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Molecular Genetics and Metabolism Reports|March 18, 2021
Favorable outcomes following early onset oral miglustat in early infantile Niemann Pick Type CShiri Curelaru, Yoav Zehavi, Tal Almagor, et al.Rheumatology International|February 25, 2014
Establishing hospital admission criteria of pediatric Henoch-Schonlein purpuraKamal Masarweh, Yoseph Horovitz, Avi Avital, et al.American Journal of Medical Genetics. Part A|September 15, 2005
A syndrome characterized by contractures and pterygia of upper body associated with umbilical hernia, short stature, and distinctive face in an Arabic familyStavit A Shalev, Ronen Spiegel, Judith G HallThe Israel Medical Association Journal : IMAJ|March 26, 2025
Molybdenum Cofactor Deficiency Type A disease in Northern IsraelEliyahu Fund, Hanna Mandel, Yoav Zehavi, et al.Journal of Pediatric Hematology/Oncology|September 16, 2003
Hypereosinophilic syndrome in a child presenting as eosinophilic pharyngitisRonen Spiegel, Luci Zalman, Herzel Gavriel, et al.The Pediatric Infectious Disease Journal|January 27, 2004
Acute neonatal suppurative parotitis: case reports and reviewRonen Spiegel, Dan Miron, Waheeb Sakran, et al.Neurogenetics|April 29, 2016
Homozygous mutation in the APOA1BP is associated with a lethal infantile leukoencephalopathyRonen Spiegel, Avraham Shaag, Stavit Shalev, et al.Journal of Pediatric Hematology/Oncology|January 18, 2005
Association of chronic symptomatic neutropenia with the triple A syndromeRonen Spiegel, Stavit Shalev, Angela Huebner, et al.European Journal of Medical Genetics|March 24, 2012
A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab familiesStavit A Shalev, Ronen Spiegel, Zvi U BorochowitzJournal of Child Neurology|June 5, 2009
Severe meningoencephalitis due to late reactivation of Varicella-Zoster virus in an immunocompetent childRonen Spiegel, Dan Miron, Dmitry Lumelsky, et al.Pageof 11