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Biochemistry Research International|July 26, 2012
The mutations associated with dilated cardiomyopathyRuti Parvari, Aviva LevitasCurrent Molecular Medicine|April 13, 2002
The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studiesShimon W Moses, Ruti ParvariEuropean Journal of Human Genetics : EJHG|July 29, 2004
Congenital deficiency of alpha feto-proteinReuven Sharony, Idit Zadik, Ruti ParvariHormone Research|September 30, 2006
Parathyroid development and the role of tubulin chaperone ERuti Parvari, George A Diaz, Eli HershkovitzHormone Research|February 9, 2008
Testicular expressed genes are missing in familial X-Linked Kallmann syndrome due to two large different deletions in daughter's X chromosomesEli Hershkovitz, Neta Loewenthal, Asaf Peretz, et al.American Journal of Medical Genetics. Part A|January 16, 2016
Phosphoglucomutase-1 deficiency: Intrafamilial clinical variability and common secondary adrenal insufficiencyNeta Loewenthal, Alon Haim, Ruti Parvari, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|January 14, 2005
Hypoparathyroidism-retardation-Dysmorphism (HRD) syndrome--a reviewEli Hershkovitz, Ruti Parvari, George A Diaz, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 17, 2015
Combined adrenal failure and testicular adrenal rest tumor in a patient with nicotinamide nucleotide transhydrogenase deficiencyEli Hershkovitz, Maram Arafat, Neta Loewenthal, et al.Pediatric Neurology|November 6, 2013
A novel mutation in SCN9A in a child with congenital insensitivity to painZamir Shorer, Einav Wajsbrot, Tamir-Hostovsky Liran, et al.Genomics|May 26, 2005
The 2p21 deletion syndrome: characterization of the transcription contentRuti Parvari, Yael Gonen, Ismael Alshafee, et al.Pageof 5