Results 151 to 160 of about 4,496,566 (351)

Puberty and Epilepsy Onset in Women

Objective: The significance of the onset of seizure based on the medical and social aspects of epilepsy. The aim of this study was to investigate the age of seizure onset based on the specific characteristics of each age of seizure onset in many epilepsy
Galina Odintsova, Nina Dengina
core   +1 more source

The Role of Calcitonin Gene‐Related Peptide in High‐Altitude Headache: A Prospective Field Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐altitude headache (HAH) is a common neurological condition associated with rapid ascent to high altitude. The pathophysiological mechanisms underlying HAH remain incompletely understood. Calcitonin gene‐related peptide (CGRP), a neuropeptide implicated in migraine pathophysiology, may play a key role in the pathophysiology of ...
Roman Schniepp, Ludwig Karrasch, Helena Breitenstein, Andreas Straube, Katharina Kamm   +4 more
wiley   +1 more source

Revisiting Childhood-Onset Systemic Lupus Erythematosus

Childhood-onset systemic lupus erythematosus (cSLE) is a chronic autoimmune disease with a multisystemic involvement diagnosed during childhood. The disease is marked by the production of autoantibodies targeting self-antigens, often before symptoms ...
Pınar Özge Avar-Aydın, Hermine I. Brunner   +1 more
core   +1 more source

Indications for the onset of deconfinement in Pb + Pb collisions at the CERN SPS from NA49 [PDF]

, 2005
Particle production in central Pb+Pb collisions was studied with the NA49 large acceptance spectrometer at the CERN SPS at beam energies of 20, 30, 40, 80, and 158 GeV per nucleon.
Vassiliou, Maria, Molnar, József, Litov, Leandr, Panayotov, Dobromir, Boimska, Bożena, Darmenov, Nikolay, Friese, Volker, Markert, Christina, Kadija, Krešo, Pálla, Gabriella, Mayes, Bill W., Sitar, Branislav, Botje, Michiel, Stefanek, Grzegorz, Lungwitz, Benjamin, Foka, Panagiota, Trainor, Thomas A., Pinsky, Lawrence, Sann, Hans, Bramm, Roland, Mischke, André, Richard, Agnes Carol Joanna, Roland, Gunther, Kowalski, Marek, Białkowska, Helena, Dinkelaker, Peter, Wetzler, Alexander Albert, Blume, Christoph, Cramer, John G., Hoehne, Claudia, Veres, Gábor I., Szentpetery, Imre, Betev, Latchezar, Sandoval, Andres, Christakoglou, Panagiotis, Chvala, Ondrej, Włodarczyk, Zbigniew, Malakhov, Aleksandr I., Roland, Christof, Schmitz, Norbert, Barna, Daniel, Grebieszkow, Katarzyna, Dimitrov, Anton, Černý, Vladimír, Leeuwen, Marco van, Karev, Alexandre, Meurer, Christine, Farantatos, Gerassimos, Rybicki, Andrzej, Vranić, Danilo, Kolesnikov, Vadim I., Yoo, In-Kwon, Skrzypczak, Ewa, Mateev, Matej D., Seyboth, Peter, Sziklai, János, Bracinik, Juraj, Mitrovski, Michael Kosta, Kraus, Ingrid, Varga, Dezsö, Kniege, Stefan, Hegyi, Sándor, Gál, József, Georgopoulos, George, Panagiotou, Apostolos D., Kornaś, Ewelina, Csató, Péter, Kreps, Michal, Makariev, Martin Vasilev, Bartke, Jerzy, Brun, René, Eckardt, Volker, Rybczyński, Maciej, Sikler, Ferenc, Freund, Peter, Bunčić, Predrag, Zaranek, Jacek, Vesztergombi, György, Baatar, B., Melkumov, Georgy L., Stock, Reinhard, Gaździcki, Marek, Ströbele, Herbert, Antičić, Tome, Kliemant, Michael, Pikna, Miroslav, Fodor, Zoltán, Gładysz-Dziaduś, Ewa, Korus, Robert, Pühlhofer, Falk, Petridis, Athanasios, Renfordt, Rainer Arno Ernst, Kollegger, Thorsten, Mrowczynski, Stanislaw, Zimanyi, József, Alt, Christopher, Lévai, Péter, Flierl, Dominik Bernhard, Šuša, Tatjana   +98 more
core  

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone, Freddy Chafota, Miguel E. Rentería, Randi J. Hagerman, Ellery Santos, Anna Atkinson, Nicholas G. Martin, Elsdon Storey, Danuta Z. Loesch   +8 more
wiley   +1 more source

[18F]Fluorodeprenyl‐D2 PET as a Tool to Monitor Disease Activity in GAD65‐Ab Autoimmune Encephalitis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate [18F]fluorodeprenyl‐D2 ([18F]F‐DED) positron‐emission tomography (PET) imaging as a biomarker of disease activity in autoimmune encephalitis (AIE) associated with glutamic acid decarboxylase 65 (GAD65) antibodies. Methods [18F]F‐DED PET was performed in 25 GAD65‐AIE patients and 8 controls using dynamic (0–60 min) and ...
Julia S. Dorneich, Jonathan A. Gernert, Hanna Zimmermann, Lisa Tagnin, Marianthi Zeinaki, Laura Sanzo, Letizia Vogler, Elisabeth Kaufmann, Justina Dargvainiene, Frank Leypoldt, Gérard N. Bischof, Robert Perneczky, Boris‐Stephan Rauchmann, Simon Lindner, Günter U. Höglinger, Rudolf A. Werner, Martin Kerschensteiner, Tania Kümpfel, Matthias Brendel, Franziska S. Thaler   +19 more
wiley   +1 more source

Prospective studies are required for assessing the outcome of a SARS-CoV-2 infection based on the symptoms at onset

Libyan Journal of Medicine, 2023
Josef Finsterer
doaj   +1 more source

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

Proceedings of the National Academy of Sciences of the United States of America, 1993
W. Strittmatter, A. Saunders, D. Schmechel, M. Pericak-Vance, J. Enghild, G. Salvesen, A. Roses   +6 more
semanticscholar   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu, Xin Duan, Fatemeh Peymani, Jia Wang, Chengjia Bao, Chaolong Xu, Ying Zou, Zixuan Zhang, Yunxi Zhang, Tongyue Li, Martin Pavlov, Junling Wang, Minhan Song, Tianyu Song, Xiaodi Han, Mingxi Sun, Danmin Shen, Ruoyu Duan, Huafang Jiang, Manting Xu, Holger Prokisch, Fang Fang   +21 more
wiley   +1 more source

High‐Resolution MRI Revealed Different Etiology‐Specific Associations With Cerebral Infarction in Adult Moyamoya Vasculopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐resolution MRI enables detailed assessment of intracranial vessel wall pathology in moyamoya vasculopathy. We aimed to classify adult moyamoya vasculopathy etiologies using high‐resolution MRI and to examine subtype‐specific associations between high‐resolution MRI features and ischemic infarction.
Guangsong Han, Jiachun Pan, Yuehui Hong, Xiaoyuan Fan, Ming Yao, Lixin Zhou, Yicheng Zhu, Feng Feng, Jun Ni   +8 more
wiley   +1 more source