The subfamily of sarcosine oxidase is a set of enzymes within the larger family of amine
oxidases. It is ubiquitously distributed among different kingdoms of life. The member …

Peroxisomal function was evaluated in a male infant with clinical features of neonatal
adrenoleukodystrophy. Very long chain fatty acid levels were elevated in both plasma and …

Le concept de l'existence d'états pathologiques humains associés à un mauvais
fonctionnement des peroxysomes est d'origine récente. Cela est partiellement dû à la …

The cerebrohepatorenal syndrome of Zellweger is a congenital syndrome of multiple
manifestations, including hepatomegaly and liver dysfunction. Treatment is generally of a …

Biochemical studies with emphasis on peroxisomal functions were conducted in six patients
with well-documented rhizomelic chondrodysplasia punctata (RCDP) and compared with …

Peroxisomal disorders are a clinically and genetically heterogeneous group of diseases
caused by defects in peroxisomal biogenesis or function, usually impairing several …

The influence of pyrene-fatty acids on the resistance of cells to ultraviolet (UV) radiation was
investigated in cultured fibroblasts from patients with five types of peroxisomal disorders. All …

As described so vividly and succinctly by Lewis Rowland in his 1983 lecture, Robert
Wartenberg was an outstanding neurologist and “peppery” teacher, and a skilled writer who …

Though peroxisomes were identified over 30 years ago, their clinical significance was not
recognized until recently. Within the last decade, five clinical syndromes definitely due to …

A high-performance liquid chromatography method for the simultaneous determination of
pipecolic acid (Pip) and lysine (Lys), a precursor of Pip, in the rumen liquor and plasma of …