| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Takahiro Seki, Naoko Adachi, Nana Abe-Seki, Takayuki Shimahara, Hideyuki Takahashi, Kazuhiro Yamamoto, Naoaki Saito, Norio Saka. Elucidation of the molecular mechanism and exploration of novel therapeutics for spinocerebellar ataxia caused by mutant protein kinase Cγ. Journal of pharmacological sciences. vol 116. issue 3. 2011-12-06. PMID:21666345. |
spinocerebellar ataxia (sca) is an inherited neurodegenerative disorder that is characterized by cerebellar atrophy and progressive ataxia and is classified into 31 types by the genetic locus. |
2011-12-06 |
2023-08-12 |
Not clear |
| J Larry Parker, Maria Santiag. Oculomotor aspects of the hereditary cerebellar ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827881. |
oculomotor aspects of the hereditary cerebellar ataxias. |
2011-12-06 |
2023-08-12 |
Not clear |
| Mario Mascalchi, Alessandra Vell. Magnetic resonance and nuclear medicine imaging in ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827882. |
fundamentally, ct has a role in the emergency evaluation of the patient with acute ataxia to ascertain brainstem or cerebellar hemorrhage and to exclude a mass lesion in the posterior cranial fossa. |
2011-12-06 |
2023-08-12 |
Not clear |
| Mario Mascalchi, Alessandra Vell. Magnetic resonance and nuclear medicine imaging in ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827882. |
in patients with inherited or sporadic chronic ataxia it reveals three fundamental patterns of atrophy of the brainstem, cerebellum, and spinal cord which match the gross neuropathological descriptions. |
2011-12-06 |
2023-08-12 |
Not clear |
| Louis R Capla. Ataxia in patients with brain infarcts and hemorrhages. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827886. |
gait and limb incoordination and ataxia are most often found in patients with brainstem and cerebellar infarcts and hemorrhages. |
2011-12-06 |
2023-08-12 |
Not clear |
| Marios Hadjivassilio. Immune-mediated acquired ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827889. |
immune-mediated ataxias include paraneoplastic cerebellar degeneration and post-infective cerebellitis, but these will be discussed elsewhere. |
2011-12-06 |
2023-08-12 |
Not clear |
| Marios Hadjivassilio. Immune-mediated acquired ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827889. |
there is particular emphasis on gluten ataxia as this is one of the commonest immune-mediated cerebellar ataxias and one of the few ataxias that are potentially treatable. |
2011-12-06 |
2023-08-12 |
Not clear |
| Marios Hadjivassilio. Immune-mediated acquired ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827889. |
the pathophysiology leading to cerebellar damage, loss of purkinje cells, and the development of ataxia remains speculative, but existing clues are discussed in detail. |
2011-12-06 |
2023-08-12 |
Not clear |
| Mario Mant. Toxic agents causing cerebellar ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827890. |
toxic agents causing cerebellar ataxias. |
2011-12-06 |
2023-08-12 |
Not clear |
| Mario Mant. Toxic agents causing cerebellar ataxias. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827890. |
although data for the prevalence and incidence of cerebellar lesions related to intoxication and poisoning are still unknown in many cases, clinicians should keep in mind the list of agents that may cause cerebellar deficits, since toxin-induced cerebellar ataxias are not rare in daily practice. |
2011-12-06 |
2023-08-12 |
Not clear |
| Isabelle Le Ber, Alexandra Dürr, Alexis Bric. Autosomal recessive cerebellar ataxias with oculomotor apraxia. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827898. |
autosomal recessive cerebellar ataxias with oculomotor apraxia. |
2011-12-06 |
2023-08-12 |
Not clear |
| Stefano Di Donato, Caterina Mariotti, Franco Taron. Spinocerebellar ataxia type 1. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827903. |
the most common presentation of sca1 is dominant ataxia 'plus', characterized by cerebellar dysfunctions variably associated with slow saccades, ophthalmoplegia, pyramidal and extrapyramidal features, mild to moderate dementia, amyotrophy, and peripheral neuropathy. |
2011-12-06 |
2023-08-12 |
Not clear |
| Ana Solodkin, Christopher M Gome. Spinocerebellar ataxia type 6. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827907. |
spinocerebellar ataxia type 6 (sca6) is the prototype of a pure cerebellar ataxia, associated with a severe form of progressive ataxia and cerebellar dysfunction. |
2011-12-06 |
2023-08-12 |
Not clear |
| Alessandra Rufa, Pamela Federigh. Fast versus slow: different saccadic behavior in cerebellar ataxias. Annals of the New York Academy of Sciences. vol 1233. 2011-11-30. PMID:21950987. |
fast versus slow: different saccadic behavior in cerebellar ataxias. |
2011-11-30 |
2023-08-12 |
Not clear |
| Gülin Oz, Isabelle Iltis, Diane Hutter, William Thomas, Khalaf O Bushara, Christopher M Gome. Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:20838948. |
hereditary and sporadic neurodegenerative ataxias are movement disorders that affect the cerebellum. |
2011-11-10 |
2023-08-12 |
human |
| Esther B E Becker, Brent L Fogel, Sanjeev Rajakulendran, Anna Dulneva, Michael G Hanna, Susan L Perlman, Daniel H Geschwind, Kay E Davie. Candidate screening of the TRPC3 gene in cerebellar ataxia. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:21321808. |
the hereditary cerebellar ataxias are a diverse group of neurodegenerative disorders primarily characterised by loss of balance and coordination due to dysfunction of the cerebellum and its associated pathways. |
2011-11-10 |
2023-08-12 |
mouse |
| Esther B E Becker, Brent L Fogel, Sanjeev Rajakulendran, Anna Dulneva, Michael G Hanna, Susan L Perlman, Daniel H Geschwind, Kay E Davie. Candidate screening of the TRPC3 gene in cerebellar ataxia. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:21321808. |
our findings suggest that mutations in trpc3 do not significantly contribute to the cause of late-onset and episodic human cerebellar ataxias. |
2011-11-10 |
2023-08-12 |
mouse |
| K Sridhar, R Sridhar, G Venkatprasann. Management of posterior fossa gliomas in children. Journal of pediatric neurosciences. vol 6. issue Suppl 1. 2011-11-10. PMID:22069433. |
cranial nerve signs, ataxia and cerebellar signs with or without symptoms and signs of raised intracranial pressure are classically described symptoms and signs. |
2011-11-10 |
2023-08-12 |
Not clear |
| Rohan Ramakrishna, Jeffrey C Mai, Tanya Filardi, Samuel R Browd, Richard G Ellenboge. Brainstem hypertrophy, acquired Chiari malformation, syringomyelia, and hydrocephalus: diagnostic dilemma. Journal of neurosurgery. Pediatrics. vol 8. issue 2. 2011-11-09. PMID:21806361. |
this 18-year-old woman presented with symptoms of right upper-extremity ataxia and imaging evidence of syringomyelia and an acquired chiari malformation after a previous suboccipital decompression for cerebellar hemorrhage. |
2011-11-09 |
2023-08-12 |
Not clear |
| Sarah Teixeira Camargos, Wilson Marques, Antonio Carlos dos Santo. Brain stem and cerebellum volumetric analysis of Machado Joseph disease patients. Arquivos de neuro-psiquiatria. vol 69. issue 2B. 2011-11-08. PMID:21625753. |
in this study we test the hypothesis that atrophy of cerebellum and brainstem in mjd/sca3 is related to clinical severity, disease duration and cag repeat length as well as to other variables such as age and icars (international cooperative ataxia rating scale). |
2011-11-08 |
2023-08-12 |
Not clear |