Variably Protease‐Sensitive Prionopathy: Two New Cases With Motor Neuron‐Dementia Syndrome
ABSTRACT We describe two patients with variably protease‐sensitive prionopathy (VPSPr) who developed progressive upper motor neuron symptoms, insomnia, behavioral and cognitive decline, compatible with primary lateral sclerosis associated with frontotemporal dementia (FTD).
María Elena Erro +10 more
wiley +1 more source
Governance for public health across health and allied sectors: a scoping review. [PDF]
Saikat S +8 more
europepmc +1 more source
ABSTRACT Objective To investigate the value of constructing models based on habitat radiomics and pathomics for predicting the risk of progression in high‐grade gliomas. Methods This study conducted a retrospective analysis of preoperative magnetic resonance (MR) images and pathological sections from 72 patients diagnosed with high‐grade gliomas (52 ...
Yuchen Zhu +14 more
wiley +1 more source
Transport stipend to facilitate cancer early detection: experiences of beneficiaries and perspectives of program personnel in Rwanda. [PDF]
Lam MCY +6 more
europepmc +1 more source
Transporting Goods in the EU:An Interplay of International, European and National Law [PDF]
Lamont-Black, Simone
core
Effects of Biological Sex and Age on Cerebrospinal Fluid Markers—A Retrospective Observational Study
ABSTRACT Objective Cerebrospinal fluid (CSF) analysis is a key diagnostic tool for neurological diseases. To date, only a few studies have investigated in larger cohorts the effect of age and biological sex on diagnostic markers extracted from CSF. Methods For this retrospective observational study, 4163 CSF findings (2012–2020) were evaluated.
Isabel‐Sophie Hafer +3 more
wiley +1 more source
Paramedic powers in mental health crises: A comparative legal analysis. [PDF]
Mordaunt DA, O'Byrne D, Jones N.
europepmc +1 more source
Incoterms 2010 and the mode of transport: how to choose the right term [PDF]
Malfliet, Jonas
core +1 more source
Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
wiley +1 more source
Epidemiological characteristics and public health responses against measles in the Ottoman empire and the early Turkish Republic. [PDF]
Erkmen A, Tüzün N, Erkmen O.
europepmc +1 more source

