Results 291 to 300 of about 9,057,553 (322)
Some of the next articles are maybe not open access.
2010
Fabry’s disease is an X-linked recessively inherited lysosomal storage disease, caused by a deficiency in catalytic activity or absence of lysosomal α-galactosidase A. This results in the lysosomal accumulation of glycosph- ingolipids with terminal α-galactosyl residues such as globotriaosylceramide and to a lesser extent of galabiosylceramide and ...
Margit Pavelka, Jürgen Roth
openaire +2 more sources
Fabry’s disease is an X-linked recessively inherited lysosomal storage disease, caused by a deficiency in catalytic activity or absence of lysosomal α-galactosidase A. This results in the lysosomal accumulation of glycosph- ingolipids with terminal α-galactosyl residues such as globotriaosylceramide and to a lesser extent of galabiosylceramide and ...
Margit Pavelka, Jürgen Roth
openaire +2 more sources
Onconephrology: The intersections between the kidney and cancer
Ca-A Cancer Journal for Clinicians, 2021Mitchell H Rosner +2 more
exaly
Multidisciplinary standards of care and recent progress in pancreatic ductal adenocarcinoma
Ca-A Cancer Journal for Clinicians, 2020Aaron J Grossberg +2 more
exaly
Fabry disease: where are we now?
International Urology and Nephrology, 2020K. Turkmen, I. Baloglu
semanticscholar +1 more source
Molecular imaging in oncology: Current impact and future directions
Ca-A Cancer Journal for Clinicians, 2022Martin G Pomper, Steven P Rowe
exaly
Management of glioblastoma: State of the art and future directions
Ca-A Cancer Journal for Clinicians, 2020Aaron C Tan +2 more
exaly