BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 10849128)

  • 1. Cutaneous and neurologic manifestations of biotinidase deficiency.
    Navarro PC; Guerra A; Alvarez JG; Ortiz FJ
    Int J Dermatol; 2000 May; 39(5):363-5. PubMed ID: 10849128
    [No Abstract]   [Full Text] [Related]  

  • 2. [Biotinidase deficiency: disease with mainly neurocutaneous manifestations responding to biotin].
    Marandian MH; Soltanabadi A; Lessani M; Kouchanfar A; Fallah A
    Ann Pediatr (Paris); 1987 Nov; 34(9):725-8. PubMed ID: 3426084
    [No Abstract]   [Full Text] [Related]  

  • 3. [Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin].
    de Parscau L; Beaufrère B; Vianey-Liaud C; Rolland MO; Langue J; Divry P; Guibaud P
    Pediatrie; 1989; 44(5):383-6. PubMed ID: 2812965
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic variation in biotinidase deficiency.
    Wolf B; Grier RE; Allen RJ; Goodman SI; Kien CL; Parker WD; Howell DM; Hurst DL
    J Pediatr; 1983 Aug; 103(2):233-7. PubMed ID: 6875714
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. Biotinidase deficiency: two cases of very early presentation.
    Haagerup A; Andersen JB; Blichfeldt S; Christensen MF
    Dev Med Child Neurol; 1997 Dec; 39(12):832-5. PubMed ID: 9433861
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype.
    Wolf B
    Eur J Pediatr; 2002 Mar; 161(3):167-8; author reply 169. PubMed ID: 11998918
    [No Abstract]   [Full Text] [Related]  

  • 8. Biotinidase deficiency: a survey of 10 cases.
    Wastell HJ; Bartlett K; Dale G; Shein A
    Arch Dis Child; 1988 Oct; 63(10):1244-9. PubMed ID: 3196050
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. Seventeen novel mutations that cause profound biotinidase deficiency.
    Wolf B; Jensen K; Hüner G; Demirkol M; Baykal T; Divry P; Rolland MO; Perez-Cerdá C; Ugarte M; Straussberg R; Basel-Vanagaite L; Baumgartner ER; Suormala T; Scholl S; Das AM; Schweitzer S; Pronicka E; Sykut-Cegielska J
    Mol Genet Metab; 2002; 77(1-2):108-11. PubMed ID: 12359137
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biotinidase deficiency: presymptomatic treatment.
    Wallace SJ
    Arch Dis Child; 1985 Jun; 60(6):574-5. PubMed ID: 4015175
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program.
    Wolf B; Heard GS; Jefferson LG; Proud VK; Nance WE; Weissbecker KA
    N Engl J Med; 1985 Jul; 313(1):16-9. PubMed ID: 4000223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complete biotinidase deficiency presenting as reversible progressive ataxia and sensorineural deafness.
    Tsao CY; Kien CL
    J Child Neurol; 2002 Feb; 17(2):146. PubMed ID: 11952077
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Biotinidase deficiency: importance of its neonatal diagnosis and early treatment].
    Couce Pico ML; Martinón-Torres F; Castiñeiras DE; Alonso-Fernández JR; Fraga JM
    An Esp Pediatr; 1999 May; 50(5):504-6. PubMed ID: 10394193
    [No Abstract]   [Full Text] [Related]  

  • 15. Biotinidase deficiency: initial clinical features and rapid diagnosis.
    Wolf B; Heard GS; Weissbecker KA; McVoy JR; Grier RE; Leshner RT
    Ann Neurol; 1985 Nov; 18(5):614-7. PubMed ID: 4073853
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. [Biotinidase deficiency. Progressive encephalopathy curable with biotin].
    Héron B; Gautier A; Dulac O; Ponsot G
    Arch Fr Pediatr; 1993 Dec; 50(10):875-8. PubMed ID: 8053766
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Normalisation of severe cranial CT scan abnormalities after biotin in a case of biotinidase deficiency.
    Bakker HD; Westra M; Overweg-Plandsoen WC; van Waveren G; Sillevis Smitt JH; Abeling NG; Wanders RJ; Schutgens RB; van Gennip AH
    Eur J Pediatr; 1994 Nov; 153(11):861-2. PubMed ID: 7843204
    [No Abstract]   [Full Text] [Related]  

  • 20. Neonatal screening for biotinidase deficiency in north eastern Italy.
    Burlina AB; Sherwood WG; Marchioro MV; Bernardina BD; Gaburro D
    Eur J Pediatr; 1988 Apr; 147(3):317-8. PubMed ID: 3391228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.