FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Anne Joutel

Research Profile

Chemicals & Drugs

Disorders

Physiology

Mutation

Concepts & Ideas

Anatomy

Living Beings

Procedures

Chromosome Mapping

Co-author Network

Publications

TOP 3
Charles Fouillade; Richard Huganir; Céline Baron-Menguy; Valérie Domenga-Denier; Kogo Takamiya; Christelle Thibault; Anne Joutel
Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculature.
Charles Fouillade; Céline Baron-Menguy; Marie Monet-Leprêtre; Anne Joutel
Notch signalling in smooth muscle cells during development and disease.
Louis R Caplan; Steven C Cramer; Anne Joutel; Eng H Lo; James Meschia; Sean Savitz; Juan Arenillas; Elizabeth Tournier-Lasserve
Stroke-related translational research.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Anne Joutel (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Charles Fouillade; Richard Huganir; Céline Baron-Menguy; Valérie Domenga-Denier; Kogo Takamiya; Christelle Thibault; Anne Joutel
Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculature.
Arteriosclerosis, thrombosis, and vascular biology 2013;33(1):76-86.
2012: Charles Fouillade; Céline Baron-Menguy; Marie Monet-Leprêtre; Anne Joutel
Notch signalling in smooth muscle cells during development and disease.
Cardiovascular research 2012;95(2):138-46.
2011: Louis R Caplan; Steven C Cramer; Anne Joutel; Eng H Lo; James Meschia; Sean Savitz; Juan Arenillas; Elizabeth Tournier-Lasserve
Stroke-related translational research.
Archives of neurology 2011;68(9):1110-23.
2011: Nada Boulos; Frank Helle; Jean-Claude Dussaule; Sandrine Placier; Paul Milliez; Sonja Djudjaj; Dominique GUERROT; Anne Joutel; Pierre Ronco; Jean-Jacques Boffa; Christos Chatziantoniou
Notch3 is essential for regulation of the renal vascular tone.
Hypertension 2011;57(6):1176-82.
2011: Katharina Eikermann-Haerter; Izumi Yuzawa; Ergin Dilekoz; Anne Joutel; Michael A Moskowitz; Cenk Ayata
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression.
Annals of neurology 2011;69(2):413-8.
2011: Anne Joutel; Stéphanie Debette
Mendelian and complex causes of migraine: bridging the gap.
Cephalalgia : an international journal of headache 2011;31(3):259-61.
2011: Anne Joutel
Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature.
BioEssays : news and reviews in molecular, cellular and developmental biology 2011;33(1):73-80.
2010: Anne Joutel; Marie Monet-Leprêtre; Claudia Gosele; Céline Baron-Menguy; Annette Hammes; Sabine Schmidt; Barbara Lemaire-Carrette; Valérie Domenga; Andreas Schedl; Pierre Lacombe; Norbert Hubner
Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease.
The Journal of clinical investigation 2010;120(2):433-45.
2009: Hugues Chabriat; Anne Joutel; Martin Dichgans; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
Cadasil.
Lancet neurology 2009;8(7):643-53.
2009: Marie Monet-Leprêtre; Boris Bardot; Barbara Lemaire; Valérie Domenga; Ophélia Godin; Martin Dichgans; Elisabeth Tournier-Lasserve; Michel Cohen-Tannoudji; Hugues Chabriat; Anne Joutel
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.
Brain : a journal of neurology 2009;132(Pt 6):1601-12.
2009: Saara Tikka; Kati Mykkänen; Marie-Magdeleine Ruchoux; Robert Bergholm; Maija Junna; Minna Pöyhönen; Hannele Yki-Järvinen; Anne Joutel; Matti Viitanen; Marc Baumann; Hannu Kalimo
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.
Brain : a journal of neurology 2009;132(Pt 4):933-9.
2008: Charles Fouillade; Hugues Chabriat; Florence Riant; Manuèle Mine; Minh Arnoud; Laurent Magy; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve; Anne Joutel
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain.
Human mutation 2008;29(3):452.
2007: Marie Monet; Valérie Domenga; Barbara Lemaire; Céline Souilhol; Francina Langa; Charles Babinet; Thomas Gridley; Elisabeth Tournier-Lasserve; Michel Cohen-Tannoudji; Anne Joutel
The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo.
Human molecular genetics 2007;16(8):982-92.
2006: Céline Souilhol; Sarah Cormier; Marie Monet; Sandrine Vandormael-Pournin; Anne Joutel; Charles Babinet; Michel Cohen-Tannoudji
Nas transgenic mouse line allows visualization of Notch pathway activity in vivo.
Genesis (New York, N.Y. : 2000) 2006;44(6):277-86.
2006: Steve Verreault; Anne Joutel; Florence Riant; Georgina Neves; Mario Rui Silva; Jacqueline Maciazek; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser; Hugues Chabriat
A novel hereditary small vessel disease of the brain.
Annals of neurology 2006;59(2):353-7.
2006: Chiho Ishida; Ken-ichi Sakajiri; Mitsuhiro Yoshita; Anne Joutel; Florence Cave-Riant; Masahito Yamada
CADASIL with a novel mutation in exon 7 of NOTCH3 (C388Y).
Internal medicine (Tokyo, Japan) 2006;45(16):981-5.
2005: Pierre Lacombe; Charleen Oligo; Valérie Domenga; Elisabeth Tournier-Lasserve; Anne Joutel
Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy.
Stroke; a journal of cerebral circulation 2005;36(5):1053-8.
2005: Caroline Dubroca; Pierre Lacombe; Valérie Domenga; Jacqueline Maciazek; Bernard Levy; Elisabeth Tournier-Lasserve; Anne Joutel; Daniel Henrion
Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy.
Stroke; a journal of cerebral circulation 2005;36(1):113-7.
2004: Valérie Domenga; Peggy Fardoux; Pierre Lacombe; Marie Monet; Jacqueline Maciazek; Luke T Krebs; Bernard Klonjkowski; Eliane Berrou; Mathias Mericskay; Zhen Li; Elisabeth Tournier-Lasserve; Thomas Gridley; Anne Joutel
Notch3 is required for arterial identity and maturation of vascular smooth muscle cells.
Genes & development 2004;18(22):2730-5.
2004: Katayoun Vahedi; Hugues Chabriat; Claude Levy; Anne Joutel; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL.
Archives of neurology 2004;61(8):1237-40.
2004: Christian Denier; Pierre Labauge; Laurent Brunereau; Florence Cavé-Riant; Florence Marchelli; Minh Arnoult; Michaelle Cecillon; Jacqueline Maciazek; Anne Joutel; Elisabeth Tournier-Lasserve
Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.
Annals of neurology 2004;55(2):213-20.
2004: Anne Joutel; Marie Monet; Valérie Domenga; Florence Riant; Elisabeth Tournier-Lasserve
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.
American journal of human genetics 2004;74(2):338-47.
2003: Luke T Krebs; Yingzi Xue; Christine R Norton; John P Sundberg; Paul Beatus; Urban Lendahl; Anne Joutel; Thomas Gridley
Characterization of Notch3-deficient mice: normal embryonic development and absence of genetic interactions with a Notch1 mutation.
Genesis (New York, N.Y. : 2000) 2003;37(3):139-43.
2003: Katayoun Vahedi; Pascale Massin; Jean-Pierre Guichard; S Miocque; Marc Polivka; F Goutières; D Dress; Françoise Chapon; Marie-Magdeleine Ruchoux; Florence Riant; Anne Joutel; alain gaudric; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.
Neurology 2003;60(1):57-63.
2003: Marie-Magdeleine Ruchoux; Valérie Domenga; Peggy Brulin; Jacqueline Maciazek; Sylvie Limol; Elisabeth Tournier-Lasserve; Anne Joutel
Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
The American journal of pathology 2003;162(1):329-42.
2002: Florence Cavé-Riant; Christian Denier; Pierre Labauge; Michaelle Cécillon; Jacqueline Maciazek; Anne Joutel; Sophie Laberge-Le Couteulx; Elisabeth Tournier-Lasserve
Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations.
European journal of human genetics : EJHG 2002;10(11):733-40.
2002: Christian Denier; J-M Gasc; Françoise Chapon; Valérie Domenga; C Lescoat; Anne Joutel; Elisabeth Tournier-Lasserve
Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult.
Mechanisms of development 2002;117(1-2):363-7.
2002: Anne Joutel; Elisabeth Tournier-Lasserve
[Molecular basis and physiopathogenic mechanisms of CADASIL: a model of small vessel diseases of the brain].
Journal de la Société de biologie 2002;196(1):109-15.
2001: Anne Joutel; Pascal Favrole; Pierre Labauge; Hugues Chabriat; C Lescoat; F Andreux; Valérie Domenga; Michaelle Cécillon; Katayoun Vahedi; Anne Ducros; Florence Cave-Riant; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis.
Lancet 2001;358(9298):2049-51.
2001: Anne Ducros; Christian Denier; Anne Joutel; Michaelle Cecillon; C Lescoat; Katayoun Vahedi; F Darcel; Eric Vicaut; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
The New England journal of medicine 2001;345(1):17-24.
2000: J L Escary; Michaelle Cécillon; Jacqueline Maciazek; M Lathrop; Elisabeth Tournier-Lasserve; Anne Joutel
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content.
Human mutation 2000;16(6):518-26.
2000: Anne Joutel; Hugues Chabriat; Katayoun Vahedi; Valérie Domenga; C Vayssière; Marie-Magdeleine Ruchoux; C Lucas; D Leys; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL.
Neurology 2000;54(9):1874-5.
2000: Anne Joutel; D D Dodick; Joseph E Parisi; Michaelle Cecillon; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
De novo mutation in the Notch3 gene causing CADASIL.
Annals of neurology 2000;47(3):388-91.
2000: Anne Joutel; F Andreux; S Gaulis; Valérie Domenga; Michaelle Cecillon; Nicole Battail; N Piga; Françoise Chapon; C Godfrain; Elisabeth Tournier-Lasserve
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients.
The Journal of clinical investigation 2000;105(5):597-605.
2000: Anne Joutel; A François; Hugues Chabriat; Katayoun Vahedi; F Andreux; Valérie Domenga; Michaelle Cecillon; Jacqueline Maciazek; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
[CADASIL: genetics and physiopathology].
Bulletin de l'Académie nationale de médecine 2000;184(7):1535-42; discussion 1542-4.
2000: Hugues Chabriat; Anne Joutel; Katayoun Vahedi; Marie-Thérèse Iba-Zizen; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging].
Bulletin de l'Académie nationale de médecine 2000;184(7):1523-31; discussion 1531-3.
2000: Olivier Heinzlef; Sonia Alamowitch; V Sazdovitch; P Chillet; Anne Joutel; Elisabeth Tournier-Lasserve; Etienne Roullet
Autoimmune diseases in families of French patients with multiple sclerosis.
Acta neurologica Scandinavica 2000;101(1):36-40.
1999: Sophie Laberge-Le Couteulx; H H Jung; Pierre Labauge; JP Houtteville; C Lescoat; Michaelle Cecillon; E Marechal; Anne Joutel; J F Bach; Elisabeth Tournier-Lasserve
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas.
Nature genetics 1999;23(2):189-93.
1999: Bernard Echenne; Anne Ducros; François Rivier; Anne Joutel; Véronique Humbertclaude; Agathe Roubertie; M Azaïs; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1.
Neuropediatrics 1999;30(4):214-7.
1999: Christian Denier; Anne Ducros; Katayoun Vahedi; Anne Joutel; P Thierry; A Ritz; Giovanni Castelnovo; T Deonna; P Gérard; J L Devoize; A Gayou; B Perrouty; T Soisson; A Autret; J M Warter; A Vighetto; P Van Bogaert; Sonia Alamowitch; Etienne Roullet; Elisabeth Tournier-Lasserve
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
Neurology 1999;52(9):1816-21.
1999: Hugues Chabriat; R Mrissa; Claude Levy; Katayoun Vahedi; H Taillia; Marie-Thérèse Iba-Zizen; Anne Joutel; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
Brain stem MRI signal abnormalities in CADASIL.
Stroke; a journal of cerebral circulation 1999;30(2):457-9.
1999: Anne Ducros; Christian Denier; Anne Joutel; Katayoun Vahedi; A Michel; F Darcel; M Madigand; D Guerouaou; F Tison; J Julien; E Hirsch; F Chedru; C Bisgård; G Lucotte; P Després; Catherine Billard; Marie-Anne Barthez; Gérard Ponsot; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
American journal of human genetics 1999;64(1):89-98.
1998: Anne Joutel; Elisabeth Tournier-Lasserve
Notch signalling pathway and human diseases.
Seminars in cell & developmental biology 1998;9(6):619-25.
1998: Alain Furby; Katayoun Vahedi; M Force; S Larrouy; Marie-Magdeleine Ruchoux; Anne Joutel; Elisabeth Tournier-Lasserve
Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening.
Journal of neurology 1998;245(11):734-40.
1998: Hugues Chabriat; Claude Levy; H Taillia; Marie-Thérèse Iba-Zizen; Katayoun Vahedi; Anne Joutel; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
Patterns of MRI lesions in CADASIL.
Neurology 1998;51(2):452-7.
1998: H Djouhri; Kathlyn Marsot-Dupuch; Anne Joutel; Michèle Kujas; M D Brette; F Artuis; Jean-Michel Tubiana
Perichiasmatic granuloma occuring after radical mastoidectomy: MR findings.
European radiology 1998;8(2):286-8.
1997: Anne Ducros; Anne Joutel; Katayoun Vahedi; Michaelle Cecillon; A Ferreira; E Bernard; A Verier; Bernard Echenne; A Lopez de Munain; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
Annals of neurology 1997;42(6):885-90.
1997: Anne Joutel; Katayoun Vahedi; C Corpechot; A Troesch; Hugues Chabriat; C Vayssière; C Cruaud; Jacqueline Maciazek; J Weissenbach; Marie-Germaine Bousser; J F Bach; Elisabeth Tournier-Lasserve
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.
Lancet 1997;350(9090):1511-5.
1997: Anne Joutel; C Corpechot; Anne Ducros; Katayoun Vahedi; Hugues Chabriat; P Mouton; Sonia Alamowitch; Valérie Domenga; M Cécillion; E Maréchal; Jacqueline Maciazek; C Vayssière; C Cruaud; Emmanuel Alain Cabanis; Marie-Magdeleine Ruchoux; J Weissenbach; J F Bach; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
Annals of the New York Academy of Sciences 1997;826():213-7.
1997: Hugues Chabriat; Anne Joutel; Katayoun Vahedi; Marie-Thérèse Iba-Zizen; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
[CADASIS. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalophathy].
Revue neurologique 1997;153(6-7):376-85.
1996: Anne Joutel; Anne Ducros; Sonia Alamowitch; C Cruaud; V Domenga; E Maréchal; Katayoun Vahedi; Hugues Chabriat; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region.
Genomics 1996;38(2):192-8.
1996: Anne Joutel; C Corpechot; Anne Ducros; Katayoun Vahedi; Hugues Chabriat; P Mouton; Sonia Alamowitch; V Domenga; M Cécillion; E Marechal; Jacqueline Maciazek; C Vayssiere; C Cruaud; E A Cabanis; Marie-Magdeleine Ruchoux; J Weissenbach; J F Bach; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.
Nature 1996;383(6602):707-10.
1996: Hugues Chabriat; Anne Joutel; Katayoun Vahedi; M T Iba-Zizen; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)].
Journal des maladies vasculaires 1996;21(5):277-82.
1996: Anne Ducros; T Nagy; Sonia Alamowitch; A Nibbio; Anne Joutel; Katayoun Vahedi; Hugues Chabriat; M T Iba-Zizen; J Julien; P Davous; J Y Goas; O Lyon-Caen; Bruno Dubois; X Ducrocq; F Salsa; Michele Ragno; P Burkhard; Claudio Bassetti; Michael Hutchinson; M Vérin; F Viader; Françoise Chapon; M Levasseur; J L Mas; O Delrieu
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.
American journal of human genetics 1996;58(1):171-81.
1995: Hugues Chabriat; Katayoun Vahedi; M T Iba-Zizen; Anne Joutel; A Nibbio; T G Nagy; M O Krebs; J Julien; Bruno Dubois; X Ducrocq
Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Lancet 1995;346(8980):934-9.
1995: Anne Ducros; Anne Joutel; Pierre Labauge; M Pagès; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
Monozygotic twins discordant for familial hemiplegic migraine.
Neurology 1995;45(6):1222.
1995: Hugues Chabriat; Elisabeth Tournier-Lasserve; Katayoun Vahedi; D Leys; Anne Joutel; A Nibbio; J P Escaillas; M T Iba-Zizen; S Bracard; A Tehindrazanarivelo
Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus.
Neurology 1995;45(6):1086-91.
1995: Katayoun Vahedi; Anne Joutel; P Van Bogaert; Anne Ducros; J Maciazeck; J F Bach; Marie-Germaine Bousser; Elisabeth Tournier-Lasserve
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.
Annals of neurology 1995;37(3):289-93.
1995: Anne Joutel; Elisabeth Tournier-Lasserve; Marie-Germaine Bousser
[Hemiplegic migraine].
Presse médicale (Paris, France : 1983) 1995;24(8):411-4.
1994: Anne Joutel; Anne Ducros; Katayoun Vahedi; Pierre Labauge; O Delrieu; N Pinsard; Josette Mancini; Gérard Ponsot; F Gouttière; J L Gastaut
Genetic heterogeneity of familial hemiplegic migraine.
American journal of human genetics 1994;55(6):1166-72.
1994: Anne Joutel; Marie-Germaine Bousser; Valérie Biousse; Pierre Labauge; Hugues Chabriat; A Nibbio; Jacqueline Maciazek; B Meyer; M A Bach; J Weissenbach
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].
Revue neurologique 1994;150(5):340-5.
1993: Anne Joutel; Marie-Germaine Bousser; Valérie Biousse; Pierre Labauge; Hugues Chabriat; A Nibbio; Jacqueline Maciazek; B Meyer; M A Bach; J Weissenbach
A gene for familial hemiplegic migraine maps to chromosome 19.
Nature genetics 1993;5(1):40-5.
1993: Elisabeth Tournier-Lasserve; Anne Joutel; J Melki; J Weissenbach; G M Lathrop; Hugues Chabriat; J L Mas; E A Cabanis; M Baudrimont; Jacqueline Maciazek
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.
Nature genetics 1993;3(3):256-9.
1993: M Baudrimont; F Dubas; Anne Joutel; Elisabeth Tournier-Lasserve; M G Bousser
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.
Stroke; a journal of cerebral circulation 1993;24(1):122-5.