Publikasjoner

Stora regionala orättvisor gällande behandling av huvudvärk. Sundal C, Tedroff J. Lakartidningen. 2018 May 9;115. pii: E6U3. Swedish.

 

CSF1R-Related Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia. Sundal C, Wszolek ZK.  In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. 2012 Aug 30 [updated 2017 Oct 5].

 

Morvan syndrome with Caspr2 antibodies. Clinical and autopsy report. Sundal C, Vedeler C, Miletic H, Andersen O.  J Neurol Sci. 2017 Jan 15;372:453-455. doi: 10.1016/j.jns.2016.10.046. Epub 2016 Oct 28.

 

Hereditary diffuse leukoencephalopathy with spheroids – a volumetric and radiological comparison with multiple sclerosis patients and healthy controls. Granberg T, Hashim F, Andersen O, Sundal C, Karrenbauer VD. Eur J Neurol. 2016 Apr;23(4):817-22. doi: 10.1111/ene.12948. Epub 2016 Jan 12.

 

A woman in her 70s with chronic walking difficulties. Flønes IH, Haugarvoll K, Sundal C, Tzoulis C.  Tidsskr Nor Laegeforen. 2015 Oct 20;135(19):1753-5. doi: 10.4045/tidsskr.15.0111. eCollection 2015 Oct 20.

 

Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis. Sundal C, Baker M, Karrenbauer V, Gustavsen M, Bedri S, Glaser A, Myhr KM, Haugarvoll K, Zetterberg H, Harbo H, Kockum I, Hillert J, Wszolek Z, Rademakers R, Andersen O.  Eur J Neurol. 2015 Feb;22(2):328-333. doi: 10.1111/ene.12572. Epub 2014 Oct 13.

 

Microglia: multiple roles in surveillance, circuit shaping, and response to injury. Sundal C. Neurology. 2014 May 20;82(20):1846.

 

An adult-onset leukoencephalopathy with axonal spheroids and pigmented glia accompanied by brain calcifications: a case report and a literature review of brain calcifications disorders. Fujioka S, Broderick DF, Sundal C, Baker MC, Rademakers R, Wszolek ZK.  J Neurol. 2013 Oct;260(10):2665-8. doi: 10.1007/s00415-013-7093-x. Epub 2013 Sep 14.

 

Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations. Sundal C, Fujioka S, Van Gerpen JA, Wider C, Nicholson AM, Baker M, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Tselis A, Swerdlow RH, Miller BB, Borjesson-Hanson A, Uitti RJ, Ross OA, Stoessl AJ, Rademakers R, Josephs KA, Dickson DW, Broderick D, Wszolek ZK.  Parkinsonism Relat Disord. 2013 Oct;19(10):869-77. doi: 10.1016/j.parkreldis.2013.05.013. Epub 2013 Jun 17.

 

Different stages of white matter changes in the original HDLS family revealed by advanced MRI techniques. Sundal C, Jönsson L, Ljungberg M, Zhong J, Tian W, Zhu T, Linden T, Börjesson-Hanson A, Andersen O, Ekholm S. J Neuroimaging. 2014 Sep-Oct;24(5):444-52. doi: 10.1111/jon.12037. Epub 2013 Jun 10.

 

Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics. Fujioka S, Sundal C, Wszolek ZK. Orphanet J Rare Dis. 2013 Jan 18;8:14. doi: 10.1186/1750-1172-8-14. Review.

 

Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia. Fujioka S, Sundal C, Strongosky AJ, Castanedes MC, Rademakers R, Ross OA, Vilariño-Güell C, Farrer MJ, Wszolek ZK, Dickson DW.  Acta Neuropathol. 2013 Mar;125(3):425-38. doi: 10.1007/s00401-012-1059-4. Epub 2012 Nov 4.

 

A novel de novo pathogenic mutation in the CACNA1A gene. Fujioka S, Rayaprolu S, Sundal C, Broderick DF, Langley WA, Shoffner J, Hyams LC, Rademakers R, Graff-Radford NR, Tatum W, Ross OA, Wszolek ZK.  Mov Disord. 2012 Oct;27(12):1578-9. doi: 10.1002/mds.25198. Epub 2012 Oct 4.

 

MRI characteristics and scoring in HDLS due to CSF1R gene mutations. Sundal C, Van Gerpen JA, Nicholson AM, Wider C, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Borjesson-Hanson A, Tselis A, Swerdlow RH, Miller BB, Fujioka S, Heckman MG, Uitti RJ, Josephs KA, Baker M, Andersen O, Rademakers R, Dickson DW, Broderick D, Wszolek ZK.  Neurology. 2012 Aug 7;79(6):566-74. doi: 10.1212/WNL.0b013e318263575a. Epub 2012 Jul 25.

 

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Rademakers R, Baker M, Nicholson AM, Rutherford NJ, Finch N, Soto-Ortolaza A, Lash J, Wider C, Wojtas A, DeJesus-Hernandez M, Adamson J, Kouri N, Sundal C, Shuster EA, Aasly J, MacKenzie J, Roeber S, Kretzschmar HA, Boeve BF, Knopman DS, Petersen RC, Cairns NJ, Ghetti B, Spina S, Garbern J, Tselis AC, Uitti R, Das P, Van Gerpen JA, Meschia JF, Levy S, Broderick DF, Graff-Radford N, Ross OA, Miller BB, Swerdlow RH, Dickson DW, Wszolek ZK.  Nat Genet. 2011 Dec 25;44(2):200-5. doi: 10.1038/ng.1027.

 

Autosomal dominant Parkinson’s disease. Sundal C, Fujioka S, Uitti RJ, Wszolek ZK. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S7-10. doi: 10.1016/S1353-8020(11)70005-0. Review.

 

Update of the original HDLS kindred: divergent clinical courses. Sundal C, Ekholm S, Nordborg C, Jönsson L, Börjesson-Hanson A, Lindén T, Zetterberg H, Viitanen M, Andersen O.  Acta Neurol Scand. 2012 Jul;126(1):67-75. doi: 10.1111/j.1600-0404.2011.01624.x. Epub 2011 Nov 18.

 

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity. Sundal C, Lash J, Aasly J, Øygarden S, Roeber S, Kretzschman H, Garbern JY, Tselis A, Rademakers R, Dickson DW, Broderick D, Wszolek ZK.  J Neurol Sci. 2012 Mar 15;314(1-2):130-7. doi: 10.1016/j.jns.2011.10.006. Epub 2011 Nov 1.

 

White matter disorders with autosomal dominant heredity: a review with personal clinical case studies and their MRI findings. Sundal C, Ekholm S, Andersen O.  Acta Neurol Scand. 2010 May;121(5):328-37. doi: 10.1111/j.1600-0404.2009.01219.x. Epub 2009 Nov 19. Review.

 

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia. Sundal. http://www.socialstyrelsen.se/ovanligadiagnoser/hereditardiffusleukoencefalopa

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