Zobrazeno 1 - 10
of 2 845
pro vyhledávání: '"Zimran, A."'
Autor:
Kfir-Erenfeld, Shlomit, Asherie, Nathalie, Lebel, Eyal, Vainstein, Vladimir, Assayag, Miri, Dubnikov Sharon, Tatyana, Grisariu, Sigal, Avni, Batia, Elias, Shlomo, Alexander-Shani, Rivka, Bessig, Nomi, Shehadeh, Alaa, Ishtay, Aseel, Zelmanovich, Veronica, Zimran, Eran, Pick, Marjorie, Roziner, Ilan, Kenett, Ron S., Cohen, Yael, Avivi, Irit, Cohen, Cyrille J., Gatt, Moshe E., Stepensky, Polina
Publikováno v:
In Blood Advances 13 August 2024 8(15):4077-4088
Autor:
Aliaksandr Skrahin, Mia Horowitz, Majdolen Istaiti, Volha Skrahina, Jan Lukas, Gilad Yahalom, Mikhal E. Cohen, Shoshana Revel-Vilk, Ozlem Goker-Alpan, Michal Becker-Cohen, Sharon Hassin-Baer, Per Svenningsson, Arndt Rolfs, Ari Zimran
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 13, p 7102 (2024)
GBA1-associated Parkinson’s disease (GBA1-PD) is increasingly recognized as a distinct entity within the spectrum of parkinsonian disorders. This review explores the unique pathophysiological features, clinical progression, and genetic underpinning
Externí odkaz:
https://doaj.org/article/e3979c57f9aa45eda829213364404fad
Autor:
Deborah Elstein, Nadia Belmatoug, Bruno Bembi, Patrick Deegan, Diego Fernandez-Sasso, Pilar Giraldo, Özlem Göker-Alpan, Derralynn Hughes, Heather Lau, Elena Lukina, Shoshana Revel-Vilk, Ida Vanessa D. Schwartz, Majdolen Istaiti, Jaco Botha, Noga Gadir, Jörn Schenk, Ari Zimran
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 12, p 3588 (2024)
Background: Long-term patient registries are important for evaluating treatment outcomes in patients with rare diseases, and can provide insights into natural disease history and progression in real-world clinical practice. Initiated in 2010, the Gau
Externí odkaz:
https://doaj.org/article/b1cc50b6372943b68cf134969c40c18d
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 11, p 3325 (2024)
Background/Objectives: Gaucher Disease type 1 (GD1) is a recessively inherited lysosomal storage disorder caused by a deficiency in the enzyme β-glucocerebrosidase. Enzyme replacement therapy (ERT) has become the standard of care for patients with G
Externí odkaz:
https://doaj.org/article/789787e2e70a4b2e846e77ea2fea14e0
Autor:
Patrick Deegan, Heather Lau, Deborah Elstein, Diego Fernandez-Sasso, Pilar Giraldo, Derralynn Hughes, Ari Zimran, Majdolen Istaiti, Noga Gadir, Jaco Botha, Shoshana Revel-Vilk
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 10, p 2782 (2024)
Background: Gaucher disease (GD) is a rare, autosomal, recessive condition characterized by hepatosplenomegaly, thrombocytopenia, anemia, and bone abnormalities, often requiring life-long treatment. Velaglucerase alfa has improved hematologic and vis
Externí odkaz:
https://doaj.org/article/52e72b7018164598a1033186e4371156
Autor:
Arslan, Muhammad, Wilkinson, Sarah, Naeth, M. Anne, Gamal El-Din, Mohamed, Khokhar, Zimran, Walker, Christopher, Lucke, Terry
Publikováno v:
In Science of the Total Environment 1 July 2023 880
Autor:
Revel-Vilk, Shoshana1,2,3 (AUTHOR) azimran@gmail.com, Zimran, Ari1,2 (AUTHOR) joleenist@szmc.org.il, Istaiti, Majdolen1 (AUTHOR), Azani, Liat4 (AUTHOR), Shalev, Varda5 (AUTHOR) chodick@tauex.tau.ac.il, Chodick, Gabriel5 (AUTHOR), Manor, Orly3 (AUTHOR), Paltiel, Ora2,3 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. Dec2023, Vol. 12 Issue 24, p7707. 9p.
Autor:
Khalid, Haris M., Rafique, Zimran, Muyeen, S.M., Raqeeb, Abdul, Said, Zafar, Saidur, R., Sopian, Kamaruzzaman
Publikováno v:
In Solar Energy February 2023 251:261-285
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Akademický článek
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