Results 81 to 90 of about 75,003 (261)

A posterior variant of corticobasal syndrome: Evidence from a longitudinal study of cognitive and functional status in a single case

Cogent Psychology, 2018
We describe a patient (CG) suffering from early onset dementia who presented with corticobasal syndrome (CBS). The aims of the study were as follows: (i) a detailed description of the cognitive phenotype; (ii) a comprehensive, longitudinal evaluation of ...
Carlo Abbate, Pietro Davide Trimarchi, Laura Manzoni, Anna Maria Quarenghi, Gian Pietro Salvi, Silvia Inglese, Fabrizio Giunco, Renzo Bagarolo, Daniela Mari, Beatrice Arosio   +9 more
doaj   +1 more source

Rapidly Progressive Corticobasal Degeneration Syndrome

Case Reports in Neurology, 2011
Introduction: Corticobasal syndrome (CBS) has a heterogeneous clinical presentation with no specific pathologic substratum. Its accurate diagnosis is a challenge for neurologists; in order to establish CBS definitively, postmortem confirmation is ...
Ana Herrero Valverde, Sónia Costa, Ângela Timoteo, Ricardo Ginestal, José Pimentel   +4 more
doaj   +1 more source

The psychosocial toll of Dublin III on asylum seekers in the Netherlands

American Journal of Community Psychology, EarlyView.
Abstract The Dublin III Regulation determines which EU Member State is responsible for examining asylum claims, but its implementation carries significant consequences for those subjected to it. This study examines how Dublin III, as implemented in the Netherlands, affects asylum seekers' psychosocial wellbeing using Silove′s Adaptation and Development
Imen El Amouri
wiley   +1 more source

Phenotypic and Positron Emission Tomography with [18F]fluordeoxyglucose (FDG PET) differences in corticobasal syndrome: comparison of two cases [PDF]

Dementia & Neuropsychologia
Corticobasal syndrome (CBS) is a rare cause of dementia and comprises varied combinations of subcortical signs (akinetic-rigid parkinsonism, dystonia, or myoclonus) with cortical signs (apraxia, alien hand or cortical sensory deficit), usually asymmetric.
Thais Winkeler Beltrão, Eduardo Barbosa de Albuquerque Maranhão, Victor Adill Gomes Correia, Pedro Mota de Albuquerque, Mariana Gonçalves Maciel Pinheiro, Rayanne Acioli Lins Santos, Luiz Eduardo Duarte Borges Nunes, Simone Cristina Soares Brandão, Breno José Alencar Pires Barbosa   +8 more
doaj   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide, Vinicius Contrucci Dantas Segarra, Siulan Vendramini‐Pittoli, Henrique Regonaschi Serigatto, Luiza Virmond, Heloisa Marcelina da Cunha Palhares, Fernanda Jehee, Ana Cristina Victorino Krepischi, Carla Rosenberg, Carlos Henrique Paiva Grangeiro, Nancy Mizue Kokitsu‐Nakata   +10 more
wiley   +1 more source

Assessment of rehabilitation of corpus callosum infarction: a case report based on functional near infrared spec-troscopy

Zhongguo kangfu lilun yu shijian
Objective To report the individualized rehabilitation protocol administered to a patient suffering from corpus callosum injury subsequent to cerebral infarction, manifesting clinically as alien hand syndrome, attention deficits, spatial neglect and gait ...
CHEN Yudong, DU Xiaoxia, HUANG Fubiao, YE Changqing, MA Lin, WANG Yunlei, WU Xiaoli   +6 more
doaj   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli, Giulia Bruna Marchetti, Maria Iascone, Maria Grazia Patricelli, Sara Giangiobbe, Gabriella Cinzia Pozzobon, Miriam Nella Savini, Fabio Giglio, Alessandro Aiuti, Paola Carrera, Francesca Ferrua, Angela Peron   +11 more
wiley   +1 more source

Which Traits Make Weeds More Successful in Maize Crops? Insights from a Three-Decade Monitoring in France

Plants, 2019
A major aim in invasion biology is identifying traits distinguishing alien invasive and alien non-invasive plants. Surprisingly, this approach has been, so far, poorly used to understand why some arable weeds are abundant and widespread while others are ...
Guillaume Fried, Bruno Chauvel, François Munoz, Xavier Reboud   +3 more
doaj   +1 more source

My left hand annoys me: When parts of your own body feel alienated [PDF]

, 2022
How the brain creates the image of the body and decides what belongs and not belongs to the body is one of the most exciting questions in neuroscience.
Kasten, Erich
core  

Inflammation Unchecked: Concurrent Kawasaki Disease and Stevens‐Johnson Syndrome in an 18‐Month‐Old Child

Arthritis Care &Research, EarlyView.
Catherine Deffendall, Jodi Backalar, Elizabeth Acevedo Zapata, Adriana Della Porta, Lorin Bibb, Tyler Reese, Charlotte M. Brown   +6 more
wiley   +1 more source