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Publications by Emmanuel Cognat

Response to Letter Regarding Article, "Archetypal Arg169Cys Mutation in NOTCH3 Does Not Drive the Pathogenesis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leucoencephalopathy via a Loss-Of-Function Mechanism"

Stroke

Cardiology

Neurology

Cardiovascular Medicine

English

Early White Matter Changes in CADASIL: Evidence of Segmental Intramyelinic Oedema in a Pre-Clinical Mouse Model

Acta neuropathologica communications

Forensic Medicine

Molecular Neuroscience

English

Related publications

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

2005

English

Response to Letters Regarding Article, "Peripheral Artery Disease as a Manifestation of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) and Practical Implications"

Circulation

Cardiovascular Medicine

Physiology

Cardiology

2013

English

Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Stroke

Cardiology

Neurology

Cardiovascular Medicine

English

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) and CADASIL-like Disorders in Japan

Internal Medicine

Medicine

2001

English

Shape and Volume of Lacunar Infarcts: A 3D MRI Study in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Stroke

Cardiology

Neurology

Cardiovascular Medicine

English

Cardiac Autonomic Nervous System and Risk of Arrhythmias in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)

Stroke

Cardiology

Neurology

Cardiovascular Medicine

English

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Progression of MR Abnormalities in Prospective 7-Year Follow-Up Study

English

Abnormal Vasoconstrictor Responses to Angiotensin II and Noradrenaline in Isolated Small Arteries From Patients With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)

Stroke

Cardiology

Neurology

Cardiovascular Medicine

English

Loss-Of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Emmanuel Cognat

Response to Letter Regarding Article, "Archetypal Arg169Cys Mutation in NOTCH3 Does Not Drive the Pathogenesis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leucoencephalopathy via a Loss-Of-Function Mechanism"

Early White Matter Changes in CADASIL: Evidence of Segmental Intramyelinic Oedema in a Pre-Clinical Mouse Model

Related publications

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Response to Letters Regarding Article, "Peripheral Artery Disease as a Manifestation of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) and Practical Implications"

Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) and CADASIL-like Disorders in Japan

Shape and Volume of Lacunar Infarcts: A 3D MRI Study in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Cardiac Autonomic Nervous System and Risk of Arrhythmias in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Progression of MR Abnormalities in Prospective 7-Year Follow-Up Study

Abnormal Vasoconstrictor Responses to Angiotensin II and Noradrenaline in Isolated Small Arteries From Patients With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)

Loss-Of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes