220 related articles for article (PubMed ID: 4947459)
1. [Early diagnosis of hereditary metabolic disorders as an effective means of preventing nervous system diseases in children].
Barashnev IuI; Kozlova SI
Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1470-4. PubMed ID: 4947459
[No Abstract] [Full Text] [Related]
2. [Mental retardation and hereditary enzymopathy (review)].
D'iachkova AIa; Lebedev BV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1588-93. PubMed ID: 5003148
[No Abstract] [Full Text] [Related]
3. [Detection of metabolic diseases].
Adriaenssens K; Van Sande M
Acta Neurol Psychiatr Belg; 1968 Oct; 68(10):719-28. PubMed ID: 4976725
[No Abstract] [Full Text] [Related]
4. Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970.
Fox JG; Hall DL; Haworth JC; Maniar A; Sekla L
Can Med Assoc J; 1971 Jun; 104(12):1085-8. PubMed ID: 5580751
[TBL] [Abstract][Full Text] [Related]
5. Newer procedures in the preconceptional, prenatal and early postnatal diagnosis of birth defects.
Nadler HL
Birth Defects Orig Artic Ser; 1970 May; 6(1):26-33. PubMed ID: 5522716
[No Abstract] [Full Text] [Related]
6. [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]
7. Genetic aspects in the diagnosis and management of mental retardation.
Stimson CW
Arch Phys Med Rehabil; 1971 Mar; 52(3):115-7. PubMed ID: 4252521
[No Abstract] [Full Text] [Related]
8. [Diagnosis of hereditary cerebral damage in children--differential diagnostic tables].
Bremer HJ
Med Welt; 1977 Oct; 28(43):1748-52. PubMed ID: 927143
[No Abstract] [Full Text] [Related]
9. Effects of early nutrition on growth of the central nervous system.
Winick M; Brasel JA; Velasco E; Rosso P
Birth Defects Orig Artic Ser; 1974; 10(2):29-36. PubMed ID: 4851745
[No Abstract] [Full Text] [Related]
10. [Prevention of congenital metabolic diseases. Early diagnosis by neonatal screening].
Giovannini M; Riva E
Minerva Med; 1979 Mar; 70(16):1137-46. PubMed ID: 440584
[No Abstract] [Full Text] [Related]
11. [Diagnosis of inborn errors of metabolism: necessity or luxury?].
Stöckler S
Wien Klin Wochenschr; 1992; 104(16):493-6. PubMed ID: 1413806
[No Abstract] [Full Text] [Related]
12. [Pre- and postnatal diagnosis of organoacidopathies].
Hoffmann GF; Jakobs C; Rating D; Sweetman L; Trefz FK
Monatsschr Kinderheilkd; 1990 Jul; 138(7):381-8. PubMed ID: 2204822
[TBL] [Abstract][Full Text] [Related]
13. [Intra-uterine diagnosis of hereditary diseases].
Cedergvist LL; Fuchs F
Nord Med; 1971 Sep; 86(35):1017-22. PubMed ID: 4257041
[No Abstract] [Full Text] [Related]
14. The use of amniocentesis for prenatal genetic counseling.
Gertner M; Hsu LY; Martin J; Hirshhorn K
Bull N Y Acad Med; 1970 Nov; 46(11):916-21. PubMed ID: 5273905
[No Abstract] [Full Text] [Related]
15. Perinatal diagnosis of the inborn errors of metabolism.
Elsas LJ
J Med Assoc Ga; 1971 Sep; 60(9):308-11. PubMed ID: 5093796
[No Abstract] [Full Text] [Related]
16. The critically ill child: acute metabolic disease in infancy and early childhood.
O'Brien D; Goodman SI
Pediatrics; 1970 Oct; 46(4):620-6. PubMed ID: 5503697
[No Abstract] [Full Text] [Related]
17. Hartnup disease in three siblings.
Nielsen EG; Vedso S; Zimmermann-Nielsen C
Dan Med Bull; 1966 Oct; 13(6):155-61. PubMed ID: 5927700
[No Abstract] [Full Text] [Related]
18. How we detect mental retardation before birth.
O'Brien JS
Med Times; 1971 Feb; 99(2):103-8. PubMed ID: 5545982
[No Abstract] [Full Text] [Related]
19. Antenatal detection of hereditary disorders.
Nadler HL
Pediatrics; 1968 Dec; 42(6):912-8. PubMed ID: 4235769
[No Abstract] [Full Text] [Related]
20. Intrauterine diagnosis of fetal disorders.
Kaback MM; Cooke RE
Paediatr Univ Tokyo; 1970 Dec; 18():79-87. PubMed ID: 5535256
[No Abstract] [Full Text] [Related]
[Next] [New Search]
