452 related articles for article (PubMed ID: 17258771)
1. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
Kobayashi S; Takuma H; Murayama S; Sakurai M; Kanazawa I
J Neurol Sci; 2007 Mar; 254(1-2):44-8. PubMed ID: 17258771
[TBL] [Abstract][Full Text] [Related]
2. Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family.
Sekijima Y; Ohara S; Nakagawa S; Tabata K; Yoshida K; Ishigame H; Shimizu Y; Yanagisawa N
J Neurol Sci; 1998 Jun; 158(1):30-7. PubMed ID: 9667774
[TBL] [Abstract][Full Text] [Related]
3. Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
Sanahuja J; Franco E; Rojas-García R; Gallardo E; Combarros O; Begué R; Granés P; Illa I
Arch Neurol; 2005 Dec; 62(12):1911-4. PubMed ID: 16344349
[TBL] [Abstract][Full Text] [Related]
4. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
Cricchi F; Di Lorenzo C; Grieco GS; Rengo C; Cardinale A; Racaniello M; Santorelli FM; Nappi G; Pierelli F; Casali C
J Neurol Sci; 2007 Mar; 254(1-2):69-71. PubMed ID: 17292920
[TBL] [Abstract][Full Text] [Related]
5. Pseudodominant inheritance of spastic ataxia of Charlevoix-Saguenay.
Terracciano A; Foulds NC; Ditchfield A; Bunyan DJ; Crolla JA; Huang S; Santorelli FM; Hammans SR
Neurology; 2010 Apr; 74(14):1152-4. PubMed ID: 20368637
[No Abstract] [Full Text] [Related]
6. Late-onset hereditary axonal neuropathies.
Bennett CL; Lawson VH; Brickell KL; Isaacs K; Seltzer W; Lipe HP; Weiss MD; Carter GT; Flanigan KM; Chance PF; Bird TD
Neurology; 2008 Jul; 71(1):14-20. PubMed ID: 18495953
[TBL] [Abstract][Full Text] [Related]
7. [Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture].
Takahashi M; Mitsui Y; Yorifuji S; Nakamura Y; Tsukamoto Y; Nishimoto K
Rinsho Shinkeigaku; 2007 Sep; 47(9):571-6. PubMed ID: 18018614
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
El Euch-Fayache G; Lalani I; Amouri R; Turki I; Ouahchi K; Hung WY; Belal S; Siddique T; Hentati F
Arch Neurol; 2003 Jul; 60(7):982-8. PubMed ID: 12873855
[TBL] [Abstract][Full Text] [Related]
9. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.
Sabatelli M; Mignogna T; Lippi G; Servidei S; Zollino M; Padua L; Lo Monaco M; De Armas L; Mereu ML; Tonali P
Am J Med Genet; 1998 Jan; 75(3):309-13. PubMed ID: 9475604
[TBL] [Abstract][Full Text] [Related]
10. Neuronal intranuclear hyaline inclusion disease showing motor-sensory and autonomic neuropathy.
Sone J; Hishikawa N; Koike H; Hattori N; Hirayama M; Nagamatsu M; Yamamoto M; Tanaka F; Yoshida M; Hashizume Y; Imamura H; Yamada E; Sobue G
Neurology; 2005 Nov; 65(10):1538-43. PubMed ID: 16301479
[TBL] [Abstract][Full Text] [Related]
11. Subtotal aplasia of myelinated nerve fibers in the sural nerve.
Schröder JM; Heide G; Ramaekers V; Mortier W
Neuropediatrics; 1993 Oct; 24(5):286-91. PubMed ID: 8309519
[TBL] [Abstract][Full Text] [Related]
12. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
Pascual-Castroviejo I; Gutierrez M; Morales C; Gonzalez-Mediero I; Martínez-Bermejo A; Pascual-Pascual SI
Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
[TBL] [Abstract][Full Text] [Related]
13. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
Eirís-Punal J; Vidal-Lijó M; Barros-Angueira F; Lopez-Fernández MJ; Pintos-Martínez E; Beiras-Iglesias A; Castro-Gago M
Rev Neurol; 2000 Sep 16-30; 31(6):506-10. PubMed ID: 11055050
[TBL] [Abstract][Full Text] [Related]
14. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
Le Ber I; Clot F; Vercueil L; Camuzat A; Viémont M; Benamar N; De Liège P; Ouvrard-Hernandez AM; Pollak P; Stevanin G; Brice A; Dürr A
Neurology; 2006 Nov; 67(10):1769-73. PubMed ID: 17130408
[TBL] [Abstract][Full Text] [Related]
15. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
Berciano J; García A; Infante J
Handb Clin Neurol; 2013; 115():907-32. PubMed ID: 23931821
[TBL] [Abstract][Full Text] [Related]
16. [Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance].
Ragno M; Curatola L; Rossi R; Salvolini U
Acta Neurol (Napoli); 1992; 14(4-6):431-9. PubMed ID: 1293986
[TBL] [Abstract][Full Text] [Related]
17. Giant axonal neuropathy in two siblings: clinical histopathological findings.
Hergüner MO; Zorludemir S; Altunbasak S
Clin Neuropathol; 2005; 24(1):48-50. PubMed ID: 15696785
[TBL] [Abstract][Full Text] [Related]
18. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.
Shimazaki H; Takiyama Y; Sakoe K; Ikeguchi K; Niijima K; Kaneko J; Namekawa M; Ogawa T; Date H; Tsuji S; Nakano I; Nishizawa M
Neurology; 2002 Aug; 59(4):590-5. PubMed ID: 12196655
[TBL] [Abstract][Full Text] [Related]
19. Dysmyelinating sensory-motor neuropathy in merosin-deficient congenital muscular dystrophy.
Di Muzio A; De Angelis MV; Di Fulvio P; Ratti A; Pizzuti A; Stuppia L; Gambi D; Uncini A
Muscle Nerve; 2003 Apr; 27(4):500-6. PubMed ID: 12661054
[TBL] [Abstract][Full Text] [Related]
20. [Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature].
Anheim M; Chaigne D; Fleury M; Santorelli FM; De Sèze J; Durr A; Brice A; Koenig M; Tranchant C
Rev Neurol (Paris); 2008 Apr; 164(4):363-8. PubMed ID: 18439928
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]