Orna Staretz-Chacham (O Staretz-Chacham)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Topics

Intellectual Disability

End Stage Renal Disease

Top Venues

Journal of inherited metabolic disease

American journal of medical genetics. Part A

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Ben Pode-Shakked, Yuval E Landau, Nava Shaul Lotan, Joshua Manor, Nitsan Haham, Eyal Kristal, Eli Hershkovitz, Guy Hazan, Yarden Haham, Shlomo Almashanu, Yair Anikster, Orna Staretz-Chacham
The natural history of dihydrolipoamide dehydrogenase deficiency in Israel. Journal of inherited metabolic disease (2024)
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Yuval Yogev, Max Drabkin, Ekaterina Eremenko, Sarit Aharoni, Ofek Freund, Matan M Jean, Nadav Agam, Noam Hadar, Neta Loewenthal, Orna Staretz-Chacham, Ohad S Birk
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation. Journal of inherited metabolic disease (2023)
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Yuval Yogev, Max Drabkin, Ekaterina Eremenko, Sarit Aharoni, Ofek Freund, Matan M Jean, Nadav Agam, Noam Hadar, Neta Loewenthal, Orna Staretz-Chacham, Ohad S Birk
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation. Journal of inherited metabolic disease (2023)
Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, Yuval Yogev, Max Drabkin, Ekaterina Eremenko, Sarit Aharoni, Ofek Freund, Matan M Jean, Nadav Agam, Noam Hadar, Neta Loewenthal, Orna Staretz-Chacham, Ohad S Birk
Hyperinsulinism / hyperammonemia syndrome caused by biallelic SLC25A36 mutation. Journal of inherited metabolic disease (2023)
Dror Kraus, Huda Abdelrahim, Orith Waisbourd-Zinman, Elena Domin, Avraham Zeharia, Orna Staretz-Chacham
Elevated Alpha-Fetoprotein in Infantile-Onset Niemann-Pick Type C Disease with Liver Involvement. Children (Basel, Switzerland) 9 (4) (2022)
Eyal Kristal, Ben Pode-Shakked, Guy Hazan, Ehud Banne, Galina Ling, Odeya David, Eilon Shany, Annick Raas-Rothschild, Yair Anikster, Katya Kneller, Eli Hershkovitz, Yuval E Landau, Ronen Spiegel, Yoav Zehavi, Orna Staretz-Chacham
The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in Israel. Orphanet journal of rare diseases 16 (1) (2021)
Yoav Bolkier, Ortal Barel, Dina Marek-Yagel, Danit Atias-Varon, Maayan Kagan, Amir Vardi, David Mishali, Uriel Katz, Yishay Salem, Tal Tirosh-Wagner, Jeffrey M Jacobson, Annick Raas-Rothschild, Odelia Chorin, Aviva Eliyahu, Yarden Sarouf, Omer Shlomovitz, Alvit Veber, Nechama Shalva, Elisheva Javasky, Yishay Ben Moshe, Orna Staretz-Chacham, Gideon Rechavi, Shrikant Mane, Yair Anikster, Asaf Vivante, Ben Pode-Shakked
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects. Journal of medical genetics (2021)
Dina Marek-Yagel, Aviva Eliyahu, Alvit Veber, Nechama Shalva, Amit Mary Philosoph, Ortal Barel, Elisheva Javasky, Ben Pode-Shakked, Neta Loewenthal, Yair Anikster, Orna Staretz-Chacham
Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux-Lamy syndrome (MPS VI). American journal of medical genetics. Part A 185 (12) (2021)
Orna Staretz-Chacham, Ben Pode-Shakked, Eyal Kristal, Smadar Yaala Abraham, Keren Porper, Ohad Wormser, Ilan Shelef, Yair Anikster
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase Deficiency. Nutrients 13 (10) (2021)
Orna Staretz-Chacham, Shirly Amar, Shlomo Almashanu, Ben Pode-Shakked, Ann Saada, Ohad Wormser, Eli Hershkovitz
Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin Tribe. Genes 12 (8) (2021)
Golan-Tripto Inbal, Jacob Bistritzer, Neta Loewenthal, Orna Staretz-Chacham, Yotam Dizitzer, Goldbart Aviv
The effect of vitamin D administration on vitamin D status and respiratory morbidity in late premature infants. Pediatric pulmonology 55 (11) (2020)
G Hazan, E Hershkovitz, Orna Staretz-Chacham
Incidence of inherited metabolic disorders in southern Israel: a comparison between consanguinity and non-consanguinity communities. Orphanet journal of rare diseases 15 (1) (2020)
Orna Staretz-Chacham, Lars Schlotawa, Ohad Wormser, Inbal Golan-Tripto, Ohad S Birk, Carlos R Ferreira, Thomas Dierks, Karthikeyan Radhakrishnan
A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. Molecular genetics & genomic medicine 8 (9) (2020)
Orna Staretz-Chacham, Suha Daas, Igor Ulanovsky, Ayala Blau, Nira Rostami, Talya Saraf-Levy, Nasser Abu Salah, Yair Anikster, Ehud Banne, Dalit Dar, Elena Dumin, Aviva Fattal-Valevski, Tzipora Falik-Zaccai, Eli Hershkovitz, Sagi Josefsberg, Hatem Khammash, Rimona Keidar, Stanley H Korman, Yuval Landau, Tally Lerman-Sagie, Dror Mandel, Hanna Mandel, Ronella Marom, Iris Morag, Erez Nadir, Naama Yosha-Orpaz, Ben Pode-Shakked, Elon Pras, Haike Reznik-Wolf, Ann Saada, Reeval Segel, Avraham Shaag, Nava Shaul Lotan, Ronen Spiegel, Galit Tal, Taly Vaisid, Avi Zeharia, Shlomo Almashanu
The role of orotic acid measurement in routine newborn screening for urea cycle disorders. Journal of inherited metabolic disease 44 (3) (2020)
Omer Kaplan, Tamar Wainstock, Eyal Sheiner, Orna Staretz-Chacham, Asnat Walfisch
Maternal anemia and offspring failure to thrive - results from a large population-based cohort. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 34 (23) (2019)
Orna Staretz-Chacham, Rachel Shukrun, Ortal Barel, Ben Pode-Shakked, Oren Pleniceanu, Yair Anikster, Nechama Shalva, Carlos R Ferreira, Admit Ben-Haim Kadosh, Justin Richardson, Shrikant M Mane, Friedhelm Hildebrandt, Asaf Vivante
Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome. American journal of medical genetics. Part A 179 (10) (2019)