BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 16541453)

  • 1. Unbalanced whole arm translocation resulting in loss of 18p in dystonia.
    Nasir J; Frima N; Pickard B; Malloy MP; Zhan L; Grünewald R
    Mov Disord; 2006 Jun; 21(6):859-63. PubMed ID: 16541453
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characteristics of dystonia in the 18p deletion syndrome, including a new case.
    Postma AG; Verschuuren-Bemelmans CC; Kok K; van Laar T
    Clin Neurol Neurosurg; 2009 Dec; 111(10):880-2. PubMed ID: 19699028
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p.
    Leube B; Hendgen T; Kessler KR; Knapp M; Benecke R; Auburger G
    Ann Neurol; 1997 Jul; 42(1):111-4. PubMed ID: 9225692
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DYT7 gene locus for cervical dystonia on chromosome 18p is questionable.
    Winter P; Kamm C; Biskup S; Köhler A; Leube B; Auburger G; Gasser T; Benecke R; Müller U
    Mov Disord; 2012 Dec; 27(14):1819-21. PubMed ID: 23115116
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and genetic evaluation in a French population presenting with primary focal dystonia.
    Dhaenens CM; Krystkowiak P; Douay X; Charpentier P; Bele S; Destée A; Sablonnière B
    Mov Disord; 2005 Jul; 20(7):822-5. PubMed ID: 15726581
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family.
    Leube B; Kessler KR; Goecke T; Auburger G; Benecke R
    Mov Disord; 1997 Nov; 12(6):1000-6. PubMed ID: 9399227
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation.
    Nazarenko SA; Ostroverkhova NV; Vasiljeva EO; Nazarenko LP; Puzyrev VP; Malet P; Nemtseva TA
    Am J Med Genet; 1999 Jul; 85(2):179-82. PubMed ID: 10406673
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.
    Grundmann K; Laubis-Herrmann U; Bauer I; Dressler D; Vollmer-Haase J; Bauer P; Stuhrmann M; Schulte T; Schöls L; Topka H; Riess O
    Arch Neurol; 2003 Sep; 60(9):1266-70. PubMed ID: 12975293
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Search for a founder mutation in idiopathic focal dystonia from Northern Germany.
    Klein C; Ozelius LJ; Hagenah J; Breakefield XO; Risch NJ; Vieregge P
    Am J Hum Genet; 1998 Dec; 63(6):1777-82. PubMed ID: 9837831
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.
    Klein C; Pramstaller PP; Castellan CC; Breakefield XO; Kramer PL; Ozelius LJ
    Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analysis of three patients with an 18p- syndrome and dystonia.
    Klein C; Page CE; LeWitt P; Gordon MF; de Leon D; Awaad Y; Breakefield XO; Brin MF; Ozelius LJ
    Neurology; 1999 Feb; 52(3):649-51. PubMed ID: 10025808
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three brothers with a very-late-onset writer's cramp.
    Bhidayasiri R; Jen JC; Baloh RW
    Mov Disord; 2005 Oct; 20(10):1375-7. PubMed ID: 15954129
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 18p monosomy with midline defects and a de novo satellite identified by FISH.
    Taine L; Goizet C; Wen ZQ; Chateil JF; Battin J; Saura R; Lacombe D
    Ann Genet; 1997; 40(3):158-63. PubMed ID: 9401105
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
    Brenk CH; Prott EC; Trost D; Hoischen A; Walldorf C; Radlwimmer B; Wieczorek D; Propping P; Gillessen-Kaesbach G; Weber RG; Engels H
    Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients.
    Portnoï MF; Gruchy N; Marlin S; Finkel L; Denoyelle F; Dubourg C; Odent S; Siffroi JP; Le Bouc Y; Houang M
    Clin Dysmorphol; 2007 Oct; 16(4):247-52. PubMed ID: 17786116
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [18p-syndrome with bilateral pyramidal tract signs, dystonia of the lower extremities and concentric visual field defect].
    Kakinuma S; Sasabe F; Negoro K; Nogaki H; Morimatsu M
    Rinsho Shinkeigaku; 1994 May; 34(5):474-8. PubMed ID: 7924061
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.
    Esposito F; Addor MC; Humm AM; Vingerhoets F; Wider C
    Parkinsonism Relat Disord; 2014 Mar; 20(3):351-2. PubMed ID: 24405754
    [No Abstract]   [Full Text] [Related]  

  • 20. Dystonia in a patient with deletion of 18p.
    Tezzon F; Zanoni T; Passarin MG; Ferrari G
    Ital J Neurol Sci; 1998 Apr; 19(2):90-3. PubMed ID: 10935843
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.