Results 281 to 290 of about 162,956 (297)

Peroxisomal leukodystrophy

Peroxisomal disorders can be classified as single-enzyme deficiencies or peroxisomal biogenesis disorders (characterized by multiple peroxisomal enzyme deficiencies or complete absence of peroxisomes). Most peroxisomal disorders give rise to complex multisystem disorders. Peroxisomal disorders associated with leukodystrophy are discussed in more detail,
openaire   +2 more sources

Peroxisome Isolation

2003
Distel, B., van der Leij, I., Kos, W.
openaire   +3 more sources

Peroxisome Mosaics

2003
Roels, Frank, Saudubray, Jean-Marie, Giros, Marisa, Mandel, Hanna, Eyskens, François, Saracibar, Nieves, Atares Pueyo, Begoña, Prats, Jose M., de Prest, Betty, de Preter, Kathleen, Pineda, Mercedes, Krystkowiak, Pierre, Gootjes, Jeannette, Wanders, Ronald J. A., Espeel, Marc, Poll-The, Bwee Tien   +15 more
openaire   +3 more sources

Peroxisomal Disorders

2003
Wanders, R. J. A., Barth, P. G., Poll-The, B. T.   +2 more
openaire   +2 more sources

Peroxisomal diseases

2007
Paul A. Watkins, Kathleen B. Schwarz
openaire   +1 more source

Peroxisomes proliferate

Trends in Cell Biology, 1995
J M, Leiper, G M, Birdsey, P B, Oatey
openaire   +2 more sources

Peroxisomal Diseases

Advances in Pediatrics, 1989
openaire   +3 more sources

Peroxisomal Disorders

2006
Poll-The, B. T., Aubourg, P., Wanders, R. J. A.   +2 more
openaire   +2 more sources

Peroxisome Biogenesis and Human Peroxisomal Disorders

Biochemical Society Transactions, 2000
openaire   +2 more sources

Interspecies Differences in Peroxisomes and Peroxisome Proliferation

Toxicology and Industrial Health, 1987
J V, Rodricks, D, Turnbull
openaire   +2 more sources