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 *

106 related articles for article (PubMed ID: 12465093)

  • 1. 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]  

  • 2. Linkage analysis with chromosome 9 markers in hereditary essential tremor.
    Conway D; Bain PG; Warner TT; Davis MB; Findley LJ; Thompson PD; Marsden CD; Harding AE
    Mov Disord; 1993 Jul; 8(3):374-6. PubMed ID: 8341306
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. 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]  

  • 5. 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]  

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

  • 7. Successful treatment of hereditary trembling chin with botulinum toxin.
    Gordon K; Cadera W; Hinton G
    J Child Neurol; 1993 Apr; 8(2):154-6. PubMed ID: 8505478
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Dutch family with 'familial cortical tremor with epilepsy'. Clinical characteristics and exclusion of linkage to chromosome 8q23.3-q24.1.
    van Rootselaar F; Callenbach PM; Hottenga JJ; Vermeulen FL; Speelman HD; Brouwer OF; Tijssen MA
    J Neurol; 2002 Jul; 249(7):829-34. PubMed ID: 12140665
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
    Kennerson M; Nicholson G; Kowalski B; Krajewski K; El-Khechen D; Feely S; Chu S; Shy M; Garbern J
    Neurology; 2009 Jan; 72(3):246-52. PubMed ID: 19153371
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary chin trembling or hereditary chin myoclonus?
    Destee A; Cassim F; Defebvre L; Guieu JD
    J Neurol Neurosurg Psychiatry; 1997 Dec; 63(6):804-7. PubMed ID: 9416823
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region.
    Hellenbroich Y; Bubel S; Pawlack H; Opitz S; Vieregge P; Schwinger E; Zühlke C
    J Neurol; 2003 Jun; 250(6):668-71. PubMed ID: 12796826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Clinical, neuropsychological, neurophysiologic, and genetic features of a new Italian pedigree with familial cortical myoclonic tremor with epilepsy.
    Suppa A; Berardelli A; Brancati F; Marianetti M; Barrano G; Mina C; Pizzuti A; Sideri G
    Epilepsia; 2009 May; 50(5):1284-8. PubMed ID: 19222544
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trembling chin--a report of this inheritable dominant character in a four-generation Canadian family.
    Alsager DE; Bowen P; Bamforth JS
    Clin Genet; 1991 Sep; 40(3):186-9. PubMed ID: 1773532
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia.
    Burns TM; Te Morsche RH; Jansen JB; Drenth JP
    Br J Dermatol; 2005 Jul; 153(1):174-7. PubMed ID: 16029345
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.
    Wolf MT; Zalewski I; Martin FC; Ruf R; Müller D; Hennies HC; Schwarz S; Panther F; Attanasio M; Acosta HG; Imm A; Lucke B; Utsch B; Otto E; Nurnberg P; Nieto VG; Hildebrandt F
    Nephrol Dial Transplant; 2005 May; 20(5):909-14. PubMed ID: 15741201
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary chin tremor in Parkinson's disease.
    Erer S; Jankovic J
    Clin Neurol Neurosurg; 2007 Nov; 109(9):784-5. PubMed ID: 17618046
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recurrent nocturnal tongue biting in a child with hereditary chin trembling.
    Goraya JS; Virdi V; Parmar V
    J Child Neurol; 2006 Nov; 21(11):985-7. PubMed ID: 17092470
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.