370 related articles for article (PubMed ID: 3318710)
1. Inborn errors of biotin metabolism.
Nyhan WL
Arch Dermatol; 1987 Dec; 123(12):1696-1698a. PubMed ID: 3318710
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Importance of biotin metabolism].
Rodríguez Meléndez R
Rev Invest Clin; 2000; 52(2):194-9. PubMed ID: 10846444
[TBL] [Abstract][Full Text] [Related]
5. Multiple carboxylase deficiency.
Nyhan WL
Int J Biochem; 1988; 20(4):363-70. PubMed ID: 3284772
[TBL] [Abstract][Full Text] [Related]
6. Inheritable biotin-treatable disorders and associated phenomena.
Sweetman L; Nyhan WL
Annu Rev Nutr; 1986; 6():317-43. PubMed ID: 3089241
[No Abstract] [Full Text] [Related]
7. [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]
8. Biotinidase deficiency.
Wolf B; Heard GS
Adv Pediatr; 1991; 38():1-21. PubMed ID: 1927696
[No Abstract] [Full Text] [Related]
9. [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]
10. [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]
11. 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]
12. [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]
13. Skin manifestations of biotin deficiency.
Mock DM
Semin Dermatol; 1991 Dec; 10(4):296-302. PubMed ID: 1764357
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities.
Holme E; Jacobson CE; Kristiansson B
J Inherit Metab Dis; 1988; 11(3):270-6. PubMed ID: 3148068
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. 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]
19. [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]
20. Ocular aspects in biotinidase deficiency. Clinical and genetic original studies.
Campana G; Valentini G; Legnaioli MI; Giovannucci-Uzielli ML; Pavari E
Ophthalmic Paediatr Genet; 1987 Jun; 8(2):125-9. PubMed ID: 3658339
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
