Results 61 to 70 of about 15,155 (248)
Epilepsia Open, EarlyView.Abstract Objective Epileptic spasms (ES) in children carry a high risk of neurodevelopmental delay, yet predictors of long‐term surgical outcome remain incompletely defined. This study aimed to evaluate seizure outcomes following epilepsy surgery and to identify independent prognostic factors for postoperative recurrence.
Hua Li +7 more
wiley +1 more source
Breast hamartomas – Differential consideration in slow developing breast asymmetry [PDF]
, 2015 Breast hamartoma is a relatively rare entity with an incidence of approximately 0.7% of benign breast masses. Hamartomas may become large and cause breast asymmetry.
Sarah Cazorla +3 more
core +1 more source
The genetic architecture of epilepsy across molecular mechanisms and clinical heterogeneity
Epilepsia Open, EarlyView.Abstract Epilepsy comprises a highly heterogeneous group of neurological disorders unified by a persistent predisposition to recurrent seizures, yet driven by remarkably diverse genetic, molecular, and network‐level mechanisms. Advances in genomic technologies have revealed that epilepsy arises from a multilayered genetic architecture encompassing rare
Mohammad Reza Seyedtaghia +4 more
wiley +1 more source
Tuberous sclerosis complex: A case report
Contemporary Clinical Dentistry, 2016 Tuberous sclerosis complex is an unusual autosomal dominant neurocutaneous syndrome characterized by the development of benign tumors affecting different body systems affecting the brain, skin, retina, and viscera.
Soumyabrata Sarkar +3 more
doaj +1 more source
The Journal of Thoracic and Cardiovascular Surgery, 1992 Eighty-nine cases of pulmonary hamartoma were studied. There were 51 men and 38 women, with a mean age of 57.5 years (range 14 to 76 years). A histologic diagnosis from examination of the resection specimens was obtained in all patients who had operations.
C P, Hansen +4 more
openaire +2 more sources
Epilepsia Open, EarlyView.This graphical abstract provides an overview of the content from this post hoc analysis evaluating the efficacy and safety of fenfluramine in patients with Dravet syndrome stratified by age, number of previously attempted antiseizure medications, and SCN1A pathogenic variant status using data pooled from the three pivotal randomized controlled trials ...
Rima Nabbout +20 more
wiley +1 more source
Clinicopathological analysis of seven breast hamartomas and review of the literature [PDF]
, 2020 Aim: Breast hamartomas are uncommon benign lesions that constitute 4.8% of benign breast tumors; they consist of mammary ducts and lobules, fatty tissue, and fibrous tissue.
Kucukkosmanoglu, Ilknur +3 more
core
Hamartomas of the Retina and Optic Disc
Türk Oftalmoloji Dergisi, 2022 Hamartomas are local malformation of cells that demonstrate abnormal proliferation in the area where they are normally present. Retinal and optic disc hamartomas include astrocytic hamartoma, congenital hypertrophy of the retinal pigment epithelium ...
Ibadulla Mirzayev, Ahmet Kaan Gündüz
doaj +1 more source
Epilepsia Open, EarlyView.Abstract Objective To determine the frequency of monogenic variants and pathogenic copy number variants (CNVs) in adults with surgically treated temporal lobe epilepsy (TLE). Methods We performed exome sequencing (ES), including CNV analysis, in 45 adults with TLE who had previously undergone epilepsy surgery.
Antonia P. Pirker +12 more
wiley +1 more source
Brunner’s Gland Hyperplasias and Hamartomas in Association with Helicobacter pylori
, 2019 Background. The proliferative lesions of the Brunner’s glands (BGs) are hyperplasia and hamartomas, and they are usually asymptomatic and very rarely diagnosed. The aetiology of these lesions is not yet clear.
Sabahattin Destek, Vahit Onur Gul
core +1 more source