BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 3196050)

  • 1. 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]  

  • 2. [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]  

  • 3. 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]  

  • 4. [Diagnosis and treatment of biotinidase deficiency-clinical study of six patients].
    Yang YL; Yamaguchi S; Tagami Y; Zhang YH; Xiong H; Hasegawa Y; Kimura M; Hanai J; Fujita K; Qian N; He XJ; Wu Y; Bao XH; Qin J; Wu X
    Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):249-51. PubMed ID: 14754524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biotinidase deficiency--a treatable entity.
    Gulati S; Passi GR; Kumar A; Kabra M; Kalra V; Verma IC
    Indian J Pediatr; 2000 Jun; 67(6):464-6. PubMed ID: 10932969
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. 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]  

  • 8. Late presentation of biotinidase deficiency with acute visual loss and gait disturbance.
    Rahman S; Standing S; Dalton RN; Pike MG
    Dev Med Child Neurol; 1997 Dec; 39(12):830-1. PubMed ID: 9433860
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

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

  • 12. 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]  

  • 13. Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases.
    Coşkun T; Tokatli A; Ozalp I
    Turk J Pediatr; 1994; 36(4):267-78. PubMed ID: 7825232
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparison of patients with complete and partial biotinidase deficiency: biochemical studies.
    Suormala TM; Baumgartner ER; Wick H; Scheibenreiter S; Schweitzer S
    J Inherit Metab Dis; 1990; 13(1):76-92. PubMed ID: 2109151
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Long-term auditory and visual complications of biotinidase deficiency.
    Taitz LS; Leonard JV; Bartlett K
    Early Hum Dev; 1985 Sep; 11(3-4):325-31. PubMed ID: 4054050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Biotin-responsive encephalopathy with myoclonus, ataxia, and seizures.
    Bressman S; Fahn S; Eisenberg M; Brin M; Maltese W
    Adv Neurol; 1986; 43():119-25. PubMed ID: 3946108
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biotinidase deficiency: a treatable genetic disorder in the Saudi population.
    Joshi S; al-Essa MA; Archibald A; Ozand PT
    East Mediterr Health J; 1999 Nov; 5(6):1213-7. PubMed ID: 11924114
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.