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Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics

Orphanet journal of rare diseases, 2013-01, Vol.8 (1), p.14-14, Article 14

2013

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Prophylactic Allogeneic Hematopoietic Stem Cell Therapy for CSF1R‐Related Leukoencephalopathy

Movement disorders, 2022-05, Vol.37 (5), p.1108-1109

2022

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

BMC neurology, 2021-01, Vol.21 (1), p.1-1, Article 1

2021

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

Acta neuropathologica communications, 2019-11, Vol.7 (1), p.188-188, Article 188

2019

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

Neurology, 2014-05, Vol.82 (20), p.1846-1846

Sundal, Christina

2014

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Different Stages of White Matter Changes in the Original HDLS Family Revealed by Advanced MRI Techniques

Journal of neuroimaging, 2014-09, Vol.24 (5), p.444-452

2014

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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Nature genetics, 2012-02, Vol.44 (2), p.200-205

2012

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Morvan syndrome with Caspr2 antibodies. Clinical and autopsy report

Journal of the neurological sciences, 2017-01, Vol.372, p.453-455

2017

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CSF Markers of Inflammation and Neurodegeneration in Two Hereditary Diffuse Leukoencephalopathy with Spheroids (HDLS) Families with Diverging Genotype and Phenotype (P5.268)

Neurology, 2016, Vol.86 (16_supplement)

2016

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Hereditary diffuse leukoencephalopathy with spheroids - a volumetric and radiological comparison with multiple sclerosis patients and healthy controls

European journal of neurology, 2016-04, Vol.23 (4), p.817-822

2016

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

BMC family practice, 2021-03, Vol.22 (1), Article 54

2021

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Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis

European journal of neurology, 2015-02, Vol.22 (2), p.328-333

2015

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MRI characteristics and scoring in HDLS due to CSF1R gene mutations

Neurology, 2012-08, Vol.79 (6), p.566-574

2012

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Autosomal dominant Parkinson's disease

Parkinsonism & related disorders, 2012, Vol.18, p.S7-S10

2012

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Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): A misdiagnosed disease entity

Journal of the neurological sciences, 2012-03, Vol.314 (1), p.130-137

2012

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

Multiple sclerosis and related disorders, 2019-06, Vol.31, p.148-150

2019

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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

Journal of neurology, 2013-10, Vol.260 (10), p.2665-2668

2013

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White matter disorders with autosomal dominant heredity: a review with personal clinical case studies and their MRI findings

Acta neurologica Scandinavica, 2010-05, Vol.121 (5), p.328-337

2010

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CSF1R Gene Screening In A Cohort Of 218 Primary Progressive Multiple Sclerosis (PPMS) Patients From The Norwegian And Swedish National PPMS Registries (S34.009)

Neurology, 2014-04, Vol.82 (10_supplement)

2014

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Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations

Parkinsonism & related disorders, 2013-10, Vol.19 (10), p.869-877

2013

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Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia

Acta neuropathologica, 2013-03, Vol.125 (3), p.425-438

2013

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A woman in her 70s with chronic walking difficulties

Tidsskrift for den Norske Lægeforening, 2015-10, Vol.135 (19), p.1753-1755

2015

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MRI Shows Unique Symmetrical Centrifugal Migration of a Low Diffusion Front from the Ventricular Horns in HDLS (P04.041)

Neurology, 2013-02, Vol.80 (7_supplement)

2013

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Update of the original HDLS kindred: divergent clinical courses

Acta neurologica Scandinavica, 2012-07, Vol.126 (1), p.67-75

2012

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Hereditary Diffuse Leukoencephalopathy with Spheroids with Phenotype of Primary Progressive MS

European journal of neurology, 2014-10, Vol.22 (2), p.328-333

2014

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Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics

Prophylactic Allogeneic Hematopoietic Stem Cell Therapy for CSF1R‐Related Leukoencephalopathy

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

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

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

Different Stages of White Matter Changes in the Original HDLS Family Revealed by Advanced MRI Techniques

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Morvan syndrome with Caspr2 antibodies. Clinical and autopsy report

CSF Markers of Inflammation and Neurodegeneration in Two Hereditary Diffuse Leukoencephalopathy with Spheroids (HDLS) Families with Diverging Genotype and Phenotype (P5.268)

Hereditary diffuse leukoencephalopathy with spheroids - a volumetric and radiological comparison with multiple sclerosis patients and healthy controls

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

Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis

MRI characteristics and scoring in HDLS due to CSF1R gene mutations

Autosomal dominant Parkinson's disease

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): A misdiagnosed disease entity

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

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

White matter disorders with autosomal dominant heredity: a review with personal clinical case studies and their MRI findings

CSF1R Gene Screening In A Cohort Of 218 Primary Progressive Multiple Sclerosis (PPMS) Patients From The Norwegian And Swedish National PPMS Registries (S34.009)

Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations

Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia

A woman in her 70s with chronic walking difficulties

MRI Shows Unique Symmetrical Centrifugal Migration of a Low Diffusion Front from the Ventricular Horns in HDLS (P04.041)

Update of the original HDLS kindred: divergent clinical courses

Hereditary Diffuse Leukoencephalopathy with Spheroids with Phenotype of Primary Progressive MS

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