Reduction of butyrylcholinesterase activity in plasma from patients with disorders of propionate metabolism is prevented by treatment with L-carnitine and protein restriction

Author:

Ribas Graziela S.,Scherer Emilene B.,Ferreira Andrea G.,Schmitz Felipe,Wyse Angela T.,Rodrigues Daiane,Nascimento Sabrina,Garcia Solange C.,Wajner Moacir,Vargas Carmen R.

Funder

FAPERGS

PROPESQ/UFRGS

CAPES

CNPq

FIPE/HCPA-Brazil

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference53 articles.

1. Disorders of propionate and methylmalonate metabolism;Fenton,2001

2. Propionic acidaemia: clinical, biochemical and therapeutic aspects. Experience in 30 patients;Lehnert;Eur J Pediatr,1994

3. Inborn metabolic diseases. Diagnosis and treatment;Ogier,1990

4. CT and MR of the brain in the diagnosis of organic acidemias. Experiences from 107 patients;Brismar;Brain Dev,1994

5. Propionic and L-methylmalonic acids induce oxidative stress in brain of young rats;Fontella;Neuroreport,2000

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