159 related articles for article (PubMed ID: 4593296)
1. Genetic screening.
Levy HL
Adv Hum Genet; 1973; 4():1-104. PubMed ID: 4593296
[No Abstract] [Full Text] [Related]
2. The value of screening in paediatrics.
Carter RA
J R Coll Physicians Lond; 1976 Jan; 10(2):153-60. PubMed ID: 54421
[No Abstract] [Full Text] [Related]
3. Neonatal screening for inborn errors of amino acid metabolism.
Levy HL
Clin Endocrinol Metab; 1974 Mar; 3(1):153-66. PubMed ID: 4609646
[No Abstract] [Full Text] [Related]
4. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
Kroll S; Zebisch P; Toussaint W
Fortschr Med; 1972 Apr; 90(11):430-1. PubMed ID: 4681731
[No Abstract] [Full Text] [Related]
5. [Dietetics in hereditary enzyme deficiencies].
Royer P
Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674
[No Abstract] [Full Text] [Related]
6. [The inborn errors of metabolism of amino acids].
Tomaszewski L
Postepy Biochem; 1973; 19(1):91-122. PubMed ID: 4697972
[No Abstract] [Full Text] [Related]
7. Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
Humangenetik; 1975 Dec; 30(4):273-86. PubMed ID: 1218857
[No Abstract] [Full Text] [Related]
8. The aminoacidurias.
Efron ML; Ampola MG
Pediatr Clin North Am; 1967 Nov; 14(4):881-903. PubMed ID: 4875467
[No Abstract] [Full Text] [Related]
9. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Kroll S; Zebisch P; Toussaint W
Fortschr Med; 1972 Apr; 90(11):423-8. PubMed ID: 4680607
[No Abstract] [Full Text] [Related]
10. [Eye manifestations of amino acid disorders].
Greco GM; Magli A
Minerva Pediatr; 1978 May; 30(10):761-80. PubMed ID: 353484
[No Abstract] [Full Text] [Related]
11. Neonatal screening tests.
Mamunes P
Pediatr Clin North Am; 1980 Nov; 27(4):733-51. PubMed ID: 7005846
[No Abstract] [Full Text] [Related]
12. INBORN ERRORS OF METABOLISM.
FINCKE ML
J Am Diet Assoc; 1965 Apr; 46():280-4. PubMed ID: 14285451
[No Abstract] [Full Text] [Related]
13. Pediatric clinical aspects of aminoacidopathies.
Hooft C; Carton D
Monogr Hum Genet; 1972; 6():50-63. PubMed ID: 4663915
[No Abstract] [Full Text] [Related]
14. Genetic screening: notes added in proof.
Levy HL
Adv Hum Genet; 1973; 4():389-94. PubMed ID: 4783333
[No Abstract] [Full Text] [Related]
15. [Paper chromatography in the detection of aminoacidopathies].
Sietti C
Minerva Pediatr; 1971 Dec; 23(51):2123-4. PubMed ID: 5136311
[No Abstract] [Full Text] [Related]
16. [Disorders of amino acids].
Aoki K
Nihon Rinsho; 1993 Jan; 51 Suppl():332-9. PubMed ID: 8459561
[No Abstract] [Full Text] [Related]
17. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
Lebedev VP; Iur'eva EA; Mukhina IuG; Buravina TA; Koroleva IA
Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437
[No Abstract] [Full Text] [Related]
18. [Systematic detection of hereditary metabolic encephalopathies].
Neimann N; Pierson M; Vidailhet M; Siest G; Badonnel Y; Humbel R; Roos F
Ann Pediatr (Paris); 1968 Oct; 15(10):635-41. PubMed ID: 4237831
[No Abstract] [Full Text] [Related]
19. [Feeble mindedness caused by genetic disorders of amino acid metabolism].
Menne F
Hippokrates; 1968 May; 39(10):357-67. PubMed ID: 4886426
[No Abstract] [Full Text] [Related]
20. Phenylketonuria and other disorders of amino acid metabolism.
Ampola MG
Pediatr Clin North Am; 1973 May; 20(2):507-36. PubMed ID: 4573597
[No Abstract] [Full Text] [Related]
[Next] [New Search]
