Lista de obras - Elisabeth Tournier-Lasserve

A case of late-onset CADASIL with interhemispheric disconnection features

article

A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French Caucasians

artículo científico publicado en 2001

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p

article

A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region

artículo científico publicado en 1996

A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13.

artículo científico publicado en 2012

A novel hereditary small vessel disease of the brain

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

artículo científico publicado en 2015

APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review

artículo científico publicado en 2016

ATP1A2 mutations in 11 families with familial hemiplegic migraine

artículo científico publicado en 2005

Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain

artículo científico publicado en 2008

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

artículo científico publicado en 2014

Advances in stroke: genetics 2012.

artículo científico publicado en 2013

Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristics.

artículo científico publicado en 2002

Antithrombotic therapy and bleeding risk in a prospective cohort study of patients with cerebral cavernous malformations

artículo científico publicado en 2012

Apports de la génétique moléculaire dans les angiomes caverneux

Autoimmune diseases in families of French patients with multiple sclerosis

article

Bases immunogénétiques du lupus systémique chez l'homme

artículo científico publicado en 1998

Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family

C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing

artículo científico publicado en 2013

CADASIS. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalophathy

artículo científico publicado el 1 de julio de 1997

CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletions

CCM1-ICAP-1 complex controls β1 integrin-dependent endothelial contractility and fibronectin remodeling

artículo científico publicado en 2013

CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas

artículo científico publicado en 2013

COL4A1 mutation in a patient with sporadic, recurrent intracerebral hemorrhage

artículo científico publicado en 2007

COL4A1 mutation revealed by an isolated brain hemorrhage.

artículo científico publicado en 2013

COL4A1 mutations associated with a characteristic pattern of intracranial calcification

artículo científico publicado en 2011

COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy

artículo científico publicado en 2014

CSF1R-related leukoencephalopathy mimicking primary progressive multiple sclerosis.

artículo científico publicado en 2016

Cadasil

artículo científico publicado en 2009

Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation

artículo científico publicado en 2013

Can whole-exome sequencing data be used for linkage analysis?

artículo científico publicado en 2015

Cerebral Cavernous Malformation-1 Protein Controls DLL4-Notch3 Signaling Between the Endothelium and Pericytes

artículo científico publicado en 2015

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

artículo científico publicado en 1993

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family ⬇️

artículo científico publicado el 1 de agosto de 1995

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: from stroke to vessel wall physiology

artículo científico publicado en 2001

Cerebral cavernous malformations arise independent of the heart of glass receptor

artículo científico publicado en 2014

Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene.

artículo científico publicado en 2015

Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasis

artículo científico publicado en 2013

Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene

artículo científico publicado en 2015

Clinical and brain MRI follow-up study of a family with COL4A1 mutation

artículo científico publicado en 2007

Clinical features of cerebral cavernous malformations patients with KRIT1 mutations

artículo científico publicado en 2004

Cognitive alterations in non-demented CADASIL patients

artículo científico publicado en 1998

De novo mutation in theNotch3 gene causing CADASIL

artículo científico publicado en 2000

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

article

De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy

artículo científico publicado en 2017

Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations

artículo científico publicado en 2013

Defective vascular integrity upon KRIT1/ICAP-1 complex loss in CCM correlates with aberrant beta 1 integrin-dependent extracellular matrix remodeling

article published in 2012

Developmental timing of CCM2 loss influences cerebral cavernous malformations in mice

artículo científico publicado en 2011

Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening.

artículo científico publicado en 1998

Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy

artículo científico publicado en 2016

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain

artículo científico publicado en 2009

Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.

artículo científico publicado en 2009

EndMT contributes to the onset and progression of cerebral cavernous malformations

artículo científico publicado en 2013

Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood

artículo científico publicado en 2009

Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q ⬇️

artículo científico publicado el 1 de julio de 1997

Familial central retinal vein occlusion.

artículo científico publicado en 2006

Familial cluster headache: a series of 186 index patients

artículo científico publicado en 2002

Familial form of typical childhood absence epilepsy in a consanguineous context

artículo científico publicado en 2010

Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)

article by Michael Hutchinson et al published November 1995 in Annals of Neurology

Familial lupus erythematosus. Clinical and immunologic features of 125 multiplex families

artículo científico publicado en 2001

Familial occurrence and heritable connective tissue disorders in cervical artery dissection

artículo científico publicado en 2014

Fetal intracerebral hemorrhage and cataract: think COL4A1

artículo científico publicado en 2014

Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations.

artículo científico publicado en 2009

Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study

artículo científico publicado en 2006

Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families

artículo científico publicado en 1999

Genetic syndromes that mimic congenital infections: report of 2 cases

artículo científico publicado en 2011

Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

artículo científico publicado en 2014

Genotype-phenotype correlations in cerebral cavernous malformations patients

artículo científico publicado en 2006

HEREDITARY PAROXYSMAL ATAXIAS

Healthy monozygous twins do not recognize identical T cell epitopes on the myelin basic protein autoantigen

artículo científico publicado en 1994

Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie

artículo científico publicado en 1998

Hereditary episodic ataxia

artículo científico publicado en 2011

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease

artículo científico publicado en 2015

Human T cell response to myelin basic protein: Is the T cell repertoire different in multiple sclerosis patients and healthy subjects?

Human T-Cell Response to Human and Heterologous Myelin Basic Proteins

artículo científico publicado en 1988

Human T-cell response to myelin basic protein in multiple sclerosis patients and healthy subjects

article

Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation

scientific article published on 01 March 2014

Identification of CACNA1A large deletions in four patients with episodic ataxia

artículo científico publicado en 2009

Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy

artículo científico publicado en 2005

Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy

artículo científico publicado en 2004

In vivo clonal expression of T lymphocytes specific for an immunodominant N-terminal myelin basic protein epitope in healthy individuals.

artículo científico publicado en 1995

Intracerebral hemorrhage and COL4A1 mutations, from preterm infants to adult patients

artículo científico publicado en 2009

Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult

artículo científico publicado en 2002

Lack of association between thrombosis in primary antiphospholipid syndrome and the recently described thrombophilic 3'-untranslated prothrombin gene polymorphism

artículo científico publicado el 1 de noviembre de 1997

Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton

scientific journal article

Large CACNA1A deletion in a family with episodic ataxia type 2.

artículo científico publicado en 2008

Late diagnosis of COL4A1 mutation and problematic vascular risk factor management.

artículo científico publicado en 2014

Late onset hereditary episodic ataxia

artículo científico publicado en 2009

Long-term improvement of paroxysmal dystonic choreathetosis with acetazolamide

Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoya

artículo científico publicado en 2011

Loss of α1β1 Soluble Guanylate Cyclase, the Major Nitric Oxide Receptor, Leads to Moyamoya and Achalasia.

artículo científico publicado en 2014

Loss of α1β1 soluble guanylate cyclase, the major nitric oxide receptor, leads to moyamoya and achalasia

artículo científico publicado en 2014

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

artículo científico publicado en 1997

Migraine With Aura and Brain Magnetic Resonance Imaging Abnormalities in Patients With CADASIL

article by Katayoun Vahedi et al published 1 August 2004 in Archives of Neurology

Migraine hémiplégique familiale

scholarly article published January 2004

Missense CACNA1A mutation causing episodic ataxia type 2

artículo científico publicado en 2001

Moyamoya disease and syndromes: from genetics to clinical management

artículo científico publicado en 2015

Multiple cerebral cavernous malformations and a novel CCM3 germline deletion in a German family

artículo científico publicado en 2010

Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy

artículo científico publicado en 2015

Mutations within the MGC4607 gene cause cerebral cavernous malformations

artículo científico publicado en 2004

Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations

artículo científico publicado en 2005

Natural history of cerebral dot-like cavernomas

artículo científico publicado en 2013

Network-based analysis of omics data: the LEAN method

artículo científico publicado en 2016

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus

artículo científico publicado en 2004

New players in the genetics of stroke

artículo científico publicado en 2002

Notch signalling pathway and human diseases

artículo científico publicado en 1998

Notch3 is required for arterial identity and maturation of vascular smooth muscle cells

artículo científico publicado en 2004

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

artículo científico publicado en 1996

Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia

artículo científico publicado en 1997

Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1.

artículo científico publicado en 2015

PDGFB Partial Deletion: a New, Rare Mechanism Causing Brain Calcification with Leukoencephalopathy

article by Gaël Nicolas et al published 7 March 2014 in Journal of Molecular Neuroscience

Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway

artículo científico publicado en 2004

Patterns of MRI lesions in CADASIL ⬇️

artículo científico publicado el 1 de agosto de 1998

Patterns of expression of the three cerebral cavernous malformation (CCM) genes during embryonic and postnatal brain development

artículo científico publicado en 2006

Phenotypic variability of episodic ataxia type 2 mutations: a family study

artículo científico publicado en 2010

Presymptomatic genetic testing in CADASIL.

artículo científico publicado en 2012

Prevalence of serum antibodies to hepatitis C virus is not increased in patients with multiple sclerosis.

artículo científico publicado en 1996

Primary antiphospholipid syndrome is not associated with activated protein C resistance caused by factor V Arg 506 -->Gln mutation

artículo científico publicado el 1 de junio de 1995

Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy

artículo científico publicado en 2013

Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians.

artículo científico publicado en 2017

Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.

artículo científico publicado en 2010

Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1

article

Regulation of β1 integrin-Klf2-mediated angiogenesis by CCM proteins.

artículo científico publicado en 2015

Research Progresses in Understanding the Pathophysiology of Moyamoya Disease

artículo científico publicado en 2016

Retinal ischemic syndrome, digestive tract small-vessel hyalinosis, and diffuse cerebral calcifications: a pediatric observation of a rare syndrome

artículo científico publicado en 2005

Role of COL4A1 in small-vessel disease and hemorrhagic stroke

artículo científico publicado en 2006

Rôle du canal calcique P/Q dans la migraine hémiplégique familiale

article by Norbert Weiss et al published January 2007 in Médecine/sciences

Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation

artículo científico publicado en 2008

Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis

artículo científico publicado en 2001

Spanish families with cavernous angiomas do not share the Hispano-American CCM1 haplotype

artículo científico publicado en 1999

Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations

artículo científico publicado en 2002

Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation

artículo científico publicado en 2009

Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

artículo científico publicado en 2001

Stroke-related translational research.

artículo científico publicado en 2011

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

artículo científico publicado en 1997

Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations: Consensus Recommendations Based on Systematic Literature Review by the Angioma Alliance Scientific Advisory Board Clinical Experts Panel

artículo científico publicado en 2017

T cell response to myelin basic protein epitopes in multiple sclerosis patients and healthy subjects

article

TREX1 Mutation in Leukodystrophy with Calcifications and Persistent Gadolinium-Enhancement

article published in 2016

The R131 low-affinity allele of the Fc gamma RIIA receptor is associated with systemic lupus erythematosus but not with other autoimmune diseases in French Caucasians

article

The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo

artículo científico publicado en 2007

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

artículo científico publicado en 2001

The control of vascular integrity by endothelial cell junctions: molecular basis and pathological implications

scientific article published on February 2009

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

artículo científico publicado en 2000

The genetics of migraine

artículo científico publicado en 2002

Tissue-specific conditional CCM2 knockout mice establish the essential role of endothelial CCM2 in angiogenesis: implications for human cerebral cavernous malformations

artículo científico publicado en 2009

Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

artículo científico publicado en 2003

Lista de obras de Elisabeth Tournier-Lasserve

A case of late-onset CADASIL with interhemispheric disconnection features

A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French Caucasians

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p

A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region

A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13.

A novel hereditary small vessel disease of the brain

APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL

APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review

ATP1A2 mutations in 11 families with familial hemiplegic migraine

Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

Advances in stroke: genetics 2012.

Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristics.

Antithrombotic therapy and bleeding risk in a prospective cohort study of patients with cerebral cavernous malformations

Apports de la génétique moléculaire dans les angiomes caverneux

Autoimmune diseases in families of French patients with multiple sclerosis

Bases immunogénétiques du lupus systémique chez l'homme

Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family

C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing

CADASIS. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalophathy

CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletions

CCM1-ICAP-1 complex controls β1 integrin-dependent endothelial contractility and fibronectin remodeling

CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas

COL4A1 mutation in a patient with sporadic, recurrent intracerebral hemorrhage

COL4A1 mutation revealed by an isolated brain hemorrhage.

COL4A1 mutations associated with a characteristic pattern of intracranial calcification

COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy

CSF1R-related leukoencephalopathy mimicking primary progressive multiple sclerosis.

Cadasil

Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation

Can whole-exome sequencing data be used for linkage analysis?

Cerebral Cavernous Malformation-1 Protein Controls DLL4-Notch3 Signaling Between the Endothelium and Pericytes

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family ⬇️

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: from stroke to vessel wall physiology

Cerebral cavernous malformations arise independent of the heart of glass receptor

Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene.

Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasis

Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene

Clinical and brain MRI follow-up study of a family with COL4A1 mutation

Clinical features of cerebral cavernous malformations patients with KRIT1 mutations

Cognitive alterations in non-demented CADASIL patients

De novo mutation in theNotch3 gene causing CADASIL

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy

Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations

Defective vascular integrity upon KRIT1/ICAP-1 complex loss in CCM correlates with aberrant beta 1 integrin-dependent extracellular matrix remodeling

Developmental timing of CCM2 loss influences cerebral cavernous malformations in mice

Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening.

Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain

Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.

EndMT contributes to the onset and progression of cerebral cavernous malformations

Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood

Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q ⬇️

Familial central retinal vein occlusion.

Familial cluster headache: a series of 186 index patients

Familial form of typical childhood absence epilepsy in a consanguineous context

Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)

Familial lupus erythematosus. Clinical and immunologic features of 125 multiplex families

Familial occurrence and heritable connective tissue disorders in cervical artery dissection

Fetal intracerebral hemorrhage and cataract: think COL4A1

Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations.

Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study

Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families

Genetic syndromes that mimic congenital infections: report of 2 cases

Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

Genotype-phenotype correlations in cerebral cavernous malformations patients

HEREDITARY PAROXYSMAL ATAXIAS

Healthy monozygous twins do not recognize identical T cell epitopes on the myelin basic protein autoantigen

Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie

Hereditary episodic ataxia

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease

Human T cell response to myelin basic protein: Is the T cell repertoire different in multiple sclerosis patients and healthy subjects?

Human T-Cell Response to Human and Heterologous Myelin Basic Proteins

Human T-cell response to myelin basic protein in multiple sclerosis patients and healthy subjects

Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation

Identification of CACNA1A large deletions in four patients with episodic ataxia

Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy