Results 41 to 50 of about 30,430 (219)
Abstract Objective This study was undertaken to evaluate whether synaptic vesicle protein 2A (SV2A) expression on peripheral immune cells predicts treatment response to levetiracetam in epilepsy. Methods High‐dimensional flow cytometry was used to prospectively assess SV2A expression on immune cells from levetiracetam responders, nonresponders, and ...
Johannes Lang +4 more
wiley +1 more source
EPILEPSY WITH GELASTIC SEIZURES AND HYPOTHALAMIC HAMARTOMA: A RARE CLINICAL CASE
Among the various types of epileptic syndromes, gelastic seizures are considered the rarest one. The condition is characterized by forced laughter and the finding of hypothalamic hamartoma.
V. A. Mikhailov +3 more
doaj +1 more source
Hamartoma Breast, Chondromatous Type. [PDF]
This case report describes an exceedingly rare case of hamartoma of breast with predominantly chondroid stroma. A 45 year old lady presented with a mobile lump in the upper outer quadrant of left breast, clinically diagnosed as fibroadenoma.
Bhat, V, Jena, M
core
Splenic hamartoma associated with abdominal discomfort and pain. Case report [PDF]
Hamartomas are benign splenic neoplasms asymptomatic in most of the cases. Symptoms, when present, may either be related to the growth of the mass with abdominal discomfort and pain or be related to a hypersplenism syndrome.
AMATUCCI, CHIARA +6 more
core +1 more source
Graphical abstract for the systematic literature review. Abstract Objective Dravet syndrome (DS) places tremendous burden on caregivers owing to the extent of required assistance and impact on daily living, as well as the risk to the individual with DS of premature mortality from sudden unexpected death in epilepsy and morbidity associated with ...
Adam Strzelczyk +8 more
wiley +1 more source
Respiratory Epithelial Adenomatoid Hamartoma of the Nasal Septum
Objective: Hamartomas are relatively uncommon, non-neoplastic malformations indigenous to the involved anatomic site. Respiratory epithelial adenomatoid hamartoma (REAH) is a subset of hamartoma characterized by prominent glandular proliferation lined by
Siti Zulaili Zulkepli +2 more
doaj +1 more source
Conus Hamartoma with Tethered Filum in a Young Male: Case Report and Review of Literature
Spinal hamartoma is an extremely rare, benign tumor, and 22 cases have been reported so far. Hereby, we report a midline conus hamartoma in a 22-year-old male with no associated systemic manifestations.
Tejaswi Vadlamani +5 more
doaj +1 more source
Epilepsy syndromes classification
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell +4 more
wiley +1 more source
Prenatal Diagnosis of Congenital Mesenchymal Hamartoma of Liver: A Case Report
Hepatic mesenchymal hamartoma is a rare benign tumor. We present an unusual case of a fetal abdominal cyst, later diagnosed histopathologically to be mesenchymal hamartoma of liver. The organ of origin was indeterminate on both prenatal and postnatal
Sreelakshmi Kodandapani +3 more
doaj +1 more source
Schwann cell hamartoma: case report [PDF]
BACKGROUND: Colorectal polyps of mesenchymal origin represent a small percentage of gastrointestinal (GI) lesions. Nevertheless, they are encountered with increasing frequency since the widespread adoption of colonoscopy screening.
Elena Guerini Rocco +8 more
core +3 more sources

