Results 71 to 80 of about 84,102 (243)

Epithelioid Enigma: Proximal‐Type Epithelioid Sarcoma in Cyst Fluid Cytology

open access: yesDiagnostic Cytopathology, EarlyView.
ABSTRACT Epithelioid sarcoma (ES) is a rare, aggressive soft tissue malignancy with substantial morphologic overlap with other epithelioid neoplasms, creating diagnostic difficulty in cytology specimens. We report proximal‐type ES identified in cyst fluid from a lesion clinically interpreted as an epidermal inclusion cyst or abscess.
Nathan McGrath   +2 more
wiley   +1 more source

Secretopathies emerge as a new class of neurocristopathies

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient embryonic population of cells that give rise to a wide range of structures, including craniofacial cartilage and bone, peripheral neurons and glia, as well as components of the cardiac outflow tract, among others.
Amanda Teixeira   +3 more
wiley   +1 more source

Progress report on new epilepsy treatments: A summary of the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVIII). II. Treatments in more advanced clinical development

open access: yesEpilepsia, EarlyView.
Abstract This article summarizes data for 13 investigational treatments for which at least preliminary seizure outcome data in patients with epilepsy were reported at the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices held in Madrid, Spain, on May 3–6, 2026.
Meir Bialer   +7 more
wiley   +1 more source

Discontinuità strutturali, mutamento strategici, performance: la ERG dopo il 1995

open access: yes, 2008
IL SAGGIO, ALL'INTERNO DI UN VOLUME CHE RIPERCORRE I 60 ANNI DELLA STORIA DELLA SOCIETA' PETROLIFERA ERG DI GENOVA, ANALIZZA STRATEGIE E RISULTATI DELLA SOCIETA' NELL'ARCO DI TEMPO DAL 1995 AL 2008, RELATIVAMENTE SOPRATUTTO ALLA POLITICA DI ...
CLO', ALBERTO
core   +1 more source

Genetic and clinical diagnosis of a Chinese family with incomplete congenital stationary night blindness caused by a novel CACNA1F mutation

open access: yesIndian Journal of Ophthalmology. Case Reports
We here describe the clinical features and identify the genetic cause of incomplete congenital stationary night blindness (CSNB) in a Chinese family. Three patients from a three-generation Chinese family were clinically examined. They exhibited nystagmus,
Zhen Qu   +5 more
doaj   +1 more source

Androgens Induce Functional CXCR4 through ERG Factor Expression in TMPRSS2-ERG Fusion-Positive Prostate Cancer Cells [PDF]

open access: yes, 2010
TMPRSS2-ERG fusion transcripts have been shown to be expressed in a majority of prostate cancer (PC) patients because of chromosomal translocations or deletions involving the TMPRSS2 gene promoter and the ERG gene coding sequence. These alterations cause
Kandagatla, Pridvi   +6 more
core   +1 more source

Hippocampal network activity changes during early epileptogenesis predict subsequent epilepsy

open access: yesEpilepsia, EarlyView.
Abstract Objective Despite decades of research, the circuit mechanisms that underlie focal epileptogenesis remain incompletely understood. In this study, we aimed to characterize the changes in hippocampal network activity induced by an epileptogenic insult.
Michael Strüber   +13 more
wiley   +1 more source

Cone dystrophy with supernormal rod response – A rare case report

open access: yesIndian Journal of Ophthalmology. Case Reports
Cone dystrophy with supernormal rod response (CDSRR), also known as potassium channel subfamily V, member 2 (KCNV2) retinopathy, is a rare autosomal recessive cone rod dystrophy, which derives its name from its characteristic full-field ...
Elizabeth Mathew   +3 more
doaj   +1 more source

The challenge of developing a shared vision: Marittime Alps-Mercantour

open access: yes, 2015
A common conservation strategy is the driving force of sustainable socio-economic development in the Marittime Alps-Mercantour Transboundary Protected Area (TBPA).
Erg, Boris   +6 more
core   +1 more source

Scn1a‐mediated developmental regulation of prefrontal cortex plasticity and cognition

open access: yesEpilepsia, EarlyView.
Abstract Objective The voltage‐gated sodium channel Nav1.1, encoded by Scn1a, is essential for γ‐aminobutyric acid (GABA)ergic function, and its alteration is associated with neurological disorders such as Dravet syndrome and Alzheimer's disease. We previously demonstrated that local Nav1.1 dysfunction in the medial prefrontal cortex (mPFC) during ...
Maurizio S. Riga   +5 more
wiley   +1 more source

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