155 related articles for article (PubMed ID: 35430109)
1. Ramsay Hunt syndrome: New impressions in the era of molecular genetics.
Teive HAG; Cassou E; Coutinho L; Camargo CHF; Munhoz RP
Parkinsonism Relat Disord; 2022 Apr; 97():101-104. PubMed ID: 35430109
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Dyssynergia cerebellaris myoclonica (Ramsay-Hunt syndrome)].
IONESESCU V; CHELCHIANU G; VOICU A
Rev Sci Med; 1962; 7():153-5. PubMed ID: 13956639
[No Abstract] [Full Text] [Related]
5. A biography of James Ramsay Hunt (1874-1937).
Louis ED; Williams M
J Hist Neurosci; 2003 Sep; 12(3):266-75. PubMed ID: 14628542
[TBL] [Abstract][Full Text] [Related]
6. PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotype.
Visser JE; Bloem BR; van de Warrenburg BP
Mov Disord; 2007 May; 22(7):1024-6. PubMed ID: 17343273
[TBL] [Abstract][Full Text] [Related]
7. [Myoclonic cerebellar dyssynergia (Ramsay Hunt). Description of 2 cases].
Fryze C; Korwin-Piotrowska T; Potemkowski A; Niezabitowski K
Neurol Neurochir Pol; 1985; 19(6):508-11. PubMed ID: 3835491
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.
Bird TD; Shaw CM
J Neurol Neurosurg Psychiatry; 1978 Feb; 41(2):140-9. PubMed ID: 632821
[TBL] [Abstract][Full Text] [Related]
11. [Action myoclonus in Ramsay Hunt myoclonic cerebellar dyssynergyand in Lance-Adams syndrome].
Tassinari CA; Roger J; Regis H; Sedan R; Lyagoubi S; Gambarelli F; Vallicioni P; Dravet C; Soulayrol R
Rev Neurol (Paris); 1970 Nov; 123(5):335-6. PubMed ID: 5513635
[No Abstract] [Full Text] [Related]
12. Herpes zoster oticus (Ramsay Hunt's syndrome) comments on an article by Johnson and Zonderman.
TSCHIASSNY K
Arch Otolaryngol (1925); 1950 Jan; 51(1):73-82, illust. PubMed ID: 15408839
[No Abstract] [Full Text] [Related]
13. 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]
14. [Progressive myoclonus epilepsy in two siblings and 5 cases with dyssynergia cerebellaris myoclonica in several generations of a kinship, a clinical and genetic study].
Diebold K; Kastner M; Penin H
Nervenarzt; 1974 Nov; 45(11):595-601. PubMed ID: 4217888
[No Abstract] [Full Text] [Related]
15. Ramsay Hunt's syndrome.
MELANT JH
N Y State J Med; 1949 Mar; 49(5):531. PubMed ID: 18111011
[No Abstract] [Full Text] [Related]
16. Symptomatic myoclonus.
Borg M
Neurophysiol Clin; 2006; 36(5-6):309-18. PubMed ID: 17336775
[TBL] [Abstract][Full Text] [Related]
17. [Ramsay-Hunt syndrome and aniridia in 2 monozygotic twins].
Chazot G; Guard O; Setiey A; Robert JM; Schott B
Rev Neurol (Paris); 1975 Jan; 131(1):43-8. PubMed ID: 1080872
[No Abstract] [Full Text] [Related]
18. Progressive myoclonus without epilepsy due to a NUS1 frameshift insertion: Dyssynergia cerebellaris myoclonica revisited.
Monfrini E; Miller C; Frucht SJ; Di Fonzo A; Riboldi GM
Parkinsonism Relat Disord; 2022 May; 98():53-55. PubMed ID: 35472621
[No Abstract] [Full Text] [Related]
19. [Familial olivo-ponto-cerebellar atrophy with myoclonus. Limits of cerebellar myoclonic dyssynergia (Ramsay-Hunt syndrome)].
Bonduelle M; Escourolle R; Bouygues P; Lormeau G; Gray F
Rev Neurol (Paris); 1976 Feb; 132(2):113-24. PubMed ID: 973068
[TBL] [Abstract][Full Text] [Related]
20. [Electroencephalographic study of myoclonic cerebellar dyssynergia with epilepsy (Ramsay-Hunt syndrome)].
Tassinari CA; Bureau-Paillas M; Grasso E; Roger J
Rev Electroencephalogr Neurophysiol Clin; 1974; 4(3):407-28. PubMed ID: 4470962
[No Abstract] [Full Text] [Related]
[Next] [New Search]
