Results 61 to 70 of about 685,470 (326)

International Veterinary Epilepsy Task Force Consensus Proposal: Diagnostic approach to epilepsy in dogs [PDF]

, 2015
This article outlines the consensus proposal on diagnosis of epilepsy in dogs by the International Veterinary Epilepsy Task Force. The aim of this consensus proposal is to improve consistency in the diagnosis of epilepsy in the clinical and research ...
A Pákozdy, Akos Pakozdy, Andrea Fischer, Andrea Tipold, AT Berg, BG Licht, C Brauer, C Brauer, CL Mariani, Clare Rusbridge, EE Patterson, EE Patterson, G Urkasemsin, Heidrun Potschka, Holger A. Volk, J Guevar, Jacques Penderis, JJ Lin, JL Gill, JW Schmidley, Karen Muñana, Kaspar Matiasek, KJ Ekenstedt, L Arrol, LM Mellema, Luisa De Risio, M Armaşu, M Berendt, M Podell, M Schwartz, M Schwartz, M Wolf, Martí Pumarola Batlle, Mette Berendt, Michael Podell, N Shihab, Ned Patterson, O Devinsky, Paul JJ. Mandigers, PM Smith, R Edwards, R Erro, R Gonçalves, R Poma, R Zimmermann, RMA Packer, Robyn Farqhuar, Rowena MA Packer, RS Fisher, RS Fisher, S Shorvon, Sam Long, Simon Platt, Sofie Bhatti, TM Ghormle, V Hülsmeyer, Veronika Stein, WB Thomas, WW Bush, YC Huang   +59 more
core   +8 more sources

Pioglitazone plus (−)‐epigallocatechin gallate: a novel approach to enhance osteogenic performance in aged bone marrow mesenchymal stem cells

FEBS Open Bio, EarlyView.
Aged human bmMSCs are seeded in the scaffold. Osteoblastic induction can slightly increase cell's bone‐forming activity to produce bone‐like tissues, shown as the sporadic xylenol orange‐stained spots (the lower left image). Notably, pioglitazone plus EGCG co‐treatment dramatically increases cell's bone‐forming activity and bone‐like tissue production (
Ching‐Yun Chen, Jia‐Ci Jhang, Chun‐Yi Peng, Quốc Cường Nguyễn, Feng‐Huei Lin, Hung‐Ming Wu, Shankung Lin   +6 more
wiley   +1 more source

Avaliação do desenvolvimento neuropsicomotor em escolares de primeira série e sua relação com o estado nutricional Evaluation of neuropsychomotor development in first grade children and its relation to nutrition

Jornal de Pediatria, 2001
OBJETIVO: estudar uma amostra representativa de escolares de 1ª série/1º grau de Porto Alegre com o intuito de estabelecer seu desempenho neurológico e investigar a associação entre o perfil neurológico e o estado nutricional.
Ana Guardiola, Cristiane Egewarth, Newra T. Rotta   +2 more
doaj   +1 more source

PENGARUH DEPRESI PADA AWAL STROKE (MINGGU I) TERHADAP WAKTU PERBAIKAN DEFISIT NEUROLOGIS PENDERITA STROKE NON HEMORAGIK [PDF]

, 2006
Introduction : Depression is the most common type of psychiatric disorder among stroke patients. It is considered as a usual reaction that frequently ignored by family and paramedic.
Yulianti, Riwanti
core  

The role of lipid metabolism in neuronal senescence

FEBS Open Bio, EarlyView.
Disrupted lipid metabolism, through alterations in lipid species or lipid droplet accumulation, can drive neuronal senescence. However, lipid dyshomeostasis can also occur alongside neuronal senescence, further amplifying tissue damage. Delineating how lipid‐induced senescence emerges in neurons and glial cells, and how it contributes to ageing and ...
Dikaia Tsagkari, Eleftheria Panagiotidou, Nektarios Tavernarakis   +2 more
wiley   +1 more source

Features of the Clinical Course and Prognosis of Severe Traumatic Brain Injury Outcomes

Неотложная медицинская помощь, 2020
BACKGROUND. Traumatic brain injury (TBI) is one of the most important contemporary health issues. According to the World Health Organization, TBI is one of three leading causes of death in the world.
Y. B. Vasilyeva, A. E. Talypov, M. V. Sinkin, S. S. Petrikov   +3 more
doaj   +1 more source

NEUROLOGICAL DISORDER AMONG PREMUTATION CARRIERS OF FRAGILE X SYNDROME AT SEMIN, GUNUNG KIDUL REGENCY [PDF]

, 2010
Background: Neurological disorder among male premutation carriers of Fragile X Syndrome (FXS) frequently occurs. In other hand, lacking of information results misdiagnosis of this disorder.
Ardiansyah, Rivaldi
core  

A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption [PDF]

, 2009
Hereditary folate malabsorption (HFM) is a rare autosomal recessive disorder which is characterized by impaired intestinal folate malabsorption and impaired folate transport into the central nervous system.
Cole, Trevor, Kurian, Manju A., Maher, Eamonn R., Meyer, Esther, Pasha, Shanaz, Trembath, Richard C.   +5 more
core   +2 more sources

Tracking Motor Progression and Device‐Aided Therapy Eligibility in Parkinson's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterise the progression of motor symptoms and identify eligibility for device‐aided therapies in Parkinson's disease, using both the 5‐2‐1 criteria and a refined clinical definition, while examining differences across genetic subgroups.
David Ledingham, Sahana Sathyanarayana, Charlotte B. Stewart, Robyn Iredale, Victoria Foster, Debra Galley, Mark Baker, Nicola Pavese   +7 more
wiley   +1 more source

Neurological Examination [PDF]

, 2012
Diagnosing neurological disorders requires accurate assessment including detailed neurological examination, which is an important step in formulating differential diagnosis and guiding laboratory investigations. Certain problems frequently face the junior physician including organizing a complete examination in a short time period, and consistently ...
  +4 more sources