Results 201 to 210 of about 35,682 (304)

[Detection of inborn errors of metabolism: guidelines in Mexico and other countries]. [PDF]

Rev Med Inst Mex Seguro Soc
Guerrero-Barrios S, Chiquillo-Domínguez M, Ayón-Aguilar J, Rodriguez-Alfaro SE, Méndez-Martínez S, García-Flores MA.   +5 more
europepmc   +1 more source

CSF Monoamine Metabolites and Cognitive Trajectory in Early Parkinson's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Imaging and postmortem studies indicate that abnormalities in monoaminergic neurotransmission contribute to cognitive impairment in Parkinson's disease (PD). However, it remains uncertain if cerebrospinal fluid (CSF) monoamine metabolites can serve as biomarkers of cognitive decline in early PD.
Jing‐Yu Shao, Rong Li, Yu‐Xiang Jiao, Kai Ma, Hong‐Qi Yang, Zheng‐Yu Sun, Jie‐Wen Zhang, Shuai Chen   +7 more
wiley   +1 more source

Writing scientific articles in the universal context of open access platforms

Edumecentro
It is necessary to deepen pedagogical research in the medical sciences, so that publications compile scientific evidence and experiences derived from teaching to create a particular didactics that perfects the teaching-learning process and lays the ...
Blanca Rosa Pérez Obregón, Yunior Mesa Reyes, Melba Menéndez Pérez, Iliana Betancourt Rodríguez   +3 more
doaj  

The Importance of a Methodological Manual for Economic Evaluations in Healthcare Decision-Making in Ecuador. [PDF]

Pharmacoecon Open
Yajamín-Villamarín R.
europepmc   +1 more source

Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi, Katharine Lee, Kerry C. Nix, Miguel Menchaca, Xiwei Shé, Lorelei Santa Maria, Wei Wu, Zihuai He, Fiona M. Baumer   +8 more
wiley   +1 more source

[Driving improvement in spinal cord injury patients using virtual reality. Systematic review]. [PDF]

Rev Neurol, 2022
De Miguel-Rubio A, Rascón-Maíz J, Alba-Rueda A, Rodrigues-de-Souza DP.   +3 more
europepmc   +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

[The commensurability of public health indicators - and the unresolved question of the incommensurableComensurabilidade de indicadores em saúde pública e o problema em aberto do incomensurável]. [PDF]

Rev Panam Salud Publica
Lozano R.
europepmc   +1 more source

[Artificial intelligence: phones smart phones and advanced technology stethoscopes]. [PDF]

Aten Primaria, 2021
Regalado Chamorro M, Medina Gamero A, Pizarro Moncada C.   +2 more
europepmc   +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