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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 7977376)

  • 1. 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]  

  • 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. 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]  

  • 4. Genetic heterogeneity in Italian families with familial hemiplegic migraine.
    Carrera P; Piatti M; Stenirri S; Grimaldi LM; Marchioni E; Curcio M; Righetti PG; Ferrari M; Gelfi C
    Neurology; 1999 Jul; 53(1):26-33. PubMed ID: 10408532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
    Nyholt DR; Lea RA; Goadsby PJ; Brimage PJ; Griffiths LR
    Neurology; 1998 May; 50(5):1428-32. PubMed ID: 9596000
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
    Terwindt GM; Ophoff RA; Lindhout D; Haan J; Halley DJ; Sandkuijl LA; Brouwer OF; Frants RR; Ferrari MD
    Epilepsia; 1997 Aug; 38(8):915-21. PubMed ID: 9579893
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.
    Ducros A; Nagy T; Alamowitch S; Nibbio A; Joutel A; Vahedi K; Chabriat H; Iba-Zizen MT; Julien J; Davous P; Goas JY; Lyon-Caen O; Dubois B; Ducrocq X; Salsa F; Ragno M; Burkhard P; Bassetti C; Hutchinson M; Vérin M; Viader F; Chapon F; Levasseur M; Mas JL; Delrieu O
    Am J Hum Genet; 1996 Jan; 58(1):171-81. PubMed ID: 8554054
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Familial hemiplegic migraine].
    Thomsen LL; Olesen J; Russell MB
    Ugeskr Laeger; 1998 Sep; 160(37):5325-9. PubMed ID: 9748855
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG.
    Terwindt GM; Ophoff RA; Haan J; Frants RR; Ferrari MD
    Cephalalgia; 1996 May; 16(3):153-5. PubMed ID: 8734765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.
    May A; Ophoff RA; Terwindt GM; Urban C; van Eijk R; Haan J; Diener HC; Lindhout D; Frants RR; Sandkuijl LA
    Hum Genet; 1995 Nov; 96(5):604-8. PubMed ID: 8530012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.
    Dichgans M; Mayer M; Müller-Myhsok B; Straube A; Gasser T
    Genomics; 1996 Feb; 32(1):151-4. PubMed ID: 8786108
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.
    Terwindt GM; Ophoff RA; Haan J; Vergouwe MN; van Eijk R; Frants RR; Ferrari MD
    Neurology; 1998 Apr; 50(4):1105-10. PubMed ID: 9566402
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.
    Münchau A; Valente EM; Shahidi GA; Eunson LH; Hanna MG; Quinn NP; Schapira AH; Wood NW; Bhatia KP
    J Neurol Neurosurg Psychiatry; 2000 May; 68(5):609-14. PubMed ID: 10766892
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.