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 *

128 related articles for article (PubMed ID: 7436398)

  • 21. Pyruvate decarboxylase activity in familial intermittent cerebellar ataxia.
    Farmer TW; Veath L; Miller AL; O'Brien JS
    Trans Am Neurol Assoc; 1973; 98():260-2. PubMed ID: 4784948
    [No Abstract]   [Full Text] [Related]  

  • 22. Biotin-responsive multiple carboxylase deficiency and immunodeficiency.
    Williams ML
    Curr Probl Dermatol; 1989; 18():89-92. PubMed ID: 2663376
    [No Abstract]   [Full Text] [Related]  

  • 23. Canine inherited ataxia.
    Cork LC; Troncoso JC; Price DL
    Ann Neurol; 1981 May; 9(5):492-8. PubMed ID: 7271243
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutrition.
    Kien CL; Kohler E; Goodman SI; Berlow S; Hong R; Horowitz SP; Baker H
    J Pediatr; 1981 Oct; 99(4):546-50. PubMed ID: 6792336
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal treatment of biotin responsive multiple carboxylase deficiency.
    Packman S; Cowan MJ; Golbus MS; Caswell NM; Sweetman L; Burri BJ; Nyhan WL; Baker H
    Lancet; 1982 Jun; 1(8287):1435-8. PubMed ID: 6123722
    [No Abstract]   [Full Text] [Related]  

  • 26. MRI-based volumetric differentiation of sporadic cerebellar ataxia.
    Burk K; Globas C; Wahl T; Bühring U; Dietz K; Zuhlke C; Luft A; Schulz JB; Voigt K; Dichgans J
    Brain; 2004 Jan; 127(Pt 1):175-81. PubMed ID: 14570820
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Biotin-responsive carboxylase deficiency associated with subnormal plasma and urinary biotin.
    Thoene J; Baker H; Yoshino M; Sweetman L
    N Engl J Med; 1981 Apr; 304(14):817-20. PubMed ID: 6782477
    [No Abstract]   [Full Text] [Related]  

  • 28. Organic aciduria in late-onset biotin-responsive multiple carboxylase deficiency.
    Erasmus C; Mienie LJ; Reinecke CJ; Wadman SK
    J Inherit Metab Dis; 1985; 8 Suppl 2():105-6. PubMed ID: 3930851
    [No Abstract]   [Full Text] [Related]  

  • 29. The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin.
    Friebel D; von der Hagen M; Baumgartner ER; Fowler B; Hahn G; Feyh P; Heubner G; Baumgartner MR; Hoffmann GF
    Neuropediatrics; 2006 Apr; 37(2):72-8. PubMed ID: 16773504
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cerebellar ataxia in systemic lupus erythematosus.
    Appenzeller S; Cendes F; Costallat LT
    Lupus; 2008 Dec; 17(12):1122-6. PubMed ID: 19029281
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Multiple carboxylase deficiency].
    Andersen JB; Haagerup A; Christensen E
    Ugeskr Laeger; 1998 Feb; 160(8):1151-7. PubMed ID: 9492625
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.
    Salih MA; Bender DA; McCreanor GM
    Pediatrics; 1985 Nov; 76(5):787-93. PubMed ID: 4058988
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal administration of biotin in biotin responsive multiple carboxylase deficiency.
    Roth KS; Yang W; Allan L; Saunders M; Gravel RA; Dakshinamurti K
    Pediatr Res; 1982 Feb; 16(2):126-9. PubMed ID: 6799930
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Familial cerebellar ataxia with sex-linked recessive inheritance.
    Spira PJ; Lance JW
    Proc Aust Assoc Neurol; 1975; 12():171-7. PubMed ID: 1215388
    [No Abstract]   [Full Text] [Related]  

  • 35. EEG findings in acetazolamide-responsive hereditary paroxysmal ataxia.
    Van Bogaert P; Szliwowski HB
    Neurophysiol Clin; 1996; 26(5):335-40. PubMed ID: 8987050
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Biotinidase deficiency in juvenile multiple carboxylase deficiency.
    Thoene J; Wolf B
    Lancet; 1983 Aug; 2(8346):398. PubMed ID: 6135890
    [No Abstract]   [Full Text] [Related]  

  • 37. A cerebellar abiotrophy of calves.
    White ME; Whitlock RH; Lahunta A
    Cornell Vet; 1975 Oct; 65(4):476-91. PubMed ID: 1192746
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
    Le Ber I; Clot F; Vercueil L; Camuzat A; Viémont M; Benamar N; De Liège P; Ouvrard-Hernandez AM; Pollak P; Stevanin G; Brice A; Dürr A
    Neurology; 2006 Nov; 67(10):1769-73. PubMed ID: 17130408
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Biotinidase deficiency--a progressive metabolic disease in children with seizures and ataxia].
    Anger H; Lorenz K; Cobet G
    Psychiatr Neurol Med Psychol (Leipz); 1990 Mar; 42(3):163-6. PubMed ID: 2356250
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Behr's syndrome. a report of seven cases].
    Pizzatto MR; Pascual-Castroviejo I
    Rev Neurol; 2001 Apr 16-30; 32(8):721-4. PubMed ID: 11391506
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.