Results 31 to 40 of about 7,233 (216)
Do patients diagnosed with a neurological disease present increased risk of suicide?
Neurología (English Edition), 2023 Introduction: Neurological diseases are the leading cause of disability and the second leading cause of death worldwide. Physical and psychological pain, despair, and disconnection with the environment are observed after the diagnosis of numerous ...
M. Alejos +4 more
doaj +1 more source
The Risk of Transmission of Genetic Prion Diseases is Greater Than 50%
European Journal of Neurology, Volume 32, Issue 12, December 2025.This study investigated whether transmission ratio distortion (TRD) occurs in inherited prion diseases, specifically familial Creutzfeldt‐Jakob disease (p.E200K variant) and fatal familial insomnia (p.D178N variant), despite the theoretical 50% autosomal dominant inheritance risk.
Izaro Kortazar‐Zubizarreta +5 more
wiley +1 more source
El papel de la terapia ocupacional en la enfermedad de Huntington [PDF]
, 2014 se analiza el papel del terapeuta ocupacional en el trabajo con las personas afectadas por la enfermedad de Huntington. se realizó una investigación por objetivos a través del diseño y puesta en práctica de un programa de intervención encaminado a ...
Fernández Hawrylak, María +2 more
core +1 more source
Attenuated Strains of Pseudomonas aeruginosa: A Promising Cell Factory for Rhamnolipid Production
Microbial Biotechnology, Volume 18, Issue 11, November 2025.PGN strains are generated by the deletion of virulence factor genes. The metabolic pathways and regulatory frameworks that lead to high‐efficiency production of rhamnolipids in P. aeruginosa are preserved in these strains. Therefore, PGN strains are promising bio‐safe cell factories for the industrial production of rhamnolipids.
Parvathy V. Das +3 more
wiley +1 more source
Revisión sistemática de los síntomas logopédicos en la enfermedad de Huntington: habla, voz, lenguaje y deglución [PDF]
, 2019 La Enfermedad de Huntington (EH) o corea de Huntington es una enfermedad genética neurodegenerativa producida por una mutación del número de repeticiones de la secuencia de nucleótidos CAG que codifica la proteína huntingtina en el brazo corto del ...
Evan García, Ángela de
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Alzheimer's &Dementia, Volume 21, Issue 8, August 2025.Abstract The landscape of Alzheimer's disease (AD) and related dementias (ADRD) diagnosis is evolving rapidly, driven by advances in disease understanding, biomarker tools, and disease‐modifying therapies. Modern diagnostic approaches emphasize biological precision, early detection, and dynamic frameworks that adapt to treatment‐induced changes in ...
Takeshi Iwatsubo +43 more
wiley +1 more source
Neurología (English Edition)Introduction: Huntington's disease (HD) is a neurodegenerative and hereditary disorder. Due to the predictive diagnosis, incipient clinical characteristics have been described in the prodromal phase.
Y. Rodríguez-Agudelo +5 more
doaj +1 more source
Enfermedad de Huntington: estado del arte [PDF]
, 2014 La enfermedad de Huntington es un desorden monogenético autosómico dominante, que genera un trastorno neurodegenerativo caracterizado por la pérdida de neuronas en diferentes partes del cerebro.
Rodas Sepúlveda, Carlos Daniel +1 more
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Psicosomática y Psiquiatría, 2021 La Enfermedad de Huntington (EH) es una afección hereditaria que produce disfunción del núcleo estriado y sus conexiones, caracterizándose clínicamente por la triada de demencia de patrón subcortical sin afasia, movimientos anormales (coreicos) y ...
Ángela Ruiz-Arcos +4 more
doaj +1 more source
A new method of molecular diagnosis for the Huntington’s disease via PCR [PDF]
, 2017 [EN] Single gene disorders are the most studied genetic diseases due to its simple inheritance pattern (recessive or dominant). Huntington’s disease (HD) is a single gene disorder which appears between the third and fifth decade of life.
Poza Villa, Jon
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