract] [Full Text] [Related]
8. Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy.
Melo TP; Ferro JM
J Neurol Neurosurg Psychiatry; 1989 Dec; 52(12):1448-9. PubMed ID: 2614456
[No Abstract] [Full Text] [Related]
9. Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease.
May DL; White HH
Arch Neurol; 1968 Sep; 19(3):331-8. PubMed ID: 5698045
[No Abstract] [Full Text] [Related]
10. Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1.
Moghadam KK; Pizza F; Tonon C; Lodi R; Carelli V; Poli F; Franceschini C; Barboni P; Seri M; Ferrari S; La Morgia C; Testa C; Cornelio F; Liguori R; Winkelmann J; Lin L; Mignot E; Plazzi G
Sleep Med; 2014 May; 15(5):582-5. PubMed ID: 24709307
[TBL] [Abstract][Full Text] [Related]
11. Cerebellar ataxia and total albinism: a kindred suggesting pleitotropism or linkage.
Skre H; Berg K
Clin Genet; 1974; 5(3):196-204. PubMed ID: 4838888
[No Abstract] [Full Text] [Related]
12. A new form of familial ataxia, deafness, and mental retardation.
Reardon W; Wilson J; Cavanagh N; Baraitser M
J Med Genet; 1993 Aug; 30(8):694-5. PubMed ID: 8411058
[TBL] [Abstract][Full Text] [Related]
13. Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
Winkelmann J; Lin L; Schormair B; Kornum BR; Faraco J; Plazzi G; Melberg A; Cornelio F; Urban AE; Pizza F; Poli F; Grubert F; Wieland T; Graf E; Hallmayer J; Strom TM; Mignot E
Hum Mol Genet; 2012 May; 21(10):2205-10. PubMed ID: 22328086
[TBL] [Abstract][Full Text] [Related]
14. Observations in a family with dominant type of cerebellar ataxia.
Frey HJ; Frey ML; Riekkinen PJ; Tuomola H
Acta Neurol Scand Suppl; 1972; 51():247-8. PubMed ID: 4514343
[No Abstract] [Full Text] [Related]
15. Arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones.
Bhaskar PA; Jagannathan K; Valmikinathan K
J Neurol Neurosurg Psychiatry; 1974 Dec; 37(12):1299-1305. PubMed ID: 4448994
[TBL] [Abstract][Full Text] [Related]
16. A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families).
Wadia NH; Swami RK
Brain; 1971; 94(2):359-74. PubMed ID: 5571047
[No Abstract] [Full Text] [Related]
17. [Autosomal recessive cerebellar ataxias].
Tranchant C; Anheim M
Presse Med; 2009 Dec; 38(12):1852-9. PubMed ID: 19442480
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary cerebellar aataxia with spinal muscular atrophies].
Hopf HC; Duensing F; Lowitzsch K; Krönke R
Z Neurol; 1971; 199(4):344-52. PubMed ID: 4104837
[No Abstract] [Full Text] [Related]
19. Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis.
D'Arrigo S; Riva D; Bulgheroni S; Chiapparini L; Castellotti B; Gellera C; Pantaleoni C
J Child Neurol; 2008 Aug; 23(8):895-900. PubMed ID: 18403580
[TBL] [Abstract][Full Text] [Related]
20. Superficial siderosis associated with anterior horn cell dysfunction.
Turner B; Wills AJ
J Neurol Neurosurg Psychiatry; 2002 Feb; 72(2):274-5. PubMed ID: 11796786
[No Abstract] [Full Text] [Related]
[Next] [New Search]
