New clinical phenotype of branched-chain acyl-CoA oxidation defect-Reference-Cited by-同舟云学术

New clinical phenotype of branched-chain acyl-CoA oxidation defect

Published:1991-12 Issue:8781 Volume:338 Page:1522-1523
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Burlina AlbertoB,Zacchello Franco,Dionisi-Vici Carlo,Bertini Enrico,Sabetta Gaetano,Bennet MichaelJ,Hale DanielE,Schmidt-Sommerfeld Eberhard,Rinaldo Piero

Publisher

Elsevier BV

Subject

General Medicine

Reference7 articles.

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2. P. Rinaldo, Rd Welch, Sf Previs, et al., Ethylmalonic/adipic aciduria: effect of oral medium chain triglycerides, carnitine and glycine on urinary excretion of organic acids, acylcamitine and acylglycines, Pediatr Res ((in press)).

3. Riboflavin responsive glutanc aciduria type II;Gregersen,1990

4. Neurodegenerative diseases of childhood: MR and CT elevation;Mirowiz;J Comput Assist Tomogr,1991

5. Analysis of acylcarnitines in normal human urine with the radioisotope exchange high performance liquid chromatography (HPLC) method;Schmidt-Sommerfeld;Clin Chim Acta,1989

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