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Results: 1 to 20 of 126

1.

Heterogeneity in genetic control of phenylalanine metabolism in man.

Rosenblatt D, Scriver CR.

Nature. 1968 May 18;218(5142):677-8. No abstract available.

PMID:
5655958
[PubMed - indexed for MEDLINE]
2.

[Some indices of phenylalanine and tyrosine metabolism in children with phenylketonuria].

D'iachkova AIa, Lebedev BV.

Vopr Okhr Materin Det. 1969;14(7):29-32. Russian. No abstract available.

PMID:
5367726
[PubMed - indexed for MEDLINE]
3.

Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals.

Thalhammer O, Pollak A, Lubec G, Königshofer H.

Hum Genet. 1980;54(2):213-6. No abstract available.

PMID:
7390492
[PubMed - indexed for MEDLINE]
4.

Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria compared with 26 normals.

Thalhammer O, Pollak A, Lubec G, Königshofer H.

J Inherit Metab Dis. 1981;4(2):73-4. No abstract available.

PMID:
6790854
[PubMed - indexed for MEDLINE]
5.

The use of deuterated phenylalanine for the elucidation of the phenylalanine-tyrosine metabolism.

Curtius HC, Völlmin JA, Baerlocher K.

Clin Chim Acta. 1972 Mar;37:277-85. No abstract available.

PMID:
5022091
[PubMed - indexed for MEDLINE]
6.

Phenylalanine and other amino acids in phenylketonuria.

Clemens PC, Burmester JG, Prankel BH, Wiegand G, Wulke AP, Plettner C.

J Inherit Metab Dis. 1993;16(6):1045-6. No abstract available.

PMID:
8127057
[PubMed - indexed for MEDLINE]
7.

Fluorometric measurement of tyrosine in serum and plasma.

Ambrose JA.

Clin Chem. 1974 Apr;20(4):505-10. No abstract available.

PMID:
4818207
[PubMed - indexed for MEDLINE]
Free Article
8.

Determination of heterozygosity for phenylketonuria on the amino acid analyzer.

Perry TL, Hansen S, Tischler B, Bunting R.

Clin Chim Acta. 1967 Oct;18(1):51-6. No abstract available.

PMID:
6064693
[PubMed - indexed for MEDLINE]
9.

Discriminant analysis for detection of phenylketonuric heterozygotes.

Christian BG.

Soc Biol. 1971 Mar;18(1):64-72. No abstract available.

PMID:
5580588
[PubMed - indexed for MEDLINE]
10.

Urinary phenylalanine excretion in hyperphenylalaninemic children.

Güttler F, Rosleff F.

Acta Paediatr Scand. 1973 Jul;62(4):333-6. No abstract available.

PMID:
4729684
[PubMed - indexed for MEDLINE]
11.

About changes of the phenylalanine-tyrosine metabolism in psoriasis vulgaris.

Knapp A.

Acta Univ Carol Med (Praha). 1986;32(3-4):203-6. No abstract available.

PMID:
3434474
[PubMed - indexed for MEDLINE]
12.

Plasma phenylalanine, tyrosine, and tryptophan in schizophrenia.

Potkin SG, Cannon-Spoor HE, DeLisi LE, Neckers LM, Wyatt RJ.

Arch Gen Psychiatry. 1983 Jul;40(7):749-52.

PMID:
6860076
[PubMed - indexed for MEDLINE]
13.

Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.

Blau K, Summer GK, Newsome HC, Edwards CH.

Clin Chim Acta. 1973 May 18;45(3):197-205. No abstract available.

PMID:
4708049
[PubMed - indexed for MEDLINE]
14.
15.

[Method of detection of heterozygotic carrier state in phenylketonuria].

Baikov AD, Sitnichenko EI.

Lab Delo. 1973;5:293-5. Russian. No abstract available.

PMID:
4129158
[PubMed - indexed for MEDLINE]
16.

The use of biochemical data in screening for mutant alleles and in genetic counselling.

Gold RJ, Maag UR, Neal JL, Scriver CR.

Ann Hum Genet. 1974 Jan;37(3):315-26. No abstract available.

PMID:
4812952
[PubMed - indexed for MEDLINE]
17.

The measurement of phenylalanine and tyrosine in blood.

Robins E.

Methods Biochem Anal. 1969;17:287-309. Review. No abstract available.

PMID:
4896502
[PubMed - indexed for MEDLINE]
18.

Detection of phenylketonuric heterozygotes.

Jackson SH, Hanley WB, Gero T, Gosse GD.

Clin Chem. 1971 Jun;17(6):538-43. No abstract available.

PMID:
5103385
[PubMed - indexed for MEDLINE]
Free Article
19.

An enzymatic assay of plasma phenylalanine and tyrosine for the detection and management of phenylketonuria.

Shen RS, Richardson CJ, Rouse BM, Abell CW.

Biochem Med. 1981 Oct;26(2):211-21. No abstract available.

PMID:
7317039
[PubMed - indexed for MEDLINE]
20.

Two siblings of hyperphenylalaninemia: suggestion to a genetic variant of phenylketonuria.

Tada K, Yoshida T, Mochizuki K, Konno T, Nakagawa H.

Tohoku J Exp Med. 1970 Mar;100(3):249-53. No abstract available.

PMID:
5442719
[PubMed - indexed for MEDLINE]
Free Article

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