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 *

131 related articles for article (PubMed ID: 5070953)

  • 1. Mendelian inheritance. Autosomal patterns.
    Gordon H
    Postgrad Med; 1972 Oct; 52(4):149-56. PubMed ID: 5070953
    [No Abstract]   [Full Text] [Related]  

  • 2. A familial study in serum dopamine-beta-hydroxylase levels in torsion dystonia.
    Ebstein RP; Freedman LS; Lieberman A; Park DH; Pasternack B; Goldstein M; Coleman M
    Neurology; 1974 Jul; 24(7):684-7. PubMed ID: 4858093
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular genetics of an autosomal dominant form of torsion dystonia.
    Kramer PL; Ozelius L; Brin MF; Fahn S; Kidd KK; Gusella J; Breakefield XO
    Adv Neurol; 1988; 50():57-66. PubMed ID: 2899954
    [No Abstract]   [Full Text] [Related]  

  • 5. Phenotypic variability in Meckel-Gruber syndrome.
    Farag TI; Usha R; Uma R; Mady SA; al-Nagdy K; el-Badramany MH
    Clin Genet; 1990 Sep; 38(3):176-9. PubMed ID: 2225527
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dystonia in 61-year-old identical twins: observations over 45 years.
    Eldridge R; Ince SE; Chernow B; Milstien S; Lake CR
    Ann Neurol; 1984 Sep; 16(3):356-8. PubMed ID: 6486739
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Formal genetics in humans: mendelian and nonmendelian inheritance.
    Pyeritz RE
    Res Publ Assoc Res Nerv Ment Dis; 1991; 69():47-73. PubMed ID: 2003164
    [No Abstract]   [Full Text] [Related]  

  • 8. The clinical behavior of genetic disease: selected aspects.
    McKusick VA; Milch RA
    Clin Orthop Relat Res; 1964; 33():22-39. PubMed ID: 5889024
    [No Abstract]   [Full Text] [Related]  

  • 9. Non-allelic genetic heterogeneity of autosomal dominant polycystic kidney disease?
    Nørby S; Sørensen AW; Boesen P
    Prog Clin Biol Res; 1989; 305():83-8. PubMed ID: 2762358
    [No Abstract]   [Full Text] [Related]  

  • 10. Tiapride as treatment for certain patients with idiopathic torsion dystonia.
    Arlazoroff A; Klein C; Meiner Z; Milo R; Theitler J; Carpel CL
    Eur Neurol; 1991; 31(6):356-9. PubMed ID: 1756758
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The genetics of primary torsion dystonia.
    Müller U; Kupke KG
    Hum Genet; 1990 Jan; 84(2):107-15. PubMed ID: 2404852
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Localization of the gene for the adult form of polycystic kidneys on the short arm of chromosome 16].
    Breuning MH; Reeders ST; Goor N; Hogewind BL; van Es LA; Pearson PL
    Ned Tijdschr Geneeskd; 1986 Apr; 130(15):689-92. PubMed ID: 3703046
    [No Abstract]   [Full Text] [Related]  

  • 13. Autosomal dominant polycystic renal disease in children.
    Kaplan BS; Rabin I; Nogrady MB; Drummond KN
    J Pediatr; 1977 May; 90(5):782-3. PubMed ID: 853340
    [No Abstract]   [Full Text] [Related]  

  • 14. Autosomal recessive idiopathic torsion dystonia in a kindred of mixed ancestry.
    Oswald A; Silber M; Goldblatt J
    S Afr Med J; 1986 Jan; 69(1):18-20. PubMed ID: 3941936
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The autosomal dominant dystonias.
    Gasser T; Fahn S; Breakefield XO
    Brain Pathol; 1992 Oct; 2(4):297-308. PubMed ID: 1341964
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rhabdomyolysis due to hereditary torsion dystonia.
    Paret G; Tirosh R; Ben-Zeev B; Vardi A; Brandt N; Barzilay Z
    Pediatr Neurol; 1995 Jul; 13(1):83-4. PubMed ID: 7575858
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal dominant torsion dystonia in a Swedish family.
    Forsgren L; Holmgren G; Almay BG; Drugge U
    Adv Neurol; 1988; 50():83-92. PubMed ID: 3400518
    [No Abstract]   [Full Text] [Related]  

  • 18. Familial dystonia musculorum deformans and tremor.
    Yanagisawa N; Goto A; Narabayashi H
    J Neurol Sci; 1972 Jun; 16(2):125-36. PubMed ID: 5037440
    [No Abstract]   [Full Text] [Related]  

  • 19. Clinical genetics: an overview.
    Nehring WM; Faux SA
    J Cardiovasc Nurs; 1999 Jul; 13(4):19-33. PubMed ID: 10386269
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution.
    Leube B; Rudnicki D; Ratzlaff T; Kessler KR; Benecke R; Auburger G
    Hum Mol Genet; 1996 Oct; 5(10):1673-7. PubMed ID: 8894706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.