|1.||Nevo, N: 1 article (06/2015)|
|2.||Cherqui, S: 1 article (06/2015)|
|3.||Van Der Smissen, P: 1 article (06/2015)|
|4.||Liao, X H: 1 article (06/2015)|
|5.||Refetoff, S: 1 article (06/2015)|
|6.||Abid, Y: 1 article (06/2015)|
|7.||Pierreux, C E: 1 article (06/2015)|
|8.||Janssens, V: 1 article (06/2015)|
|9.||Courtoy, P J: 1 article (06/2015)|
|10.||Gaide Chevronnay, H P: 1 article (06/2015)|
07/01/1956 - "[Genetics of cystinosis (cystine storage disease) and its relation to cystinuria and hyperaminoaciduria]."
06/01/2015 - "Cystinosis is a lysosomal cystine storage disease due to defective cystine exporter, cystinosin. "
10/01/1951 - "Cystinosis (cystine-storage disease); report of a case with chemical isolation and quantitative determination of cystine in lymph nodes, spleen, and liver."
01/01/1980 - "These deposits are possibly immune complexes being deposited in the glomeruli unrelated to the cystine-storage disease or they may represent a localized activation of the complement system induced by the glomerular injury of cystinosis."
|3.||X-Linked Dominant Hypophosphatemic Rickets (X-Linked Hypophosphatemia)
|3.||Complement System Proteins (Complement)
|4.||Antigen-Antibody Complex (Immune Complex)