Angioendotheliomatosis of the central nervous system

Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies.

Journal of neurology, neurosurgery, and psychiatry·1995

Lewy bodies in the lateral hypothalamus: do they imply neuronal loss?

Movement disorders : official journal of the Movement Disorder Society·1993

Distribution of beta/A4 protein and amyloid precursor protein in hereditary cerebral hemorrhage with amyloidosis-Dutch type and Alzheimer's disease.

The American journal of pathology·1993

Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings.

Journal of the neurological sciences·1992

Acute phase proteins but not activated microglial cells are present in parenchymal beta/A4 deposits in the brains of patients with hereditary cerebral hemorrhage with amyloidosis-Dutch type.

Neuroscience letters·1992

Neuropathological findings in cerebral B-protein amyloidosis. Differences and similarities in those cases presenting as a cerebral hemorrhage and those presenting as a dementia of the Alzheimer type.

Clinical neurology and neurosurgery·1992

Oligodendroglial somatic SNCA copy number gains are associated with inclusions and disease onset in multiple system atrophy.

Acta neuropathologica·2026

Familial, neuropathological and cellular analysis identify ARPP21 as a major amyotrophic lateral sclerosis associated gene in French cohorts.

Acta neuropathologica·2026

Changes in five cerebrospinal fluid and three plasma Alzheimer's disease biomarkers across increasing brain amyloid-beta and tau pathology burden.

Acta neuropathologica·2026

Seeds from ALS patients homozygous for the SOD1 D90A mutation transmit two types of SOD1 aggregation and motor neuron disease.

Acta neuropathologica·2026

High levels of cell-free hemoglobin and iron in cerebral thrombi of pre-Omicron COVID-19 stroke patients: novel drivers of SARS-CoV-2-induced prothrombotic state.

Acta neuropathologica·2026

Distinctive properties of the prion protein in the brain and retina in the amyloidosis associated with the PRNP F198S mutation.

Acta neuropathologica·2026

Metabolic dysfunction-associated fatty liver disease exacerbates hematoma expansion in intracerebral hemorrhage: an explainable machine learning approach.

Frontiers in endocrinology·2026

Diagnostic Accuracy of Magnetic Resonance Urography Compared With Computed Tomography Urography in Patients With Hematuria.

Cureus·2026

Peripheral administration of 11.7% hypertonic saline and phlebitis risk in acute ischemic stroke requiring hyperosmolar therapy in South Korea.

Acute and critical care·2026

Patient Preferences for the Treatment of Haemophilia A and B in France.

Haemophilia : the official journal of the World Federation of Hemophilia·2026

EXPRESS: Covert cerebral small vessel disease and outcomes after spontaneous intracerebral hemorrhage.

Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism·2026

Association Between Platelet Transfusion and ICU Mortality Within 28 Days Among Patients With Intracranial Hemorrhage Complicated by Thrombocytopenia: A Propensity Score-Matched Cohort Study.

Medical science monitor : international medical journal of experimental and clinical research·2026

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Angioendotheliomatosis of the central nervous system

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Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies.

Lewy bodies in the lateral hypothalamus: do they imply neuronal loss?

Distribution of beta/A4 protein and amyloid precursor protein in hereditary cerebral hemorrhage with amyloidosis-Dutch type and Alzheimer's disease.

Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings.

Acute phase proteins but not activated microglial cells are present in parenchymal beta/A4 deposits in the brains of patients with hereditary cerebral hemorrhage with amyloidosis-Dutch type.

Neuropathological findings in cerebral B-protein amyloidosis. Differences and similarities in those cases presenting as a cerebral hemorrhage and those presenting as a dementia of the Alzheimer type.

Oligodendroglial somatic SNCA copy number gains are associated with inclusions and disease onset in multiple system atrophy.

Familial, neuropathological and cellular analysis identify ARPP21 as a major amyotrophic lateral sclerosis associated gene in French cohorts.

Changes in five cerebrospinal fluid and three plasma Alzheimer's disease biomarkers across increasing brain amyloid-beta and tau pathology burden.

Seeds from ALS patients homozygous for the SOD1 D90A mutation transmit two types of SOD1 aggregation and motor neuron disease.

High levels of cell-free hemoglobin and iron in cerebral thrombi of pre-Omicron COVID-19 stroke patients: novel drivers of SARS-CoV-2-induced prothrombotic state.

Distinctive properties of the prion protein in the brain and retina in the amyloidosis associated with the PRNP F198S mutation.

Metabolic dysfunction-associated fatty liver disease exacerbates hematoma expansion in intracerebral hemorrhage: an explainable machine learning approach.

Diagnostic Accuracy of Magnetic Resonance Urography Compared With Computed Tomography Urography in Patients With Hematuria.

Peripheral administration of 11.7% hypertonic saline and phlebitis risk in acute ischemic stroke requiring hyperosmolar therapy in South Korea.

Patient Preferences for the Treatment of Haemophilia A and B in France.

EXPRESS: Covert cerebral small vessel disease and outcomes after spontaneous intracerebral hemorrhage.

Association Between Platelet Transfusion and ICU Mortality Within 28 Days Among Patients With Intracranial Hemorrhage Complicated by Thrombocytopenia: A Propensity Score-Matched Cohort Study.

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Angioendotheliomatosis of the central nervous system

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