BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 7695228)

  • 1. 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]  

  • 2. Genetic heterogeneity of familial hemiplegic migraine.
    Ophoff RA; van Eijk R; Sandkuijl LA; Terwindt GM; Grubben CP; Haan J; Lindhout D; Ferrari MD; Frants RR
    Genomics; 1994 Jul; 22(1):21-6. PubMed ID: 7959770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
    Cevoli S; Pierangeli G; Monari L; Valentino ML; Bernardoni P; Mochi M; Cortelli P; Montagna P
    Neurol Sci; 2002 Apr; 23(1):7-10. PubMed ID: 12111614
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
    Ducros A; Joutel A; Vahedi K; Cecillon M; Ferreira A; Bernard E; Verier A; Echenne B; Lopez de Munain A; Bousser MG; Tournier-Lasserve E
    Ann Neurol; 1997 Dec; 42(6):885-90. PubMed ID: 9403481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.
    Elliott MA; Peroutka SJ; Welch S; May EF
    Ann Neurol; 1996 Jan; 39(1):100-6. PubMed ID: 8572654
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
    Benomar A; Krols L; Stevanin G; Cancel G; LeGuern E; David G; Ouhabi H; Martin JJ; Dürr A; Zaim A
    Nat Genet; 1995 May; 10(1):84-8. PubMed ID: 7647798
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A gene for familial hemiplegic migraine maps to chromosome 19.
    Joutel A; Bousser MG; Biousse V; Labauge P; Chabriat H; Nibbio A; Maciazek J; Meyer B; Bach MA; Weissenbach J
    Nat Genet; 1993 Sep; 5(1):40-5. PubMed ID: 8220421
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p.
    Hovatta I; Kallela M; Färkkilä M; Peltonen L
    Genomics; 1994 Oct; 23(3):707-9. PubMed ID: 7851903
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
    Alonso I; Barros J; Tuna A; Coelho J; Sequeiros J; Silveira I; Coutinho P
    Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
    Takashima M; Ishikawa K; Nagaoka U; Shoji S; Mizusawa H
    J Hum Genet; 2001; 46(4):167-71. PubMed ID: 11322654
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
    Verbeek DS; Schelhaas JH; Ippel EF; Beemer FA; Pearson PL; Sinke RJ
    Hum Genet; 2002 Oct; 111(4-5):388-93. PubMed ID: 12384780
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.
    Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Mohrenweiser H; Litt M; Hofker MH; Haan J; Ferrari MD; Frants RR
    Eur J Hum Genet; 1996; 4(6):321-8. PubMed ID: 9043864
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
    Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J
    Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.
    Jones KW; Ehm MG; Pericak-Vance MA; Haines JL; Boyd PR; Peroutka SJ
    Genomics; 2001 Dec; 78(3):150-4. PubMed ID: 11735221
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z; Fernandez M; Matsushita M; Lipe H; Wolff J; Bird TD; Raskind WH
    Am J Med Genet; 2002 May; 114(4):450-7. PubMed ID: 11992570
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].
    Joutel A; Bousser MG; Biousse V; Labauge P; Chabriat H; Nibbio A; Maciazek J; Meyer B; Bach MA; Weissenbach J
    Rev Neurol (Paris); 1994; 150(5):340-5. PubMed ID: 7878319
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p.
    Baloh RW; Yue Q; Furman JM; Nelson SF
    Ann Neurol; 1997 Jan; 41(1):8-16. PubMed ID: 9005860
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic heterogeneity of familial hemiplegic migraine.
    Joutel A; Ducros A; Vahedi K; Labauge P; Delrieu O; Pinsard N; Mancini J; Ponsot G; Gouttière F; Gastaut JL
    Am J Hum Genet; 1994 Dec; 55(6):1166-72. PubMed ID: 7977376
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.