158 related articles for article (PubMed ID: 337387)
1. [Disorders of amino acid metabolism (author's transl)].
Hirano S
Tanpakushitsu Kakusan Koso; 1977; 22(6):776-83. PubMed ID: 337387
[No Abstract] [Full Text] [Related]
2. The assessment of serum amino acids.
Swallow WH; Carrell RW
N Z Med J; 1970 Feb; 71(453):85-8. PubMed ID: 5267129
[No Abstract] [Full Text] [Related]
3. Phenylalaninemia or classical phenylketonuria.
Menkes JH; Holtzman NA
Neuropadiatrie; 1970 Aug; 2(1):121-2. PubMed ID: 5538091
[No Abstract] [Full Text] [Related]
4. [Brain function in inborn error of amino acid metabolism].
Takada G
Tanpakushitsu Kakusan Koso; 1984 Dec; 29(14):1783-93. PubMed ID: 6398464
[No Abstract] [Full Text] [Related]
5. Phenylalaninaemia or classical phenylketonuria (PKU)?
Bickel H
Neuropadiatrie; 1970 Apr; 1(4):379-82. PubMed ID: 5538079
[No Abstract] [Full Text] [Related]
6. [Inborn errors of amino acid metabolism--pathogenesis of mental retardation].
Tada K; Yoshida T
Shinkei Kenkyu No Shimpo; 1968; 12(1):137-46. PubMed ID: 4881483
[No Abstract] [Full Text] [Related]
7. [Hyperaminoaciduria].
Prader A
Schweiz Med Wochenschr; 1966 Jan; 96(2):53-6. PubMed ID: 5985557
[No Abstract] [Full Text] [Related]
8. [Amino acid metabolism of neuro-muscular diseases].
Yoshikawa M; Hirai S
Nihon Rinsho; 1966 Jan; 24(1):39-49. PubMed ID: 5336583
[No Abstract] [Full Text] [Related]
9. Abnormal amino acid metabolism and brain protein synthesis during neural development.
Hughes JV; Johnson TC
Neurochem Res; 1978 Aug; 3(4):381-99. PubMed ID: 34113
[No Abstract] [Full Text] [Related]
10. [Brain protein synthesis in experimental hyperaminoacidemia--an approach to the pathogenesis of mental retardation in inborn errors of amino acid metabolism].
Tada K; Takada G
Shinkei Kenkyu No Shimpo; 1971; 15(2):359-66. PubMed ID: 5106846
[No Abstract] [Full Text] [Related]
11. [Early detection of inborne errors of metabolism in Switzerland: the problems of hyperphenylanalinemia (author's transl)].
Colombo JP
Ther Umsch; 1974 Aug; 31(8):545-52. PubMed ID: 4848540
[No Abstract] [Full Text] [Related]
12. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies].
Segni G
Minerva Nipiol; 1970; 20(4):83-110. PubMed ID: 4396023
[No Abstract] [Full Text] [Related]
13. The transport of metabolizable substances into the living brain.
Pratt OE
Adv Exp Med Biol; 1976; 69():55-75. PubMed ID: 7929
[No Abstract] [Full Text] [Related]
14. [Physiological and pathological aminoacidurias].
Brodehl J
Monatsschr Kinderheilkd (1902); 1973 May; 121(5):190-200. PubMed ID: 4713389
[No Abstract] [Full Text] [Related]
15. [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]
16. 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. PubMed ID: 5022091
[No Abstract] [Full Text] [Related]
17. Hyperphenylalaninemias and tyrosinemias.
Berry HK
Clin Perinatol; 1976 Mar; 3(1):15-40. PubMed ID: 954342
[No Abstract] [Full Text] [Related]
18. [Metabolism of amino acids and brain proteins in phenylketonuria].
Borkowska I
Postepy Biochem; 1979; 25(2):159-68. PubMed ID: 574271
[No Abstract] [Full Text] [Related]
19. [Biochemical studies on inherited disorders of amino acid metabolism in pediatrics].
Antener I
Z Klin Chem Klin Biochem; 1970 Sep; 7(5):427-39. PubMed ID: 5505952
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
