Publikasjoner Dr. Christina Sundal:

1.

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.
PMID: 22166459 Review.

2.

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.
PMID: 23331413 Free PMC article. Review.

3.

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.
PMID: 23787135 Free PMC article.

4.

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.
PMID: 22050953 Free PMC article.

5.

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.
PMID: 22843259 Free PMC article.

6.

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.
PMID: 23124435 Free PMC article.

7.

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.
PMID: 24036850 Free PMC article. Review. No abstract available.

8.

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.
PMID: 22197934 Free PMC article.

9.

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.
PMID: 25311247 Free PMC article.

10.

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.
PMID: 23038654 Free PMC article. No abstract available.

11.

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.
PMID: 19925533 Review.

12.

A SCA7 premutation may be a novel Mendelian modifier of MS course: A case report

Sundal C, Axelsson M, Wiklund L, Lindberg C, Andersen O.

Mult Scler Relat Disord. 2019 Jun;31:148-150. doi: 10.1016/j.msard.2019.04.009. Epub 2019 Apr 13.
PMID: 30999137

13.

Prophylactic Allogeneic Hematopoietic Stem Cell Therapy for CSF1R-Related Leukoencephalopathy

Horn MA, Myhre AE, Prescott T, Aasly J, Sundal CH, Gedde-Dahl T.

Mov Disord. 2022 May;37(5):1108-1109. doi: 10.1002/mds.29011.
PMID: 35587623 Free PMC article. No abstract available.

14.

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.
PMID: 26486671 English, Norwegian. No abstract available.

15.

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.
PMID: 23751174

16.

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.
PMID: 22098561

17.

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.
PMID: 26756564

18.

Microglia: multiple roles in surveillance, circuit shaping, and response to injury

Sundal C.

Neurology. 2014 May 20;82(20):1846. doi: 10.1212/WNL.0000000000000399.
PMID: 24843036 No abstract available.

19.

An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids

Sundal C, Carmona S, Yhr M, Almström O, Ljungberg M, Hardy J, Hedberg-Oldfors C, Fred Å, Brás J, Oldfors A, Andersen O, Guerreiro R.

Acta Neuropathol Commun. 2019 Nov 27;7(1):188. doi: 10.1186/s40478-019-0843-y.
PMID: 31775912 Free PMC article.

20.

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.
PMID: 27802867 No abstract available.

21.

Current clinical practice in disabling and chronic migraine in the primary care setting: results from the European My-LIFE anamnesis survey

Ryvlin P, Skorobogatykh K, Negro A, Sanchez-De La Rosa R, Israel-Willner H, Sundal C, MacGregor EA, Guerrero AL.

BMC Neurol. 2021 Jan 4;21(1):1. doi: 10.1186/s12883-020-02014-6.
PMID: 33390161 Free PMC article.

22.

Need of guidance in disabling and chronic migraine identification in the primary care setting, results from the european MyLife anamnesis survey

Guerrero AL, Negro A, Ryvlin P, Skorobogatykh K, Sanchez-De La Rosa R, Israel-Willner H, Sundal C, MacGregor EA.

BMC Fam Pract. 2021 Mar 20;22(1):54. doi: 10.1186/s12875-021-01402-2.
PMID: 33743604 Free PMC article.

23.

Redefining migraine prevention: early treatment with anti-CGRP monoclonal antibodies enhances response in the real world

Caronna E, Gallardo VJ, Egeo G, Vázquez MM, Castellanos CN, Membrilla JA, Vaghi G, Rodríguez-Montolio J, Fabregat Fabra N, Sánchez-Caballero F, Jaimes Sánchez A, Muñoz-Vendrell A, Oliveira R, Gárate G, González-Osorio Y, Guisado-Alonso D, Ornello R, Thunstedt C, Fernández-Lázaro I, Torres-Ferrús M, Alpuente A, Torelli P, Aurilia C, Pére RL, Castrillo MJR, Icco R, Sances G, Broadhurst S, Ong HC, García AG, Campoy S, Sanahuja J, Cabral G, Beltrán Blasco I, Waliszewska-Prosół M, Pereira L, Layos-Romero A, Luzeiro I, Dorado L, Álvarez Escudero MR, May A, López-Bravo A, Martins IP, Sundal C, Irimia P, Lozano Ros A, Gago-Veiga AB, Juanes FV, Ruscheweyh R, Sacco S, Cuadrado-Godia E, García-Azorín D, Pascual J, Gil-Gouveia R, Huerta-Villanueva M, Rodriguez-Vico J, Viguera Romero J, Obach V, Santos-Lasaosa S, Ghadiri-Sani M, Tassorelli C, Díaz-de-Terán J, Díaz Insa S, Oria CG, Barbanti P, Pozo-Rosich P; EUREkA study group.

J Neurol Neurosurg Psychiatry. 2024 Sep 17;95(10):927-937. doi: 10.1136/jnnp-2023-333295.
PMID: 38777579

24.

CSF1R-Related Disorder

Dulski J, Sundal C, Wszolek ZK.

2012 Aug 30 [updated 2024 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID: 22934315 Free Books & Documents. Review.

25.

Stora regionala orättvisor gällande behandling av huvudvärk

Sundal C, Tedroff J.

Lakartidningen. 2018 May 9;115:E6U3.
PMID: 29762814 Swedish. No abstract available.