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Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Brain (London, England : 1878), 2009-04, Vol.132 (4), p.933-939

2009

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CADASIL: a Common Form of Hereditary Arteriopathy Causing Brain Infarcts and Dementia

Brain pathology (Zurich, Switzerland), 2002-07, Vol.12 (3), p.371-384

2002

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

Nature (London), 1996-10, Vol.383 (6602), p.707-710

1996

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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, Vol.162 (1), p.329-342

2003

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Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease

Neurology, 2005-11, Vol.65 (10), p.1636-1638

2005

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CADASIL: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Journal of neuropathology and experimental neurology, 1997-09, Vol.56 (9), p.947-964

1997

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Progression-Free Survival in Children With Optic Pathway Tumors: Dependence on Age and the Quality of the Response to Chemotherapy—Results of the First French Prospective Study for the French Society of Pediatric Oncology

Journal of clinical oncology, 2003-12, Vol.21 (24), p.4572-4578

2003

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Galectin-1 is highly expressed in human gliomas with relevance for modulation of invasion of tumor astrocytes into the brain parenchyma

Glia, 2001-03, Vol.33 (3), p.241-255

2001

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Galectins Are Differentially Expressed in Supratentorial Pilocytic Astrocytomas, Astrocytomas, Anaplastic Astrocytomas and Glioblastomas, and Significantly Modulate Tumor Astrocyte Migration

Brain pathology (Zurich, Switzerland), 2001-01, Vol.11 (1), p.12-26

2001

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Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy

Neurology, 2003-01, Vol.60 (1), p.57-63

2003

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Pineal Parenchymal Tumors: A Correlation of Histological Features with Prognosis in 66 Cases

Brain pathology (Zurich, Switzerland), 2000-01, Vol.10 (1), p.49-60

2000

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Retinal involvement in dementia with Lewy bodies: A clue to hallucinations?

Annals of neurology, 2003-10, Vol.54 (4), p.542-547

2003

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MR Imaging in the Diagnosis of Desmoplastic Infantile Tumor: Retrospective Study of Six Cases

American journal of neuroradiology : AJNR, 2004-06, Vol.25 (6), p.1028-1033

2004

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Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient Children

American journal of human genetics, 2003, Vol.72 (1), p.213-216

2003

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Morphometric analysis of ultrastructural vascular changes in CADASIL: analysis of 50 skin biopsy specimens and pathogenic implications

Acta neuropathologica, 2002-09, Vol.104 (3), p.241-248

2002

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Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Acta neuropathologica, 1995, Vol.89 (6), p.500-512

1995

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Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL

Neurology, 2000-05, Vol.54 (9), p.1874-1875

2000

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Tumour necrosis and microvascular proliferation are associated with 9p deletion and CDKN2A alterations in 1p/19q-deleted oligodendrogliomas

Neuropathology and applied neurobiology, 2003-10, Vol.29 (5), p.462-471

2003

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Small vessel abnormalities in alternating hemiplegia of childhood: pathophysiologic implications

Neurology, 2006-02, Vol.66 (4), p.499-504

2006

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Specific tau variants in the brains of patients with myotonic dystrophy

Neurology, 1996-09, Vol.47 (3), p.711-717

1996

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Supratentorial Pilocytic Astrocytomas, Astrocytomas, Anaplastic Astrocytomas and Glioblastomas are Characterized by a Differential Expression of S100 Proteins

Brain pathology (Zurich, Switzerland), 1999-01, Vol.9 (1), p.1-19

1999

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Phosphorylated serine 199 of microtubule-associated protein tau is a neuronal epitope abundantly expressed in youth and an early marker of tau pathology

Acta neuropathologica, 2003-02, Vol.105 (2), p.89-97

2003

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Diffuse form of argyrophilic grain disease: a new variant of four-repeat tauopathy different from limbic argyrophilic grain disease

Acta neuropathologica, 2003-12, Vol.106 (6), p.575-583

2003

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Endothelial changes in muscle and skin biopsies in patients with CADASIL

Neuropathology and applied neurobiology, 1998-02, Vol.24 (1), p.60-65

1998

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Management of delayed intracranial and intraspinal metastases of intradural spinal paragangliomas

Acta neurochirurgica, 2006-01, Vol.148 (1), p.63-66

2006

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Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

CADASIL: a Common Form of Hereditary Arteriopathy Causing Brain Infarcts and Dementia

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

Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease

CADASIL: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Progression-Free Survival in Children With Optic Pathway Tumors: Dependence on Age and the Quality of the Response to Chemotherapy—Results of the First French Prospective Study for the French Society of Pediatric Oncology

Galectin-1 is highly expressed in human gliomas with relevance for modulation of invasion of tumor astrocytes into the brain parenchyma

Galectins Are Differentially Expressed in Supratentorial Pilocytic Astrocytomas, Astrocytomas, Anaplastic Astrocytomas and Glioblastomas, and Significantly Modulate Tumor Astrocyte Migration

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy

Pineal Parenchymal Tumors: A Correlation of Histological Features with Prognosis in 66 Cases

Retinal involvement in dementia with Lewy bodies: A clue to hallucinations?

MR Imaging in the Diagnosis of Desmoplastic Infantile Tumor: Retrospective Study of Six Cases

Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient Children

Morphometric analysis of ultrastructural vascular changes in CADASIL: analysis of 50 skin biopsy specimens and pathogenic implications

Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL

Tumour necrosis and microvascular proliferation are associated with 9p deletion and CDKN2A alterations in 1p/19q-deleted oligodendrogliomas

Small vessel abnormalities in alternating hemiplegia of childhood: pathophysiologic implications

Specific tau variants in the brains of patients with myotonic dystrophy

Supratentorial Pilocytic Astrocytomas, Astrocytomas, Anaplastic Astrocytomas and Glioblastomas are Characterized by a Differential Expression of S100 Proteins

Phosphorylated serine 199 of microtubule-associated protein tau is a neuronal epitope abundantly expressed in youth and an early marker of tau pathology

Diffuse form of argyrophilic grain disease: a new variant of four-repeat tauopathy different from limbic argyrophilic grain disease

Endothelial changes in muscle and skin biopsies in patients with CADASIL

Management of delayed intracranial and intraspinal metastases of intradural spinal paragangliomas

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