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Age-related iron deposition in the basal ganglia: quantitative analysis in healthy subjects

Radiology, 2009-07, Vol.252 (1), p.165-172

2009

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The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature review

Journal of the neurological sciences, 2016-05, Vol.364, p.77-83

2016

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Case 159: cerebral amyloid angiopathy-related inflammation

Radiology, 2010-07, Vol.256 (1), p.323-327

2010

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Angiographically proven cervical venous engorgement: a possible concurrent cause in the pathophysiology of Hirayama’s myelopathy

Neurological sciences, 2010-12, Vol.31 (6), p.845-848

2010

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Brainstem signs with progressing atrophy of medulla oblongata and upper cervical spinal cord

Lancet neurology, 2007-06, Vol.6 (6), p.562-570

2007

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Marjorie LeMay

American journal of roentgenology (1976), 2009-09, Vol.193 (3), p.906-907

Savoiardo, Mario

2009

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Anti-amyloid β autoantibodies in cerebral amyloid angiopathy-related inflammation: Implications for amyloid-modifying therapies

Annals of neurology, 2013-04, Vol.73 (4), p.449-458

2013

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Novel (ovario) leukodystrophy related to AARS2 mutations

Neurology, 2014-06, Vol.82 (23), p.2063-2071

2014

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Iron-related MRI images in patients with pantothenate kinase-associated neurodegeneration (PKAN) treated with deferiprone: Results of a phase II pilot trial

Movement disorders, 2011-08, Vol.26 (9), p.1755-1759

2011

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MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

American journal of neuroradiology : AJNR, 2000-09, Vol.21 (8), p.1478-1482

2000

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Combined treatment with oral metronidazole and N -acetylcysteine is effective in ethylmalonic encephalopathy

Nature medicine, 2010-08, Vol.16 (8), p.869-871

2010

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Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

Neurology, 2014-09, Vol.83 (13), p.1217-1218

2014

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Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

Brain (London, England : 1878), 2008-09, Vol.131 (9), p.2321-2331

2008

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Spontaneous intracranial hypotension with deep brain swelling

Brain (London, England : 1878), 2007-07, Vol.130 (7), p.1884-1893

2007

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Prodromal Alzheimer's disease presenting as cerebral amyloid angiopathy-related inflammation with spontaneous amyloid-related imaging abnormalities and high cerebrospinal fluid anti-Aβ autoantibodies

Journal of Alzheimer's disease, 2015-01, Vol.45 (2), p.363-367

2015

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Brain fluorodeoxyglucose PET in adrenoleukodystrophy

Neurology, 2014-09, Vol.83 (11), p.981-989

2014

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Prognostic factors for survival in 676 consecutive patients with newly diagnosed primary glioblastoma

Neuro-oncology (Charlottesville, Va.), 2008-02, Vol.10 (1), p.79-87

2008

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A 52-Year-Old Man with Myoclonic Jerks

Brain pathology (Zurich, Switzerland), 2016-03, Vol.26 (2), p.291-292

2016

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Schizencephaly: Neuroradiologic and Epileptologic Findings

Epilepsia (Copenhagen), 1996-12, Vol.37 (12), p.1185-1193

1996

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Constrained spherical deconvolution-based tractography to depict and characterize a case of “hyperplastic fornix dorsalis”

Magnetic resonance imaging, 2014-12, Vol.32 (10), p.1428-1433

2014

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Superficial siderosis due to dural defect with thoracic spinal cord herniation

Journal of the neurological sciences, 2012-01, Vol.312 (1), p.170-172

2012

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Frontal cortex BOLD signal changes in premanifest Huntington disease: a possible fMRI biomarker

Neurology, 2014-07, Vol.83 (1), p.65-72

2014

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Sagging and swelling of the midbrain suggest spontaneous intracranial hypotension rather than a malformation

Brain (London, England : 1878), 2010-08, Vol.133 (8), p.e148-e148

2010

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Case 159

Radiology, 2010-03, Vol.254 (3), p.982-984

2010

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Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant

Orphanet journal of rare diseases, 2013-05, Vol.8 (1), p.66-66, Article 66

2013

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Age-related iron deposition in the basal ganglia: quantitative analysis in healthy subjects

The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature review

Case 159: cerebral amyloid angiopathy-related inflammation

Angiographically proven cervical venous engorgement: a possible concurrent cause in the pathophysiology of Hirayama’s myelopathy

Brainstem signs with progressing atrophy of medulla oblongata and upper cervical spinal cord

Marjorie LeMay

Anti-amyloid β autoantibodies in cerebral amyloid angiopathy-related inflammation: Implications for amyloid-modifying therapies

Novel (ovario) leukodystrophy related to AARS2 mutations

Iron-related MRI images in patients with pantothenate kinase-associated neurodegeneration (PKAN) treated with deferiprone: Results of a phase II pilot trial

MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

Combined treatment with oral metronidazole and N -acetylcysteine is effective in ethylmalonic encephalopathy

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

Spontaneous intracranial hypotension with deep brain swelling

Prodromal Alzheimer's disease presenting as cerebral amyloid angiopathy-related inflammation with spontaneous amyloid-related imaging abnormalities and high cerebrospinal fluid anti-Aβ autoantibodies

Brain fluorodeoxyglucose PET in adrenoleukodystrophy

Prognostic factors for survival in 676 consecutive patients with newly diagnosed primary glioblastoma

A 52-Year-Old Man with Myoclonic Jerks

Schizencephaly: Neuroradiologic and Epileptologic Findings

Constrained spherical deconvolution-based tractography to depict and characterize a case of “hyperplastic fornix dorsalis”

Superficial siderosis due to dural defect with thoracic spinal cord herniation

Frontal cortex BOLD signal changes in premanifest Huntington disease: a possible fMRI biomarker

Sagging and swelling of the midbrain suggest spontaneous intracranial hypotension rather than a malformation

Case 159

Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant

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