Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Mustafa Kabha"'
Autor:
Hava Peretz, Michael Korostishevsky, David M. Steinberg, Mustafa Kabha, Sali Usher, Irit Krause, Hannah Shalev, Daniel Landau, David Levartovsky
Publikováno v:
JIMD Reports, Vol 51, Iss 1, Pp 45-52 (2020)
Abstract Classical xanthinuria is a rare autosomal recessive metabolic disorder characterized by lack of xanthine dehydrogenase activity that often manifests as xanthine urolithiasis and risk of drug toxicity. Variants in the XDH or HMCS gene underli
Externí odkaz:
https://doaj.org/article/4b3823acbf6f42c58b33cb8b0c6f9357
Autor:
Hava Peretz, Ayala Lagziel, Florian Bittner, Mustafa Kabha, Meirav Shtauber-Naamati, Vicki Zhuravel, Sali Usher, Steffen Rump, Silke Wollers, Bettina Bork, Hanna Mandel, Tzipora Falik-Zaccai, Limor Kalfon, Juergen Graessler, Avraham Zeharia, Nasser Heib, Hannah Shalev, Daniel Landau, David Levartovsky
Publikováno v:
Biomedicines, Vol 9, Iss 7, p 788 (2021)
Classical xanthinuria is a rare autosomal recessive metabolic disorder caused by variants in the XDH (type I) or MOCOS (type II) genes. Thirteen Israeli kindred (five Jewish and eight Arab) and two isolated cases from Germany were studied between the
Externí odkaz:
https://doaj.org/article/39f61b1380a64273a9863f181879c35b
Autor:
Mustafa Kabha, Nahum Karlinsky
The Palestinian Nakba (catastrophe) of 1948, devastated Palestinian lives and shattered Palestinian society, culture, and economy. It also nipped in the bud a nascent grassroots, binational alliance between Arab and Jewish citrus growers.This signifi
Autor:
Mustafa Kabha
Mustafa Kabha plumbs the complex story of the Palestinian people, from the revolts of 1936-1939 to the present, focusing on their efforts to establish a viable independent state--and the internal factors that have thwarted them. With unparalleled acc
Autor:
Ayala Lagziel, Avraham Zeharia, Sali Usher, Mustafa Kabha, Nasser Heib, David Levartovsky, Limor Kalfon, Hava Peretz, Bettina Bork, Daniel Landau, Tzipora C Falik-Zaccai, Juergen Graessler, Florian Bittner, Vicki Zhuravel, Silke Wollers, Hannah Shalev, Hanna Mandel, Meirav Shtauber-Naamati, Steffen Rump
Publikováno v:
Biomedicines, Vol 9, Iss 788, p 788 (2021)
Biomedicines
Volume 9
Issue 7
Biomedicines
Volume 9
Issue 7
Classical xanthinuria is a rare autosomal recessive metabolic disorder caused by variants in the XDH (type I) or MOCOS (type II) genes. Thirteen Israeli kindred (five Jewish and eight Arab) and two isolated cases from Germany were studied between the
Autor:
Daniel Landau, David M. Steinberg, Hava Peretz, Michael Korostishevsky, Sali Usher, David Levartovsky, Mustafa Kabha, Irit Krause, Hannah Shalev
Publikováno v:
JIMD Reports
JIMD Reports, Vol 51, Iss 1, Pp 45-52 (2020)
JIMD Reports, Vol 51, Iss 1, Pp 45-52 (2020)
Classical xanthinuria is a rare autosomal recessive metabolic disorder characterized by lack of xanthine dehydrogenase activity that often manifests as xanthine urolithiasis and risk of drug toxicity. Variants in the XDH or HMCS gene underlie classic
Publikováno v:
Journal of Holy Land and Palestine Studies. 16:99-123
Mass communication media technologies influence the structuring of reality, consolidation of value systems, and construction of common social denominators, and thus contribute to the formation of personal and national identities. While, as Edward Sai
Autor:
Mustafa Kabha
Publikováno v:
Journal of Palestine Studies. 47:119-121
Autor:
Mustafa Kabha
Publikováno v:
The Holocaust and the Nakba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766d6ee377febf3826bfa5617476c2bf
https://doi.org/10.7312/bash18296-009
https://doi.org/10.7312/bash18296-009