Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Eliezer J. Holtzman"'
Publikováno v:
Advances in experimental medicine and biology. 1360
Preeclampsia is a pregnancy-induced complex of multiple pathological changes. Numerous stresses during pregnancy, including hypoxia, immune activation, inflammatory cytokines, and oxidative stress were reported as contributing factors to the preeclam
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783030948030
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a94eb094c527abfd991793f1a05fcc16
https://doi.org/10.1007/978-3-030-94804-7_7
https://doi.org/10.1007/978-3-030-94804-7_7
Autor:
Nabil Abu-Amer, Olga L. Kukuy, Margarita Kunin, Eliezer J. Holtzman, Uri Rimon, Dganit Dinour, Pazit Beckerman
Publikováno v:
Journal of Vascular and Interventional Radiology. 33:707-714.e2
To evaluate the outcomes of percutaneous transluminal renal angioplasty with stent implantation (PTRAS) among patients with renal artery stenosis (RAS) who become dialysis-dependent due to acute deterioration of renal function.This was a single-cente
Autor:
Liat Ganon, Aaron Hanukoglu, Eias Massalha, Eliezer J. Holtzman, Orit Kliuk-Ben Bassat, Zvi Farfel, Haim Mayan, Vered Carmon
Publikováno v:
Nephron. 137:77-84
Background: Familial hyperkalemia and hypertension (FHHt) is an inherited disorder manifested by hyperkalemia and hypertension. The following four causative genes were identified: WNK1, WNK4, CUL3, and KLHL3. For the first 3 genes, inheritance is aut
Autor:
Yardena Tenenbaum-Rakover, Vered Carmon, Kira Oleinikov, Aaron Hanukoglu, Eliezer J. Holtzman, Haim Mayan, Shira London, Raphael Halevy, Zvi Farfel
Publikováno v:
Nephron. 130:59-65
Background: Familial hyperkalemia and hypertension (FHHt) is a rare genetic disorder manifested by hyperkalemia and early hypertension. Hypercalciuria is another accompanying feature. Mutations in WNK4 and WNK1 were found initially, and recently addi
Autor:
Adi Leiba, Dganit Dinour, Merav Leiba, Michal Shani, Eliezer J. Holtzman, Shlomo Vinker, Gilad Twig
Publikováno v:
The Journal of clinical endocrinology and metabolism. 101(10)
The risk associated with serum uric acid (SUA) levels within the normal range is unknown, especially among lean and apparently healthy adults.Evaluating whether high-normal SUA levels, 6.8 mg/dL and below, are associated with an increased diabetes ri
Autor:
Olga, Kukuy, Avi, Livneh, Liran, Mendel, Ariel, Benor, Eitan, Giat, Oleg, Perski, Olga, Feld, Yonatan, Kassel, Ilan, Ben-Zvi, Merav, Lidar, Eliezer J, Holtzman, Adi, Leiba
Publikováno v:
Clinical and experimental rheumatology. 35(6)
Familial Mediterranean fever (FMF) is an autoinflammatory disorder with episodic and persistent inflammation, which is only partially suppressed by continuous colchicine treatment. While chronic inflammation is considered an important cardiovascular
Autor:
Dan A. Liebermann, Barbara Hoffman, Ossie Geifman-Holtzman, Yali Xiong, Stacey Jeronis, Eliezer J. Holtzman
Publikováno v:
Journal of Cellular Physiology. 228:362-370
Accumulating evidence suggests that placental stresses during pregnancy can play an important role in the pathogenesis of preeclampsia. A common signal pathway that senses and converts placental stresses into intracellular stress response may be cont
Publikováno v:
European Journal of Clinical Investigation. 41:1113-1120
Background Cyclosporine is used for treatment of transplanted patients and for immune-mediated diseases. Cyclosporine is known to cause a combination of metabolic side effects including hypertension, hyperkalemia, hypercalciuria and hypomagnesemia. T
Autor:
Uzi Gafter, Liat Ganon, Ruth Rachamimov, Andrew Bahn, Rotem Ron, Ossie Geifman-Holtzman, Eliezer J. Holtzman, Aaron Knecht, Gerhard Burckhardt, Ben-Ami Sela, Dganit Dinour
Publikováno v:
Nephrology Dialysis Transplantation. 26:2175-2181
BACKGROUND: Hereditary renal hypouricemia may be complicated by nephrolithiasis or exercise-induced acute renal failure. Most patients described so far are of Japanese origin and carry the truncating mutation W258X in the uric acid transporter URAT1