Stéphanie Guey

INSERM

France

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Articles (18)

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2025

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2022

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2020

Collaborators (7)

Saskia A.J. Lesnik Oberstein

Leiden University Medical Center

NETHERLANDS

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Chaker ALOUI

Laureate Institute for Brain Research

FRANCE

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Minne Cerfontaine

Leiden University Medical Center

NETHERLANDS

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Sam Neilson

University of Glasgow

UNITED KINGDOM

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Hugues Chabriat

Professor of Neurology

Université Paris-Saclay

FRANCE

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Raj N. Kalaria

UNITED KINGDOM

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Hyunjin Kim

Assistant professor

Asan Medical Center

SOUTH KOREA

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Stéphanie Guey

Research Interests

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Articles (18)

ASSESSMENT OF RETINAL ARTERIOLAR TORTUOSITY IN PATIENTS WITH COL4A1 OR COL4A2 MUTATIONS.

Improving methodology of radiosurgery for posterior fossa cavernomas: higher volume, lower dose.

Disease Severity Staging System for NOTCH3-Associated Small Vessel Disease, Including CADASIL.

Determining Clinical Disease Progression in Symptomatic Patients With CADASIL.

Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System: A Multicentric Cohort Study.

CADA-PRO: A Patient Questionnaire Measuring Key Cognitive, Motor, Emotional, and Behavioral Outcomes in CADASIL.

Spinal Anterior Dural Dissection: Moving From Differential to Unifying Diagnosis.

Monogenic causes of cerebral small vessel disease and stroke.

Phenotypic variability in 446 CADASIL patients: Impact of NOTCH3 gene mutation location in addition to the effects of age, sex and vascular risk factors

Border-Zone Cerebral Infarcts Associated with COVID-19 in CADASIL: A Report of 3 Cases and Literature Review.

Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease.

Elderly CADASIL patients with intact neurological status

Trajectory Pattern of Cognitive Decline in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Natural history of Myhre syndrome.

Main features of <i>COL4A1-COL4A2</i> related cerebral microangiopathies.

Cerebrospinal Fluid Profile of Tau, Phosphorylated Tau, Aβ42, and Aβ40 in Probable Cerebral Amyloid Angiopathy.

Hereditary Cerebral Small Vessel Diseases and Stroke: A Guide for Diagnosis and Management.

Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome.

Collaborators (7)

Saskia A.J. Lesnik Oberstein

Chaker ALOUI

Minne Cerfontaine

Sam Neilson

Hugues Chabriat

Raj N. Kalaria

Hyunjin Kim

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