| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| H Sasaki, I Yabe, K Tashir. The hereditary spinocerebellar ataxias in Japan. Cytogenetic and genome research. vol 100. issue 1-4. 2004-01-30. PMID:14526181. |
from this cluster, pure cerebellar ataxias linked with the sca4, sca14, and sca16 locus have been isolated. |
2004-01-30 |
2023-08-12 |
Not clear |
| Yousef Tizabi, Mashael Al-Namaeh, Kebreten F Manaye, Robert E Taylo. Protective effects of nicotine on ethanol-induced toxicity in cultured cerebellar granule cells. Neurotoxicity research. vol 5. issue 5. 2004-01-28. PMID:14715450. |
the cerebellum is believed to play an important role in ethanol-induced ataxia. |
2004-01-28 |
2023-08-12 |
rat |
| S H Subramony, Kelly Schott, Robert S Raike, Joel Callahan, Leigh R Langford, Peka S Christova, John H Anderson, Christopher M Gome. Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits. Annals of neurology. vol 54. issue 6. 2004-01-14. PMID:14681882. |
novel cacna1a mutation causes febrile episodic ataxia with interictal cerebellar deficits. |
2004-01-14 |
2023-08-12 |
human |
| A Chakravarty, S C Mukherje. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations. Neurology India. vol 51. issue 2. 2004-01-07. PMID:14571010. |
primary degenerative cerebellar ataxias in ethnic bengalees in west bengal: some observations. |
2004-01-07 |
2023-08-12 |
human |
| A Chakravarty, S C Mukherje. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations. Neurology India. vol 51. issue 2. 2004-01-07. PMID:14571010. |
seventy cases of primary degenerative cerebellar ataxias in ethnic bengalees from southern west bengal, india, were studied by the authors. |
2004-01-07 |
2023-08-12 |
human |
| Kiyoko Sugita, Sadao Suga, Yoko Tanak. A juvenile case of cerebellar arteriovenous malformation (AVM) with gradual onset of headache and ataxia. The Bulletin of Tokyo Dental College. vol 44. issue 1. 2003-12-19. PMID:12772582. |
a juvenile case of cerebellar arteriovenous malformation (avm) with gradual onset of headache and ataxia. |
2003-12-19 |
2023-08-12 |
Not clear |
| Kiyoko Sugita, Sadao Suga, Yoko Tanak. A juvenile case of cerebellar arteriovenous malformation (AVM) with gradual onset of headache and ataxia. The Bulletin of Tokyo Dental College. vol 44. issue 1. 2003-12-19. PMID:12772582. |
this case suggests that cerebellar hemorrhage caused by avm should be considered as a possible diagnosis when mild symptoms of headache and ataxia proceed gradually. |
2003-12-19 |
2023-08-12 |
Not clear |
| Julien Falk, Carine Bonnon, Jean-Antoine Girault, Catherine Faivre-Sarrail. F3/contactin, a neuronal cell adhesion molecule implicated in axogenesis and myelination. Biology of the cell. vol 94. issue 6. 2003-12-18. PMID:12500940. |
the f3/contactin deficient mice display a severe ataxia correlated with defects in axonal and dendritic projections in the cerebellum. |
2003-12-18 |
2023-08-12 |
mouse |
| Kh T Abdulkerimo. [Clinical manifestations of cerebellar ataxias]. Vestnik otorinolaringologii. issue 2. 2003-12-16. PMID:12958853. |
[clinical manifestations of cerebellar ataxias]. |
2003-12-16 |
2023-08-12 |
Not clear |
| Isabelle Le Ber, Maria-Ceù Moreira, Sophie Rivaud-Péchoux, Céline Chamayou, François Ochsner, Thierry Kuntzer, Marc Tardieu, Gérard Saïd, Marie-Odile Habert, Geneviève Demarquay, Christian Tannier, Jean-Marie Beis, Alexis Brice, Michel Koenig, Alexandra Dür. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies. Brain : a journal of neurology. vol 126. issue Pt 12. 2003-12-12. PMID:14506070. |
the presence of chorea, sensorimotor neuropathy, oculomotor anomalies, biological abnormalities, cerebellar atrophy on mri and absence of the babinski sign can help to distinguish aoa1 from friedreich's ataxia on a clinical basis. |
2003-12-12 |
2023-08-12 |
Not clear |
| José Gazulla, José Errea, Isabel Benavente, Carlos Tordesilla. Improvement of ataxia in cortical cerebellar atrophy with the drug gabapentin. Clinical neuropharmacology. vol 26. issue 5. 2003-12-12. PMID:14520159. |
improvement of ataxia in cortical cerebellar atrophy with the drug gabapentin. |
2003-12-12 |
2023-08-12 |
Not clear |
| C Monaca-Charley, T Stojkovic, A Duhamel, J De Seze, D Ferriby, P Vermersc. Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosis. Journal of neurology. vol 250. issue 10. 2003-12-12. PMID:14586600. |
previous studies found that a levorotatory form of 5-hydroxytryptophan, a 5-ht precursor, and ondansetron, a 5-ht(3) receptor antagonist, decreased cerebellar symptoms in friedreich's ataxia and ms. we studied the effect of another 5-ht(3) receptor antagonist, dolasetron mesilate, on cerebellar syndrome in ms patients.thirty-four ms patients were included in a placebo-controlled double-blind crossover study. |
2003-12-12 |
2023-08-12 |
Not clear |
| C Monaca-Charley, T Stojkovic, A Duhamel, J De Seze, D Ferriby, P Vermersc. Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosis. Journal of neurology. vol 250. issue 10. 2003-12-12. PMID:14586600. |
a quantitative evaluation of cerebellar syndrome using the nine-hole peg test and an ataxia score comprising static and kinetic parameters were performed before and after each treatment. |
2003-12-12 |
2023-08-12 |
Not clear |
| V Soussan, B Husson, M Tardie. [Description and prognostic value of cerebellar MRI lesions in children with severe acute ataxia]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. vol 10. issue 7. 2003-11-04. PMID:12907067. |
[description and prognostic value of cerebellar mri lesions in children with severe acute ataxia]. |
2003-11-04 |
2023-08-12 |
Not clear |
| V Soussan, B Husson, M Tardie. [Description and prognostic value of cerebellar MRI lesions in children with severe acute ataxia]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. vol 10. issue 7. 2003-11-04. PMID:12907067. |
the aim of this work was to evaluate nmr cerebellar abnormalities in children with severe acute ataxia. |
2003-11-04 |
2023-08-12 |
Not clear |
| T Connelly, J M Farmer, D R Lynch, R L Dot. Olfactory dysfunction in degenerative ataxias. Journal of neurology, neurosurgery, and psychiatry. vol 74. issue 10. 2003-11-04. PMID:14570842. |
in this study, we administered the university of pennsylvania smell identification test (upsit), a standardised test of olfactory function, to patients with ataxias primarily due to cerebellar pathology (spinocerebellar ataxias and related disorders) and to patients with friedreich ataxia, an ataxia associated mainly with loss of afferent cerebellar pathways. |
2003-11-04 |
2023-08-12 |
human |
| Arndt Rolfs, Arnulf H Koeppen, Ingrid Bauer, Peter Bauer, Sven Buhlmann, Helge Topka, Ludger Schöls, Olaf Ries. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). Annals of neurology. vol 54. issue 3. 2003-10-23. PMID:12953269. |
the neuropathology of sca17 can be classified as a "pure cerebellar" or "cerebello-olivary" form of ataxia. |
2003-10-23 |
2023-08-12 |
Not clear |
| Evangeline Wassmer, Paul Davies, William P Whitehouse, Stuart H Gree. Clinical spectrum associated with cerebellar hypoplasia. Pediatric neurology. vol 28. issue 5. 2003-09-17. PMID:12878295. |
of the 45 children with cerebellar hypoplasia, 39 exhibited developmental delay; 24, speech delay; 25, seizures; nine, microcephaly; 22, hypotonia; 22, ataxia and impaired coordination; four, abnormal movements (tremor or titubation); 13, hypertonia; eight, autistic features; and 18, ocular signs (nystagmus, strabismus, and abnormal ocular movements). |
2003-09-17 |
2023-08-12 |
Not clear |
| Evangeline Wassmer, Paul Davies, William P Whitehouse, Stuart H Gree. Clinical spectrum associated with cerebellar hypoplasia. Pediatric neurology. vol 28. issue 5. 2003-09-17. PMID:12878295. |
statistically significant clinical features of children with cerebellar hypoplasia compared with those without were development and speech delay, microcephaly, abnormal movements, ataxia and impaired coordination, autistic features, hypotonia, and ocular signs. |
2003-09-17 |
2023-08-12 |
Not clear |
| Umberto Pea, Francesco de Luca, Massimiliano Nicola, Luigi Gall. [Anatomical and clinical correlations in the cerebellar eredodegeneration]. Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica. vol 75. issue 2. 2003-09-15. PMID:12868150. |
during a 4-year period, we studied 14 patients (42-61 years old) suffering cerebellar eredodegeneration (hereditary ataxia). |
2003-09-15 |
2023-08-12 |
Not clear |