Clinical Validation of Plasma p‐217tau in Neurological Diseases
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi +13 more
wiley +1 more source
Elecciones y poder local en Bilbao entre 1917 y 1936: una perspectiva urbana y social
La presente investigación plantea un ejercicio que cruza cuatro variables claves: procedencia geográfica, espacios urbanos, grupos sociales, y política.
José María Beascoechea Gangoiti +1 more
doaj +1 more source
Un análisis del perfil del cuidador y su impacto sobre la situación laboral: cuidadores principales de enfermos de Alzheimer y otras demencias en el Sur Oeste de España [PDF]
The aim of this paper is to analyse the main demographic and socio-economic conditions of the primary caregivers of Alzheimer's and dementia sufferers, and their relationship to the employment situation of the caregiver.
González Camacho, María del Carmen +2 more
core
Determinantes sociais da não-adesão ao tratamento de tuberculose em Buenos Aires, Argentina [PDF]
El objetivo fue identificar los determinantes individuales y de área de la no adherencia al tratamiento de la tuberculosis (TB) en municipios de Buenos Aires, Argentina. Se realizó un estudio transversal con un modelo jerarquizado. El análisis se llevó a
Arrossi, Silvina +3 more
core +3 more sources
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
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 +19 more
wiley +1 more source
Patrones de dinámica industrial en la industria manufacturera del Partido de General Pueyrredon en el período 1994-2005 [PDF]
Este trabajo analiza los patrones de natalidad, mortalidad y supervivencia de empresas manufactureras en el Partido de General Pueyrredon entre los años 1994 y 2005.
Calá, Carla Daniela +4 more
core
Sertraline Treatment Can Mimic Niemann‐Pick Type C Biomarker Profile: A Diagnostic Pitfall
ABSTRACT Background Oxysterols (cholestane‐3β,5α,6β‐triol and 7‐ketocholesterol) and N‐palmitoyl‐O‐phosphocholineserine (PPCS) are sensitive biomarkers for Niemann‐Pick disease type C (NPC) screening. However, false‐positive results occur, with a biomarker profile suggestive of NPC despite the absence of pathogenic variants in genes involved in NPC or ...
Maria Makrygianni +19 more
wiley +1 more source
Helping a visually impaired student to improve her social interaction skills at Andrés Bello University, Viña del Mar, Chile : an action research [PDF]
Tesis (Pedagogía en Inglés)During the last decade, inclusion that is “Something which cannot be done to people, it is something in which people are actively involved” (Norwich, 1999), has been used by different educational institutions to define or ...
Aguirre Reyes, Ivette Lissette +3 more
core
Impact of Plasma p‐tau181 on Cognition, Motor Phenotypes, and Disease Course in ALS
ABSTRACT Phosphorylated tau181 (p‐tau181), an Alzheimer's disease biomarker, was recently evaluated in amyotrophic lateral sclerosis (ALS). We investigated plasma p‐tau181 in 202 ALS/ALS‐FTD patients and 94 healthy controls, assessing cognitive performance, motor function, and longitudinal dynamics.
Elisabeth Kasper +25 more
wiley +1 more source

