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.
3. Hyperphenylalaninemia syndromes: current status of diagnosis and management. Matsuo N Keio J Med; 1988 Mar; 37(1):1-9. PubMed ID: 3286956 [No Abstract] [Full Text] [Related]
4. [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]
5. [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]
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. [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]
8. Tetrahydrobiopterin deficiencies: preliminary analysis from an international survey. Dhondt JL J Pediatr; 1984 Apr; 104(4):501-8. PubMed ID: 6142937 [TBL] [Abstract][Full Text] [Related]
9. [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]
14. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood. Güttler F Acta Paediatr Scand Suppl; 1980; 280():1-80. PubMed ID: 7006308 [No Abstract] [Full Text] [Related]