60 related articles for article (PubMed ID: 2121121)
1. ILAE Genetics Literacy series: Progressive myoclonus epilepsies.
Cameron JM; Ellis CA; Berkovic SF; ;
Epileptic Disord; 2023 Oct; 25(5):670-680. PubMed ID: 37616028
[TBL] [Abstract][Full Text] [Related]
2. The natural history of progressive myoclonus ataxia.
van der Veen S; Eggink H; Elting JWJ; Sival D; Verschuuren-Bemelmans CC; de Koning TJ; Tijssen MAJ
Neurobiol Dis; 2024 Jun; 199():106555. PubMed ID: 38844245
[TBL] [Abstract][Full Text] [Related]
3. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia.
Godeiro Junior CO; Vale TC; Afonso COM; Kok F; Pedroso JL; Barsottini OG
Mov Disord Clin Pract; 2018; 5(3):330-332. PubMed ID: 30800706
[No Abstract] [Full Text] [Related]
4. The Nosologic Term "Conversive" Disorder Should Be Abandoned.
Lizarazo DA; Guarnizo A
AJNR Am J Neuroradiol; 2022 Aug; 43(8):E17. PubMed ID: 35863778
[No Abstract] [Full Text] [Related]
5. Ramsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation.
van Egmond ME; Verschuuren-Bemelmans CC; Nibbeling EA; Elting JW; Sival DA; Brouwer OF; de Vries JJ; Kremer HP; Sinke RJ; Tijssen MA; de Koning TJ
Mov Disord; 2014 Jan; 29(1):139-43. PubMed ID: 24458321
[TBL] [Abstract][Full Text] [Related]
6. Progressive myoclonus ataxia: Time for a new definition?
van der Veen S; Zutt R; Elting JWJ; Becker CE; de Koning TJ; Tijssen MAJ
Mov Disord; 2018 Aug; 33(8):1281-1286. PubMed ID: 30145808
[TBL] [Abstract][Full Text] [Related]
7. Movement Disorders Related to Gluten Sensitivity: A Systematic Review.
Vinagre-Aragón A; Zis P; Grunewald RA; Hadjivassiliou M
Nutrients; 2018 Aug; 10(8):. PubMed ID: 30096784
[TBL] [Abstract][Full Text] [Related]
8. The man who walks backwards.
Brown AR; Peet M
J R Soc Med; 2002 Mar; 95(3):137. PubMed ID: 11872766
[No Abstract] [Full Text] [Related]
9. Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNA(Lys)(8344) (MERRF) mutation.
Thompson PD; Hammans SR; Harding AE
J Neurol; 1994 Mar; 241(5):335-40. PubMed ID: 8006688
[TBL] [Abstract][Full Text] [Related]
10. Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome).
Vaamonde J; Muruzabal J; Tuñón T; Perez N; Artieda J; Rodriguez M; Obeso JA
J Neurol Neurosurg Psychiatry; 1992 Feb; 55(2):128-32. PubMed ID: 1538218
[TBL] [Abstract][Full Text] [Related]
11. Progressive myoclonic ataxia without ragged red fibres: Unverricht-Lundborg disease vs Ramsay Hunt syndrome.
Shakir RA; Khan RA; al-Zuhair AG
Acta Neurol Scand; 1992 Nov; 86(5):470-3. PubMed ID: 1336290
[TBL] [Abstract][Full Text] [Related]
12. The Ramsay Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalomyopathy with ragged-red fibers and Baltic myoclonus.
Genton P; Michelucci R; Tassinari CA; Roger J
Acta Neurol Scand; 1990 Jan; 81(1):8-15. PubMed ID: 2109922
[TBL] [Abstract][Full Text] [Related]
13. Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Harding AE
Mov Disord; 1989; 4(1):18-9. PubMed ID: 2494437
[No Abstract] [Full Text] [Related]
14. Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.
Guazzi GC; Federico A
Acta Neurol (Napoli); 1992; 14(4-6):469-84. PubMed ID: 1293989
[TBL] [Abstract][Full Text] [Related]
15. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
Lance JW
Adv Neurol; 1986; 43():33-55. PubMed ID: 3080851
[TBL] [Abstract][Full Text] [Related]
16. Progressive myoclonic ataxia (the Ramsay Hunt syndrome).
Marsden CD; Harding AE; Obeso JA; Lu CS
Arch Neurol; 1990 Oct; 47(10):1121-5. PubMed ID: 2121121
[TBL] [Abstract][Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]