ライフサイエンスコーパス: cerebellar atrophy

1 xhibited moderately progressive brain and/or cerebellar atrophy.

2 nia, non-progressive ataxia, and progressive cerebellar atrophy.

3 ted in neurodegenerative processes including cerebellar atrophy.

4 sal cerebellar sulci widening, supportive of cerebellar atrophy.

5 seases involving progressive gait ataxia and cerebellar atrophy.

6 f the brains of our patients revealed marked cerebellar atrophy.

7 ive children showed generalised cerebral and cerebellar atrophy.

8 Neuroimaging showed isolated cerebellar atrophy.

9 drome, hallmarks of which include ataxia and cerebellar atrophy.

10 p1 resulted in age-dependent and progressive cerebellar atrophy.

11 ght be considered in the etiopathogenesis of cerebellar atrophy: (1) transneuronal degeneration and n

12 , and magnetic resonance imaging evidence of cerebellar atrophy (33%).

13 son, who died at age 3 years) had pronounced cerebellar atrophy and a renal biopsy specimen that show

14 atter fraction, T2 lesion volume, metrics of cerebellar atrophy and cerebellar lesion volume) and mot

15 impairment was predicted by a combination of cerebellar atrophy and decreased cerebellar-sensorimotor

16 nically by ataxia and neuropathologically by cerebellar atrophy and granule cell loss, gliosis, and P

17 an absent or disappearing putamen, variable cerebellar atrophy and highly variable cerebral atrophy.

18 ble for ARCA that is mainly characterized by cerebellar atrophy and lack of peripheral neuropathy.

19 tage-gated calcium channel, Cacna1a, develop cerebellar atrophy and mutations in the homologous human

20 degenerative syndrome associated with marked cerebellar atrophy and peripheral neuropathy.

21 heterogeneous group of disorders exhibiting cerebellar atrophy and Purkinje cell degeneration whose

22 pes arising from Purkinje cell degeneration, cerebellar atrophy and varying degrees of degeneration o

23 a significant correlation with MRI scores of cerebellar atrophy, and a significant correlation with c

24 ities, ipsilateral thalamic or contralateral cerebellar atrophy, and compensatory calvarial changes.

25 ntal delay, hypotonia, early-onset seizures, cerebellar atrophy, and osteopenia.

26 developmental delay, hypotonia, strabismus, cerebellar atrophy, and variable short stature.

27 and intellectual disability, with prominent cerebellar atrophy as a key neuroradiographic finding.

28 gly efficient in preventing motor neuron and cerebellar atrophy, as demonstrated in mouse models, fli

29 her displays later-onset encephalopathy with cerebellar atrophy, ataxia and dystonia.

30 als with ataxia-telangiectasia have reported cerebellar atrophy; but abnormalities of motor control c

31 lizumab treatment, especially in cases where cerebellar atrophy can be visualized by magnetic resonan

32 The extent of cerebellar atrophy correlated with decreased resting-sta

33 ed with volumetric measures of T2 lesions or cerebellar atrophy, diffusivity measures of middle or su

34 sive encephalopathy characterized by extreme cerebellar atrophy due to almost total granule neuron lo

35 30s and 40s and show predominant ataxia and cerebellar atrophy features on imaging.

36 oencephalopathy, and on its possible role in cerebellar atrophy in HIV-infected individuals.

37 ated with midbrain atrophy in PSP, and ponto-cerebellar atrophy in MSA-P.

38 ailability of coordinate data of grey matter cerebellar atrophy in patients were included.

39 the cerebellum, and the particularly severe cerebellar atrophy in some of the patients.

40 velopmental delay, hypotonia, scoliosis, and cerebellar atrophy in three families.

41 ll death in culture, and leads to ataxia and cerebellar atrophy in transgenic mice.

42 These findings demonstrate that cerebellar atrophy is related to both increases and decr

43 tural abnormalities (eg, rapidly progressive cerebellar atrophy), myopathies (including congenital mu

44 gies, including motor coordination disorder, cerebellar atrophy, neuronal loss in the cerebellum and

45 Intellectual disability and cerebellar atrophy occur together in a large number of g

46 , mild oculomotor abnormalities, and diffuse cerebellar atrophy on brain imaging.

47 eurological features including ataxia and/or cerebellar atrophy on brain MRI.

48 itive/psychiatric features, and cerebral and cerebellar atrophy on magnetic resonance imaging but abs

49 Six patients had evidence of cerebellar atrophy on magnetic-resonance imaging.

50 Pathologically, SCA2 presents as olivo-ponto-cerebellar atrophy (OPCA).

51 e ataxia with Purkinje cell degeneration and cerebellar atrophy, partially resembling the consequence

52 early onset epileptic seizures, optic nerve/cerebellar atrophy, pedal oedema, and early death.

53 with infantile spinal motor neuron disease, cerebellar atrophy, progressive microcephaly and profoun

54 Cerebellar atrophy rates were better discriminators of M

55 These cerebellar atrophied regions share robust and selective

56 he functional connectivity patterns of these cerebellar atrophy regions.

57 hat coexpress cyPrP and PrP(C) exhibit focal cerebellar atrophy, scratching behavior, and gait abnorm

58 l disability, cerebellar ataxia, early-onset cerebellar atrophy, sensorineural hearing loss, and the

59 hable recessive syndrome in 12 families with cerebellar atrophy together with ataxia, coarsened facia

60 lido-pyramidal syndrome, iron deposition and cerebellar atrophy, we identified a homozygous p.G53R mu

61 Across 54 studies, clusters of cerebellar atrophy were found for AD, ALS, FTD, MSA, and

62 netic resonance imaging revealed symmetrical cerebellar atrophy, which appeared progressive, and a pr

63 Chi3 Tg mice exhibit severe cerebellar atrophy with a significant loss of granule ce

64 severe and progressive brain, brainstem and cerebellar atrophy, with hypomyelination in most.

65 Magnetic resonance imaging demonstrated cerebellar atrophy without white matter lesions and ster