| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Maitane García, Idoia Rouco-Axpe, Imanol Amayra, Alfredo Rodríguez-Antigüedad, Claudio Catalli, Alberto Cabrera-Zubizarreta, Alicia Aurora Rodríguez, Manuel Pére. Neuropsychological Profile of Hereditary Ataxias: Study of 38 Patients. Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists. 2022-04-29. PMID:35484833. |
hereditary ataxias are a heterogeneous group of disorders characterized by degeneration of the cerebellum and its connections. |
2022-04-29 |
2023-08-13 |
Not clear |
| Hui Chen, Limeng Dai, Yuhan Zhang, Liu Feng, Zhenzhen Jiang, Xingang Wang, Dongjing Xie, Jing Guo, Huafu Chen, Jian Wang, Chen Li. Network Reconfiguration Among Cerebellar Visual, Frontiers in aging neuroscience. vol 14. 2022-04-28. PMID:35478700. |
network reconfiguration among cerebellar visual, spinocerebellar ataxia type 3 (sca3) is a rare movement disorder characterized with ataxia. |
2022-04-28 |
2023-08-13 |
Not clear |
| Mahmoud Reza Ashrafi, Elham Pourbakhtyaran, Mohammad Rohani, Bita Shalbafan, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinezhad, Zahra Rezaei, Ali Zare Dehnavi, Seyyed Mohammad Mahdi Hosseiny, Roya Haghighi, Homa Ghabeli, Morteza Heidar. Follow-up of 25 patients with treatable ataxia: A comprehensive case series study. Clinical case reports. vol 10. issue 4. 2022-04-27. PMID:35474986. |
autosomal recessive cerebellar ataxias are a group of heterogeneous early-onset progressive disorders that some of them are treatable. |
2022-04-27 |
2023-08-13 |
Not clear |
| Manish Bhartiya, Amit Kumar, Rakesh K Singh, Divya M Radhakrishnan, Roopa Rajan, Achal Kumar Srivastav. Mesenchymal Stem Cell Therapy in the Treatment of Neurodegenerative Cerebellar Ataxias: a Systematic Review and Meta-analysis. Cerebellum (London, England). 2022-04-22. PMID:35451803. |
mesenchymal stem cell therapy in the treatment of neurodegenerative cerebellar ataxias: a systematic review and meta-analysis. |
2022-04-22 |
2023-08-13 |
Not clear |
| Manish Bhartiya, Amit Kumar, Rakesh K Singh, Divya M Radhakrishnan, Roopa Rajan, Achal Kumar Srivastav. Mesenchymal Stem Cell Therapy in the Treatment of Neurodegenerative Cerebellar Ataxias: a Systematic Review and Meta-analysis. Cerebellum (London, England). 2022-04-22. PMID:35451803. |
the objective of this study is to synthesise the findings of clinical studies in order to derive evidence for use of the mesenchymal stem cell (msc) therapy in the treatment of neurodegenerative cerebellar ataxias. |
2022-04-22 |
2023-08-13 |
Not clear |
| Manish Bhartiya, Amit Kumar, Rakesh K Singh, Divya M Radhakrishnan, Roopa Rajan, Achal Kumar Srivastav. Mesenchymal Stem Cell Therapy in the Treatment of Neurodegenerative Cerebellar Ataxias: a Systematic Review and Meta-analysis. Cerebellum (London, England). 2022-04-22. PMID:35451803. |
no l rcts was available in the literature to test efficacy; therefore, well-designed rcts are needed to ascertain the effectiveness of mscs in patients with neurodegenerative cerebellar ataxias. |
2022-04-22 |
2023-08-13 |
Not clear |
| Yang Tian, Zhen Shi, Chi Hou, Wenjuan Li, Haixia Zhu, Xiaojing Li, Wenxiong Che. [Diagnosis of a child with mitochondrial myopathy and cerebellar atrophy with ataxia due to compound heterozygous variants of MSTO1 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. vol 39. issue 4. 2022-04-21. PMID:35446979. |
[diagnosis of a child with mitochondrial myopathy and cerebellar atrophy with ataxia due to compound heterozygous variants of msto1 gene]. |
2022-04-21 |
2023-08-13 |
Not clear |
| Yang Tian, Zhen Shi, Chi Hou, Wenjuan Li, Haixia Zhu, Xiaojing Li, Wenxiong Che. [Diagnosis of a child with mitochondrial myopathy and cerebellar atrophy with ataxia due to compound heterozygous variants of MSTO1 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. vol 39. issue 4. 2022-04-21. PMID:35446979. |
to explore the genetic basis for a child with myopathy and cerebellar atrophy with ataxia. |
2022-04-21 |
2023-08-13 |
Not clear |
| b' Ikhlass Haj Salem, Marie Beaudin, Christopher J Klein, Nicolas Dupr\\xc3\\xa. Treatment and Management of Autosomal Recessive Cerebellar Ataxias: Current Advances and Future Perspectives. CNS & neurological disorders drug targets. 2022-04-20. PMID:35440322.' |
treatment and management of autosomal recessive cerebellar ataxias: current advances and future perspectives. |
2022-04-20 |
2023-08-13 |
Not clear |
| b' Ikhlass Haj Salem, Marie Beaudin, Christopher J Klein, Nicolas Dupr\\xc3\\xa. Treatment and Management of Autosomal Recessive Cerebellar Ataxias: Current Advances and Future Perspectives. CNS & neurological disorders drug targets. 2022-04-20. PMID:35440322.' |
the autosomal recessive cerebellar ataxias (arcas) compose a clinically and genetically heterogeneous group of neurodegenerative diseases characterized by prominent cerebellar ataxia, dysmetria, dysarthria, and nystagmus that are inherited in an autosomal recessive fashion. |
2022-04-20 |
2023-08-13 |
Not clear |
| Jin Zhao, Huan Zhang, Xueyu Fan, Xue Yu, Jisen Hua. Lipid Dyshomeostasis and Inherited Cerebellar Ataxia. Molecular neurobiology. 2022-04-14. PMID:35420383. |
cerebellar ataxia is a form of ataxia that originates from dysfunction of the cerebellum, but may involve additional neurological tissues. |
2022-04-14 |
2023-08-13 |
Not clear |
| Pierre Cabaraux, Sunil K Agrawal, Huaying Cai, Rocco Salvatore Calabro, Casali Carlo, Damm Loic, Doss Sarah, Christophe Habas, Anja K E Horn, Winfried Ilg, Elan D Louis, Hiroshi Mitoma, Vito Monaco, Maria Petracca, Alberto Ranavolo, Ashwini K Rao, Serena Ruggieri, Tommaso Schirinzi, Mariano Serrao, Susanna Summa, Michael Strupp, Olivia Surgent, Matthis Synofzik, Shuai Tao, Hiroo Terasi, Diego Torres-Russotto, Brittany Travers, Jaimie A Roper, Mario Mant. Consensus Paper: Ataxic Gait. Cerebellum (London, England). 2022-04-13. PMID:35414041. |
ataxia of stance/gait is amongst the first cerebellar deficits in cerebellar disorders such as degenerative ataxias and is a disabling symptom with a high risk of falls. |
2022-04-13 |
2023-08-13 |
human |
| Pierre Cabaraux, Sunil K Agrawal, Huaying Cai, Rocco Salvatore Calabro, Casali Carlo, Damm Loic, Doss Sarah, Christophe Habas, Anja K E Horn, Winfried Ilg, Elan D Louis, Hiroshi Mitoma, Vito Monaco, Maria Petracca, Alberto Ranavolo, Ashwini K Rao, Serena Ruggieri, Tommaso Schirinzi, Mariano Serrao, Susanna Summa, Michael Strupp, Olivia Surgent, Matthis Synofzik, Shuai Tao, Hiroo Terasi, Diego Torres-Russotto, Brittany Travers, Jaimie A Roper, Mario Mant. Consensus Paper: Ataxic Gait. Cerebellum (London, England). 2022-04-13. PMID:35414041. |
tandem gait is impaired in the early stages of cerebellar disorders and may be particularly useful in the evaluation of pre-ataxic stages of progressive ataxias. |
2022-04-13 |
2023-08-13 |
human |
| Pierre Cabaraux, Sunil K Agrawal, Huaying Cai, Rocco Salvatore Calabro, Casali Carlo, Damm Loic, Doss Sarah, Christophe Habas, Anja K E Horn, Winfried Ilg, Elan D Louis, Hiroshi Mitoma, Vito Monaco, Maria Petracca, Alberto Ranavolo, Ashwini K Rao, Serena Ruggieri, Tommaso Schirinzi, Mariano Serrao, Susanna Summa, Michael Strupp, Olivia Surgent, Matthis Synofzik, Shuai Tao, Hiroo Terasi, Diego Torres-Russotto, Brittany Travers, Jaimie A Roper, Mario Mant. Consensus Paper: Ataxic Gait. Cerebellum (London, England). 2022-04-13. PMID:35414041. |
the panel of experts agree that the understanding of the cerebellar contribution to gait control will lead to a better management of cerebellar ataxias in general and will likely contribute to use gait parameters as robust biomarkers of future clinical trials. |
2022-04-13 |
2023-08-13 |
human |
| Eva M Müller-Oehring, Tilman Schulte, Adolf Pfefferbaum, Edith V Sulliva. Disruption of cerebellar-cortical functional connectivity predicts balance instability in alcohol use disorder. Drug and alcohol dependence. vol 235. 2022-04-08. PMID:35395501. |
whether disruption of neural communication between cerebellar and cortical brain regions exerts an influence on ataxia in alcohol use disorder (aud) was the focus of this study. |
2022-04-08 |
2023-08-13 |
Not clear |
| Marinela Vavla, Filippo Arrigoni, Denis Peruzzo, Domenico Montanaro, Francesca Frijia, Silvia Pizzighello, Alberto De Luca, Emma Della Libera, Federica Tessarotto, Paola Guerra, Ian H Harding, Andrea Martinuzz. Functional MRI Studies in Friedreich's Ataxia: A Systematic Review. Frontiers in neurology. vol 12. 2022-04-01. PMID:35360279. |
friedreich's ataxia (frda) is an inherited neurodegenerative movement disorder with early onset, widespread cerebral and cerebellar pathology, and no cure still available. |
2022-04-01 |
2023-08-13 |
Not clear |
| Masamichi Yamashita, Yusuke Murahata, Inoru Yokoe, Yoshiharu Okamoto, Tomohiro Imagaw. Imaging findings and outcomes after traumatic cerebellar injury: a canine case report. BMC veterinary research. vol 18. issue 1. 2022-04-01. PMID:35361210. |
the cerebellum facilitates movement coordination and provides a sense of equilibrium; damage to this structure can cause a wide variety of symptoms, including ataxia or dystaxia, ocular motor dysfunction, and disequilibrium. |
2022-04-01 |
2023-08-13 |
Not clear |
| Maria S Protasova, Fedor E Gusev, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey N Illarioshkin, Evgeny I Rogae. Novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia. European journal of human genetics : EJHG. 2022-03-30. PMID:35351988. |
novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia. |
2022-03-30 |
2023-08-13 |
human |
| Maria S Protasova, Fedor E Gusev, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey N Illarioshkin, Evgeny I Rogae. Novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia. European journal of human genetics : EJHG. 2022-03-30. PMID:35351988. |
here, we present rare clinical forms of early ataxia with cerebellar hypoplasia. |
2022-03-30 |
2023-08-13 |
human |
| S Catelan, B Santini, F Sala, A Felett. Cerebellar mutism syndrome: the importance of preoperative language assessment. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 2022-03-26. PMID:35338372. |
children undergoing surgical removal of tumors in the posterior cranial fossa can encounter a varied and complex constellation of neurological symptoms, called cerebellar mutism, defined as a disturbance in the planning and programming of motor language with preserved understanding, behavioral disorders such as inattention, visual-spatial disorganization, personality change, as well as ataxia and dysmetria. |
2022-03-26 |
2023-08-13 |
Not clear |