| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Roy Turner, Alessandra Schiavett. The cerebellum in schizophrenia: a case of intermittent ataxia and psychosis--clinical, cognitive, and neuroanatomical correlates. The Journal of neuropsychiatry and clinical neurosciences. vol 16. issue 4. 2005-01-26. PMID:15616166. |
the cerebellum in schizophrenia: a case of intermittent ataxia and psychosis--clinical, cognitive, and neuroanatomical correlates. |
2005-01-26 |
2023-08-12 |
Not clear |
| Richard J Naftalin, Philip Cunningham, Iram Afzal-Ahme. Piracetam and TRH analogues antagonise inhibition by barbiturates, diazepam, melatonin and galanin of human erythrocyte D-glucose transport. British journal of pharmacology. vol 142. issue 3. 2005-01-25. PMID:15148255. |
thyrotropin-releasing hormone, trh, which has a chemical structure similar to nootropics increases cerebellar uptake of glucose in murine rolling ataxia. |
2005-01-25 |
2023-08-12 |
human |
| Tetsutaro Ozawa, Dominic Paviour, Niall P Quinn, Keith A Josephs, Hardev Sangha, Linda Kilford, Daniel G Healy, Nick W Wood, Andrew J Lees, Janice L Holton, Tamas Reves. The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations. Brain : a journal of neurology. vol 127. issue Pt 12. 2005-01-19. PMID:15509623. |
our finding that relatively mild involvement of the substantia nigra is associated clinically with manifest parkinsonism, while more advanced cerebellar pathology is required for ataxia, may explain why the parkinsonian presentation is predominant over ataxia in msa. |
2005-01-19 |
2023-08-12 |
Not clear |
| Maria Spadaro, Simona Ursu, Frank Lehmann-Horn, Liana Veneziano, Veneziano Liana, Giovanni Antonini, Antonini Giovanni, Paola Giunti, Giunti Paola, Marina Frontali, Karin Jurkat-Rot. A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. Neurogenetics. vol 5. issue 3. 2005-01-06. PMID:15459825. |
in over 50% of cases the causative gene is cacna1a (fhm1), which in some cases produces a phenotype with cerebellar signs, including ataxia and nystagmus. |
2005-01-06 |
2023-08-12 |
Not clear |
| Martin Viau, Yvan Boulange. Characterization of ataxias with magnetic resonance imaging and spectroscopy. Parkinsonism & related disorders. vol 10. issue 6. 2004-11-19. PMID:15261875. |
magnetic resonance imaging (mri) and magnetic resonance spectroscopy (mrs) generally show cerebellar or cerebral atrophy and perturbed metabolite levels which differ between ataxias. |
2004-11-19 |
2023-08-12 |
Not clear |
| Jeremy D Schmahman. Disorders of the cerebellum: ataxia, dysmetria of thought, and the cerebellar cognitive affective syndrome. The Journal of neuropsychiatry and clinical neurosciences. vol 16. issue 3. 2004-11-19. PMID:15377747. |
the universal cerebellar impairment manifests as ataxia when the sensorimotor cerebellum is involved and as the ccas when pathology is in the lateral hemisphere of the posterior cerebellum (involved in cognitive processing) or in the vermis (limbic cerebellum). |
2004-11-19 |
2023-08-12 |
Not clear |
| U Wüllner, B Evert, T Klockgethe. Mechanisms of cell death in cerebellar disorders. Restorative neurology and neuroscience. vol 13. issue 1-2. 2004-10-22. PMID:12671288. |
trinucleotide repeat expansions have been identified as an important cause of inherited cerebellar ataxias and mechanisms involved in apoptotic cell death have become centerstage of scientific interest. |
2004-10-22 |
2023-08-12 |
Not clear |
| J R M Cruysberg, A F Deutma. [From gene to disease; autosomal dominant cerebellar ataxias]. Nederlands tijdschrift voor geneeskunde. vol 148. issue 31. 2004-10-05. PMID:15366729. |
[from gene to disease; autosomal dominant cerebellar ataxias]. |
2004-10-05 |
2023-08-12 |
Not clear |
| José Gazulla, José M Errea, Isabel Benavente, Carlos J Tordesilla. Treatment of ataxia in cortical cerebellar atrophy with the GABAergic drug gabapentin. A preliminary study. European neurology. vol 52. issue 1. 2004-09-30. PMID:15218338. |
treatment of ataxia in cortical cerebellar atrophy with the gabaergic drug gabapentin. |
2004-09-30 |
2023-08-12 |
Not clear |
| José Gazulla, José M Errea, Isabel Benavente, Carlos J Tordesilla. Treatment of ataxia in cortical cerebellar atrophy with the GABAergic drug gabapentin. A preliminary study. European neurology. vol 52. issue 1. 2004-09-30. PMID:15218338. |
an ataxia scale based on clinical findings was used to evaluate the cerebellar signs at baseline and after administration of the drug. |
2004-09-30 |
2023-08-12 |
Not clear |
| Sergey V Ivanov, Jerrold M Ward, Lino Tessarollo, Dorothea McAreavey, Vandana Sachdev, Lameh Fananapazir, Melissa K Banks, Nicole Morris, Draginja Djurickovic, Deborah E Devor-Henneman, Ming-Hui Wei, Gregory W Alvord, Boning Gao, James A Richardson, John D Minna, Michael A Rogawski, Michael I Lerma. Cerebellar ataxia, seizures, premature death, and cardiac abnormalities in mice with targeted disruption of the Cacna2d2 gene. The American journal of pathology. vol 165. issue 3. 2004-09-30. PMID:15331424. |
in summary, our findings provide genetic evidence that the alpha2delta-2 subunit serves in vivo as a component of p/q-type calcium channels, is indispensable for the central nervous system function, and may be involved in hereditary cerebellar ataxias and epileptic disorders in humans. |
2004-09-30 |
2023-08-12 |
mouse |
| T J DANARA. The cerebellar aspect of nutritional spinal ataxia. Transactions of the Royal Society of Tropical Medicine and Hygiene. vol 43. issue 3. 2004-09-30. PMID:15395882. |
the cerebellar aspect of nutritional spinal ataxia. |
2004-09-30 |
2023-08-12 |
Not clear |
| Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, Naima Bouslam, Michel Gouttard, Caroline Soumphonphakdy, Marie-Laure Welter, Elisabeth Ollagnon-Roman, Arnaud Lemainque, Merle Ruberg, Alexis Brice, Alexandra Dur. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14. Archives of neurology. vol 61. issue 8. 2004-09-07. PMID:15313841. |
autosomal dominant cerebellar ataxias comprise a clinically, neuropathologically, and genetically heterogeneous group of neurodegenerative disorders. |
2004-09-07 |
2023-08-12 |
Not clear |
| L A Martin, T Escher, D Goldowitz, G Mittlema. A relationship between cerebellar Purkinje cells and spatial working memory demonstrated in a lurcher/chimera mouse model system. Genes, brain, and behavior. vol 3. issue 3. 2004-08-26. PMID:15140011. |
through histological examination of chimeric mice and observations of motor ability, we showed that ataxia is dependent upon both the number and distribution of purkinje cells in the cerebellum. |
2004-08-26 |
2023-08-12 |
mouse |
| Michisuke Yuzak. The delta2 glutamate receptor: a key molecule controlling synaptic plasticity and structure in Purkinje cells. Cerebellum (London, England). vol 3. issue 2. 2004-08-23. PMID:15233575. |
the orphan glutamate receptor delta2 (glurdelta2) is predominantly expressed in cerebellar purkinje cells and plays a crucial role in cerebellar functions; mice that lack the glurdelta2 gene display ataxia and impaired motor-related learning tasks. |
2004-08-23 |
2023-08-12 |
mouse |
| Riccardo Della Nave, Silvia Foresti, Carlo Tessa, Marco Moretti, Andrea Ginestroni, Cinzia Gavazzi, Laura Guerrini, Fabrizio Salvi, Silvia Piacentini, Mario Mascalch. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. NeuroImage. vol 22. issue 2. 2004-08-19. PMID:15193598. |
adc mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. |
2004-08-19 |
2023-08-12 |
Not clear |
| Riccardo Della Nave, Silvia Foresti, Carlo Tessa, Marco Moretti, Andrea Ginestroni, Cinzia Gavazzi, Laura Guerrini, Fabrizio Salvi, Silvia Piacentini, Mario Mascalch. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. NeuroImage. vol 22. issue 2. 2004-08-19. PMID:15193598. |
a correlation between clinical severity as assessed with the inherited ataxias clinical rating scale (iacrs) and the 50th percentile of the d value in the brainstem and cerebellum histogram (r = 0.69) was observed in patients with sca1 or sca2. |
2004-08-19 |
2023-08-12 |
Not clear |
| Riccardo Della Nave, Silvia Foresti, Carlo Tessa, Marco Moretti, Andrea Ginestroni, Cinzia Gavazzi, Laura Guerrini, Fabrizio Salvi, Silvia Piacentini, Mario Mascalch. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. NeuroImage. vol 22. issue 2. 2004-08-19. PMID:15193598. |
diffusion mr imaging reveals variable patterns of increase of d in the brainstem, cerebellum, and cerebral hemispheres in degenerative ataxias that match the known distribution of the neuropathological changes. |
2004-08-19 |
2023-08-12 |
Not clear |
| Fatiha Boukhtouche, Jean Mariani, Alain Tedgu. The "CholesteROR" protective pathway in the vascular system. Arteriosclerosis, thrombosis, and vascular biology. vol 24. issue 4. 2004-08-05. PMID:14751813. |
the homozygous rora(sg/sg) mutant mouse, of which the most obvious phenotype is ataxia associated with cerebellar degeneration, also displays a variety of other phenotypes, including several vascular ones; in particular, dysfunction of smooth muscle cells and enhanced susceptibility to atherosclerosis. |
2004-08-05 |
2023-08-12 |
mouse |
| Yosuke Ando, Nobutsune Ichihara, Shigehito Takeshita, Yoshiaki Saito, Takeki Kikuchi, Noboru Wakasug. Histological and ultrastructural features in the early stage of Purkinje cell degeneration in the cerebellar calcification (CC) rat. Experimental animals. vol 53. issue 2. 2004-07-20. PMID:15153669. |
the cerebellar calcification (cc) rat is a new neurodegenerative mutant with severe purkinje cell loss and symmetrical calcifications in the cerebellar cortex manifesting ataxia: lack of coordination in body movements. |
2004-07-20 |
2023-08-12 |
rat |