| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Abbas Aliaghaei, Mahdi Eskandarian Boroujeni, Houssein Ahmadi, Amir-Hossein Bayat, Mostafa Rezaei Tavirani, Mohammad Amin Abdollahifar, Mohammad H Pooyafar, Vahid Mansour. Dental pulp stem cell transplantation ameliorates motor function and prevents cerebellar atrophy in rat model of cerebellar ataxia. Cell and tissue research. vol 376. issue 2. 2019-08-30. PMID:30635776. |
cerebellar ataxias (ca) include a range of neurodegenerative disorders hallmarked by deterioration of the cerebellum. |
2019-08-30 |
2023-08-13 |
human |
| Abbas Aliaghaei, Mahdi Eskandarian Boroujeni, Houssein Ahmadi, Amir-Hossein Bayat, Mostafa Rezaei Tavirani, Mohammad Amin Abdollahifar, Mohammad H Pooyafar, Vahid Mansour. Dental pulp stem cell transplantation ameliorates motor function and prevents cerebellar atrophy in rat model of cerebellar ataxia. Cell and tissue research. vol 376. issue 2. 2019-08-30. PMID:30635776. |
then, experimental ataxia was induced in 20 male adult rats by a single injection of 3-ap and bilateral dpsc transplantation was performed 3 days after 3-ap administration, followed by stereological analysis of cerebellar layers along with assessment of motor skills and inflammatory response. |
2019-08-30 |
2023-08-13 |
human |
| Abbas Aliaghaei, Mahdi Eskandarian Boroujeni, Houssein Ahmadi, Amir-Hossein Bayat, Mostafa Rezaei Tavirani, Mohammad Amin Abdollahifar, Mohammad H Pooyafar, Vahid Mansour. Dental pulp stem cell transplantation ameliorates motor function and prevents cerebellar atrophy in rat model of cerebellar ataxia. Cell and tissue research. vol 376. issue 2. 2019-08-30. PMID:30635776. |
the findings showed that transplantation of dpscs in a 3-ap model of ataxia ameliorated motor coordination and muscle activity, increased cerebellar volumes of molecular and granular layers plus white matter, reduced the levels of inflammatory cytokines and thwarted the degeneration of purkinje cells against 3-ap toxicity. |
2019-08-30 |
2023-08-13 |
human |
| Jessica M Bake. Gait Disorders. The American journal of medicine. vol 131. issue 6. 2019-08-29. PMID:29288631. |
we review gaits due to lesions of motor systems (spasticity and neuromuscular weakness), the cerebellum and sensory systems (ataxia), parkinsonism, and frontal lobes and discuss the remarkably diverse phenomenology of functional (psychogenic) gait disorders. |
2019-08-29 |
2023-08-13 |
Not clear |
| K Feil, N Böttcher, O Kremmyda, C Muth, J Teufel, A Zwergal, T Brandt, M Strup. [Pharmacotherapy of Vestibular Disorders, Nystagmus and Cerebellar Disorders]. Laryngo- rhino- otologie. vol 97. issue 1. 2019-08-28. PMID:29301160. |
there are ongoing rcts on treatment of vestibular paroxysmia with carbamazepine (vespa), acute unilateral vestibulopathy with betahistine (betavest), vestibular migraine with metoprolol (provemig), benign paroxysmal positional vertigo with vitamin d (vitd@bppv), ea2 with 4-aminopyridine versus acetazolamide (eat-2-treat), and cerebellar ataxias with acetyl-dl-leucine (alcat). |
2019-08-28 |
2023-08-13 |
Not clear |
| Igor de Assis Franco, Marcelo de Melo Aragão, Pedro Braga-Neto, Marcela Amaral Avelino, José Luiz Pedroso, Victor Hugo Rocha Marussi, Leonardo Furtado Freitas, Marcelo Rodrigues Masruha, Orlando G P Barsottin. The cerebellar histiocytosis: Progressive ataxia is not always a genetic disease. Neurology. vol 91. issue 8. 2019-08-27. PMID:30021921. |
the cerebellar histiocytosis: progressive ataxia is not always a genetic disease. |
2019-08-27 |
2023-08-13 |
Not clear |
| Malco Rossi, Mathieu Anheim, Alexandra Durr, Christine Klein, Michel Koenig, Matthis Synofzik, Connie Marras, Bart P van de Warrenbur. The genetic nomenclature of recessive cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 33. issue 7. 2019-08-26. PMID:29756227. |
the genetic nomenclature of recessive cerebellar ataxias. |
2019-08-26 |
2023-08-13 |
Not clear |
| Malco Rossi, Mathieu Anheim, Alexandra Durr, Christine Klein, Michel Koenig, Matthis Synofzik, Connie Marras, Bart P van de Warrenbur. The genetic nomenclature of recessive cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 33. issue 7. 2019-08-26. PMID:29756227. |
the recessive cerebellar ataxias are a large group of degenerative and metabolic disorders, the diagnostic management of which is difficult because of the enormous clinical and genetic heterogeneity. |
2019-08-26 |
2023-08-13 |
Not clear |
| Malco Rossi, Mathieu Anheim, Alexandra Durr, Christine Klein, Michel Koenig, Matthis Synofzik, Connie Marras, Bart P van de Warrenbur. The genetic nomenclature of recessive cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 33. issue 7. 2019-08-26. PMID:29756227. |
here, we propose a new nomenclature for the genetically confirmed recessive cerebellar ataxias according to the principles and criteria laid down by the international parkinson and movement disorder society task force on classification and nomenclature of genetic movement disorders. |
2019-08-26 |
2023-08-13 |
Not clear |
| Malco Rossi, Mathieu Anheim, Alexandra Durr, Christine Klein, Michel Koenig, Matthis Synofzik, Connie Marras, Bart P van de Warrenbur. The genetic nomenclature of recessive cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 33. issue 7. 2019-08-26. PMID:29756227. |
the newly proposed list of recessively inherited cerebellar ataxias includes 62 disorders that were assigned an atx prefix, followed by the gene name, because these typically present with ataxia as a predominant and/or consistent feature. |
2019-08-26 |
2023-08-13 |
Not clear |
| Malco Rossi, Mathieu Anheim, Alexandra Durr, Christine Klein, Michel Koenig, Matthis Synofzik, Connie Marras, Bart P van de Warrenbur. The genetic nomenclature of recessive cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 33. issue 7. 2019-08-26. PMID:29756227. |
this new, transparent and adaptable nomenclature of the recessive cerebellar ataxias will facilitate the clinical recognition of recessive ataxias, guide diagnostic testing in ataxia patients, and help in interpreting genetic findings. |
2019-08-26 |
2023-08-13 |
Not clear |
| Matthis Synofzik, Hélène Puccio, Fanny Mochel, Ludger Schöl. Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies. Neuron. vol 101. issue 4. 2019-08-26. PMID:30790538. |
autosomal recessive cerebellar ataxias: paving the way toward targeted molecular therapies. |
2019-08-26 |
2023-08-13 |
Not clear |
| Matthis Synofzik, Hélène Puccio, Fanny Mochel, Ludger Schöl. Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies. Neuron. vol 101. issue 4. 2019-08-26. PMID:30790538. |
autosomal-recessive cerebellar ataxias (arcas) comprise a heterogeneous group of rare degenerative and metabolic genetic diseases that share the hallmark of progressive damage of the cerebellum and its associated tracts. |
2019-08-26 |
2023-08-13 |
Not clear |
| R Mohammadi, M H Heidari, Y Sadeghi, M A Abdollahifar, A Aghae. Evaluation of the spatial arrangement of Purkinje cells in ataxic rat's cerebellum after Sertoli cells transplantation. Folia morphologica. vol 77. issue 2. 2019-08-13. PMID:29064552. |
purkinje cells (pcs) pathology is important in cerebellar disorders like ataxia. |
2019-08-13 |
2023-08-13 |
rat |
| R Mohammadi, M H Heidari, Y Sadeghi, M A Abdollahifar, A Aghae. Evaluation of the spatial arrangement of Purkinje cells in ataxic rat's cerebellum after Sertoli cells transplantation. Folia morphologica. vol 77. issue 2. 2019-08-13. PMID:29064552. |
immunohistochemistry (ihc) analysis of cerebellum can give a proper tool for explaining the pathophysiology of pcs in ataxia. |
2019-08-13 |
2023-08-13 |
rat |
| R Mohammadi, M H Heidari, Y Sadeghi, M A Abdollahifar, A Aghae. Evaluation of the spatial arrangement of Purkinje cells in ataxic rat's cerebellum after Sertoli cells transplantation. Folia morphologica. vol 77. issue 2. 2019-08-13. PMID:29064552. |
here we stereologically analysed the 3-dimensional spatial arrangement of pcs in the cerebellum of rats after ataxia induction with 3-acetylpyridine (3-ap). |
2019-08-13 |
2023-08-13 |
rat |
| Theresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, Susan Perlman, Patricia E Greenstein, Sarah H Ying, Tetsuo Ashizawa, S H Subramony, Jeremy D Schmahmann, K P Figueroa, Hidehiro Mizusawa, Ludger Schöls, Jessica D Shaw, Richard M Dubinsky, Melissa J Armstrong, Gary S Gronseth, Kelly L Sulliva. Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology. Neurology. vol 90. issue 10. 2019-08-08. PMID:29440566. |
comprehensive systematic review summary: treatment of cerebellar motor dysfunction and ataxia: report of the guideline development, dissemination, and implementation subcommittee of the american academy of neurology. |
2019-08-08 |
2023-08-13 |
Not clear |
| Chih-Chun Lin, Shi-Rui Gan, Deepak Gupta, Armin Alaedini, Peter H Green, Sheng-Han Ku. Hispanic Spinocerebellar Ataxia Type 35 (SCA35) with a Novel Frameshift Mutation. Cerebellum (London, England). vol 18. issue 2. 2019-07-30. PMID:30229425. |
an immune-mediated ataxia previously found to be associated with autoantibody reactivity to tg6 may share a similar pathomechanism to sca35, suggesting a converging role for tg6 in cerebellar function. |
2019-07-30 |
2023-08-13 |
Not clear |
| Ilse Eidhof, Bart P van de Warrenburg, Annette Schenc. SnapShot: Biology of Genetic Ataxias. Cell. vol 175. issue 3. 2019-07-29. PMID:30340048. |
genetic ataxias are a clinically important group of disabling, mostly neurodegenerative, diseases of the cerebellum. |
2019-07-29 |
2023-08-13 |
Not clear |
| Ilse Eidhof, Bart P van de Warrenburg, Annette Schenc. SnapShot: Biology of Genetic Ataxias. Cell. vol 175. issue 3. 2019-07-29. PMID:30340048. |
this snapshot shows that the vast majority of established monogenic causes of dominant and recessive ataxias can be captured by a limited number of affected cellular components and biological processes in the cerebellum. |
2019-07-29 |
2023-08-13 |
Not clear |