Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syn...
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Δευτέρα 23 Απριλίου 2018
Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency
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This protocol presents an in vitro live-imaging phagocytosis assay to measure the phagocytic capacity of astrocytes. Purified rat astrocyt...
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A Case of Miller Fisher Syndrome Due to the Use of Cemiplimab : No abstract available Miller Fisher syndrome is a rare, acquired n...
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