Cairo University

HLA HHaplotypes In 250 Families: The Baylor Laboratory Results And A Aerspective On A Core NGS Testing Model For The 17th International HLA And Immunogenetics Workshop (2019) Askar M, Madbouly A, Zhrebker L, Willis A, Kennedy S, Padros K, Rodriguez MB, et al. Journal article, Review article Studies on Pd(1,4-bis(2-hydroxyethyl)piperazine)-dicarboxylic acid complexes as models for carboplatin with structural features enhancing the interaction with DNA (2019) Shehata MR, Shoukry MM, Mabrouk MA, Kozakiewicz A, van Eldik R Journal article Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children (2019) Vivante A, Chacham OS, Shril S, Schreiber R, Mane SM, Pode-Shakked B, Soliman NA, et al. Journal article Association of Intrathecal Immunoglobulin G Synthesis with Disability Worsening in Multiple Sclerosis (2019) Gasperi C, Salmen A, Antony G, Bayas A, Heesen C, Kümpfel T, Linker R, et al. Journal article A homozygous splice site mutation in SLC25A42, encoding the mitochondrial transporter of coenzyme a, causes metabolic crises and epileptic encephalopathy (2019) Iuso A, Alhaddad B, Weigel C, Kotzaeridou U, Mastantuono E, Schwarzmayr T, Graf E, et al. Book chapter / Article in edited volumes Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment (2018) Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, et al. Journal article Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract (2018) Van Der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, et al. Journal article Preparation and in vitro characterization of silver-doped bioactive glass nanoparticles fabricated using a sol-gel process and modified Stöber method (2018) El-Rashidy AA, Waly G, Gad A, Hashem AA, Balasubramanian P, Kaya S, Boccaccini AR, Sami I Journal article Composition and diameter modulation of magnetic nanowire arrays fabricated by a novel approach (2018) Salem MS, Tejo F, Zierold R, Sergelius P, Moreno JMM, Goerlitz D, Nielsch K, Escrig J Journal article Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis (2018) Daga A, Majmundar AJ, Braun DA, Gee HY, Lawson JA, Shril S, Jobst-Schwan T, et al. Journal article