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Comparing the Prognostic Value of BAP1 Mutation Pattern, Chromosome 3 Status, and BAP1 Immunohistochemistry in Uveal Melanoma

The American journal of surgical pathology, 2016-06, Vol.40 (6), p.796-805

2016

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Integrated Genomic Classification of Melanocytic Tumors of the Central Nervous System Using Mutation Analysis, Copy Number Alterations, and DNA Methylation Profiling

Clinical cancer research, 2018-09, Vol.24 (18), p.4494-4504

2018

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Immunocytochemical analysis of glucose transporter protein-1 (GLUT-1) in typical, brain invasive, atypical and anaplastic meningioma

Neuropathology, 2015-02, Vol.35 (1), p.24-36

2015

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Comparison between optical coherence tomography imaging and histological sections of peripheral nerves

Journal of neurosurgery, 2021-01, Vol.134 (1), p.270-277

2021

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SF3B1 and BAP1 mutations in blue nevus-like melanoma

Modern pathology, 2017-07, Vol.30 (7), p.928-939

2017

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Activating cysteinyl leukotriene receptor 2 (CYSLTR2) mutations in blue nevi

Modern pathology, 2017-03, Vol.30 (3), p.350-356

2017

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Frequent GNAQ, GNA11, and EIF1AX Mutations in Iris Melanoma

Investigative ophthalmology & visual science, 2017-07, Vol.58 (9), p.3464-3470

2017

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Intraventricular melanocytoma diagnosis confirmed by gene mutation profile

Neuropathology, 2018-06, Vol.38 (3), p.288-292

2018

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Activating CYSLTR2 and PLCB4 Mutations in Primary Leptomeningeal Melanocytic Tumors

Journal of investigative dermatology, 2017-09, Vol.137 (9), p.2033-2035

2017

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Proliferation Activity Is Significantly Elevated in Partially Embolized Cerebral Arteriovenous Malformations

Cerebrovascular diseases (Basel, Switzerland), 2010-09, Vol.30 (4), p.396-401

2010

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MET overexpressing chordomas frequently exhibit polysomy of chromosome 7 but no MET activation through sarcoma-specific gene fusions

Tumor biology, 2010-06, Vol.31 (3), p.157-163

2010

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A broad spectrum of posterior reversible encephalopathy syndrome - a case series with clinical and paraclinical characterisation, and histopathological findings

BMC neurology, 2021-10, Vol.21 (1), p.1-386, Article 386

2021

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AVM resection after radiation therapy—clinico-morphological features and microsurgical results

Neurosurgical review, 2010-01, Vol.33 (1), p.53-61

2010

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Methylation analysis of SST and SSTR4 promoters in the neocortex of Alzheimer's disease patients

Neuroscience letters, 2014-04, Vol.566, p.241-246

2014

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Surgical treatment of primary intracranial myxoma in a child following radiotherapy: case report and review of the literature

Child's nervous system, 2010-06, Vol.26 (6), p.829-834

2010

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Never Too Old? Occurrence of Medulloblastoma in the Elderly beyond the 70th Year of Life

Case reports in neurological medicine, 2018-01, Vol.2018, p.8639404-4

2018

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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

Nature genetics, 2013-08, Vol.45 (8), p.933-936

2013

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Targeted next generation sequencing reveals unique mutation profile of primary melanocytic tumors of the central nervous system

Journal of neuro-oncology, 2016-05, Vol.127 (3), p.435-444

2016

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A 33‐Year‐Old Male with Five Years of Neck Pain

Brain pathology (Zurich, Switzerland), 2019-01, Vol.29 (1), p.141-142

2019

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New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

European journal of human genetics : EJHG, 2017-08, Vol.25 (8), p.935-945

2017

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Genetic and clinico-pathologic analysis of metastatic uveal melanoma

Modern pathology, 2014-02, Vol.27 (2), p.175-183

2014

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Absence of TERT promoter mutations in primary melanocytic tumours of the central nervous system

Neuropathology and applied neurobiology, 2014-10, Vol.40 (6), p.794-797

2014

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Diagnosing a Primary Leptomeningeal Melanoma by Gene Mutation Signature

Journal of investigative dermatology, 2016-07, Vol.136 (7), p.1526-1528

2016

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A 68-Year Old Man with A Cerebellopontine Angle Tumor

Brain pathology (Zurich, Switzerland), 2013-07, Vol.23 (4), p.483-484

2013

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A 32-year-old male with brainstem lesions

Brain pathology (Zurich, Switzerland), 2013-01, Vol.23 (1), p.101-104

2013

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Comparing the Prognostic Value of BAP1 Mutation Pattern, Chromosome 3 Status, and BAP1 Immunohistochemistry in Uveal Melanoma

Integrated Genomic Classification of Melanocytic Tumors of the Central Nervous System Using Mutation Analysis, Copy Number Alterations, and DNA Methylation Profiling

Immunocytochemical analysis of glucose transporter protein-1 (GLUT-1) in typical, brain invasive, atypical and anaplastic meningioma

Comparison between optical coherence tomography imaging and histological sections of peripheral nerves

SF3B1 and BAP1 mutations in blue nevus-like melanoma

Activating cysteinyl leukotriene receptor 2 (CYSLTR2) mutations in blue nevi

Frequent GNAQ, GNA11, and EIF1AX Mutations in Iris Melanoma

Intraventricular melanocytoma diagnosis confirmed by gene mutation profile

Activating CYSLTR2 and PLCB4 Mutations in Primary Leptomeningeal Melanocytic Tumors

Proliferation Activity Is Significantly Elevated in Partially Embolized Cerebral Arteriovenous Malformations

MET overexpressing chordomas frequently exhibit polysomy of chromosome 7 but no MET activation through sarcoma-specific gene fusions

A broad spectrum of posterior reversible encephalopathy syndrome - a case series with clinical and paraclinical characterisation, and histopathological findings

AVM resection after radiation therapy—clinico-morphological features and microsurgical results

Methylation analysis of SST and SSTR4 promoters in the neocortex of Alzheimer's disease patients

Surgical treatment of primary intracranial myxoma in a child following radiotherapy: case report and review of the literature

Never Too Old? Occurrence of Medulloblastoma in the Elderly beyond the 70th Year of Life

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

Targeted next generation sequencing reveals unique mutation profile of primary melanocytic tumors of the central nervous system

A 33‐Year‐Old Male with Five Years of Neck Pain

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

Genetic and clinico-pathologic analysis of metastatic uveal melanoma

Absence of TERT promoter mutations in primary melanocytic tumours of the central nervous system

Diagnosing a Primary Leptomeningeal Melanoma by Gene Mutation Signature

A 68-Year Old Man with A Cerebellopontine Angle Tumor

A 32-year-old male with brainstem lesions

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