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.
6. Sibling disability risk at onset and during disease progression in familial multiple sclerosis. Wellek A; Korsukewitz C; Bach JP; Schock S; Eienbröker C; Seitz F; Spengler A; Hemmer B; Schlegel K; Oertel WH; Sommer N; Tackenberg B Mult Scler; 2011 Sep; 17(9):1060-6. PubMed ID: 21561958 [TBL] [Abstract][Full Text] [Related]
7. Comparison of clinical and demographic features between affected pairs of Italian multiple sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms. Trojano M; Liguori M; De Robertis F; Stella A; Guanti G; Avolio C; Livrea P J Neurol Sci; 1999 Jan; 162(2):194-200. PubMed ID: 10202987 [TBL] [Abstract][Full Text] [Related]
8. Concordance for disease course and age of onset in Scandinavian multiple sclerosis coaffected sib pairs. Oturai AB; Ryder LP; Fredrikson S; Myhr KM; Celius EG; Harbo HF; Andersen O; Akesson E; Hillert J; Madsen HO; Nyland H; Spurkland A; Datta P; Svejgaard A; Sorensen PS Mult Scler; 2004 Feb; 10(1):5-8. PubMed ID: 14760946 [TBL] [Abstract][Full Text] [Related]
9. Age of onset in siblings concordant for multiple sclerosis. Bulman DE; Sadovnick AD; Ebers GC Brain; 1991 Apr; 114 ( Pt 2)():937-50. PubMed ID: 2043958 [TBL] [Abstract][Full Text] [Related]
14. The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen. Chataway J; Feakes R; Coraddu F; Gray J; Deans J; Fraser M; Robertson N; Broadley S; Jones H; Clayton D; Goodfellow P; Sawcer S; Compston A Brain; 1998 Oct; 121 ( Pt 10)():1869-87. PubMed ID: 9798743 [TBL] [Abstract][Full Text] [Related]
15. Multiple sclerosis in sibling pairs: an analysis of 250 families. Chataway J; Mander A; Robertson N; Sawcer S; Deans J; Fraser M; Broadley S; Clayton D; Compston A J Neurol Neurosurg Psychiatry; 2001 Dec; 71(6):757-61. PubMed ID: 11723196 [TBL] [Abstract][Full Text] [Related]
16. An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. Dyment DA; Sadovnick AD; Willer CJ; Armstrong H; Cader ZM; Wiltshire S; Kalman B; Risch N; Ebers GC; Hum Mol Genet; 2004 May; 13(10):1005-15. PubMed ID: 15069025 [TBL] [Abstract][Full Text] [Related]
17. The genetic epidemiology of multiple sclerosis. Compston A Philos Trans R Soc Lond B Biol Sci; 1999 Oct; 354(1390):1623-34. PubMed ID: 10603615 [TBL] [Abstract][Full Text] [Related]
18. Genetic factors and the founder effect explain familial MS in Sardinia. Marrosu MG; Lai M; Cocco E; Loi V; Spinicci G; Pischedda MP; Massole S; Marrosu G; Contu P Neurology; 2002 Jan; 58(2):283-8. PubMed ID: 11805258 [TBL] [Abstract][Full Text] [Related]
19. Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group. Haines JL; Terwedow HA; Burgess K; Pericak-Vance MA; Rimmler JB; Martin ER; Oksenberg JR; Lincoln R; Zhang DY; Banatao DR; Gatto N; Goodkin DE; Hauser SL Hum Mol Genet; 1998 Aug; 7(8):1229-34. PubMed ID: 9668163 [TBL] [Abstract][Full Text] [Related]
20. [Familial multiple sclerosis in Tomsk region]. Alifirova VM; Titova MA; Terskikh EV; Musina NF; Sjomkina AA; Gumenyuk YS Zh Nevrol Psikhiatr Im S S Korsakova; 2016; 116(10 Pt 2):6-9. PubMed ID: 28139604 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]