All Relations between Neurodegenerative Diseases and cerebellum

Reference Sentence Publish Date Extraction Date Species
Federica Morani, Stefano Doccini, Daniele Galatolo, Francesco Pezzini, Rabah Soliymani, Alessandro Simonati, Maciej M Lalowski, Federica Gemignani, Filippo M Santorell. Integrative Organelle-Based Functional Proteomics: In Silico Prediction of Impaired Functional Annotations in Biomolecules vol 12 issue 8 2022 35892334 integrative organelle-based functional proteomics: in silico prediction of impaired functional annotations in autosomal recessive spastic ataxia of charlevoix-saguenay (arsacs) is an inherited neurodegenerative disease characterized by early-onset spasticity in the lower limbs, axonal-demyelinating sensorimotor peripheral neuropathy, and cerebellar ataxia. 2022-07-27 2022-08-08 Not clear
Jo\\xc3\\xa3o Br\\xc3\\xa1s, Daniel Henriques, Ricardo Moreira, Magda M Santana, Rita Silva-Pedrosa, Diana Ad\\xc3\\xa3o, Sandra Braz, Ana Rita \\xc3\\x81lvaro, Lu\\xc3\\xads Pereira de Almeida, Liliana S Mendon\\xc3\\xa7. Establishment and characterization of human pluripotent stem cells-derived brain organoids to model cerebellar diseases. Scientific reports vol 12 issue 1 2022 35869235 machado-joseph disease (mjd) is a cerebellar hereditary neurodegenerative disease, without therapeutic options able to prevent the disease progression. 2022-07-22 2022-07-25 Not clear
Giulia Lazzeri, Giulia Franco, Teresa Difonzo, Angelica Carandina, Chiara Gramegna, Maurizio Vergari, Federica Arienti, Anisa Naci, Costanza Scat\\xc3\\xa0, Edoardo Monfrini, Gabriel Dias Rodrigues, Nicola Montano, Giacomo P Comi, Maria Cristina Saetti, Eleonora Tobaldini, Alessio Di Fonz. Cognitive and Autonomic Dysfunction in Multiple System Atrophy Type P and C: A Comparative Study. Frontiers in neurology vol 13 issue 2022 35785342 multiple system atrophy (msa) is a rare neurodegenerative disease, clinically defined by a combination of autonomic dysfunction and motor involvement, that may be predominantly extrapyramidal (msa-p) or cerebellar (msa-c). 2022-07-05 2022-07-07 Not clear
Mutaz Amin, Cedric Vignal, Ahlam A A Hamed, Inaam N Mohammed, Maha A Elseed, Rayan Abubaker, Yousuf Bakhit, Arwa Babai, Eman Elbadi, Esraa Eltaraifee, Doua Mustafa, Ashraf Yahia, Melka Osman, Mahmoud Koko, Mohamed Mustafa, Mohamed Alsiddig, Sahwah Haroun, Azza Elshafea, Severine Drunat, Liena E O Elsayed, Ammar E Ahmed, Odile Boespflug-Tanguy, Imen Dorbo. Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan. Frontiers in genetics vol 13 issue 2022 35719383 pontocerebellar hypoplasia type 10 (pch10) is a very rare autosomal recessive neurodegenerative disease characterized by intellectual disability, microcephaly, severe developmental delay, pyramidal signs, mild cerebellar atrophy, and white matter changes in the brain, as shown by magnetic resonance imaging (mri). 2022-06-20 2022-07-04 Not clear
Kurt A Jellinge. Heterogeneity of Multiple System Atrophy: An Update. Biomedicines vol 10 issue 3 2022 35327402 multiple system atrophy (msa) is a fatal, rapidly progressing neurodegenerative disease of uncertain etiology, clinically characterized by various combinations of levodopa unresponsive parkinsonism, cerebellar, autonomic and motor dysfunctions. 2022-03-25 2022-04-14 Not clear
Li Xu, Zichen Sun, Zhiyao Xing, Yutong Liu, Hongting Zhao, Zhongmin Tang, Yu Luo, Shuangying Hao, Kuanyu L. Cur@SF NPs alleviate Friedreich's ataxia in a mouse model through synergistic iron chelation and antioxidation. Journal of nanobiotechnology vol 20 issue 1 2022 35264205 abnormal iron metabolism, mitochondrial dysfunction and the derived oxidative damage are the main pathogeneses of friedrich's ataxia (frda), a single-gene inherited recessive neurodegenerative disease characterized by progressive cerebellar and sensory ataxia. 2022-03-10 2022-04-14 Not clear
Ryuji Sakakibar. [Autonomic Disorder in Multiple System Atrophy]. Brain and nerve = Shinkei kenkyu no shinpo vol 74 issue 3 2022 35260523 multiple system atrophy (msa) is a neurodegenerative disease characterized by both autonomic and motor dysfunction (cerebellar ataxia and/or parkinsonism). 2022-03-09 2022-04-14 Not clear
Javier Miranda, Esther Cub. Spinocerebellar ataxia type 3: response to levodopa infusion in two cases. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol issue 2022 35199253 spinocerebellar ataxia type 3 (sca-atxn3) is a genetic neurodegenerative disease characterized by progressive cerebellar ataxia and other variable findings, including parkinsonian syndrome. 2022-02-24 2022-02-27 Not clear
Anne Pavy-Le Traon, Alexandra Foubert-Samier, Fabienne Ory-Magne, Margherita Fabbri, Jean-Michel Senard, Wassilios G Meissner, Olivier Rascol, Jacques Ama. Ambulatory blood pressure and drug treatment for orthostatic hypotension as predictors of mortality in patients with Multiple System Atrophy. European journal of neurology vol issue 2021 34971021 multiple system atrophy (msa) is a rare fatal neurodegenerative disease characterized by parkinsonism, cerebellar ataxia and autonomic failure. 2022-01-28 2022-01-13 Not clear
Anne Pavy-Le Traon, Alexandra Foubert-Samier, Fabienne Ory-Magne, Margherita Fabbri, Jean-Michel Senard, Wassilios G Meissner, Olivier Rascol, Jacques Ama. Ambulatory blood pressure and drug treatment for orthostatic hypotension as predictors of mortality in patients with Multiple System Atrophy. European journal of neurology vol issue 2021 34971021 multiple system atrophy (msa) is a rare fatal neurodegenerative disease characterized by parkinsonism, cerebellar ataxia and autonomic failure. 2021-12-31 2022-01-13 Not clear
Katharina Feil, Christine Adrion, Sylvia Boesch, Sarah Doss, Ilaria Giordano, Holger Hengel, Heike Jacobi, Thomas Klockgether, Thomas Klopstock, Wolfgang Nachbauer, Ludger Sch\\xc3\\xb6ls, Katharina Marie Steiner, Claudia Stendel, Dagmar Timmann, Ivonne Naumann, Ulrich Mansmann, Michael Strup. Safety and Efficacy of Acetyl-DL-Leucine in Certain Types of Cerebellar Ataxia: The ALCAT Randomized Clinical Crossover Trial. JAMA network open vol 4 issue 12 2021 34905009 cerebellar ataxia is a neurodegenerative disease impairing motor function characterized by ataxia of stance, gait, speech, and fine motor disturbances. 2021-12-14 2022-01-13 Not clear
David G Coughlin, Ian Dryden, Vanessa S Goodwill, Donald P Pizzo, Brenton Wright, Stephanie Lessig, Douglas Galasko, Ian R MacKenzie, Annie Hinike. Longstanding Multiple System Atrophy-Parkinsonism with Limbic and FTLD-type \\xce\\xb1-Synuclein Pathology. Neuropathology and applied neurobiology vol issue 2021 34847258 multiple system atrophy (msa) is a sporadic neurodegenerative disease clinically marked by autonomic failure and variable degrees of parkinsonism and cerebellar ataxias. 2021-11-30 2022-01-13 Not clear
Anna Niewiadomska-Cimicka, Fr\\xc3\\xa9d\\xc3\\xa9ric Doussau, Jean-Baptiste Perot, Michel J Roux, Celine Keime, Antoine Hache, Fran\\xc3\\xa7oise Piguet, Ariana Novati, Chantal Weber, Binnaz Yalcin, Hamid Meziane, Marie-France Champy, Erwan Grandgirard, Alice Karam, Nadia Messaddeq, Aur\\xc3\\xa9lie Eisenmann, Emmanuel Brouillet, Hoa Huu Phuc Nguyen, Julien Flament, Philippe Isope, Yvon Trottie. SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2. The Journal of neuroscience : the official journal of the Society for Neuroscience vol 41 issue 22 2021 33888607 spinocerebellar ataxia type 7 (sca7) is an inherited neurodegenerative disease mainly characterized by motor incoordination because of progressive cerebellar degeneration. 2021-11-19 2022-01-13 Not clear
Sharif I Kronemer, Mitchell B Slapik, Jessica R Pietrowski, Michael J Margron, Owen P Morgan, Catherine C Bakker, Liana S Rosenthal, Chiadi U Onyike, Cherie L Marve. Neuropsychiatric Symptoms as a Reliable Phenomenology of Cerebellar Ataxia. Cerebellum (London, England) vol 20 issue 2 2021 33000380 while cerebellar ataxia (ca) is a neurodegenerative disease known for motor impairment, changes in mood have also been reported. 2021-11-05 2022-01-13 Not clear
Matthew R Burns, Nikolaus R McFarlan. Current Management and Emerging Therapies in Multiple System Atrophy. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics vol 17 issue 4 2021 32767032 multiple system atrophy (msa) is a progressive neurodegenerative disease variably associated with motor, nonmotor, and autonomic symptoms, resulting from putaminal and cerebellar degeneration and associated with glial cytoplasmic inclusions enriched with \xce\xb1-synuclein in oligodendrocytes and neurons. 2021-10-28 2022-01-13 Not clear
Kristine Joyce Porto, Makito Hirano, Jun Mitsui, Ayaka Chikada, Takashi Matsukawa, Hiroyuki Ishiura, Tatsushi Toda, Susumu Kusunoki, Shoji Tsuj. COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population. Journal of the neurological sciences vol 429 issue 2021 34455210 multiple system atrophy (msa) is a rare, late-onset, and devastating neurodegenerative disease characterized by autonomic failure, alongside with various combination of parkinsonism, cerebellar ataxia, and pyramidal dysfunction. 2021-10-27 2022-01-14 Not clear
Louisa P Selvadurai, Nellie Georgiou-Karistianis, Rosita Shishegar, Cathlin Sheridan, Gary F Egan, Martin B Delatycki, Ian H Harding, Louise A Corbe. Longitudinal structural brain changes in Friedreich ataxia depend on disease severity: the IMAGE-FRDA study. Journal of neurology vol 268 issue 11 2021 33860369 friedreich ataxia is an inherited neurodegenerative disease, with cerebral and cerebellar pathology evident. 2021-10-13 2022-01-13 Not clear
Milvia Alata, Arturo Gonz\\xc3\\xa1lez-Vega, Valeria Piazza, Anke Kleinert-Altamirano, Carmen Cortes, Juan C Ahumada-Ju\\xc3\\xa1rez, Jose R Eguibar, Alejandra L\\xc3\\xb3pez-Ju\\xc3\\xa1rez, Victor H Hernande. Longitudinal Evaluation of Cerebellar Signs of H-ABC Tubulinopathy in a Patient and in the Frontiers in neurology vol 12 issue 2021 34335454 longitudinal evaluation of cerebellar signs of h-abc tubulinopathy in a patient and in the hypomyelination with atrophy of the basal ganglia and cerebellum (h-abc) is a central neurodegenerative disease due to mutations in the tubulin beta-4a (tubb4a) gene, characterized by motor development delay, abnormal movements, ataxia, spasticity, dysarthria, and cognitive deficits. 2021-08-03 2022-01-13 Not clear
Yusuke Tokuhara, Shohei Watanabe, Hiroo Yoshikaw. Changes in clinical features of multiple system atrophy in Japan. Clinical parkinsonism & related disorders vol 3 issue 2021 34316637 multiple system atrophy (msa) is an adult-onset progressive neurodegenerative disease that causes parkinsonism, cerebellar ataxia, and/or autonomic failure. 2021-07-29 2022-01-13 Not clear
Philip W Tipton, Dale C Ekbom, Amy L Rutt, Jay A van Gerpe. Vocal Fold \"Paralysis\": An Early Sign in Multiple System Atrophy. Journal of voice : official journal of the Voice Foundation vol 34 issue 6 2021 31324432 multiple system atrophy (msa) is a neurodegenerative disease characterized by a cerebellar syndrome, autonomic dysfunction, and extrapyramidal signs. 2021-07-28 2022-01-13 Not clear
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