Results 141 to 150 of about 261,427 (263)

Cross-Cultural Beliefs and Stigmatization in Vitiligo: A Systematic Review. [PDF]

J Cosmet Dermatol
Ma S, Zieneldien T, Tan IJ, Jafferany M.
europepmc   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza, Arun Meyyazhagan, Eliseo Picchi, Gustavo Ribas, Ingrid Faber, Ryosuke Miyamoto, Preethi Basavaraju, Paolo Eusebi, Haripriya Kuchi Bhotla, Mario Stasi, Fabrizio Gaudiello, Francesco Patti, Filippo Maria Santorelli, Marcondes Cavalcante França Jr, José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Hélio Afonso Ghizoni Teive, Peter Henry St George‐Hyslop, Toshitaka Kawarai, Antonio Orlacchio   +19 more
wiley   +1 more source

International conference “The Caucasus at the crossroads of international trade and cultural exchange (from ancient times to the present)”

Banber Arevelagitut'yan Instituti
The International Conference "The Caucasus at the Crossroads of Internation-al Trade and Cultural Exchange (from ancient times to the present)" was held at the National Academy of Sciences of RA on September 5-6, 2022.
Monika Mirzoyan
doaj  

Meta-analysis reveals apolipoprotein ε4 confers higher susceptibility to Parkinson's disease dementia in Asian populations. [PDF]

Front Aging Neurosci
Akhter N, Ho NBP, Nangreave R, Ahmad S, Ducruet AF, Bhatia K.   +5 more
europepmc   +1 more source

THE PROBLEM OF CULTURAL-HISTORIC SYNTHESIS IN CAUCASIAN STUDIES [PDF]

Kavkazologiya, 2017
openaire   +1 more source

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

Philipp Ammon, Georgien zwischen Eigenstaatlichkeit und russischer Okkupation. Die Wurzeln des Konflikts vom 18. Jahrhundert bis 1924. Neuauflage mit einem Nachwort v. Uwe Halbach. Frankfurt am Main, Klostermann 2020

Historische Zeitschrift
Reisner Oliver
doaj   +1 more source

Anatomy of a Cohort: 40-Year Follow-Up of a Sjögren's Cohort. [PDF]

J Clin Med
Viejo-Sosa B, Couto-Lareo U, Angerri-Nadal M, Isenberg DA.   +3 more
europepmc   +1 more source

Review: “Caucasian studies: Symposium”

Bulletin of Taras Shevchenko National University of Kyiv. History, 2018
openaire   +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