Zobrazeno 1 - 10
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pro vyhledávání: '"A, Zimran"'
Akademický článek
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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:
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:
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:
Zimran, Ari1,2 (AUTHOR) azimran@gmail.com, Szer, Jeff3,4 (AUTHOR), Becker-Cohen, Michal1 (AUTHOR), Jens, Sjoerd5,6 (AUTHOR), Cozma, Claudia7 (AUTHOR), Revel-Vilk, Shoshana1,2 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. Mar2023, Vol. 12 Issue 6, p2220. 7p.
Akademický článek
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Publikováno v:
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Zaguán. Repositorio Digital de la Universidad de Zaragoza
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Background : Gaucher disease (GD) is an autosomal recessive disorder produced by mutations in the glucocerebrosidase gene (GBA), causing storage of glucosylceramide in reticuloendothelial cells in multiple organs. Traditionally, the prediction of the