318 related articles for article (PubMed ID: 7432385)
1. Phenylketonuria: epitome of human biochemical genetics (second of two parts).
Scriver CR; Clow CL
N Engl J Med; 1980 Dec; 303(24):1394-400. PubMed ID: 7432385
[No Abstract] [Full Text] [Related]
2. Phenylketonuria: epitome of human biochemical genetics (first of two parts).
Scriver CR; Clow CL
N Engl J Med; 1980 Dec; 303(23):1336-42. PubMed ID: 7001231
[No Abstract] [Full Text] [Related]
3. Treated phenylketonuria: intelligence and blood phenylalanine levels.
Fuller R; Shuman J
Am J Ment Defic; 1971 Mar; 75(5):539-45. PubMed ID: 5551499
[No Abstract] [Full Text] [Related]
4. 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]
5. Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria.
Hennermann JB; Loui A; Weber A; Mönch E
J Perinat Med; 2004; 32(4):383-5. PubMed ID: 15346830
[TBL] [Abstract][Full Text] [Related]
6. [Our experiences with treatment of phenylketonuria].
Tresohlavá Z; Brachfeld K; Svatý J
Cesk Pediatr; 1969 Jun; 24(6):522-8. PubMed ID: 5792287
[No Abstract] [Full Text] [Related]
7. Phenylketonuria and its variants.
Kaufman S
Adv Hum Genet; 1983; 13():217-97. PubMed ID: 6362361
[No Abstract] [Full Text] [Related]
8. Neonatal hyperphenylalaninemia: a differential diagnosis.
Menkes JH; Holtzman NA
Neuropadiatrie; 1970 Apr; 1(4):434-46. PubMed ID: 5538081
[No Abstract] [Full Text] [Related]
9. Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.
Cunningham GC; Day RW; Berman JL; Hsia DY
Am J Dis Child; 1969 Jun; 117(6):626-35. PubMed ID: 5771502
[No Abstract] [Full Text] [Related]
10. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.
Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
J Pediatr Gastroenterol Nutr; 2008 May; 46(5):561-9. PubMed ID: 18493213
[TBL] [Abstract][Full Text] [Related]
11. The problem of maternal phenylketonuria.
MacCready RA; Levy HL
Am J Obstet Gynecol; 1972 May; 113(1):121-8. PubMed ID: 5024993
[No Abstract] [Full Text] [Related]
12. Phenylketonemia in phenylketonuria.
Partington MW; Vickery SK
Neuropadiatrie; 1974 May; 5(2):125-37. PubMed ID: 4407755
[No Abstract] [Full Text] [Related]
13. Phenylketonuria: intellectual developmental and early treatment.
O'Grady DJ; Berry HK; Sutherland BS
Dev Med Child Neurol; 1970 Jun; 12(3):343-7. PubMed ID: 5433150
[No Abstract] [Full Text] [Related]
14. The correlation of genotype and phenotype in Portuguese hyperphenylalaninemic patients.
Rivera I; Cabral A; Almeida M; Leandro P; Carmona C; Eusébio F; Tasso T; Vilarinho L; Martins E; Lechner MC; de Almeida IT; Konecki DS; Lichter-Konecki U
Mol Genet Metab; 2000 Mar; 69(3):195-203. PubMed ID: 10767174
[TBL] [Abstract][Full Text] [Related]
15. A new variant form of phenylketonuria.
Watts RW; Purkiss P; Chalmers RA
Q J Med; 1979 Jul; 48(191):403-17. PubMed ID: 317358
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders.
Ledley FD; Levy HL; Woo SL
N Engl J Med; 1986 May; 314(20):1276-80. PubMed ID: 3702929
[TBL] [Abstract][Full Text] [Related]
17. Newborn screening for phenylketonuria: thirty years of progress.
O'Flynn ME
Curr Probl Pediatr; 1992 Apr; 22(4):159-65. PubMed ID: 1576829
[No Abstract] [Full Text] [Related]
18. Prenatal diagnosis of classical phenylketonuria by gene mapping.
Woo SL; Lidsky AS; Güttler F; Thirumalachary C; Robson KJ
JAMA; 1984 Apr; 251(15):1998-2002. PubMed ID: 6700105
[No Abstract] [Full Text] [Related]
19. [Congenital errors of metabolism: phenylketonuria and hyperphenylalanemias].
Laguna Serrano C
An R Acad Nac Med (Madr); 1982; 99(4):783-814. PubMed ID: 7185286
[No Abstract] [Full Text] [Related]
20. [Current problems in the diagnosis and treatment of phenylketonuria].
Sanielevici-Marinov S; Anagnoste V; Mark E; Tomescu E; Iordache C
Pediatria (Bucur); 1973; 22(1):1-12. PubMed ID: 4733556
[No Abstract] [Full Text] [Related]
[Next] [New Search]