Results 61 to 70 of about 2,574,835 (312)

Patient-Reported Disability Measures Do Not Correlate with Electrodiagnostic Severity in Carpal Tunnel Syndrome. [PDF]

, 2017
BACKGROUND: Electrophysiologic studies including electromyography and nerve conduction studies play a role in the evaluation of carpal tunnel syndrome (CTS), despite evidence that these studies do not correlate with CTS-specific symptom scores.
Atroshi, Bakhsh, Bessette, Chan, Changulani, Cohen, Das De, de la Llave-Rincón, de-la-Llave-Rincon, Graham, Itsubo, Jablecki, Jordan, Kimura, Kronlage, Levine, Makanji, Niekel, Nunez, Robinson, Sandin, Sucher, Ware, Watson, Werner, Wilder-Smith   +25 more
core   +2 more sources

Oligodendrogenesis in Evolution, Development and Adulthood

Glia, EarlyView.
Oligodendrocytes and myelin took shape in jawed vertebrates. During development, OPCs are originated from NSCs and then undergo differentiation into mature oligodendrocytes that supply myelin. OPCs persist in the adult CNS and continue to produce oligodendrocytes and myelin. Adaptive myelination, which fine‐tunes neural circuits in response to neuronal
Hao Hu, Tianhao Gao, Jingwei Zhao, Huiliang Li   +3 more
wiley   +1 more source

A De Novo POLD1 Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome

Journal of Investigative Medicine High Impact Case Reports, 2018
Background. Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy (MDPL) syndrome is a recently recognized genetic disorder comprised of mandibular hypoplasia, deafness, progeroid features, and lipodystrophy. It is caused by an autosomal
Linda R. Wang, Aleksandar Radonjić, A. Dilliott, A. McIntyre, R. Hegele   +4 more
semanticscholar   +1 more source

Attention Deficit Disorder, Residual Type- A Case Study [PDF]

, 2011
The syndrome of Minimal Brain Dysfunction (MBD) in children has been well described by a number of authors. Such children were first described in 1941 by Werner and Strauss(1) who made a distinction between brain injury and -simple- mental retardation ...
Stanch, MD, James
core   +1 more source

The prognostic potential of RNA in stage II colon cancer: Insights from a screened multicenter population‐based cohort study

International Journal of Cancer, EarlyView.
What's New? Patients with stage II colon cancer exhibit considerable variation in prognosis. Consequently, decisions regarding the necessity of adjuvant chemotherapy in this population often rely on imperfect high‐risk criteria. Here, the authors developed a novel RNA‐based risk score, using NanoString nCounter technology, to stratify recurrence risk ...
Ulrik Korsgaard, Maria P. Kristensen, Juan L. García‐Rodríguez, Sanne Kjær‐Frifeldt, Jan Lindebjerg, Torben F. Hansen, Jørgen Kjems, Henrik Hager, Lasse S. Kristensen   +8 more
wiley   +1 more source

TELOMERES AND TELOMERASE COMPLEX. THE MAIN CLINICAL MANIFESTATION OF GENETIC MALFUNCTIONING

Кардиоваскулярная терапия и профилактика, 2015
Telomeres and telomerase complex have got be known by scientists not long ago. At the current moment there quite large data on this topic collected.
О. М. Drapkina, R. N. Shepel
doaj   +1 more source

Clinical features and surgical options of obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome: A systematic review and a meta‐analysis of prevalence

International Journal of Gynecology &Obstetrics, EarlyView.
Abstract Background OHVIRA syndrome, a urogenital malformation, lacks standardized management. Narrative reviews exist, but there is no a comprehensive meta‐analysis. Objectives The aim of this first systematic review and meta‐analysis is to evaluate the current literature and inform management strategies.
Emma Bonetti, Gloria Anderson, Simona Duranti, Federico Ferrari, Franco Odicino, Antonia Testa, Francesco Fanfani, Giovanni Scambia, Ursula Catena   +8 more
wiley   +1 more source

Herlyn-Werner-Wunderlich syndrome: Case report

Revista de la Facultad de Medicina, 2021
Introduction: Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation of the urogenital tract characterized by the triad of uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis, which is usually diagnosed after ...
Laura Catalina López-Alza, Mario Santiago Mesa-Espinel   +1 more
doaj   +1 more source

Uterus Didelphys with Hematocervix in the Unilateral Obstructed Hemivagina and Ipsilateral Renal Agenesis: A Case Report of Herlyn–Werner–Wunderlich Syndrome

Reproductive Medicine
Background: Mullerian duct anomalies include a broad spectrum of genital tract defects that arise from developmental abnormalities of the genital tract.
Cristina Taliento, Alba Rondoni, Gennaro Scutiero, Matteo Pavone, Matteo Mordenti, Giuseppe Vizzielli, Pantaleo Greco   +6 more
doaj   +1 more source

The Werner syndrome protein is distinguished from the Bloom syndrome protein by its capacity to tightly bind diverse DNA structures. [PDF]

PLoS ONE, 2012
Loss of Werner syndrome helicase-exonuclease (WRN) or of its homolog Bloom syndrome helicase (BLM) results in different inherited disorders. Whereas Werner syndrome is characterized by premature onset of aging and age-associated diseases, Bloom syndrome ...
Ashwini Kamath-Loeb, Lawrence A Loeb, Michael Fry   +2 more
doaj   +1 more source