Egypt (EG)

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 NAFLD-Associated Comorbidities in Advanced Stage HCC Do Not Alter the Safety and Efficacy of Yttrium-90 Radioembolization (2019) Schotten C, Bechmann LP, Manka P, Theysohn J, Dechêne A, El Fouly A, Barbato F, et al. Journal article Protein biomarker discovery using human blood plasma microparticles (2019) Taleb RSZ, Moez P, Younan D, Eisenacher M, Tenbusch M, Sitek B, Bracht T Book chapter / Article in edited volumes 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 CT-derived left ventricular global strain: a head-to-head comparison with speckle tracking echocardiography (2019) Ammon F, Bittner D, Hell M, Mansour H, Achenbach S, Marwan M, Arnold M Journal article A new strategy for developing chitosan conversion coating on magnesium substrates for orthopedic implants (2019) Francis A, Yang Y, Boccaccini AR Journal article, Original article 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