BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

295 related articles for article (PubMed ID: 16009908)

  • 1. 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]  

  • 2. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
    Waters MF; Fee D; Figueroa KP; Nolte D; Müller U; Advincula J; Coon H; Evidente VG; Pulst SM
    Neurology; 2005 Oct; 65(7):1111-3. PubMed ID: 16135769
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
    Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR
    Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.
    Deprez L; Peeters K; Van Paesschen W; Claeys KG; Claes LR; Suls A; Audenaert D; Van Dyck T; Goossens D; Del-Favero J; De Jonghe P
    Neurology; 2007 Jun; 68(23):1995-2002. PubMed ID: 17460155
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
    Schüle R; Bonin M; Dürr A; Forlani S; Sperfeld AD; Klimpe S; Mueller JC; Seibel A; van de Warrenburg BP; Bauer P; Schöls L
    Neurology; 2009 Jun; 72(22):1893-8. PubMed ID: 19357379
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A;
    Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740
    [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. A mutation in myotilin causes spheroid body myopathy.
    Foroud T; Pankratz N; Batchman AP; Pauciulo MW; Vidal R; Miravalle L; Goebel HH; Cushman LJ; Azzarelli B; Horak H; Farlow M; Nichols WC
    Neurology; 2005 Dec; 65(12):1936-40. PubMed ID: 16380616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
    Diaz GA; Khan KT; Gelb BD
    Genomics; 1998 Nov; 54(1):13-8. PubMed ID: 9806825
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG; McLean DE; Nyholt DR; Mowry BJ
    Arch Gen Psychiatry; 2009 Oct; 66(10):1058-67. PubMed ID: 19805696
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.
    Dick KJ; Al-Mjeni R; Baskir W; Koul R; Simpson MA; Patton MA; Raeburn S; Crosby AH
    Neurology; 2008 Jul; 71(4):248-52. PubMed ID: 18463364
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia.
    Jen JC; Lee H; Cha YH; Nelson SF; Baloh RW
    Neurology; 2006 Nov; 67(9):1704-6. PubMed ID: 17101914
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
    Wilson SG; Adam G; Langdown M; Reneland R; Braun A; Andrew T; Surdulescu GL; Norberg M; Dudbridge F; Reed PW; Sambrook PN; Kleyn PW; Spector TD
    Eur J Hum Genet; 2006 Mar; 14(3):340-8. PubMed ID: 16391564
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency.
    Indo Y; Mardy S; Miura Y; Moosa A; Ismail EA; Toscano E; Andria G; Pavone V; Brown DL; Brooks A; Endo F; Matsuda I
    Hum Mutat; 2001 Oct; 18(4):308-18. PubMed ID: 11668614
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of a susceptibility locus for SLE, SLEB5, on chromosome 4p14-13.
    Johansson CM; Kristjánsdottir H; Gröndal G; Steinsson K; Alarcón-Riquelme ME
    Scand J Immunol; 2006 Sep; 64(3):308-13. PubMed ID: 16918700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
    de Vries B; Mamsa H; Stam AH; Wan J; Bakker SL; Vanmolkot KR; Haan J; Terwindt GM; Boon EM; Howard BD; Frants RR; Baloh RW; Ferrari MD; Jen JC; van den Maagdenberg AM
    Arch Neurol; 2009 Jan; 66(1):97-101. PubMed ID: 19139306
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset.
    Valente EM; Bentivoglio AR; Cassetta E; Dixon PH; Davis MB; Ferraris A; Ialongo T; Frontali M; Wood NW; Albanese A
    Ann Neurol; 2001 Mar; 49(3):362-6. PubMed ID: 11261511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
    Pang CP; Fan BJ; Canlas O; Wang DY; Dubois S; Tam PO; Lam DS; Raymond V; Ritch R
    Mol Vis; 2006 Feb; 12():85-92. PubMed ID: 16518310
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.