Results 261 to 270 of about 337,645 (313)

Seroprevalence of <i>Mycobacterium leprae</i> <i>antibodies</i> among school children in Indonesia in 2023: a cross-sectional study. [PDF]

Lancet Reg Health Southeast Asia
Pierneef L, Muhammad M, Wassenaar G, Edbert D, Krismawati H, Wahyuni S, Ali S, Martini Kaisar MM, Corstjens P, Geluk A.   +9 more
europepmc   +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

Voices from the classroom: Teachers' perspectives on collaboration with speech-language therapists in learners with special educational needs schools. [PDF]

S Afr J Commun Disord
Mahomed Joosub H, De Jongh M, Mothapo R.
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

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

The evolution and improvement of medical-vocational education policies: a perspective based on the IAD framework. [PDF]

Front Public Health
Liu X, Liu J, Mukundan J.
europepmc   +1 more source

Conceptualising equity in basic medical education accreditation standards: A qualitative study of expert perspectives. [PDF]

Pak J Med Sci
Shaheen N, Mahboob U, Sethi A, Irfan M.
europepmc   +1 more source

Integrating AI and digital medicine into undergraduate medical education. [PDF]

Korean J Med Educ
Dharmasaroja P.
europepmc   +1 more source

The status of interprofessional medical and nursing education in wound care at German higher education institutions. [PDF]

GMS J Med Educ
Weiß A, Richters C, Kiriakidou R, Hausen A, Fischer MR, Stadler M, Witti MJ.   +6 more
europepmc   +1 more source

The digital transformation of medical education collaborative governance in the era of smart education: an innovative management restructuring of medical talent cultivation systems. [PDF]

Front Med (Lausanne)
Zhang X, Shi P.
europepmc   +1 more source