Results 91 to 100 of about 1,135,071 (192)

A brief history of the human liver peroxisome. [PDF]

Histochem Cell Biol
De Craemer D, Van den Branden C, Roels F.   +2 more
europepmc   +1 more source

Peroxisomes, Peroxisomal Diseases, and the Hepatotoxicity Induced by Peroxisomal Metabolites

, 2012
The group of peroxisomal disorders represents a growing number of genetically determined diseases in humans in which there is an impairment in one or more peroxisomal functions.
Wanders, Ronald J. A., Ferdinandusse, Sacha   +1 more
core  

Adult-Onset Recessive Cerebellar Ataxia and Severe Multisystem Disease-Associated Genes: Hypomorphic Alleles and Clinical Interpretation Pitfalls. [PDF]

Genes (Basel)
Cipriano L, Petillo R, Priolo M, D'Ambrosio P.   +3 more
europepmc   +1 more source

Early hypotonia and visual regression as presenting features of peroxisome biogenesis disorder: an Egyptian case report. [PDF]

BMC Pediatr
Sadek AA, Aladawy MA, Hassan K, Mansour TMM, Naser M, Elmoursy MM, Hedewy S, Hagag A, Mohamed KR, Abdelkreem E.   +9 more
europepmc   +1 more source

Heimler Syndrome Caused by Novel <i>PEX6</i> Variants: Clinical and Genetic Characterization in a Saudi Cohort. [PDF]

Genes (Basel)
AlMoallem B.
europepmc   +1 more source

Peroxisome Biogenesis Disorder 6B [PDF]

, 2020
openaire   +1 more source

Visualisation of peroxisomes: a journey through seven decades. [PDF]

Histochem Cell Biol
Tang X, Islinger M, Schrader M.
europepmc   +1 more source

Peroxisome Biogenesis Disorder 1B [PDF]

, 2020
openaire   +1 more source

Unraveling PEX6: insights into very-long-chain fatty acid levels and peroxisome biogenesis disorders in pediatric populations. [PDF]

Ann Pediatr Endocrinol Metab
Ahangari N, Shirvan BB, Ashrafzadeh F, Karimiani EG, Hashemi N, Imannezhad S, Kalat HL, Ebrahimzadeh F, Akhondian J, Toosi MB.   +9 more
europepmc   +1 more source

Peroxisome Biogenesis Disorder 5A [PDF]

, 2020
openaire   +1 more source