| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| W Zhang, W H Lee, L C Triarho. Grafted cerebellar cells in a mouse model of hereditary ataxia express IGF-I system genes and partially restore behavioral function. Nature medicine. vol 2. issue 1. 1996-03-05. PMID:8564845. |
grafted cerebellar cells in a mouse model of hereditary ataxia express igf-i system genes and partially restore behavioral function. |
1996-03-05 |
2023-08-12 |
mouse |
| W Zhang, W H Lee, L C Triarho. Grafted cerebellar cells in a mouse model of hereditary ataxia express IGF-I system genes and partially restore behavioral function. Nature medicine. vol 2. issue 1. 1996-03-05. PMID:8564845. |
bilateral cerebellar grafts led to an improvement of motor behaviors in balance rod tests and in the open field, providing evidence for functional integration into the atrophic mouse cerebellum and underscoring the potential of neural transplantation for counteracting the human cerebellar ataxias. |
1996-03-05 |
2023-08-12 |
mouse |
| X Qiao, F Hefti, B Knusel, J L Noebel. Selective failure of brain-derived neurotrophic factor mRNA expression in the cerebellum of stargazer, a mutant mouse with ataxia. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 16. issue 2. 1996-02-22. PMID:8551348. |
selective failure of brain-derived neurotrophic factor mrna expression in the cerebellum of stargazer, a mutant mouse with ataxia. |
1996-02-22 |
2023-08-12 |
mouse |
| G Cancel, G Stevanin, A Dürr, H Chneiweiss, C Penet, Y Pothin, Y Agid, A Bric. SCA2 is not a major locus for ADCA type I in French families. American journal of medical genetics. vol 60. issue 5. 1996-02-13. PMID:8546150. |
autosomal dominant cerebellar ataxias (adca) of type i, a group of clinically heterogeneous neurodegenerative disorders, are known to be genetically heterogeneous since a second locus for adca type i (sca2) has been identified on the long arm of chromosome 12. |
1996-02-13 |
2023-08-12 |
Not clear |
| S Spieker, J B Schulz, D Petersen, M Fetter, T Klockgether, J Dichgan. Fixation instability and oculomotor abnormalities in Friedreich's ataxia. Journal of neurology. vol 242. issue 8. 1996-01-29. PMID:8530980. |
eye movements were studied in 13 patients with friedreich's ataxia and correlated with mri findings to investigate whether oculomotor abnormalities can be traced to cerebellar disturbances in this disease. |
1996-01-29 |
2023-08-12 |
Not clear |
| C C Verschuuren-Bemelmans, E R Brunt, M Burton, R G Mensink, M A van der Meulen, N H Smit, I Stolte-Dijkstra, C H Buys, H Scheffe. Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I. Human genetics. vol 96. issue 6. 1996-01-22. PMID:8522329. |
the autosomal dominant cerebellar ataxias (adca) are clinically and genetically heterogeneous. |
1996-01-22 |
2023-08-12 |
Not clear |
| G Haberhausen, M S Damian, F Leweke, U Mülle. Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD). Journal of the neurological sciences. vol 132. issue 1. 1996-01-19. PMID:8523034. |
spinocerebellar ataxia, type 3 (sca3) and machado-joseph disease (mjd) are two clinically distinct representatives of the heterogeneous group of autosomal dominant cerebellar ataxias. |
1996-01-19 |
2023-08-12 |
Not clear |
| J O Larsen, H Braendgaar. Structural preservation of cerebellar granule cells following neurointoxication with methyl mercury: a stereological study of the rat cerebellum. Acta neuropathologica. vol 90. issue 3. 1996-01-19. PMID:8525798. |
however, it is still unclear whether the ataxia is of cerebellar or peripheral origin. |
1996-01-19 |
2023-08-12 |
rat |
| P Giunti, M G Sweeney, A E Hardin. Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth. Brain : a journal of neurology. vol 118 ( Pt 5). 1996-01-18. PMID:7496771. |
affected members of 63 families with a variety of autosomal dominant late onset cerebellar ataxias (adca), and 29 patients with similar phenotypes but no affected relatives, were investigated for the trinucleotide (cag) repeat expansion described in japanese families with machado-joseph disease (mjd). |
1996-01-18 |
2023-08-12 |
Not clear |
| Y Trottier, Y Lutz, G Stevanin, G Imbert, D Devys, G Cancel, F Saudou, C Weber, G David, L Tor. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature. vol 378. issue 6555. 1995-12-28. PMID:7477379. |
polyglutamine expansion as a pathological epitope in huntington's disease and four dominant cerebellar ataxias. |
1995-12-28 |
2023-08-12 |
Not clear |
| Y Ugawa, Y Terao, C Nagai, K Nakamura, I Kanazaw. Electrical stimulation of the cerebellum normally suppresses motor cortical excitability in a patient with ataxia due to a lesion of the middle cerebellar peduncle. European neurology. vol 35. issue 4. 1995-10-19. PMID:7671991. |
electrical stimulation of the cerebellum normally suppresses motor cortical excitability in a patient with ataxia due to a lesion of the middle cerebellar peduncle. |
1995-10-19 |
2023-08-12 |
Not clear |
| A Benomar, L Krols, G Stevanin, G Cancel, E LeGuern, G David, H Ouhabi, J J Martin, A Dürr, A Zai. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1. Nature genetics. vol 10. issue 1. 1995-09-25. PMID:7647798. |
our results show that adca type ii is a genetically homogenous disorder, independent of the heterogeneous group of type i cerebellar ataxias. |
1995-09-25 |
2023-08-12 |
Not clear |
| A Riva, G B Brada. Primary cerebellar and spino-cerebellar ataxia an MRI study on 63 cases. Journal of neuroradiology = Journal de neuroradiologie. vol 22. issue 2. 1995-09-05. PMID:7629572. |
primary cerebellar and spino-cerebellar ataxia an mri study on 63 cases. |
1995-09-05 |
2023-08-12 |
Not clear |
| A Dürr, A Brice, A Lepage-Lezin, G Cancel, D Smadja, J C Vernant, Y Agi. Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2). Clinical neuroscience (New York, N.Y.). vol 3. issue 1. 1995-08-24. PMID:7614088. |
spinocerebellar ataxia 2 (sca2) is one of the loci for the clinically and genetically heterogeneous group of autosomal dominant type i cerebellar ataxias. |
1995-08-24 |
2023-08-12 |
Not clear |
| L J Ptáce. Autosomal dominant spinocerebellar atrophy with retinal degeneration. Clinical neuroscience (New York, N.Y.). vol 3. issue 1. 1995-08-24. PMID:7614091. |
the autosomal dominant cerebellar ataxias are a clinically and genetically heterogeneous group of disorders. |
1995-08-24 |
2023-08-12 |
Not clear |
| S Belal, F Hentati, C Ben Hamida, M Ben Hamid. Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus. Clinical neuroscience (New York, N.Y.). vol 3. issue 1. 1995-08-24. PMID:7614093. |
the most common autosomal recessive ataxia is friedreich's ataxia (fa), characterized mainly by an early onset, absent tendon reflexes, deep sensory loss, cerebellar and babinski signs. |
1995-08-24 |
2023-08-12 |
Not clear |
| B Bonnefoi-Kyriacou, E Trouche, E Legallet, F Vialle. Planning and execution of pointing movements in cerebellar patients. Movement disorders : official journal of the Movement Disorder Society. vol 10. issue 2. 1995-06-21. PMID:7753059. |
twelve patients with cerebellar dysfunction including a limb ataxia and 12 age-matched controls performed pointing movements with an arm. |
1995-06-21 |
2023-08-12 |
Not clear |
| P Haggard, R C Miall, D Wade, S Fowler, A Richardson, P Anslow, J Stei. Damage to cerebellocortical pathways after closed head injury: a behavioural and magnetic resonance imaging study. Journal of neurology, neurosurgery, and psychiatry. vol 58. issue 4. 1995-06-05. PMID:7738549. |
all patients had had a closed head injury and all had cerebellar type ataxia. |
1995-06-05 |
2023-08-12 |
Not clear |
| P Haggard, R C Miall, D Wade, S Fowler, A Richardson, P Anslow, J Stei. Damage to cerebellocortical pathways after closed head injury: a behavioural and magnetic resonance imaging study. Journal of neurology, neurosurgery, and psychiatry. vol 58. issue 4. 1995-06-05. PMID:7738549. |
ataxia seen after severe head injury can arise from damage to the superior cerebellar peduncle, which may interfere with the cerebellocortical circuits involved in coordinated movement. |
1995-06-05 |
2023-08-12 |
Not clear |
| H Ackermann, I Hertrich, T Heh. Oral diadochokinesis in neurological dysarthrias. Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP). vol 47. issue 1. 1995-06-01. PMID:7728177. |
the present study performed an acoustic analysis of rapid syllable repetitions in patients suffering from idiopathic parkinson's disease (n = 17), huntington's chorea (n = 14), friedreich's ataxia (n = 9), or from a purely cerebellar syndrome (n = 13). |
1995-06-01 |
2023-08-12 |
human |