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[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
Ann Biol Clin (Paris). 1979; 37(5):259-70.AB

Abstract

The authors define the main stages of the biochemical study of hereditary abnormalities of galactose metabolism. They review laboratory examinations for detection, enzyme examinations which provide the diagnostic proof, further examinations which permit one to follow the course and efficacy of a galactose-free diet, the demonstration of genetic variants, the technics of antenatal diagnosis and routine neonatal detection.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Review

Language

fre

PubMed ID

232826

Citation

Brivet, M, et al. "[Hereditary Abnormalities of Galactose Metabolism: Diagnosis and Biochemical Supervision (author's Transl)]." Annales De Biologie Clinique, vol. 37, no. 5, 1979, pp. 259-70.
Brivet M, Moatti N, Lemonnier A. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)]. Ann Biol Clin (Paris). 1979;37(5):259-70.
Brivet, M., Moatti, N., & Lemonnier, A. (1979). [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)]. Annales De Biologie Clinique, 37(5), 259-70.
Brivet M, Moatti N, Lemonnier A. [Hereditary Abnormalities of Galactose Metabolism: Diagnosis and Biochemical Supervision (author's Transl)]. Ann Biol Clin (Paris). 1979;37(5):259-70. PubMed PMID: 232826.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)]. AU - Brivet,M, AU - Moatti,N, AU - Lemonnier,A, PY - 1979/1/1/pubmed PY - 1979/1/1/medline PY - 1979/1/1/entrez SP - 259 EP - 70 JF - Annales de biologie clinique JO - Ann Biol Clin (Paris) VL - 37 IS - 5 N2 - The authors define the main stages of the biochemical study of hereditary abnormalities of galactose metabolism. They review laboratory examinations for detection, enzyme examinations which provide the diagnostic proof, further examinations which permit one to follow the course and efficacy of a galactose-free diet, the demonstration of genetic variants, the technics of antenatal diagnosis and routine neonatal detection. SN - 0003-3898 UR - https://www.unboundmedicine.com/medline/citation/232826/[Hereditary_abnormalities_of_galactose_metabolism:_diagnosis_and_biochemical_supervision__author's_transl_]_ DB - PRIME DP - Unbound Medicine ER -