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  Fabry Disease - Google Books

  https://books.google.de/books?id=GAwHNttd8McC

  Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathological disease, occurs preferentially in renal glomerular and tubular…

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  Anthony Cerami - Google Scholar Citations

  https://scholar.google.de/citations?user=ZC57OsIAAAAJ&hl=de&oi=ao

  Keine Beschreibung vorhanden.

• 

  Fabry Disease - Google Books

  https://books.google.de/books?id=GAwHNttd8McC&pg=PA293#v=onepage

  Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathological disease, occurs preferentially in renal glomerular and tubular…

• 

  Fabry Disease - Google Books

  https://books.google.de/books?id=GAwHNttd8McC&pg=PA3#v=onepage

  Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathological disease, occurs preferentially in renal glomerular and tubular…

• 

  Fabry Disease - Google Books

  https://books.google.de/books?id=GAwHNttd8McC&pg=PAXIX#v=onepage

  Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathological disease, occurs preferentially in renal glomerular and tubular…

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  Niere Dr.Jastrows EM-Atlas

  http://www.uni-mainz.de/FB/Medizin/Anatomie/workshop/EM/EMNiere.html

  Keine Beschreibung vorhanden.

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