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 *

133 related articles for article (PubMed ID: 88555)

  • 1. Biotin-responsive alopecia and developmental regression.
    Charles BM; Hosking G; Green A; Pollitt R; Bartlett K; Taitz LS
    Lancet; 1979 Jul; 2(8134):118-20. PubMed ID: 88555
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
    Bartlett K; Ng H; Leonard JV
    Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency: long-term outcome in a case with neonatal onset.
    Lehnert W; Niederhoff H; Suormala T; Baumgartner ER
    Eur J Pediatr; 1996 Jul; 155(7):568-72. PubMed ID: 8831079
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Holocarboxylase synthetase deficiency: early diagnosis and management of a new case.
    Fuchshuber A; Suormala T; Roth B; Duran M; Michalk D; Baumgartner ER
    Eur J Pediatr; 1993 May; 152(5):446-9. PubMed ID: 8319716
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts.
    Saunders M; Sweetman L; Robinson B; Roth K; Cohn R; Gravel RA
    J Clin Invest; 1979 Dec; 64(6):1695-702. PubMed ID: 115903
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.
    Burri BJ; Sweetman L; Nyhan WL
    J Clin Invest; 1981 Dec; 68(6):1491-5. PubMed ID: 6798072
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria.
    Weyler W; Sweetman L; Maggio DC; Nyhan WL
    Clin Chim Acta; 1977 May; 76(3):321-8. PubMed ID: 858206
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency.
    Elpeleg ON; Havkin S; Barash V; Jakobs C; Glick B; Shalev RS
    J Pediatr; 1992 Sep; 121(3):407-10. PubMed ID: 1517917
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fatty-acid-responsive alopecia in multiple carboxylase deficiency.
    Munnich A; Saudubray JM; Coude FX; Charpentier C; Saurat JH; Frezal J
    Lancet; 1980 May; 1(8177):1080-1. PubMed ID: 6103410
    [No Abstract]   [Full Text] [Related]  

  • 10. [Multiple biotin-dependent carboxylase deficiencies (author's transl)].
    Munnich A; Saudubray JM; Ogier H; Coude FX; Marsac C; Roccichioli F; Labarthe JC; Cazenave C; Laugier J; Charpentier C; Frézal J
    Arch Fr Pediatr; 1981 Feb; 38(2):83-90. PubMed ID: 6112972
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stimulation of propionyl CoA and beta-methylcrotonyl CoA carboxylase activities in human leukocytes and cultured fibroblasts by biotin.
    Wolf B; Rosenberg LE
    Pediatr Res; 1979 Nov; 13(11):1275-9. PubMed ID: 514693
    [No Abstract]   [Full Text] [Related]  

  • 12. Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitro.
    Suormala T; Fowler B; Duran M; Burtscher A; Fuchshuber A; Tratzmüller R; Lenze MJ; Raab K; Baur B; Wick H; Baumgartner R
    Pediatr Res; 1997 May; 41(5):666-73. PubMed ID: 9128289
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biotin-reversible neurodegenerative disease in infancy.
    Low LC; Stephenson JB; Bartlett K; Seakins JW; Shaikh SA
    Aust Paediatr J; 1986 Feb; 22(1):65-8. PubMed ID: 3087340
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Organic aciduria. Treatable cause of floppy infant syndrome.
    Keeton BR
    Arch Dis Child; 1976 Aug; 51(8):636-8. PubMed ID: 962376
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and metabolic abnormalities in a boy with dietary deficiency of biotin.
    Sweetman L; Surh L; Baker H; Peterson RM; Nyhan WL
    Pediatrics; 1981 Oct; 68(4):553-8. PubMed ID: 7322688
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiency.
    Packman S; Caswell NM; Baker H
    Biochem Genet; 1982 Feb; 20(1-2):17-28. PubMed ID: 6807281
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis.
    Munnich A; Saudubray JM; Cotisson A; Coudĕ FX; Ogier H; Charpentier C; Marsac C; Carrĕ G; Bourgeay-Causse M; Frĕzal J
    Eur J Pediatr; 1981 Oct; 137(2):203-6. PubMed ID: 7198043
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment.
    Wolf B; Hsia YE; Sweetman L; Feldman G; Boychuk RB; Bart RD; Crowell DH; Di Mauro RM; Nyhan WL
    Pediatrics; 1981 Jul; 68(1):113-8. PubMed ID: 6787561
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome.
    Bannwart C; Wermuth B; Baumgartner R; Suormala T; Weismann UN
    J Inherit Metab Dis; 1992; 15(6):863-8. PubMed ID: 1293382
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.