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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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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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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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Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy

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

2003

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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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Standard-Risk Medulloblastoma Treated by Adjuvant Chemotherapy Followed by Reduced-Dose Craniospinal Radiation Therapy: A French Society of Pediatric Oncology Study

Journal of clinical oncology, 2005-07, Vol.23 (21), p.4726-4734

2005

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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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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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Could the pale, soft, and exudative condition be explained by distinctive histological characteristics?

Journal of animal science, 2007-03, Vol.85 (3), p.746

2007

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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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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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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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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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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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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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Outcome of children treated with preradiation chemotherapy for a high-grade glioma: Results of a French Society of Pediatric Oncology (SFOP) pilot study

Pediatric Blood & Cancer, 2007-11, Vol.49 (6), p.803-807

2007

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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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Tau aggregates are abnormally phosphorylated in inclusion body myositis and have an immunoelectrophoretic profile distinct from other tauopathies

Neuropathology and applied neurobiology, 2004-12, Vol.30 (6), p.624-634

2004

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Cathepsin B, D and K expression in adamantinomatous craniopharyngiomas relates to their levels of differentiation as determined by the patterns of retinoic acid receptor expression

Histopathology, 2003-12, Vol.43 (6), p.563-572

2003

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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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Systemic activation of the vascular endothelial growth factor receptor KDR/flk-1 selectively triggers endothelial cells with an angiogenic phenotype

The American journal of pathology, 1997-11, Vol.151 (5), p.1215-1224

1997

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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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Cerebellar gliomas in children with NF1 : pathology and surgery

Child's nervous system, 2000-07, Vol.16 (7), p.417-420

2000

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Lipomatous differentiation in ependymomas: a report of three cases and comparison with similar changes reported in other central nervous system neoplasms of neuroectodermal origin

The American journal of surgical pathology, 1998-03, Vol.22 (3), p.338-346

1998

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

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

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy

CADASIL: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Standard-Risk Medulloblastoma Treated by Adjuvant Chemotherapy Followed by Reduced-Dose Craniospinal Radiation Therapy: A French Society of Pediatric Oncology Study

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

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

Could the pale, soft, and exudative condition be explained by distinctive histological characteristics?

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

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

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

Small vessel abnormalities in alternating hemiplegia of childhood: pathophysiologic implications

Specific tau variants in the brains of patients with myotonic dystrophy

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

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

Outcome of children treated with preradiation chemotherapy for a high-grade glioma: Results of a French Society of Pediatric Oncology (SFOP) pilot study

Endothelial changes in muscle and skin biopsies in patients with CADASIL

Tau aggregates are abnormally phosphorylated in inclusion body myositis and have an immunoelectrophoretic profile distinct from other tauopathies

Cathepsin B, D and K expression in adamantinomatous craniopharyngiomas relates to their levels of differentiation as determined by the patterns of retinoic acid receptor expression

Management of delayed intracranial and intraspinal metastases of intradural spinal paragangliomas

Systemic activation of the vascular endothelial growth factor receptor KDR/flk-1 selectively triggers endothelial cells with an angiogenic phenotype

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

Cerebellar gliomas in children with NF1 : pathology and surgery

Lipomatous differentiation in ependymomas: a report of three cases and comparison with similar changes reported in other central nervous system neoplasms of neuroectodermal origin

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