| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Massimo Pandolfo, Mario Mant. Cerebellar and afferent ataxias. Continuum (Minneapolis, Minn.). vol 19. issue 5 Movement Disorders. 2014-05-15. PMID:24092292. |
ataxia is the predominant manifestation of many acquired and inherited neurologic disorders affecting the cerebellum, its connections, and the afferent proprioceptive pathways. |
2014-05-15 |
2023-08-12 |
Not clear |
| Massimo Pandolfo, Mario Mant. Cerebellar and afferent ataxias. Continuum (Minneapolis, Minn.). vol 19. issue 5 Movement Disorders. 2014-05-15. PMID:24092292. |
this article reviews the phenomenology and etiologies of cerebellar and afferent ataxias and provides indications for a rational approach to diagnosis and management. |
2014-05-15 |
2023-08-12 |
Not clear |
| Yasushi Iwasaki, Keiko Mori, Masumi Ito, Shinsui Tatsumi, Maya Mimuro, Mari Yoshid. An autopsied case of progressive supranuclear palsy presenting with cerebellar ataxia and severe cerebellar involvement. Neuropathology : official journal of the Japanese Society of Neuropathology. vol 33. issue 5. 2014-05-12. PMID:23320789. |
he was initially diagnosed as having olivopontocerebellar atrophy because dysarthria and ataxia gradually developed, and head ct scan showed apparent atrophy of the cerebellum and brainstem and dilatation of the fourth ventricle. |
2014-05-12 |
2023-08-12 |
Not clear |
| Michael Strupp, Olympia Kremmyda, Thomas Brand. Pharmacotherapy of vestibular disorders and nystagmus. Seminars in neurology. vol 33. issue 3. 2014-05-02. PMID:24057832. |
the use of aminopyridines is a well-established therapeutic principle in the treatment of downbeat and upbeat nystagmus as well as episodic ataxia type 2 and cerebellar gait disorders. |
2014-05-02 |
2023-08-12 |
Not clear |
| Osamu Onoder. [What is ataxia? - Towards developing a new scale for ataxia]. Rinsho shinkeigaku = Clinical neurology. vol 52. issue 11. 2014-04-21. PMID:23196493. |
in this symposium, we will learn the recent advance of physiological role of cerebellum and imagine a new continuous scale for evaluation for ataxias. |
2014-04-21 |
2023-08-12 |
human |
| Makoto Yoned. [Ataxic form of Hashimoto's encephalopathy]. Rinsho shinkeigaku = Clinical neurology. vol 52. issue 11. 2014-04-21. PMID:23196621. |
when a pure cerebellar ataxic patient who presents with truncal ataxia without nystagmus and cerebellar atrophy on brain mri, he should be considered as a differential diagnosis and anti-nae abs should be examined for the screening of this disease. |
2014-04-21 |
2023-08-12 |
Not clear |
| Iselin Marie Wedding, Jeanette Koht, Espen Dietrichs, Nils Inge Landrø, Chantal M E Tallakse. Cognition is only minimally impaired in Spinocerebellar ataxia type 14 (SCA14): a neuropsychological study of ten Norwegian subjects compared to intrafamilial controls and population norm. BMC neurology. vol 13. 2014-04-04. PMID:24289098. |
spinocerebellar ataxia type 14 (sca14) is an autosomal dominant hereditary ataxia characterized by a relatively pure cerebellar phenotype. |
2014-04-04 |
2023-08-12 |
human |
| Rong-Ni Chang, Guang-Zhi Yuan, Jian-Qiang Tan, Qing-Niao Lai, Jun Ma, Yi-Jin Yang, Wei Shu, Wei Hou, Zhi-Gang Yua. [Analysis of SCA3/MJD3 gene mutation and genetic polymorphism in a guangxi family with spinocerebellar ataxia 3]. Yi chuan = Hereditas. vol 35. issue 11. 2014-04-01. PMID:24579313. |
autosomal dominant cerebellar ataxias (adcas) comprise a group of genetically heterogeneous neurodegenerative disorders among which spinocerebellar ataxia type 3 (sca3) represents the most common form of scas worldwide. |
2014-04-01 |
2023-08-12 |
Not clear |
| Sara Winchester, Piyush K Singh, Mohamad A Mikat. Ataxia. Handbook of clinical neurology. vol 112. 2014-03-27. PMID:23622331. |
the differential of acute and recurring ataxia covered in this chapter includes intoxication (e.g., antiepileptics, lead, alcohol), postinfectious cerebellitis, hemorrhage, ischemic stroke, tumor (posterior fossa or cerebellum), brainstem encephalitis, occult neuroblastoma, miller fisher syndrome, conversion reaction, multiple sclerosis, epileptic pseudoataxia, vasculitis (e.g., kawasaki), metabolic etiologies (e.g., maple syrup urine disease, pyruvate dehydrogenase deficiency, ornithine transcarbamylase deficiency, biotinidase deficiency, hartnup disease, and argininosuccinic aciduria), migraine, migraine equivalents (benign paroxysmal positional vertigo), autosomal dominant episodic ataxias (with seven types currently identified), and hypothyroidism. |
2014-03-27 |
2023-08-12 |
Not clear |
| Nicole I Wolf, Michel Koeni. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration. Handbook of clinical neurology. vol 113. 2014-03-27. PMID:23622410. |
progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration. |
2014-03-27 |
2023-08-12 |
Not clear |
| Suman Jayadev, Thomas D Bir. Hereditary ataxias: overview. Genetics in medicine : official journal of the American College of Medical Genetics. vol 15. issue 9. 2014-03-10. PMID:23538602. |
the hereditary ataxias are a highly heterogeneous group of disorders phenotypically characterized by gait ataxia, incoordination of eye movements, speech, and hand movements, and usually associated with atrophy of the cerebellum. |
2014-03-10 |
2023-08-12 |
Not clear |
| Kotaro Kawanishi, Mitsuya Morita, Keiichi Nakahara, Syuichi Tetsuka, Tom Kouki, Kaoru Tominaga, Hitoshi Endo, Takashi Yashiro, Keiko Tanaka, Imaharu Nakan. [Paraneoplastic cerebellar degeneration with bladder cancer confirmed the existence of an anti-neural antibody: a case report]. Brain and nerve = Shinkei kenkyu no shinpo. vol 65. issue 11. 2014-03-06. PMID:24200618. |
three months later, he developed subacute progressive cerebellar limb ataxia and truncal oscillation. |
2014-03-06 |
2023-08-12 |
mouse |
| Clévio Nóbrega, Isabel Nascimento-Ferreira, Isabel Onofre, David Albuquerque, Mariana Conceição, Nicole Déglon, Luís Pereira de Almeid. Overexpression of mutant ataxin-3 in mouse cerebellum induces ataxia and cerebellar neuropathology. Cerebellum (London, England). vol 12. issue 4. 2014-03-03. PMID:23242710. |
overexpression of mutant ataxin-3 in mouse cerebellum induces ataxia and cerebellar neuropathology. |
2014-03-03 |
2023-08-12 |
mouse |
| Fiore Manganelli, Raffaele Dubbioso, Chiara Pisciotta, Antonella Antenora, Maria Nolano, Giuseppe De Michele, Alessandro Filla, Alfredo Berardelli, Lucio Santor. Somatosensory temporal discrimination threshold is increased in patients with cerebellar atrophy. Cerebellum (London, England). vol 12. issue 4. 2014-03-03. PMID:23288507. |
the degree of cerebellar dysfunction was measured by the international cooperative ataxia rating scale. |
2014-03-03 |
2023-08-12 |
Not clear |
| Arnulf H Koeppen, R Liane Ramirez, Sarah T Bjork, Peter Bauer, Paul J Feuste. The reciprocal cerebellar circuitry in human hereditary ataxia. Cerebellum (London, England). vol 12. issue 4. 2014-03-03. PMID:23389921. |
the reciprocal cerebellar circuitry in human hereditary ataxia. |
2014-03-03 |
2023-08-12 |
human |
| Muriel Panouillères, Solène Frismand, Olivier Sillan, Christian Urquizar, Alain Vighetto, Denis Pélisson, Caroline Tiliket. Saccades and eye-head coordination in ataxia with oculomotor apraxia type 2. Cerebellum (London, England). vol 12. issue 4. 2014-03-03. PMID:23475383. |
ataxia with oculomotor apraxia type 2 (aoa2) is one of the most frequent autosomal recessive cerebellar ataxias. |
2014-03-03 |
2023-08-12 |
human |
| Xiaowei Wang, Benjamin J Whalley, Gary J Stephen. The du(2J) mouse model of ataxia and absence epilepsy has deficient cannabinoid CB₁ receptor-mediated signalling. The Journal of physiology. vol 591. issue 16. 2014-03-03. PMID:23732642. |
cerebellar ataxias are a group of progressive, debilitating diseases often associated with abnormal purkinje cell (pc) firing and/or degeneration. |
2014-03-03 |
2023-08-12 |
mouse |
| Hiroshi Doi, Chihiro Ohba, Yoshinori Tsurusaki, Satoko Miyatake, Noriko Miyake, Hirotomo Saitsu, Yuko Kawamoto, Tamaki Yoshida, Shigeru Koyano, Yume Suzuki, Yoshiyuki Kuroiwa, Fumiaki Tanaka, Naomichi Matsumot. Identification of a novel homozygous SPG7 mutation in a Japanese patient with spastic ataxia: making an efficient diagnosis using exome sequencing for autosomal recessive cerebellar ataxia and spastic paraplegia. Internal medicine (Tokyo, Japan). vol 52. issue 14. 2014-03-03. PMID:23857099. |
autosomal recessive cerebellar ataxias and autosomal recessive hereditary spastic paraplegias are clinically and genetically heterogeneous disorders with diverse neurological and non-neurological features. |
2014-03-03 |
2023-08-12 |
Not clear |
| Fatih Bayrakli, Mehmet Canpolat, Huseyin Per, Hakan Gumus, Sefer Kumandas, Ugur Kartal, Hatice Balaba. A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23. Case reports in neurology. vol 6. issue 1. 2014-02-27. PMID:24575028. |
the molecular pathogenesis of the autosomal recessive cerebellar ataxias has a wide range of mechanisms. |
2014-02-27 |
2023-08-12 |
Not clear |
| Anne Noreau, Cynthia V Bourassa, Anna Szuto, Annie Levert, Sylvia Dobrzeniecka, Julie Gauthier, Sylvie Forlani, Alexandra Durr, Mathieu Anheim, Giovanni Stevanin, Alexis Brice, Jean-Pierre Bouchard, Patrick A Dion, Nicolas Dupré, Guy A Roulea. SYNE1 mutations in autosomal recessive cerebellar ataxia. JAMA neurology. vol 70. issue 10. 2014-02-14. PMID:23959263. |
autosomal recessive cerebellar ataxia type i, also known as recessive ataxia of beauce, is a slowly progressive ataxia that leads to moderate disability with gait ataxia, dysarthria, dysmetria, mild oculomotor abnormalities, and diffuse cerebellar atrophy on brain imaging. |
2014-02-14 |
2023-08-12 |
Not clear |