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 *

83 related articles for article (PubMed ID: 2835027)

  • 1. [Tetrahydrobiopterin deficiency. Lessons from the analysis of 90 patients collected in the international register].
    Dhondt JL
    Arch Fr Pediatr; 1987; 44 Suppl 1():655-9. PubMed ID: 2835027
    [No Abstract]   [Full Text] [Related]  

  • 2. [Detection, differential diagnosis, and prenatal diagnosis of tetrahydrobiopterin deficiency].
    Niederwieser A; Curtius HC
    Arch Fr Pediatr; 1987; 44 Suppl 1():661-4. PubMed ID: 2452621
    [No Abstract]   [Full Text] [Related]  

  • 3. Hyperphenylalaninaemia due to tetrahydrobiopterin deficiency: a report of 16 cases.
    Coskun T; Ozalp I; Tokatli A; Blau N; Niederwieser A
    J Inherit Metab Dis; 1993; 16(3):605-7. PubMed ID: 7609463
    [No Abstract]   [Full Text] [Related]  

  • 4. Hyperphenylalaninemia due to inherited deficiencies of tetrahydrobiopterin.
    Matalon R; Michals K; Blau N; Rouse B
    Adv Pediatr; 1989; 36():67-89. PubMed ID: 2675577
    [No Abstract]   [Full Text] [Related]  

  • 5. [Malignant hyperphenylalaninemia--tetrahydrobiopterin (BH4) deficiency].
    Shintaku H
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):493-6. PubMed ID: 3270853
    [No Abstract]   [Full Text] [Related]  

  • 6. Tetrahydrobiopterin and inherited hyperphenylalaninemias.
    Blau N; Thony B; Spada M; Ponzone A
    Turk J Pediatr; 1996; 38(1):19-35. PubMed ID: 8819618
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Trial of indirect screening of tetrahydrobiopterin deficiency].
    Ferraris S; Guardamagna O; Bracco G; Ponzone A
    Pediatrie; 1987; 42(7):549-55. PubMed ID: 3444720
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Disorders of tetrahydrobiopterin homeostasis].
    Shintaku H; Asada M; Isshiki G; Sawada Y
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):125-9. PubMed ID: 9590005
    [No Abstract]   [Full Text] [Related]  

  • 9. Tetrahydrobiopterin and maternal PKU.
    Koch R; Moseley K; Guttler F
    Mol Genet Metab; 2005 Dec; 86 Suppl 1():S139-41. PubMed ID: 16338627
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Evaluation of 6-years' experience of screening for hyperphenylalaninemia caused by cofactor deficiency].
    Dhondt JL; Farriaux JP; Hayte JM
    Arch Fr Pediatr; 1986 Dec; 43(10):785-9. PubMed ID: 3827510
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Measurement in samples of dry blood of dihydropteridine reductase and ratio of total biopterin in hyperphenylalaninemia and other neurological diseases].
    Leeming RJ; Karim AR; Sahota AS; Blair JA; Green A
    Arch Fr Pediatr; 1987; 44 Suppl 1():649-54. PubMed ID: 3449009
    [No Abstract]   [Full Text] [Related]  

  • 12. Liver enzyme activities in hyperphenylalaninaemia due to a defective synthesis of tetrahydrobiopterin.
    Dhondt JL; Cotton RG; Danks DM
    J Inherit Metab Dis; 1985; 8(2):47-8. PubMed ID: 3939528
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Outcome of the patients detected by newborn screening in Japan.
    Aoki K; Wada Y
    Acta Paediatr Jpn; 1988 Aug; 30(4):429-34. PubMed ID: 3150232
    [No Abstract]   [Full Text] [Related]  

  • 14. The origin of red blood cell biopterin.
    Leeming RJ; Hall SK; Green A
    Mol Genet Metab; 1998 Dec; 65(4):291-7. PubMed ID: 9889016
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tetrahydrobiopterin protects phenylalanine hydroxylase activity in vivo: implications for tetrahydrobiopterin-responsive hyperphenylalaninemia.
    Thöny B; Ding Z; Martínez A
    FEBS Lett; 2004 Nov; 577(3):507-11. PubMed ID: 15556637
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biopterin synthesis defects: problems in diagnosis.
    Hoganson G; Berlow S; Kaufman S; Milstien S; Schuett V; Matalon R; Naylor E; Seifert W
    Pediatrics; 1984 Dec; 74(6):1004-11. PubMed ID: 6150460
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neonatal hyperphenylalaninaemia presumably caused by a new variant of biopterin synthetase deficiency.
    Dhondt JL; Guibaud P; Rolland MO; Dorche C; Andre S; Forzy G; Hayte JM
    Eur J Pediatr; 1988 Feb; 147(2):153-7. PubMed ID: 3366132
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Screening of tetrahydrobiopterin deficiency among hyperphenylalaninemic patients].
    Dhondt JL; Hayte JM
    Ann Biol Clin (Paris); 2002; 60(2):165-71. PubMed ID: 11937441
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenylketonuria detected by the neonatal screening program in Thailand.
    Pangkanon S; Ratrisawadi V; Charoensiriwatana W; Techasena W; Boonpuan K; Srisomsap C; Svasti J
    Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():179-81. PubMed ID: 15906730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tetrahydrobiopterin deficiencies without hyperphenylalaninemia: diagnosis and genetics of dopa-responsive dystonia and sepiapterin reductase deficiency.
    Blau N; Bonafé L; Thöny B
    Mol Genet Metab; 2001; 74(1-2):172-85. PubMed ID: 11592814
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.