| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Renu Kumari, Deepak Kumar, Samir K Brahmachari, Achal K Srivastava, Mohammed Faruq, Mitali Mukerj. Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias. Journal of genetics. vol 97. issue 3. 2018-10-29. PMID:30027898. |
cerebellar ataxias are a group of rare progressive neurodegenerative disorders with an average prevalence ranges from 4.8 to 13.8 in 100,000 individuals. |
2018-10-29 |
2023-08-13 |
Not clear |
| Renu Kumari, Deepak Kumar, Samir K Brahmachari, Achal K Srivastava, Mohammed Faruq, Mitali Mukerj. Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias. Journal of genetics. vol 97. issue 3. 2018-10-29. PMID:30027898. |
in a unique research collaboration spanning over 20 years, we have been able to develop a paradigm for studying cerebellar ataxias in the indian population which would also be relevant in other rare diseases. |
2018-10-29 |
2023-08-13 |
Not clear |
| Minh-Ha Tran, Haik Mkhikian, Michael Sy, Ingrid Perez-Alvarez, Michael Demetrio. Long-term plasma exchange as maintenance therapy for cerebellar-type Hashimoto's encephalopathy, a case report. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. vol 57. issue 3. 2018-10-25. PMID:29891220. |
a sub-type of he is associated with cerebellar dysfunction and ataxia. |
2018-10-25 |
2023-08-13 |
Not clear |
| Idoia Rouco Axpe, Javier Almeida Velasco, Jose Guillermo Barreiro Garcia, Jose Manuel Urbizu Gallardo, Beatriz Mateos Goñ. Hypomagnesemia: a Treatable Cause of Ataxia with Cerebellar Edema. Cerebellum (London, England). vol 16. issue 5-6. 2018-10-22. PMID:28656525. |
hypomagnesemia: a treatable cause of ataxia with cerebellar edema. |
2018-10-22 |
2023-08-13 |
Not clear |
| Hui Zhou, Shuo Sun, Hui Shi, Kui M. Cavernous Sinus Aneurysm Associated With Cerebellar Hemangioblastoma in an Adult With von Hippel-Lindau Disease. The Journal of craniofacial surgery. vol 29. issue 5. 2018-10-22. PMID:29608473. |
a 60-year-old woman presented with a cerebellar solid tumor manifesting as headache of 4 months, progressive vomiting, and ataxia of half a month. |
2018-10-22 |
2023-08-13 |
Not clear |
| Wu Xing, Xinxin Liao, Tingting Guan, Fangfang Xie, Lu Shen, Weihua Liao, Xiaoyi Wan. [Value of 1H-MRS on SCA3/MJD diagnosis and clinical course]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. vol 42. issue 3. 2018-10-15. PMID:28364102. |
the onset patients with sca3/mjd were evaluated with the international cooperative ataxia rating scale and scale for the assessment and rating of ataxia, the correlation between naa/cr, cho/cr or mi/cr ratio and the clinical score was calculated.
results: the naa/cr in the pons and cerebellar dentate nucleus from the onset patients with sca3/mjd was significantly reduced compared to that in the normal control group. |
2018-10-15 |
2023-08-13 |
human |
| Carlo Wilke, Friedemann Bender, Stefanie N Hayer, Kathrin Brockmann, Ludger Schöls, Jens Kuhle, Matthis Synofzi. Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study. Journal of neurology. vol 265. issue 7. 2018-10-04. PMID:29737427. |
specifically, as a marker of neuronal damage, nfl might (1) help to differentiate multiple system atrophy of cerebellar type (msa-c) from sporadic adult-onset ataxia (saoa), and (2) show increases in repeat-expansion spinocerebellar ataxias (scas) which might be amenable to treatment in the future. |
2018-10-04 |
2023-08-13 |
human |
| Etsuko Shimobayashi, Josef P Kapfhamme. Calcium Signaling, PKC Gamma, IP3R1 and CAR8 Link Spinocerebellar Ataxias and Purkinje Cell Dendritic Development. Current neuropharmacology. vol 16. issue 2. 2018-10-01. PMID:28554312. |
spinocerebellar ataxias (scas) are a group of cerebellar diseases characterized by progressive ataxia and cerebellar atrophy. |
2018-10-01 |
2023-08-13 |
Not clear |
| Grace Yoon, Keith W Caldecot. Nonsyndromic cerebellar ataxias associated with disorders of DNA single-strand break repair. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891053. |
nonsyndromic cerebellar ataxias associated with disorders of dna single-strand break repair. |
2018-10-01 |
2023-08-13 |
Not clear |
| Grace Yoon, Keith W Caldecot. Nonsyndromic cerebellar ataxias associated with disorders of DNA single-strand break repair. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891053. |
hereditary cerebellar ataxias are genetically and clinically heterogeneous, and an important subgroup of these disorders are caused by defects in dna repair. |
2018-10-01 |
2023-08-13 |
Not clear |
| Grace Yoon, Keith W Caldecot. Nonsyndromic cerebellar ataxias associated with disorders of DNA single-strand break repair. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891053. |
these conditions are inherited in an autosomal-recessive fashion, with the main clinical feature being ataxia due to cerebellar degeneration. |
2018-10-01 |
2023-08-13 |
Not clear |
| Hilary J Vernon, Laurence A Bindof. Mitochondrial ataxias. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891055. |
mitochondrial ataxias can be caused by disturbance of the cerebellum and its connections, involvement of proprioception (i.e., sensory ataxia) or a combination of both (spinocerebellar). |
2018-10-01 |
2023-08-13 |
Not clear |
| Ginevra Zanni, Enrico Bertin. X-linked ataxias. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891057. |
x-linked cerebellar ataxias (xlca) are an expanding group of genetically heterogeneous and clinically variable conditions characterized by cerebellar dysgenesis (hypoplasia, atrophy, or dysplasia) caused by gene mutations or genomic imbalances on the x chromosome. |
2018-10-01 |
2023-08-13 |
Not clear |
| b' Olena Bereznyakova, Nicolas Dupr\\xc3\\xa. Spastic ataxias. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891058.' |
certain spastic paraplegias, such as spastic paraplegia 7, may present as an ataxic phenotype and often share common pathophysiologic pathways with cerebellar ataxias. |
2018-10-01 |
2023-08-13 |
Not clear |
| Thomas Klockgethe. Sporadic adult-onset ataxia. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891060. |
sporadic adult-onset ataxia (saoa) is a nongenetic neurodegenerative disorder of the cerebellum of unknown cause which manifests with progressive ataxia. |
2018-10-01 |
2023-08-13 |
Not clear |
| Mario Manto, Christiane S Hamp. Endocrine disorders and the cerebellum: from neurodevelopmental injury to late-onset ataxia. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891071. |
endocrine disorders and the cerebellum: from neurodevelopmental injury to late-onset ataxia. |
2018-10-01 |
2023-08-13 |
Not clear |
| Mario Manto, Christiane S Hamp. Endocrine disorders and the cerebellum: from neurodevelopmental injury to late-onset ataxia. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891071. |
disturbances of thyroid hormone may also impact on cerebellar ataxias of other origin, decompensating or aggravating the pre-existing ataxia manifesting with motor ataxia, oculomotor ataxia, and/or schmahmann syndrome. |
2018-10-01 |
2023-08-13 |
Not clear |
| Susan Perlman, Eugen Boltshause. Drug treatment. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891072. |
there are no approved disease-modifying therapies for any of the inherited cerebellar ataxias. |
2018-10-01 |
2023-08-13 |
Not clear |
| Jan Cendelin, Hiroshi Mitom. Neurotransplantation therapy. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891073. |
neurotransplantation therapy in cerebellar ataxias is still at the stage of experimental studies. |
2018-10-01 |
2023-08-13 |
Not clear |
| Roberta Ferrucci, Alberto Prior. Noninvasive stimulation. Handbook of clinical neurology. vol 155. 2018-10-01. PMID:29891074. |
nibs is a promising approach not only to elucidate the numerous cerebellar functions, but also to improve the management of cerebellar ataxias in children and in adults. |
2018-10-01 |
2023-08-13 |
human |