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Pediatrics|August 3, 1999
Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative StudyF Güttler, C Azen, P Guldberg, et al.Human Immunology|May 4, 2004
HLA-DRB1 alleles and HLA-DRB1 shared epitopes are markers for juvenile rheumatoid arthritis subgroups in Colombian mestizosGloria Garavito, Edmond J Yunis, Eduardo Egea, et al.Oncogene|April 8, 2014
SUMOylation regulates AKT1 activityC F de la Cruz-Herrera, M Campagna, V Lang, et al.International Journal of Experimental Pathology|October 31, 2015
Altered expression of CKs 14/20 is an early event in a rat model of multistep bladder carcinogenesisRui M Gil da Costa, Paula A Oliveira, Carmen Vasconcelos-Nóbrega, et al.American Journal of Obstetrics and Gynecology|February 29, 2000
The international study of pregnancy outcome in women with maternal phenylketonuria: report of a 12-year studyL D Platt, R Koch, W B Hanley, et al.Prenatal Diagnosis|May 1, 1992
Risk factors associated with transcervical CVS lossesM S Golbus, J L Simpson, S E Fowler, et al.Epilepsia Open|July 3, 2023
Postsurgical outcomes in a cohort of patients with hippocampal sclerosis: Initial experience in a referral epilepsy center in PeruWalter F De La Cruz Ramirez, Denisse E Chacón Zuñiga, Sofía S Sánchez-Boluarte, et al.Cell Cycle (Georgetown, Tex.)|January 22, 2015
KSHV latent protein LANA2 inhibits sumo2 modification of p53Marcos-Villar Laura, Carlos F de la Cruz-Herrera, Alba Ferreirós, et al.Physical Review Letters|March 14, 2003
Melting of "porous" vortex matterS S Banerjee, A Soibel, Y Myasoedov, et al.Pediatric Research|May 1, 2001
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative StudyH L Levy, P Guldberg, F Güttler, et al.Pageof 26