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 *

181 related articles for article (PubMed ID: 9616944)

  • 1. [Biotinidase deficiency].
    Casado de Frías E
    An R Acad Nac Med (Madr); 1997; 114(4):817-27; discussion 827-8. PubMed ID: 9616944
    [No Abstract]   [Full Text] [Related]  

  • 2. [Biotinidase deficiency. Its form of presentation and response to treatment].
    Campistol J; Vilaseca MA; Ribes A; Riudor E
    An Esp Pediatr; 1996 Apr; 44(4):389-92. PubMed ID: 8796946
    [No Abstract]   [Full Text] [Related]  

  • 3. Neurological deterioration and lactic acidemia in biotinidase deficiency. A treatable condition mimicking Leigh's disease.
    Mitchell G; Ogier H; Munnich A; Saudubray JM; Shirrer J; Charpentier C; Rocchiccioli F
    Neuropediatrics; 1986 Aug; 17(3):129-31. PubMed ID: 3762868
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biotinidase deficiency.
    Wolf B; Heard GS
    Adv Pediatr; 1991; 38():1-21. PubMed ID: 1927696
    [No Abstract]   [Full Text] [Related]  

  • 5. [Biotinidase deficiency (late-onset multiple carboxylase deficiency)].
    Sakamoto O; Narisawa K
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):223-4. PubMed ID: 9645048
    [No Abstract]   [Full Text] [Related]  

  • 6. Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome.
    Baumgartner ER; Suormala TM; Wick H; Probst A; Blauenstein U; Bachmann C; Vest M
    Pediatr Res; 1989 Sep; 26(3):260-6. PubMed ID: 2587127
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism.
    Baumgartner ER; Suormala T
    Int J Vitam Nutr Res; 1997; 67(5):377-84. PubMed ID: 9350481
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biotinidase deficiency: result of treatment with biotin from age 12 years.
    Casado de Frías E; Campos-Castelló J; Careaga Maldonado J; Pérez Cerdá C
    Eur J Paediatr Neurol; 1997; 1(5-6):173-6. PubMed ID: 10728214
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Importance of biotin metabolism].
    Rodríguez Meléndez R
    Rev Invest Clin; 2000; 52(2):194-9. PubMed ID: 10846444
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inborn errors of biotin metabolism.
    Nyhan WL
    Arch Dermatol; 1987 Dec; 123(12):1696-1698a. PubMed ID: 3318710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Multiple carboxylase deficiency.
    Nyhan WL
    Int J Biochem; 1988; 20(4):363-70. PubMed ID: 3284772
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: the usefulness of multiple study designs.
    Weissbecker KA; Wolf B; Eaves LJ; Marazita ML; Nance WE
    Am J Med Genet; 1993 Aug; 47(2):231-40. PubMed ID: 8213911
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deficient biotinidase activity in late-onset multiple carboxylase deficiency.
    Wolf B; Grier RE; Parker WD; Goodman SI; Allen RJ
    N Engl J Med; 1983 Jan; 308(3):161. PubMed ID: 6848914
    [No Abstract]   [Full Text] [Related]  

  • 15. [Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H].
    Nothjunge J; Krägeloh-Mann I; Suormala TM; Baumgartner ER
    Monatsschr Kinderheilkd; 1989 Nov; 137(11):737-40. PubMed ID: 2608075
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biotinidase deficiency: early neurological presentation.
    Collins JE; Nicholson NS; Dalton N; Leonard JV
    Dev Med Child Neurol; 1994 Mar; 36(3):268-70. PubMed ID: 8138076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple carboxylase deficiency due to deficiency of biotinidase.
    Thuy LP; Zielinska B; Zammarchi E; Pavari E; Vierucci A; Sweetman F; Sweetman L; Nyhan WL
    J Neurogenet; 1986 Nov; 3(6):357-63. PubMed ID: 3783319
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Results of a pilot study of neonatal screening for congenital biotinidase deficiency].
    Sander J; Niehaus C
    Monatsschr Kinderheilkd; 1986 Oct; 134(10):729-32. PubMed ID: 3796633
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Biotinidase deficiency. Results of neonatal screening 1985-1989 in Lower Saxony].
    Schweitzer S; Sander J; Suormala T; Baumgartner R; Byrd DJ; Brodehl J
    Monatsschr Kinderheilkd; 1991 Jun; 139(6):349-54. PubMed ID: 1896047
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations causing profound biotinidase deficiency in children ascertained by newborn screening in the United States occur at different frequencies than in symptomatic children.
    Norrgard KJ; Pomponio RJ; Hymes J; Wolf B
    Pediatr Res; 1999 Jul; 46(1):20-7. PubMed ID: 10400129
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.