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.
3. A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Hadano S; Hand CK; Osuga H; Yanagisawa Y; Otomo A; Devon RS; Miyamoto N; Showguchi-Miyata J; Okada Y; Singaraja R; Figlewicz DA; Kwiatkowski T; Hosler BA; Sagie T; Skaug J; Nasir J; Brown RH; Scherer SW; Rouleau GA; Hayden MR; Ikeda JE Nat Genet; 2001 Oct; 29(2):166-73. PubMed ID: 11586298 [TBL] [Abstract][Full Text] [Related]
4. [From gene to disease: amyotrophic lateral sclerosis]. van Vught PW; Veldink JH; Baas F; van Muiswinkel FL; van den Berg LH Ned Tijdschr Geneeskd; 2004 Oct; 148(43):2125-7. PubMed ID: 15553356 [TBL] [Abstract][Full Text] [Related]
5. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Yang Y; Hentati A; Deng HX; Dabbagh O; Sasaki T; Hirano M; Hung WY; Ouahchi K; Yan J; Azim AC; Cole N; Gascon G; Yagmour A; Ben-Hamida M; Pericak-Vance M; Hentati F; Siddique T Nat Genet; 2001 Oct; 29(2):160-5. PubMed ID: 11586297 [TBL] [Abstract][Full Text] [Related]
6. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers. Rosen DR; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf KS; Haines JL; Gusella JF; Horvitz HR; Brown RH Am J Med Genet; 1994 May; 51(1):61-9. PubMed ID: 7913294 [TBL] [Abstract][Full Text] [Related]
7. Identification of three mutations in the Cu,Zn-superoxide dismutase (Cu,Zn-SOD) gene with familial amyotrophic lateral sclerosis: transduction of human Cu,Zn-SOD into PC12 cells by HIV-1 TAT protein basic domain. Chou CM; Huang CJ; Shih CM; Chen YP; Liu TP; Chen CT Ann N Y Acad Sci; 2005 May; 1042():303-13. PubMed ID: 15965076 [TBL] [Abstract][Full Text] [Related]
8. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. Hentati A; Bejaoui K; Pericak-Vance MA; Hentati F; Speer MC; Hung WY; Figlewicz DA; Haines J; Rimmler J; Ben Hamida C Nat Genet; 1994 Jul; 7(3):425-8. PubMed ID: 7920663 [TBL] [Abstract][Full Text] [Related]
9. [What is the role of the genetic survey in amyotrophic lateral sclerosis?]. Camu W Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S91-4S95. PubMed ID: 17128094 [TBL] [Abstract][Full Text] [Related]
10. Gender difference in levels of Cu/Zn superoxide dismutase (SOD1) in cerebrospinal fluid of patients with amyotrophic lateral sclerosis. Frutiger K; Lukas TJ; Gorrie G; Ajroud-Driss S; Siddique T Amyotroph Lateral Scler; 2008 Jun; 9(3):184-7. PubMed ID: 18574763 [TBL] [Abstract][Full Text] [Related]
11. Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: homozygous NAIP deletion in a sporadic case. Jackson M; Morrison KE; Al-Chalabi A; Bakker M; Leigh PN Ann Neurol; 1996 Jun; 39(6):796-800. PubMed ID: 8651652 [TBL] [Abstract][Full Text] [Related]
12. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation. Tan CF; Piao YS; Hayashi S; Obata H; Umeda Y; Sato M; Fukushima T; Nakano R; Tsuji S; Takahashi H Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802 [TBL] [Abstract][Full Text] [Related]
13. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. Siddique T; Figlewicz DA; Pericak-Vance MA; Haines JL; Rouleau G; Jeffers AJ; Sapp P; Hung WY; Bebout J; McKenna-Yasek D N Engl J Med; 1991 May; 324(20):1381-4. PubMed ID: 2020294 [TBL] [Abstract][Full Text] [Related]