Similar articles for PMID: 22723063

Year	Number of Results
1968	2
1978	1
1989	2
1992	1
1993	3
1994	1
1995	9
1996	1
1997	1
1998	3
1999	3
2001	3
2002	1
2003	2
2004	2
2005	2
2006	4
2007	6
2008	4
2009	7
2010	6
2011	2
2012	6
2013	3
2014	2
2015	5
2016	5
2017	6
2018	4
2019	4
2020	4
2021	2
2022	1
2024	0

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 PMC 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

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.

4

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

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

Non-progressive familial congenital cerebellar hypoplasia.

al Shahwan SA, Bruyn GW, al Deeb SM. al Shahwan SA, et al. J Neurol Sci. 1995 Jan;128(1):71-7. doi: 10.1016/0022-510x(94)00209-7. J Neurol Sci. 1995. PMID: 7722536

7

Diagnostic approach to cerebellar disease in children.

D'Arrigo S, Viganò L, Grazia Bruzzone M, Marzaroli M, Nikas I, Riva D, Pantaleoni C. D'Arrigo S, et al. J Child Neurol. 2005 Nov;20(11):859-66. doi: 10.1177/08830738050200110101. J Child Neurol. 2005. PMID: 16417854

8

Localized proton magnetic resonance spectroscopy of cerebral abnormalities in children with carbohydrate-deficient glycoprotein syndrome.

Holzbach U, Hanefeld F, Helms G, Hänicke W, Frahm J. Holzbach U, et al. Acta Paediatr. 1995 Jul;84(7):781-6. doi: 10.1111/j.1651-2227.1995.tb13756.x. Acta Paediatr. 1995. PMID: 7549297

9

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

10

Posterior fossa imaging in 158 children with ataxia.

Boddaert N, Desguerre I, Bahi-Buisson N, Romano S, Valayannopoulos V, Saillour Y, Seidenwurm D, Grevent D, Berteloot L, Lebre AS, Zilbovicius M, Puget S, Salomon R, Attie-Bitach T, Munnich A, Brunelle F, de Lonlay P. Boddaert N, et al. J Neuroradiol. 2010 Oct;37(4):220-30. doi: 10.1016/j.neurad.2009.12.009. Epub 2010 Apr 7. J Neuroradiol. 2010. PMID: 20378176

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

97 results

Results by year