These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia. Cader MZ; Steckley JL; Dyment DA; McLachlan RS; Ebers GC Neurology; 2005 Jul; 65(1):156-8. PubMed ID: 16009908 [TBL] [Abstract][Full Text] [Related]
3. Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo). Brandt T; Strupp M Audiol Neurootol; 1997; 2(6):373-83. PubMed ID: 9390841 [TBL] [Abstract][Full Text] [Related]
4. Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13. Calandriello L; Veneziano L; Francia A; Sabbadini G; Colonnese C; Mantuano E; Jodice C; Trettel F; Viviani P; Manfredi M; Frontali M Brain; 1997 May; 120 ( Pt 5)():805-12. PubMed ID: 9183251 [TBL] [Abstract][Full Text] [Related]
6. [Familial periodic ataxia with myokymia sensitive to acetazolamide: a family case]. Gómez-Gosálvez F; Smeyers P; Escrivá P; Clemente F; Mallada J; Mulas F; Palao F; Millet E Rev Neurol; 1997 Dec; 25(148):1925-7. PubMed ID: 9528033 [TBL] [Abstract][Full Text] [Related]
7. Episodic ataxia and channelopathies. Gordon N Brain Dev; 1998 Jan; 20(1):9-13. PubMed ID: 9533553 [TBL] [Abstract][Full Text] [Related]
8. A new episodic ataxia syndrome with linkage to chromosome 19q13. Kerber KA; Jen JC; Lee H; Nelson SF; Baloh RW Arch Neurol; 2007 May; 64(5):749-52. PubMed ID: 17502476 [TBL] [Abstract][Full Text] [Related]
9. Linkage analysis of Alzheimer's disease with methods using relative pairs. Blossey H; Commenges D; Olson JM Genet Epidemiol; 1993; 10(6):377-82. PubMed ID: 8314030 [TBL] [Abstract][Full Text] [Related]
10. Familial episodic ataxia type II. Mugundhan K; Thiruvarutchelvan K; Sivakumar S J Assoc Physicians India; 2011 Oct; 59():668-70. PubMed ID: 22479753 [TBL] [Abstract][Full Text] [Related]
11. Hereditary episodic ataxias. Jen JC Ann N Y Acad Sci; 2008 Oct; 1142():250-3. PubMed ID: 18990130 [TBL] [Abstract][Full Text] [Related]
12. A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p. Vahedi K; Joutel A; Van Bogaert P; Ducros A; Maciazeck J; Bach JF; Bousser MG; Tournier-Lasserve E Ann Neurol; 1995 Mar; 37(3):289-93. PubMed ID: 7695228 [TBL] [Abstract][Full Text] [Related]
19. Episodic ataxias. Jen JC; Wan J Handb Clin Neurol; 2018; 148():521-529. PubMed ID: 29478597 [TBL] [Abstract][Full Text] [Related]
20. A novel mutation in KCNA1 causes episodic ataxia without myokymia. Lee H; Wang H; Jen JC; Sabatti C; Baloh RW; Nelson SF Hum Mutat; 2004 Dec; 24(6):536. PubMed ID: 15532032 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]