Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Aaron Knecht"'
Publikováno v:
Asian Spine Journal, Vol 11, Iss 1, Pp 99-104 (2017)
Study DesignProspective cohort study.PurposeThis study was to investigate interside asymmetries of three lower extremity somatosensory evoked potentials (SSEPs) in anesthetized patients with unilateral lumbosacral radiculopathy.Overview of Literature
Externí odkaz:
https://doaj.org/article/1c85d1d67df049c6bc22a9f7c0fb4cd7
Publikováno v:
Journal of Back and Musculoskeletal Rehabilitation. 32:841-845
BACKGROUND Within the thenar eminence, the median nerve innervates three muscles: abductor pollicis brevis (APB), flexor pollicis brevis (FPB), and opponens pollicis (OP). Of these muscles, APB was often considered as the sole contributor to the then
Publikováno v:
The Neurodiagnostic Journal. 59:212-218
Paradoxical cortical potential polarity of the upper extremity somatosensory evoked potential (SSEP) has been reported in cases of polymicrogyria (PMG) syndrome. To date, the pathophysiological basis of this electrophysiological aberration remains un
Publikováno v:
World neurosurgery. 97
Background Footdrop secondary to L5 root injury is a rare complication associated with lumbar surgery. It is unclear whether intraoperative neuromonitoring can detect such an injury. Case Description A 54-year-old man who had had bilateral chronic L5
Publikováno v:
Asian Spine Journal
Asian Spine Journal, Vol 11, Iss 1, Pp 99-104 (2017)
Asian Spine Journal, Vol 11, Iss 1, Pp 99-104 (2017)
Study DesignProspective cohort study.PurposeThis study was to investigate interside asymmetries of three lower extremity somatosensory evoked potentials (SSEPs) in anesthetized patients with unilateral lumbosacral radiculopathy.Overview of Literature
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
Autor:
Dganit Dinour, Danny Lotan, Aaron Knecht, Roxana Cleper, Miriam Davidovitz, Eli J. Holtzman, Irith Weissman, Nomy Levin-Iaina
Publikováno v:
Nephron Clinical Practice. 112:c262-c267
Dent’s disease is an X-linked hereditary renal tubular disorder characterized by low-molecular-weight proteinuria (LMWP), hypercalciuria, nephrocalcinosis, nephrolithiasis, rickets and progressive renal failure. About 60% of patients have mutations
Autor:
Eli J. Holtzman, Brenda L. Smith, Min Hwang Chang, Dganit Dinour, Michael F. Romero, Aaron Knecht, Nathan Angle, I. Serban, Jun Ichi Satoh
Publikováno v:
Journal of Biological Chemistry. 279:52238-52246
In humans and terrestrial vertebrates, the kidney controls systemic pH in part by absorbing filtered bicarbonate in the proximal tubule via an electrogenic Na+/HCO3- cotransporter (NBCe1/SLC4A4). Recently, human genetics revealed that NBCe1 is the ma
Autor:
Shai Rosenberg, Andrew P. Levy, Farid Nakhoul, Irit Hochberg, Zvi Burbea, Rachel Miller-Lotan, Sidney Benchetrit, David Tovbin, Joshua Weissgarten, Karl Skorecki, Aaron Knecht, Nina S. Levy, Roaa Zoabi
Publikováno v:
Nephron Experimental Nephrology. 97:e71-e76
Background: We recently reported that haptoglobin (Hp) phenotype 1-1 is protective against the development of nephropathy in normal creatinine diabetics. In the present study, we sought to determine if Hp phenotype also plays a role in renal deterior
Publikováno v:
Journal of Chromatography B. 796:141-153
According to the “middle molecule” (MM) hypothesis, the uremic solutes ranging from 500 to 5000 Da are insufficiently eliminated by conventional hemodialysis and may act as uremic toxins. However, because of the methodological difficulties of MM