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159 related items for PubMed ID: 7825578
1. The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2. Stevanin G, Cancel G, Dürr A, Chneiweiss H, Dubourg O, Weissenbach J, Cann HM, Agid Y, Brice A. Am J Hum Genet; 1995 Jan; 56(1):193-201. PubMed ID: 7825578 [Abstract] [Full Text] [Related]
2. Mapping of the gene for Machado-Joseph disease within a 3.6-cM interval flanked by D14S291/D14S280 and D14S81, on the basis of studies of linkage and linkage disequilibrium in 24 Japanese families. Sasaki H, Wakisaka A, Takada A, Yoshiki T, Ihara T, Suzuki Y, Hamada T, Iwabuchi K, Onari K, Tada J. Am J Hum Genet; 1995 Jan; 56(1):231-42. PubMed ID: 7825583 [Abstract] [Full Text] [Related]
3. Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus. Twist EC, Casaubon LK, Ruttledge MH, Rao VS, Macleod PM, Radvany J, Zhao Z, Rosenberg RN, Farrer LA, Rouleau GA. J Med Genet; 1995 Jan; 32(1):25-31. PubMed ID: 7897622 [Abstract] [Full Text] [Related]
5. The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q. Stevanin G, Sousa PS, Cancel G, Dürr A, Dubourg O, Nicholson GA, Weissenbach J, Jardim E, Agid Y, Cassa E. Neurobiol Dis; 1994 Nov; 1(1-2):79-82. PubMed ID: 9216989 [Abstract] [Full Text] [Related]
7. Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I. Verschuuren-Bemelmans CC, Brunt ER, Burton M, Mensink RG, van der Meulen MA, Smit NH, Stolte-Dijkstra I, Buys CH, Scheffer H. Hum Genet; 1995 Dec; 96(6):691-4. PubMed ID: 8522329 [Abstract] [Full Text] [Related]
8. The gene for Machado-Joseph disease maps to human chromosome 14q. Takiyama Y, Nishizawa M, Tanaka H, Kawashima S, Sakamoto H, Karube Y, Shimazaki H, Soutome M, Endo K, Ohta S. Nat Genet; 1993 Jul; 4(3):300-4. PubMed ID: 8358439 [Abstract] [Full Text] [Related]
9. The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. Jodice C, Frontali M, Persichetti F, Novelletto A, Pandolfo M, Spadaro M, Giunti P, Schinaia G, Lulli P, Malaspina P. Hum Mol Genet; 1993 Sep; 2(9):1383-7. PubMed ID: 8242061 [Abstract] [Full Text] [Related]
10. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families. Lezin A, Cancel G, Stevanin G, Smadja D, Vernant JC, Dürr A, Martial J, Buisson GG, Bellance R, Chneiweiss H, Agid Y, Brice A. Hum Genet; 1996 May; 97(5):671-6. PubMed ID: 8655151 [Abstract] [Full Text] [Related]
11. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12. Nechiporuk A, Lopes-Cendes I, Nechiporuk T, Starkman S, Andermann E, Rouleau GA, Weissenbach JS, Kort E, Pulst SM. Neurology; 1996 Jun; 46(6):1731-5. PubMed ID: 8649579 [Abstract] [Full Text] [Related]
12. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C. Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438 [Abstract] [Full Text] [Related]
13. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. Zu L, Figueroa KP, Grewal R, Pulst SM. Am J Hum Genet; 1999 Feb; 64(2):594-9. PubMed ID: 9973298 [Abstract] [Full Text] [Related]
14. Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD). Haberhausen G, Damian MS, Leweke F, Müller U. J Neurol Sci; 1995 Sep; 132(1):71-5. PubMed ID: 8523034 [Abstract] [Full Text] [Related]
15. Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus. Twells R, Yenchitsomanus PT, Sirinavin C, Allotey R, Poungvarin N, Viriyavejakul A, Cemal C, Weber J, Farrall M, Rodprasert P. Hum Mol Genet; 1994 Jan; 3(1):177-80. PubMed ID: 8162021 [Abstract] [Full Text] [Related]
16. Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14. St George-Hyslop P, Rogaeva E, Huterer J, Tsuda T, Santos J, Haines JL, Schlumpf K, Rogaev EI, Liang Y, McLachlan DR. Am J Hum Genet; 1994 Jul; 55(1):120-5. PubMed ID: 8023841 [Abstract] [Full Text] [Related]
17. The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1). Carson WJ, Radvany J, Farrer LA, Vincent D, Rosenberg RN, MacLeod PM, Rouleau GA. Genomics; 1992 Jul; 13(3):852-5. PubMed ID: 1639414 [Abstract] [Full Text] [Related]
18. A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia. Nagaoka U, Takashima M, Ishikawa K, Yoshizawa K, Yoshizawa T, Ishikawa M, Yamawaki T, Shoji S, Mizusawa H. Neurology; 2000 May 23; 54(10):1971-5. PubMed ID: 10822439 [Abstract] [Full Text] [Related]
19. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Neurology; 1994 Aug 23; 44(8):1423-6. PubMed ID: 8058142 [Abstract] [Full Text] [Related]
20. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23. Chung MY, Lu YC, Cheng NC, Soong BW. Brain; 2003 Jun 23; 126(Pt 6):1293-9. PubMed ID: 12764052 [Abstract] [Full Text] [Related] Page: [Next] [New Search]