Suchergebnisse - "Huntington's disease"

Estudio de signos clínicos y biomarcadores en taupatías primarias, secundarias y atrofia multisistémica

Autoren: Ruiz Barrio, Iñigo

Thesis Advisors: Kulisevsky, Jaime, Pagonabarraga Mora, Javier

Quelle: TDX (Tesis Doctorals en Xarxa)

Schlagwörter: Paràlisi supranuclear progress, Progressive supranuclear palsy, Parálisis supranuclear progres, Atròfia multisistèmica, Multiple system atrophy, Atrofia multisistémica, Malaltia de Huntington, Huntington's disease, Enfermedad de Huntington, Ciències de la Salut

Time: 616.8

Dateibeschreibung: application/pdf

Zugangs-URL: http://hdl.handle.net/10803/693553

Desarrollo y validación de nuevas herramientas para la evaluación cognitiva en la enfermedad de Huntington

Autoren: Horta Barba, Andrea

Thesis Advisors: Kulisevsky, Jaime, Pagonabarraga Mora, Javier

Quelle: TDX (Tesis Doctorals en Xarxa)

Schlagwörter: Malaltia de Huntington, Huntington's disease, Enfermedad de Huntington, Cognició, Cognition, Cognición, Neuropsicologia, Neuropsychology, Neuropsicología, Ciències de la Salut

Time: 616.8

Dateibeschreibung: application/pdf

Zugangs-URL: http://hdl.handle.net/10803/691596

Study of two analogues of pituitary adenylate cyclase-activating polypeptide as novel therapeutic compounds for Huntington’s disease

Autoren: Solés Tarrés, Irene

Weitere Verfasser: University/Department: Universitat de Girona. Departament de Ciències Mèdiques

Thesis Advisors: Xifró i Collsamata, Xavier

Quelle: TDX (Tesis Doctorals en Xarxa)

Schlagwörter: Pituitary adenylate cyclase-activating polypeptide (PACAP), Malaltia de Huntington, Enfermedad de Huntington, Huntington's disease, Neuroprotecció, Neuroprotección, Neuroprotection, Plasticitat sinàptica, Plasticidad sináptica, Synaptic plasticity, Neurotròfic, Neurotrófico, Neurotrophic, Dèficits motors, Déficits motores, Motor deficits, Disfunció cognitiva, Disfunción cognitiva, Cognitive dysfunction

Time: 616.8

Dateibeschreibung: application/pdf

Zugangs-URL: http://hdl.handle.net/10803/688973

Distinct molecular patterns in R6/2 HD mouse brain: Insights from spatiotemporal transcriptomics

Autoren: Burns, Mara S Miramontes, Ricardo Wu, Jie et al.

Quelle: Neuron. 113(15)

Schlagwörter: 32 Biomedical and Clinical Sciences (for-2020), 3209 Neurosciences (for-2020), Neurosciences (rcdc), Human Genome (rcdc), Genetics (rcdc), Huntington's Disease (rcdc), Biotechnology (rcdc), Brain Disorders (rcdc), Rare Diseases (rcdc), Neurodegenerative (rcdc), 2.1 Biological and endogenous factors (hrcs-rac), 1.1 Normal biological development and functioning (hrcs-rac), Neurological (hrcs-hc), Animals (mesh), Mice (mesh), Huntington Disease (mesh), Transcriptome (mesh), Brain (mesh), Mice, Transgenic (mesh), Corpus Striatum (mesh), Male (mesh), Receptors, Dopamine D2 (mesh), Disease Models, Animal (mesh), Gene Expression Profiling (mesh), Brain (mesh), Corpus Striatum (mesh), Animals (mesh), Mice, Transgenic (mesh), Mice (mesh), Huntington Disease (mesh), Disease Models, Animal (mesh), Receptors, Dopamine D2 (mesh), Gene Expression Profiling (mesh), Male (mesh), Transcriptome (mesh), Huntington’s disease, R62 transgenic, cell-cell signaling, metabolism, neuropeptide Y, protein kinase A, snRNA-seq, spatial transcriptomics, transcription factor 4, transcriptional dysregulation, Animals (mesh), Mice (mesh), Huntington Disease (mesh), Transcriptome (mesh), Brain (mesh), Mice, Transgenic (mesh), Corpus Striatum (mesh), Male (mesh), Receptors, Dopamine D2 (mesh), Disease Models, Animal (mesh), Gene Expression Profiling (mesh), 1109 Neurosciences (for), 1701 Psychology (for), 1702 Cognitive Sciences (for), Neurology & Neurosurgery (science-metrix), 3209 Neurosciences (for-2020), 5202 Biological psychology (for-2020)

Zugangs-URL: https://escholarship.org/uc/item/9ds7r658

Two mental disorders as disease models of language: linguistic (dis)organisation in schizophrenia and Huntington's disease

Autoren: Tovar, Antonia

Weitere Verfasser: University/Department: Universitat Pompeu Fabra. Departament de Traducció i Ciències del llenguatge

Thesis Advisors: Hinzen, Wolfram

Quelle: TDX (Tesis Doctorals en Xarxa)

Schlagwörter: Mental disorders, Trastornos mentales, Schizophrenia, Huntington’s disease, Enfermedad de Huntington, Esquizofrenia

Dateibeschreibung: application/pdf

Zugangs-URL: http://hdl.handle.net/10803/687810

Dopamine receptor D3 induces transient, mTORC1-dependent autophagy that becomes persistent, AMPK-mediated, and neuroprotective in experimental models of Huntington’s disease

Autoren: Luis-Ravelo, Diego Fumagallo-Reading, Felipe Febles-Casquero, Alejandro et al.

Quelle: Cells. 14(9)

Schlagwörter: AMPK, dopamine receptors, Huntington’s disease, mTORC1, neuroprotection, ULK1

Dateibeschreibung: electronic

Zugangs-URL: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-239118
https://doi.org/10.3390/cells14090652

Correlatos neuronales y neuropsicológicos de las alteraciones cognitivas y conductuales en las fases prodrómica e inicial de la enfermedad de Huntington

Autoren: Martínez Horta, Saul

Thesis Advisors: Kulisevsky, Jaime, Pagonabarraga Mora, Javier

Quelle: TDX (Tesis Doctorals en Xarxa)

Schlagwörter: Malaltia de Huntington, Enfermedad de Huntington, Huntington's disease, Neuropsicologia, Neuropsicología, Neuropsychology, Neuroimatge, Neuroimagen, Neuroimage, Ciències de la Salut

Time: 616.8

Dateibeschreibung: application/pdf

Zugangs-URL: http://hdl.handle.net/10803/671898

Mesenchymal Stem Cell-Derived Extracellular Vesicles: Emerging Therapies for Neurodegenerative Diseases

Autoren: Chen P Wang F Ling B et al.

Quelle: Int J Nanomedicine
International Journal of Nanomedicine, Vol Volume 20, Iss Issue 1, Pp 8547-8565 (2025)

Schlagwörter: Medicine (General), R5-920, Parkinson's disease, Huntington's disease, Review, Alzheimer's disease, Amyotrophic lateral sclerosis, extracellular vesicles, Mesenchymal stem cell

Zugangs-URL: https://doaj.org/article/54bf0f4228f743cd8add54a790893448

Dysregulation of protein SUMOylation networks in Huntingtons disease R6/2 mouse striatum.

Autoren: Kachemov, Marketta Vaibhav, Vineet Smith, Charlene et al.

Quelle: Brain. 148(4)

Schlagwörter: E3 SUMO ligase, Huntington’s disease, PIAS1, SUMO, mGLUR7, proteomics, synaptic, Animals, Huntington Disease, Sumoylation, Mice, Transgenic, Mice, Corpus Striatum, Huntingtin Protein, Neurons, Disease Models, Animal, Cells, Cultured, Receptors, Metabotropic Glutamate, Male

Dateibeschreibung: application/pdf

Zugangs-URL: https://escholarship.org/uc/item/0d8525ws
https://escholarship.org/content/qt0d8525ws/qt0d8525ws.pdf

A phase I, open-label study of intravenous human dental pulp stem cells (NestaCell®) at two dose levels in patients with Huntington’s disease

Autoren: Joyce Macedo Sanches Fernandes Eduardo Pagani Cristiane Valverde Wenceslau et al.

Quelle: Stem Cell Research & Therapy, Vol 16, Iss 1, Pp 1-11 (2025)

Schlagwörter: Huntington’s disease, Stem cells, Unified Huntington’s disease rating scale, Dental pulp stem cell, Medicine (General), R5-920, Biochemistry, QD415-436

Dateibeschreibung: electronic resource

Relation: https://doaj.org/toc/1757-6512

Zugangs-URL: https://doaj.org/article/8fbf8f46d85d409487d3de117a1ba7a2

Protocol considerations for multigenerational blinding of preimplantation genetic testing for a monogenic condition for Huntington disease: a case report

Autoren: Samuel Raine Dana R. Siegel Liya Rabkina et al.

Quelle: F S Rep
F&S Reports, Vol 6, Iss 2, Pp 201-205 (2025)

Schlagwörter: PGT-M, exclusion-based PGT, Nondisclosure, IVF, RG1-991, Huntington's disease, RC870-923, Gynecology and obstetrics, Original Articles, Diseases of the genitourinary system. Urology

Zugangs-URL: https://doaj.org/article/80f8fa7c2da941939c39c0eb6228ee55

Potential common pathogenesis of several neurodegenerative diseases

Autoren: Ting Fan Jiaman Peng Huiting Liang et al.

Quelle: Neural Regen Res
Neural Regeneration Research, Vol 21, Iss 3, Pp 972-988 (2026)

Schlagwörter: frontotemporal lobar dementia, amyotrophic lateral sclerosis, parkinson's disease, huntington's disease, aging, lewy body disease, alzheimer's disease, genetics, Neurology. Diseases of the nervous system, Review, protein misfolding, RC346-429, progressive neuron dysfunction and death

Zugangs-URL: https://doaj.org/article/c85f963888ae42dc8ab11592c5a2611d

Gene Silencing Therapies for Huntington’s Disease

Autoren: Chunlan Hao Hanfeng Ji

Quelle: Neurology Letters, Vol 4, Iss 1, Pp 69-75 (2025)

Schlagwörter: rna interference, huntington's disease, huntingtin, htt lowering, Neurology. Diseases of the nervous system, antisense oligonucleotides, crispr, RC346-429

Zugangs-URL: https://doaj.org/article/0326aec5e74548bfbd088fb8bc9122bc

A 14‐Year Study of Serum Glial Fibrillary Acidic Protein and Total Tau in Premanifest Huntington's

Autoren: Owen, Natalia E Voysey, Zanna J Holbrook, Jonathan A et al.

Weitere Verfasser: Owen, Natalia E Voysey, Zanna J Holbrook, Jonathan A et al.

Quelle: Ann Clin Transl Neurol
Annals of Clinical and Translational Neurology, Vol 12, Iss 6, Pp 1296-1301 (2025)

Schlagwörter: Male, Adult, blood‐based biomarkers, Neurosciences. Biological psychiatry. Neuropsychiatry, Huntington's disease, tau Proteins, Middle Aged, Brief Communication, prognostic biomarkers, Huntington Disease, Neurofilament Proteins, glial fibrillary acidic protein, Glial Fibrillary Acidic Protein, Humans, Female, Neurology. Diseases of the nervous system, tau, Longitudinal Studies, RC346-429, Biomarkers, RC321-571

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/40256911
https://doaj.org/article/48eded7a692d4adaa442b0b7de8898bc
https://ueaeprints.uea.ac.uk/id/eprint/99056/
https://www.repository.cam.ac.uk/handle/1810/382814
https://doi.org/10.17863/cam.117442
https://doi.org/10.1002/acn3.70057

Early Language Impairment as an Integral Part of the Cognitive Phenotype in Huntington's Disease

Autoren: Arnau Puig‐Davi Carla Franch‐Marti Iñigo Ruiz‐Barrio et al.

Quelle: Ann Clin Transl Neurol
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Annals of Clinical and Translational Neurology, Vol 12, Iss 6, Pp 1201-1213 (2025)

Schlagwörter: cognitive phenotype, language, neuroimaging, brain structure, Neurosciences. Biological psychiatry. Neuropsychiatry, Huntington's disease, Neuroimaging, Cognitive phenotype, Brain structure, Neurology. Diseases of the nervous system, RC346-429, RC321-571, Language, Research Article

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/40244831
https://doaj.org/article/0bc537a5b55d4272bcc8c4d945d7ac0f
https://ddd.uab.cat/record/313507

Malestar psicológico en portadores y no portadores de la mutación causante de enfermedad de Huntington y su relación con la carga de la enfermedad

Autoren: Y. Rodríguez-Agudelo M. Chávez-Oliveros A. Ochoa-Morales et al.

Quelle: Neurología, Vol 40, Iss 1, Pp 1-9 (2025)

Schlagwörter: 03 medical and health sciences, 0302 clinical medicine, Huntington's disease, Psychological distress, Disease burden, Neurology. Diseases of the nervous system, Huntington's disease prodrome, RC346-429

Zugangs-URL: https://doaj.org/article/b33ad3217b0c4438a9440bbaa02a43e8

Language in Huntington’s disease

Autoren: Saldert, Charlotta Cummings, Louise, book editor

Weitere Verfasser: Saldert, Charlotta Cummings, Louise, book editor

Quelle: The Oxford Handbook of Communication Disorders in Neurodegenerative Diseases.

Verfügbarkeit: https://doi.org/10.1093/oxfordhb/9780198888482.013.0014

Stuttering and cluttering in neurodegenerative disorders

Autoren: Scaler Scott, Kathleen Cummings, Louise, book editor

Weitere Verfasser: Scaler Scott, Kathleen Cummings, Louise, book editor

Quelle: The Oxford Handbook of Communication Disorders in Neurodegenerative Diseases.

Verfügbarkeit: https://doi.org/10.1093/oxfordhb/9780198888482.013.0009

Dysarthria in Huntington’s disease

Autoren: de Riesthal, Michael Diehl, Sarah K. Cummings, Louise, book editor

Weitere Verfasser: de Riesthal, Michael Diehl, Sarah K. Cummings, Louise, book editor

Quelle: The Oxford Handbook of Communication Disorders in Neurodegenerative Diseases.

Verfügbarkeit: https://doi.org/10.1093/oxfordhb/9780198888482.013.0005

Corrigendum to “Differential electrophysiological and morphological alterations of thalamostriatal and corticostriatal projections in the R6/2 mouse model of Huntington's disease” [Neurobiology of Disease 108 (2017) Pages 29-44]

Autoren: Parievsky, Anna Moore, Cindy Kamdjou, Talia et al.

Schlagwörter: Biological Sciences, Genetics, Neurosciences, Huntington's Disease, Brain Disorders, Rare Diseases, Neurodegenerative, Clinical Sciences, Neurology & Neurosurgery, Biochemistry and cell biology

Dateibeschreibung: application/pdf

Zugangs-URL: https://escholarship.org/uc/item/0j49p32f
https://escholarship.org/content/qt0j49p32f/qt0j49p32f.pdf