| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Yoko Takahashi, Masaya Kubota, Rika Kosaki, Kenjiro Kosaki, Akira Ishigur. A severe form of autosomal recessive spinocerebellar ataxia associated with novel PMPCA variants. Brain & development. vol 43. issue 3. 2021-10-04. PMID:33272776. |
spinocerebellar ataxia, autosomal recessive 2 (scar2) [mim:213200] is a rare autosomal recessive disease of spinocerebellar ataxia associated with degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. |
2021-10-04 |
2023-08-13 |
Not clear |
| Roderick P P W M Maas, Bart P C van de Warrenburg, Dennis J L G Schutte. Inverse associations between cerebellar inhibition and motor impairment in spinocerebellar ataxia type 3. Brain stimulation. vol 14. issue 2. 2021-10-04. PMID:33535082. |
inverse associations between cerebellar inhibition and motor impairment in spinocerebellar ataxia type 3. |
2021-10-04 |
2023-08-13 |
Not clear |
| Polina A Egorova, Aleksandra V Gavrilova, Ilya B Bezprozvann. In vivo analysis of the spontaneous firing of cerebellar Purkinje cells in awake transgenic mice that model spinocerebellar ataxia type 2. Cell calcium. vol 93. 2021-09-24. PMID:33248384. |
cerebellar purkinje cells (pcs) fire spontaneously in a tonic mode, although the precision of this pacemaking activity is disturbed in many abnormal conditions involving cerebellar atrophy, such as many spinocerebellar ataxias (scas). |
2021-09-24 |
2023-08-13 |
mouse |
| Jan Cendelin, Marija Cvetanovic, Mandi Gandelman, Hirokazu Hirai, Harry T Orr, Stefan M Pulst, Michael Strupp, Filip Tichanek, Jan Tuma, Mario Mant. Consensus Paper: Strengths and Weaknesses of Animal Models of Spinocerebellar Ataxias and Their Clinical Implications. Cerebellum (London, England). 2021-09-23. PMID:34378174. |
spinocerebellar ataxias (scas) represent a large group of hereditary degenerative diseases of the nervous system, in particular the cerebellum, and other systems that manifest with a variety of progressive motor, cognitive, and behavioral deficits with the leading symptom of cerebellar ataxia. |
2021-09-23 |
2023-08-13 |
mouse |
| Jianping Hu, Xinyuan Chen, Mengcheng Li, Hao-Ling Xu, Ziqiang Huang, Naping Chen, Yuqing Tu, Qunlin Chen, Shirui Gan, Dairong Ca. Pattern of cerebellar grey matter loss associated with ataxia severity in spinocerebellar ataxias type 3: a multi-voxel pattern analysis. Brain imaging and behavior. 2021-08-21. PMID:34417969. |
pattern of cerebellar grey matter loss associated with ataxia severity in spinocerebellar ataxias type 3: a multi-voxel pattern analysis. |
2021-08-21 |
2023-08-13 |
human |
| Jianping Hu, Xinyuan Chen, Mengcheng Li, Hao-Ling Xu, Ziqiang Huang, Naping Chen, Yuqing Tu, Qunlin Chen, Shirui Gan, Dairong Ca. Pattern of cerebellar grey matter loss associated with ataxia severity in spinocerebellar ataxias type 3: a multi-voxel pattern analysis. Brain imaging and behavior. 2021-08-21. PMID:34417969. |
spinocerebellar ataxias type 3 (sca3) patients are clinically characterized by progressive cerebellar ataxia combined with degeneration of the cerebellum. |
2021-08-21 |
2023-08-13 |
human |
| Giulia Coarelli, Frederic Darios, Emilien Petit, Karim Dorgham, Isaac Adanyeguh, Elodie Petit, Alexis Brice, Fanny Mochel, Alexandra Dur. Plasma neurofilament light chain predicts cerebellar atrophy and clinical progression in spinocerebellar ataxia. Neurobiology of disease. vol 153. 2021-08-20. PMID:33636389. |
plasma neurofilament light chain predicts cerebellar atrophy and clinical progression in spinocerebellar ataxia. |
2021-08-20 |
2023-08-13 |
Not clear |
| Mohamed A Elsaey, Kazuhiko Namikawa, Reinhard W Köste. Genetic Modeling of the Neurodegenerative Disease Spinocerebellar Ataxia Type 1 in Zebrafish. International journal of molecular sciences. vol 22. issue 14. 2021-08-17. PMID:34298970. |
dominant spinocerebellar ataxias (scas) are progredient neurodegenerative diseases commonly affecting the survival of purkinje cells (pcs) in the human cerebellum. |
2021-08-17 |
2023-08-13 |
human |
| Cleo J L M Smeets, Kai Yu Ma, Simon E Fisher, Dineke S Verbee. Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23. Brain pathology (Zurich, Switzerland). vol 31. issue 2. 2021-08-11. PMID:33043513. |
cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23. |
2021-08-11 |
2023-08-13 |
Not clear |
| Roberto Rodríguez-Labrada, Alejandro Batista-Izquierdo, Zuleyra González-Melix, Lorenzo Reynado-Cejas, Yaimeé Vázquez-Mojena, Yuri Arsenio Sanz, Nalia Canales-Ochoa, Yanetza González-Zaldívar, Imis Dogan, Kathrin Reetz, Luis Velázquez-Pére. Cognitive Decline Is Closely Associated with Ataxia Severity in Spinocerebellar Ataxia Type 2: a Validation Study of the Schmahmann Syndrome Scale. Cerebellum (London, England). 2021-07-27. PMID:34313938. |
the cerebellar cognitive affective syndrome scale (ccas-s) was designed to detect specific cognitive dysfunctions in cerebellar patients but is scarcely validated in spinocerebellar ataxias (sca). |
2021-07-27 |
2023-08-13 |
Not clear |
| Qing Lin, Yichen Chang, Peng Liu, Jeffery A Jones, Xi Chen, Danhua Peng, Mingyuan Chen, Chao Wu, Hanjun Li. Cerebellar Continuous Theta Burst Stimulation Facilitates Auditory-Vocal Integration in Spinocerebellar Ataxia. Cerebral cortex (New York, N.Y. : 1991). 2021-07-09. PMID:34240142. |
cerebellar continuous theta burst stimulation facilitates auditory-vocal integration in spinocerebellar ataxia. |
2021-07-09 |
2023-08-13 |
Not clear |
| Thomas P Zwaka, Marta Skowronska, Ronald Richman, Marion Dejose. Ronin overexpression induces cerebellar degeneration in a mouse model of ataxia. Disease models & mechanisms. vol 14. issue 6. 2021-07-08. PMID:34165550. |
spinocerebellar ataxias (scas) are a group of genetically heterogeneous inherited neurodegenerative disorders characterized by progressive ataxia and cerebellar degeneration. |
2021-07-08 |
2023-08-13 |
mouse |
| Roderick P P W M Maas, Ivan Toni, Jonne Doorduin, Thomas Klockgether, Dennis J L G Schutter, Bart P C van de Warrenbur. Correction to: Cerebellar transcranial direct current stimulation in spinocerebellar ataxia type 3 (SCA3-tDCS): rationale and protocol of a randomized, double-blind, sham-controlled study. BMC neurology. vol 21. issue 1. 2021-07-03. PMID:34187386. |
correction to: cerebellar transcranial direct current stimulation in spinocerebellar ataxia type 3 (sca3-tdcs): rationale and protocol of a randomized, double-blind, sham-controlled study. |
2021-07-03 |
2023-08-13 |
Not clear |
| Sally Rowland, Xiaofei Du, Christopher M Gome. Commentary to: "The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6" by Rentiya et al., Cerebellum 2020;19(3):459-464). Cerebellum (London, England). vol 20. issue 3. 2021-06-22. PMID:33219436. |
commentary to: "the pathophysiology and clinical manifestations of spinocerebellar ataxia type 6" by rentiya et al., cerebellum 2020;19(3):459-464). |
2021-06-22 |
2023-08-13 |
Not clear |
| Sara AlHilali, Nada H AlMadhi, Eman D AlBalaw. Ophthalmic Features of Spinocerebellar Ataxia Type 7: A Case Report. The American journal of case reports. vol 22. 2021-06-22. PMID:34148052. |
background spinocerebellar ataxia (sca) is an inherited progressive neurodegenerative disorder characterized by late-onset cerebellar and brainstem dysfunction. |
2021-06-22 |
2023-08-13 |
Not clear |
| Taro Ishiguro, Yoshitaka Nagai, Kinya Ishikaw. Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From Frontiers in neuroscience. vol 15. 2021-06-12. PMID:34113230. |
insight into spinocerebellar ataxia type 31 (sca31) from spinocerebellar ataxia type 31 (sca31) is a progressive neurodegenerative disease characterized by degeneration of purkinje cells in the cerebellum. |
2021-06-12 |
2023-08-13 |
Not clear |
| Etsuko Shimobayashi, Josef P Kapfhamme. A New Mouse Model Related to SCA14 Carrying a Pseudosubstrate Domain Mutation in PKCγ Shows Perturbed Purkinje Cell Maturation and Ataxic Motor Behavior. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 41. issue 9. 2021-06-11. PMID:33478986. |
spinocerebellar ataxias (scas) are diseases characterized by cerebellar atrophy and loss of purkinje neurons caused by mutations in diverse genes. |
2021-06-11 |
2023-08-13 |
mouse |
| R Palvadeau, Z E Kaya-Güleç, G Şimşir, A Vural, Ö Öztop-Çakmak, G Genç, M S Aygün, O Falay, A Nazlı Başak, S Erta. Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family. Neurogenetics. vol 21. issue 1. 2021-05-28. PMID:31741143. |
sca48 is a novel spinocerebellar ataxia (sca) originally and recently characterized by prominent cerebellar cognitive-affective syndrome (ccas) and late-onset ataxia caused by mutations on the stub1 gene. |
2021-05-28 |
2023-08-13 |
Not clear |
| Fatima Zahra Bouzid, Maria Mansouri, Chaikhy Abdelaziz, Nisrine Louhab, Sablonniere Bernard, Isabelle Strubi-Vuillaume, Kenza Dafir, Nisrine Aboussai. Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report). The Pan African medical journal. vol 38. 2021-05-25. PMID:33995769. |
the cag repeat expansion in the ataxin-7 gene (atxn7) causes spinocerebellar ataxia type 7 - a mutation that results in the degeneration of the brain stem cells, retina and cerebellum. |
2021-05-25 |
2023-08-13 |
Not clear |
| Marina P Hommersom, Ronald A M Buijsen, Willeke M C van Roon-Mom, Bart P C van de Warrenburg, Hans van Bokhove. Human Induced Pluripotent Stem Cell-Based Modelling of Spinocerebellar Ataxias. Stem cell reviews and reports. 2021-05-25. PMID:34031815. |
dominant spinocerebellar ataxias (scas) constitute a large group of phenotypically and genetically heterogeneous disorders that mainly present with dysfunction of the cerebellum as their main hallmark. |
2021-05-25 |
2023-08-13 |
human |