Results 231 to 240 of about 9,130,139 (414)

Ejecución neuropsicológica y carga de enfermedad en sujetos en riesgo de desarrollar enfermedad de Huntington

Neurología
Resumen: Introducción: La enfermedad de Huntington (EH) es un trastorno neurodegenerativo y hereditario. Gracias al diagnóstico predictivo se han descrito características clínicas incipientes en la fase prodrómica.
F. Paz-Rodríguez, M. Chávez-Oliveros, A. Bernal-Pérez, A. Ochoa-Morales, L. Martínez-Ruano, A. Camacho-Molina, Y. Rodríguez-Agudelo   +6 more
doaj  

Stem cell‐based cell therapy for Huntington disease: A review [PDF]

, 2007
Manho Kim, Soon‐Tae Lee, Kon Chu, Seung Up Kim   +3 more
openalex   +1 more source

Proteomic Profiling Informs Mechanisms of Esophageal Adenocarcinoma Inhibition by Cranberry Proanthocyanidins

Molecular Nutrition &Food Research, EarlyView.
In this study we utilized proteomic profiling to investigate mechanisms linked to the cancer‐inhibitory effect of cranberry proanthocyanidins (CPACs) on reflux‐induced esophageal adenocarcinoma in a rat model. The results indicate that CPAC inhibits cancer through targeting multiple hallmarks of cancer known to be dysregulated in progression to ...
Yun Zhang, Michelle Lee, Erika de Jesus, Katherine Weh, Connor Howard, Henriette Remmer, Amy B. Howell, Laura A. Kresty   +7 more
wiley   +1 more source

Clostridium sporogenes bacteremia in an immunocompetent patient

IDCases, 2019
Of the 200 Clostridium spp. known to exist, approximately 30 have been associated with human disease. Commonly found in soil, marine sediment and mammalian intestinal tracts, these gram-positive bacilli are known to cause infections ranging from ...
Waiel Abusnina, Mena Shehata, Emhemmid Karem, Zeynep Koc, Elie Khalil   +4 more
doaj  

Understanding the psychiatric prodrome of Huntington disease [PDF]

, 2007
Adam Rosenblatt
openalex   +1 more source

A Systematic Review of Attributes Influencing Preferences for Treatments and Interventions in People With Amyotrophic Lateral Sclerosis (ALS)

Muscle &Nerve, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that has no cure, and treatments predominantly focus on improving quality of life. Patient‐centred care is central to bringing about meaningful improvements to quality of life.
A. Clift, D. Rowen, L. Knox, A. W. Griffiths, C. J. McDermott   +4 more
wiley   +1 more source

Suicidal Ideation and Sleep Disturbances Among People With Huntington Disease: Evidence From the HDBOI Study. [PDF]

Neurol Clin Pract
Rodríguez Santana I, Frank SA, Mestre TA, Arnesen A, Hamilton JL, Hubberstey H, Winkelmann M, Hernandez-Jimenez E, Frimpter J, Dolmetsch R, Ali TM.   +10 more
europepmc   +1 more source

Humanistic Burden of Huntington Disease: Evidence From the Huntington Disease Burden of Illness Study. [PDF]

Neurol Clin Pract, 2022
Rodriguez Santana I, Frank S, Doherty M, Willock R, Hamilton J, Hubberstey H, Stanley C, Vetter L, Winkelmann M, Dolmetsch RE, Li N, Ratsch S, Ali TM.   +12 more
europepmc   +1 more source

Huntington Disease [PDF]

Journal of Neuropathology and Experimental Neurology, 1998
J P, Vonsattel, M, DiFiglia
openaire   +2 more sources

Neuroleptic malignant syndrome in Huntington disease. [PDF]

Eur J Neurol
Funcis A, Ravera B, Zinzi P, Solito M, Petracca M, Calabresi P, Bentivoglio AR.   +6 more
europepmc   +1 more source