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Dive into the research topics where Orna Staretz is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Bioenergetic Signatures of DLD Deficiency: Dissecting PDHc- and α-KGDHc-Linked Defects
Haham Zarbib, Y., Huri Ohev-Shalom, S., Lyskov, S. K., Mazor, Y., Anekstein-Spigel, M., Shalva, N., Spiegel, R., Staretz-Chacham, O., Manor, J., Saada, A., Rock, R., Anikster, Y. & Yardeni, T., 1 Jan 2026, In: Antioxidants. 15, 1, 19.Research output: Contribution to journal › Article › peer-review
Open Access -
Pyruvate Dehydrogenase Complex Deficiency: A Review of Treatments and Case Series
Betesh-Abay, B., Shany, E., Staretz-Chacham, O., Shelef, I. & Azab, A. N., 1 Mar 2026, In: International Journal of Molecular Sciences. 27, 6, 2732.Research output: Contribution to journal › Review article › peer-review
Open Access -
Newborn screening algorithm distinguishing potential symptomatic isovaleric acidemia from asymptomatic newborns
Rock, R., Rock, O., Daas, S., Biton-Regev, V., Sagiv, N., Salah, N. A., Anikster, Y., Barel, O., Cohen, R. H., Dumin, E., Fattal-Valevski, A., Falik-Zaccai, T., Herskovitz, E., Josefsberg, S., Khammash, H., Kneller, K., Korman, S. H., Landau, Y. E., Lerman-Sagie, T. & Mandel, H. & 9 others, , 1 Jan 2025, In: Journal of Inherited Metabolic Disease. 48, 1, e12800.Research output: Contribution to journal › Article › peer-review
Open Access -
Predischarge Betamethasone in Infants Diagnosed With Bronchopulmonary Dysplasia
Ernest, T. E., Ozalvo, D., Staretz-Chacham, O., Marks, K. A., Shany, E., Landau, D. & Richardson, J., 1 Jul 2025, In: Pediatric Pulmonology. 60, 7, e71201.Research output: Contribution to journal › Article › peer-review
Open Access -
Severe neonatal hypotonia due to SLC30A5 variant affecting function of ZnT5 zinc transporter
Dolgin, V., Chabosseau, P., Bistritzer, J., Noyman, I., Staretz-Chacham, O., Wormser, O., Hadar, N., Eskin-Schwartz, M., Kanengisser-Pines, B., Narkis, G., Abramsky, R., Shany, E., Rutter, G. A., Marks, K. & Birk, O. S., 1 Jan 2025, In: JIMD Reports. 66, 1, e12465.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Biochemical and neurophysiological effects of deficiency of the mitochondrial import protein TIMM50
Paz, E., Jain, S., Gottfried, I., Staretz-Chacham, O., Mahajnah, M., Bagchi, P., Seyfried, N. T., Ashery, U. & Azem, A., 16 Dec 2024, In: eLife. 13Research output: Contribution to journal › Article › peer-review
Open Access -
The natural history of dihydrolipoamide dehydrogenase deficiency in Israel
Pode-Shakked, B., Landau, Y. E., Shaul Lotan, N., Manor, J., Haham, N., Kristal, E., Hershkovitz, E., Hazan, G., Haham, Y., Almashanu, S., Anikster, Y. & Staretz-Chacham, O., 1 Sep 2024, In: Journal of Inherited Metabolic Disease. 47, 5, p. 895-902 8 p.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
Addition of galactose-1-phosphate measurement enhances newborn screening for classical galactosemia
Daas, S., Abu Salah, N., Anikster, Y., Barel, O., Damseh, N. S., Dumin, E., Fattal-Valevski, A., Falik-Zaccai, T. C., Habib, C., Josefsberg, S., Korman, S. H., Kneller, K., Landau, Y., Lerman-Sagie, T., Mandel, H., Manor, Y., Moady Abdalla, T., Rock, R., Rostami, N. & Saada, A. & 9 others, , 1 Mar 2023, In: Journal of Inherited Metabolic Disease. 46, 2, p. 232-242 11 p.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Hereditary orotic aciduria identified by newborn screening
Staretz-Chacham, O., Damseh, N. S., Daas, S., Abu Salah, N., Anikster, Y., Barel, O., Dumin, E., Fattal-Valevski, A., Falik-Zaccai, T. C., Hershkovitz, E., Josefsberg, S., Landau, Y., Lerman-Sagie, T., Mandel, H., Rock, R., Rostami, N., Saraf-Levy, T., Shaul Lotan, N., Spiegel, R. & Tal, G. & 4 others, , 1 Jan 2023, In: Frontiers in Genetics. 14, 1135267.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation
Safran, A., Proskorovski-Ohayon, R., Eskin-Schwartz, M., Yogev, Y., Drabkin, M., Eremenko, E., Aharoni, S., Freund, O., Jean, M. M., Agam, N., Hadar, N., Loewenthal, N., Staretz-Chacham, O. & Birk, O. S., 1 Jul 2023, In: Journal of Inherited Metabolic Disease. 46, 4, p. 744-755 12 p.Research output: Contribution to journal › Article › peer-review
7 Scopus citations
Press/Media
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Recent Findings in Drug Research Described by Researchers from Soroka University Medical Center (Pyruvate Dehydrogenase Complex Deficiency: A Review of Treatments and Case Series)
Staretz, O., Shelef, I., Shany, E., Azab, A. N. & Betesh - Abay, B. T.
15/04/26
1 item of Media coverage
Press/Media
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Recent Research from Ben-Gurion University of the Negev Highlight Findings in Hyperinsulinism (Hyperinsulinism/hyperammonemia Syndrome Caused By Biallelic Slc25a36 Mutation)
Birk, O., Safran, A., Staretz, O., Freund, O., Agam, N., Jean, M. M. & Eremenko, E.
16/03/23
1 item of Media coverage
Press/Media