Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mirra Manevich Mazor"'
Delivery of second breech twin.Comparison between vaginal delivery of vertex and breech second twins
Autor:
Ronnie Cohen, Lior Kashani Ligumsky, Miriam Lopian, null avshalom elmalech, Ioana Olteanu, Joseph B. Lessing, null michael cohen, Mirra Manevich Mazor, null gabi haran
Publikováno v:
American Journal of Obstetrics and Gynecology. 226:S129-S130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f20a68484354dd381be92a09be2190b0
https://doi.org/10.1016/j.ajog.2021.11.229
https://doi.org/10.1016/j.ajog.2021.11.229
Autor:
Mariela Mosheva, Roei D Mazor, Chen Hoffmann, Mirra Manevich-Mazor, Alina Weissmann-Brenner, Omer Bar Yosef, Reuven Achiron, Eldad Katorza
Publikováno v:
Ultraschall in der Medizin (Stuttgart, Germany : 1980). 39(5)
To evaluate the added value of fetal MRI to ultrasound in detecting and specifying callosal anomalies, and its impact on clinical decision making.Fetuses with a sonographic diagnosis of an anomalous corpus callosum (CC) who underwent a subsequent fet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::463cbd6d84cef465309a65e227ba1ac0
https://pubmed.ncbi.nlm.nih.gov/29879745
https://pubmed.ncbi.nlm.nih.gov/29879745
Publikováno v:
Expert Opinion on Orphan Drugs. 1:891-899
6. Radiation therapy 7. Bisphosphonates 8. Imatinib mesylate 9. Infliximab 10. Anakinra 11. Vemurafenib 12. Hematopoietic stem cell transplantation 13. Conclusion 14. Expert opinion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86bb1e2f7a931084292ede013376bf51
https://doi.org/10.1517/21678707.2013.847785
https://doi.org/10.1517/21678707.2013.847785
Autor:
Ronald Jaffe, Anat Kesler, Chezi Ganzel, Eli Sprecher, Yakov Pessach, Iris Yaish, Orna Aizenstein, Ilan Goldberg, Iris Eshed, Mirra Manevich-Mazor, Yehuda Shoenfeld, Roei D Mazor, Alexander Gural
Publikováno v:
BMC Medicine
Background Erdheim-Chester Disease (ECD), a non Langerhans’ cell histiocytosis of orphan nature and propensity for multi-systemic presentations, comprises an intricate medical challenge in terms of diagnosis, treatment and complication management.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec9b6bf745a2abaebbb2ca5c40393192
https://doi.org/10.1186/s12916-014-0221-3
https://doi.org/10.1186/s12916-014-0221-3
Publikováno v:
Orphanet Journal of Rare Diseases
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected. The multi systemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc5aada6455f35c5e6bc680c62000f34