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Literature DB >> 5936868

Hypersarcosinemia: an inborn error of metabolism.

T Gerritsen, H A Waisman.

Abstract

Entities: Disease

Mesh：

Substances：
Glycine

Year: 1966 PMID： 5936868 DOI： 10.1056/NEJM196607142750202

Source DB: PubMed Journal: N Engl J Med ISSN： 0028-4793 Impact factor: 91.245

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Cited

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10 in total

1. Hypersarcosinemia with craniostenosis-syndactylism syndrome.

Authors: R Minami; K Olek; P Wardenbach
Journal: Humangenetik Date: 1975-06-19

2. Evaluation of Oxidative Stress Parameters and Energy Metabolism in Cerebral Cortex of Rats Subjected to Sarcosine Administration.

Authors: Rodrigo Binkowski de Andrade; Tanise Gemelli; Denise Bertin Rojas; Tomas Duk Hwa Kim; Ângela Zanatta; Felipe Schmitz; André Felipe Rodrigues; Angela T S Wyse; Moacir Wajner; Carlos Severo Dutra-Filho; Clovis Milton Duval Wannmacher
Journal: Mol Neurobiol Date: 2016-06-29 Impact factor: 5.590

3. A young adult with sarcosinemia. No benefit from long duration treatment with memantine.

Authors: A Benarrosh; R Garnotel; A Henry; C Arndt; P Gillery; J Motte; S Bakchine
Journal: JIMD Rep Date: 2012-10-21

4. Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.

Authors: B A Binzak; R A Wevers; S H Moolenaar; Y M Lee; W L Hwu; J Poggi-Bach; U F Engelke; H M Hoard; J G Vockley; J Vockley
Journal: Am J Hum Genet Date: 2001-02-28 Impact factor: 11.025

5. Sarcosinaemia in a retarded, amaurotic child.

Authors: A C Sewell; M Krille; I Wilhelm
Journal: Eur J Pediatr Date: 1986-02 Impact factor: 3.183

6. Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia.

Authors: Ifat Bar-joseph; Elon Pras; Haike Reznik-Wolf; Dina Marek-Yagel; Almogit Abu-Horvitz; Maya Dushnitzky; Nurit Goldstein; Shlomit Rienstein; Michal Dekel; Ben Pode-Shakked; Joseph Zlotnik; Anelia Benarrosh; Philippe Gillery; Niklaus Hofliger; Christiane Auray-Blais; Roselyne Garnotel; Yair Anikster
Journal: Hum Genet Date: 2012-07-24 Impact factor: 4.132

Hypersarcosinemia: an inborn error of metabolism.

1. Hypersarcosinemia with craniostenosis-syndactylism syndrome.

2. Evaluation of Oxidative Stress Parameters and Energy Metabolism in Cerebral Cortex of Rats Subjected to Sarcosine Administration.

3. A young adult with sarcosinemia. No benefit from long duration treatment with memantine.

4. Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.

5. Sarcosinaemia in a retarded, amaurotic child.

6. Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia.

7. sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis.

8. Variability in the phenotypic expression of abnormal sarcosine metabolism in a family.

9. Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes.

10. Chemically induced acute model of sarcosinemia in wistar rats.