Page last updated: 2024-08-26

nsc-172755 and Hyperphosphatemia

nsc-172755 has been researched along with Hyperphosphatemia in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adjagba, M; Alao, MJ; Arveiler, B; Ayivi, B; Coupry, I; Darboux, RB; Gbessi, G; Lacombe, D; Laleye, A; Lepreux, S; Marche, M; Redonnet-Vernhet, I	1

Other Studies

1 other study(ies) available for nsc-172755 and Hyperphosphatemia

Article	Year
Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African family. Genetic counseling (Geneva, Switzerland), 2008, Volume: 19, Issue:2 Topics: Adolescent; Adult; Amelogenesis Imperfecta; Apatites; Benin; Black People; Calcinosis; Fibroblast Growth Factor-23; Humans; Hyperphosphatemia; Joint Diseases; Male; Mutation; N-Acetylgalactosaminyltransferases; Pedigree; Polypeptide N-acetylgalactosaminyltransferase; Siblings	2008

Article

Year

Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African family.

Genetic counseling (Geneva, Switzerland), 2008, Volume: 19, Issue:2

Topics: Adolescent; Adult; Amelogenesis Imperfecta; Apatites; Benin; Black People; Calcinosis; Fibroblast Growth Factor-23; Humans; Hyperphosphatemia; Joint Diseases; Male; Mutation; N-Acetylgalactosaminyltransferases; Pedigree; Polypeptide N-acetylgalactosaminyltransferase; Siblings

2008