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 *

451 related articles for article (PubMed ID: 5771502)

  • 1. 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]  

  • 2. Hyperphenylalaninemia or phenylketonuria (PKU)? Problems of early distinction in 15 and 34 cases respectively.
    Scheibenreiter S; Thalhammer O
    Z Kinderheilkd; 1972; 112(2):153-62. PubMed ID: 5023843
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. [The traps of Guthrie's test].
    Saudubray JM; Charpentier C
    Arch Fr Pediatr; 1976 Nov; 33(G):915-20. PubMed ID: 827271
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hyperphenylalaninemia in Polish children's population.
    Cabalska B; Duczynska N; Nowaczewska I; Bozkowa K
    Acta Anthropogenet; 1985; 9(1-3):91-102. PubMed ID: 3843752
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia].
    Dhondt JL; Cartigny B; Farriaux JP
    Ann Biol Clin (Paris); 1974; 32(6):499-506. PubMed ID: 4468743
    [No Abstract]   [Full Text] [Related]  

  • 8. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R
    Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976
    [No Abstract]   [Full Text] [Related]  

  • 9. Analysis of the "report on a cooperative study of various fluorometric procedures and the Guthrie Bacterial Inhibition Assay in the determination of hyperphenylalaninemia" and the significance of this study in the detection, diagnosis, and management of phenylketonuria (PKU).
    Ambrose JA
    Health Lab Sci; 1973 Jul; 10(3):188-94. PubMed ID: 4720477
    [No Abstract]   [Full Text] [Related]  

  • 10. [Phenylketonuria and hyperphenylalaninemia. Introduction to the subject].
    Romano C
    Minerva Nipiol; 1970; 20(5):112-43. PubMed ID: 5566887
    [No Abstract]   [Full Text] [Related]  

  • 11. Neonatal hyperphenylalaninemia: a differential diagnosis.
    Menkes JH; Holtzman NA
    Neuropadiatrie; 1970 Apr; 1(4):434-46. PubMed ID: 5538081
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. [Detection of heterozygotes of typical phenylketonuria].
    Farriaux JP; Delabre M
    Arch Fr Pediatr; 1972 Apr; 29(4):365-72. PubMed ID: 5053206
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. [Evaluation of the activity of a phenylketonuria detection center. Analysis of the results of 500,000 tests].
    Barbesier J; Boisse J; Charpentier C; Lemonnier A; Mozziconacci P; Saudubray JM
    Presse Med (1893); 1971 Feb; 79(9):395-7. PubMed ID: 5546799
    [No Abstract]   [Full Text] [Related]  

  • 16. [Follow-up in mild hyperphenylalaninemia].
    Theile H; Machill G
    Kinderarztl Prax; 1980 Mar; 48(3):124-9. PubMed ID: 7392429
    [No Abstract]   [Full Text] [Related]  

  • 17. [Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages].
    Simková M; Hyánek J; Karger P; Hoza J; Holub J; Viletová H
    Cesk Pediatr; 1976 Nov; 31(11):619-21. PubMed ID: 1035139
    [No Abstract]   [Full Text] [Related]  

  • 18. [Differentiation of hyperphenylalaninemia by means of dietary loading].
    Zammarchi E; Bardini MR; De Nigris L; Vierucci A
    Minerva Pediatr; 1978 May; 30(9):713-26. PubMed ID: 661780
    [No Abstract]   [Full Text] [Related]  

  • 19. [Phenylalanine metabolites in the urine after oral phenylalanine loading. Significance for the discrimination between classical phenylketonuria and variations of hyperphenylalaninemia (heterozygotes and homozygotes)].
    Koepp P
    Fortschr Med; 1977 Mar; 95(10):627-31. PubMed ID: 844759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Early blood sampling in neonatal programs for the detection of phenylketonuria.
    Szeinberg A; Cohen BE
    Padiatr Padol; 1982; 17(2):287-92. PubMed ID: 7099682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.