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 *

98 related articles for article (PubMed ID: 8914107)

  • 1. Hereditary geniospasm: two new families.
    Soland VL; Bhatia KP; Sheean GL; Marsden CD
    Mov Disord; 1996 Nov; 11(6):744-6. PubMed ID: 8914107
    [No Abstract]   [Full Text] [Related]  

  • 2. Variable onset of adult inherited focal dystonia: a problem for genetic studies.
    Micheli S; Fernández-Pardal M; Quesada P; Brannan T; Obeso JA
    Mov Disord; 1994 Jan; 9(1):64-8. PubMed ID: 8139606
    [No Abstract]   [Full Text] [Related]  

  • 3. Treatment of hereditary trembling chin with botulinum toxin.
    Bakar M; Zarifoglu M; Bora I; Turan F; Sen C; Ogul E
    Mov Disord; 1998 Sep; 13(5):845-6. PubMed ID: 9756157
    [No Abstract]   [Full Text] [Related]  

  • 4. Geniospasm: hereditary chin trembling.
    Danek A
    Mov Disord; 1993 Jul; 8(3):335-8. PubMed ID: 8341298
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary chin trembling: a new family with exclusion of the chromosome 9q13-q21 Locus.
    Grimes DA; Han F; Bulman D; Nicolson ML; Suchowersky O
    Mov Disord; 2002 Nov; 17(6):1390-2. PubMed ID: 12465093
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evidence that a gene for essential tremor maps to chromosome 2p in four families.
    Higgins JJ; Loveless JM; Jankovic J; Patel PI
    Mov Disord; 1998 Nov; 13(6):972-7. PubMed ID: 9827627
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance].
    Wszolek ZK; Cordes M; Calne DB; Münter MD; Cordes I; Pfeifer RF
    Nervenarzt; 1993 May; 64(5):331-5. PubMed ID: 8321342
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary quivering of the chin in a West Spanish family].
    Becker H
    Arch Psychiatr Nervenkr (1970); 1982; 231(6):509-18. PubMed ID: 7138277
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.
    Jarman PR; Wood NW; Davis MT; Davis PV; Bhatia KP; Marsden CD; Davis MB
    Am J Hum Genet; 1997 Oct; 61(4):928-33. PubMed ID: 9382105
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Chin tremor in a peruvian family].
    Torres L; Vélez M; Cosentino C
    Rev Neurol; 2001 Nov 16-30; 33(10):958-9. PubMed ID: 11785009
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)].
    Lefèvre A; Hiroz C; Zografos L; Schorderet DF; Munier FL
    Klin Monbl Augenheilkd; 1998 May; 212(5):301-4. PubMed ID: 9677562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Pedigree analysis of two families with Alport's syndrome].
    Wässer S; Theile H; Schöne D; Lemme B
    Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376
    [No Abstract]   [Full Text] [Related]  

  • 13. Hereditary hemorrhagic telangiectasia with juvenile polyposis--coincidence or linked autosomal dominant inheritance?
    Ballauff A; Koletzko S
    Z Gastroenterol; 1999 May; 37(5):385-8. PubMed ID: 10413846
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Syndactyly of the ring and small finger.
    De Smet L; Mulier T; Fabry G
    Genet Couns; 1994; 5(1):45-9. PubMed ID: 8031535
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A gene (ETM) for essential tremor maps to chromosome 2p22-p25.
    Higgins JJ; Pho LT; Nee LE
    Mov Disord; 1997 Nov; 12(6):859-64. PubMed ID: 9399207
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A Dutch family with hereditary pancreatitis].
    Lawson JA
    Ned Tijdschr Geneeskd; 1981 Feb; 125(8):309-12. PubMed ID: 7219588
    [No Abstract]   [Full Text] [Related]  

  • 17. Acute megaloblastic reaction in hereditary spherocytosis.
    Shukla J; Mishra OP; Katiyar GP; Dube B
    J Assoc Physicians India; 1993 Mar; 41(3):177. PubMed ID: 8226606
    [No Abstract]   [Full Text] [Related]  

  • 18. [A case of hereditary hypodontia of all the molars in the upper jaw].
    Spetalen E
    Nor Tannlaegeforen Tid; 1971 Feb; 81(2):118-21. PubMed ID: 5279905
    [No Abstract]   [Full Text] [Related]  

  • 19. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family.
    Moens P; De Smet L; Fabry G; Fryns JP
    Genet Couns; 1993; 4(4):277-80. PubMed ID: 8110414
    [No Abstract]   [Full Text] [Related]  

  • 20. [Familial idiopathic atrial fibrillation with bradyarrhythmia].
    Beyer F; Paul T; Luhmer I; Bertram H; Kallfelz HC
    Z Kardiol; 1993 Nov; 82(11):674-7. PubMed ID: 8291288
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.