[The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders]
- PMID: 9507277
[The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders]
Similar articles
-
High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:130-3. Southeast Asian J Trop Med Public Health. 1995. PMID: 8629091
-
Diagnosis and therapy of organic acidurias.Padiatr Padol. 1993;28(1):3-8. Padiatr Padol. 1993. PMID: 8446425 Review.
-
[Biochemistry of the blood and urine in members of families suspected of having hereditary metabolic defects].Physiologie. 1980 Apr-Jun;17(2):101-11. Physiologie. 1980. PMID: 6770382 French. No abstract available.
-
Screening urine of 3-week-old newborns: lack of association between sudden infant death syndrome and some metabolic disorders.Pediatrics. 1993 May;91(5):986-8. Pediatrics. 1993. PMID: 8474821 No abstract available.
-
Screening for genetic disorders.Fed Proc. 1975 Nov;34(12):2134-9. Fed Proc. 1975. PMID: 1102335 Review. No abstract available.