Similar articles for PMID: 22723063

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1

The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a.

Feraco P, Mirabelli-Badenier M, Severino M, Alpigiani MG, Di Rocco M, Biancheri R, Rossi A. Feraco P, et al. AJNR Am J Neuroradiol. 2012 Dec;33(11):2062-7. doi: 10.3174/ajnr.A3151. Epub 2012 Jun 21. AJNR Am J Neuroradiol. 2012. PMID: 22723063 Free article.

2

Measuring brain stem and cerebellar damage in parkinsonian syndromes using diffusion tensor MRI.

Blain CR, Barker GJ, Jarosz JM, Coyle NA, Landau S, Brown RG, Chaudhuri KR, Simmons A, Jones DK, Williams SC, Leigh PN. Blain CR, et al. Neurology. 2006 Dec 26;67(12):2199-205. doi: 10.1212/01.wnl.0000249307.59950.f8. Neurology. 2006. PMID: 17190944

3

Middle cerebellar peduncles and Pontine T2 hypointensities in ARSACS.

Shimazaki H, Takiyama Y, Honda J, Sakoe K, Namekawa M, Tsugawa J, Tsuboi Y, Suzuki C, Baba M, Nakano I. Shimazaki H, et al. J Neuroimaging. 2013 Jan;23(1):82-5. doi: 10.1111/j.1552-6569.2011.00647.x. Epub 2012 Jan 23. J Neuroimaging. 2013. PMID: 22268491

4

Cerebellar atrophy: an important feature of carbohydrate deficient glycoprotein syndrome type 1.

Antoun H, Villeneuve N, Gelot A, Panisset S, Adamsbaum C. Antoun H, et al. Pediatr Radiol. 1999 Mar;29(3):194-8. doi: 10.1007/s002470050571. Pediatr Radiol. 1999. PMID: 10201039

5

[Norman type congenital atrophy of the granular layer. Observation of 2 sisters; neuro-pathological examination of a case].

Goulon M, Escourolle R, Barois A, Grosbuis S. Goulon M, et al. Rev Neurol (Paris). 1968 Jan;118(1):87-8. Rev Neurol (Paris). 1968. PMID: 5697569 French. No abstract available.

6

Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.

van der Knaap MS, Linnankivi T, Paetau A, Feigenbaum A, Wakusawa K, Haginoya K, Köhler W, Henneke M, Dinopoulos A, Grattan-Smith P, Brockmann K, Schiffmann R, Blaser S. van der Knaap MS, et al. Neurology. 2007 Jul 10;69(2):166-71. doi: 10.1212/01.wnl.0000265592.74483.a6. Neurology. 2007. PMID: 17620549

7

Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?

Lev D, Michelson-Kerman M, Vinkler C, Blumkin L, Shalev SA, Lerman-Sagie T. Lev D, et al. Eur J Paediatr Neurol. 2008 Mar;12(2):97-101. doi: 10.1016/j.ejpn.2007.06.005. Epub 2007 Jul 30. Eur J Paediatr Neurol. 2008. PMID: 17681808

8

Cerebellar lesions in multiple system atrophy: postmortem MR imaging-pathologic correlations.

Matsusue E, Fujii S, Kanasaki Y, Kaminou T, Ohama E, Ogawa T. Matsusue E, et al. AJNR Am J Neuroradiol. 2009 Oct;30(9):1725-30. doi: 10.3174/ajnr.A1662. Epub 2009 Jun 18. AJNR Am J Neuroradiol. 2009. PMID: 19541777 Free PMC article.

9

In vivo voxel-based morphometry in multiple system atrophy of the cerebellar type.

Specht K, Minnerop M, Abele M, Reul J, Wüllner U, Klockgether T. Specht K, et al. Arch Neurol. 2003 Oct;60(10):1431-5. doi: 10.1001/archneur.60.10.1431. Arch Neurol. 2003. PMID: 14568814 Clinical Trial.

10

Hyperintensity of the middle cerebellar peduncles on fluid-attenuated inversion recovery imaging: variation with age and implications for the diagnosis of multiple system atrophy.

Ngai S, Tang YM, Du L, Stuckey S. Ngai S, et al. AJNR Am J Neuroradiol. 2006 Nov-Dec;27(10):2146-8. AJNR Am J Neuroradiol. 2006. PMID: 17110685 Free article.

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