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Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk

Journal of lipid research, 2011-11, Vol.52 (11), p.1885-1926

2011

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Somatostatin Receptor PET/MR Imaging of Inflammation in Patients With Large Vessel Vasculitis and Atherosclerosis

Journal of the American College of Cardiology, 2023-01, Vol.81 (4), p.336-354

2023

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Periocular Amyloidosis Manifesting as Pseudopemphigoid Treated With Mitomycin C

Cornea, 2017-04, Vol.36 (4), p.518-520

2017

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Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 Mutations

Journal of neuropathology and experimental neurology, 2015-07, Vol.74 (7), p.688-703

2015

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Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

Journal of general virology, 2007-03, Vol.88 (3), p.1068-1072

2007

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Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?

Journal of neurology, neurosurgery and psychiatry, 2007-07, Vol.78 (7), p.750-753

2007

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'Radiologically compatible CLIPPERS' may conceal a number of pathologies

Brain (London, England : 1878), 2011-08, Vol.134 (8), p.e187-e187

2011

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Giant intracranial hemangioma in a neonate

Acta neurochirurgica, 2014-06, Vol.156 (6), p.1151-1154

2014

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Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

HGG advances, 2022-04, Vol.3 (2), p.100097-100097, Article 100097

2022

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Internal auditory canal metastasis mimicking a vestibular schwannoma at presentation - a case report and review of the literature

International seminars in surgical oncology, 2009-03, Vol.6 (8), p.8-8, Article 8

2009

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Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNAGlu (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Journal of neuropathology and experimental neurology, 2013-02, Vol.72 (2), p.164-175

2013

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The genome of the sparganosis tapeworm Spirometra erinaceieuropaei isolated from the biopsy of a migrating brain lesion

Genome biology, 2014, Vol.15 (11), p.510-510

2014

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Atypical Presentation of Low-Grade Small Lymphocytic Lymphoma of the Lacrimal Sac

Ophthalmic plastic and reconstructive surgery, 2015-11, Vol.31 (6), p.e163-e165

2015

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A 73 Year-Old Man with a Mass at the Foramen Magnum

Brain pathology (Zurich, Switzerland), 2013-11, Vol.23 (6), p.699-702

2013

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Reversible parkinsonism in a patient with progressive multifocal leucoencephalopathy

Journal of neurology, neurosurgery and psychiatry, 2007-04, Vol.78 (4), p.408-410

2007

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The genome of the sparganosis tapeworm Spirometra erinaceieuropaeiisolated from the biopsy of a migrating brain lesion

Genome biology, 2014-11, Vol.15 (11), Article 510

2014

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Extracellular matrix-modulated differential invasion of human meningioma cell lines in vitro

Neuroscience letters, 1999-03, Vol.263 (2), p.214-216

1999

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Chromosomal imbalances in meningeal solitary fibrous tumors

Cancer genetics and cytogenetics, 2002-06, Vol.135 (2), p.160-164

2002

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Histologic, molecular, and radiologic characterization of resolving cerebral posttransplant lymphoproliferative disorder

Pediatric research, 1997-05, Vol.41 (5), p.651-656

1997

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Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA Glu ( MT - TE ) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Journal of neuropathology and experimental neurology, 2013-02, Vol.72 (2), p.164-175

2013

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Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA^sup Glu^ (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Journal of neuropathology and experimental neurology, 2013-02, Vol.72 (2), p.164

2013

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Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA super( Glu) (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Journal of neuropathology and experimental neurology, 2013-02, Vol.72 (2), p.164-164

2013

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Solitary fibrous tumours of the meninges : case series and literature review

Journal of neuro-oncology, 2001-08, Vol.54 (1), p.57-69

2001

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'Radiologically compatible CLIPPERS' may conceal a number of pathologies

Brain : a journal of neurology, 2011, Vol.134, p.e187-e187

2011

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THE CLASSICAL INVESTIGATION

Journal of education (Boston, Mass.), 1923-08, Vol.98 (5 (2441)), p.122-122

WEST, DEAN ANDREW F.

1923

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Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk

Somatostatin Receptor PET/MR Imaging of Inflammation in Patients With Large Vessel Vasculitis and Atherosclerosis

Periocular Amyloidosis Manifesting as Pseudopemphigoid Treated With Mitomycin C

Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 Mutations

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?

'Radiologically compatible CLIPPERS' may conceal a number of pathologies

Giant intracranial hemangioma in a neonate

Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

Internal auditory canal metastasis mimicking a vestibular schwannoma at presentation - a case report and review of the literature

Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNAGlu (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

The genome of the sparganosis tapeworm Spirometra erinaceieuropaei isolated from the biopsy of a migrating brain lesion

Atypical Presentation of Low-Grade Small Lymphocytic Lymphoma of the Lacrimal Sac

A 73 Year-Old Man with a Mass at the Foramen Magnum

Reversible parkinsonism in a patient with progressive multifocal leucoencephalopathy

The genome of the sparganosis tapeworm Spirometra erinaceieuropaeiisolated from the biopsy of a migrating brain lesion

Extracellular matrix-modulated differential invasion of human meningioma cell lines in vitro

Chromosomal imbalances in meningeal solitary fibrous tumors

Histologic, molecular, and radiologic characterization of resolving cerebral posttransplant lymphoproliferative disorder

Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA Glu ( MT - TE ) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA^sup Glu^ (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA super( Glu) (MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study

Solitary fibrous tumours of the meninges : case series and literature review

'Radiologically compatible CLIPPERS' may conceal a number of pathologies

THE CLASSICAL INVESTIGATION

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