[Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing encephalopathy]

Paroxysmal extreme pain disorder (previously familial rectal pain syndrome).

Neurology·2007

[Aicardi-Goutieres syndrome: an oft unrecognised familial early-onset encephalopathy].

Revue neurologique·2005

[The effect of refractory epileptic seizures on cognitive processes].

Revista de neurologia·2003

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.

Neurology·2003

Dreamy state: a case report from the selected writings of John Hughlings Jackson. Brain 1874.

Epileptic disorders : international epilepsy journal with videotape·2001

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.

Annals of neurology·2001

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

Astrocytic PDE7B Drives Blood-Brain Barrier Breakdown via Extracellular Vesicles in Demyelinating Disease.

Glia·2026

miRNA-34b overexpression alleviates neuromyelitis optica spectrum disorders by regulating the TIA-1-stress granule pathway.

Pakistan journal of pharmaceutical sciences·2026

Validation and interpretation of the Persian Multiple Sclerosis Neuropsychological Screening Questionnaire.

Journal of clinical and experimental neuropsychology·2026

Disease-Associated Mutations Impact DNA Methyltransferase 1 Function through Dynamic Allosteric Effects and Solvent Exposure.

Journal of chemical theory and computation·2026

Risk of radial nerve injury during deltoid intramuscular injection in shoulder internal rotation and abduction position-cadaveric anatomical study.

Human vaccines & immunotherapeutics·2026

BetaII-spectrin gaps and patches emerge from the patterned assembly of the actin/spectrin membrane skeleton in human motor neuron axons.

eLife·2026

Related Experiment Videos

[Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing

Related Concept Videos

Paroxysmal extreme pain disorder (previously familial rectal pain syndrome).

[Aicardi-Goutieres syndrome: an oft unrecognised familial early-onset encephalopathy].

[The effect of refractory epileptic seizures on cognitive processes].

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.

Dreamy state: a case report from the selected writings of John Hughlings Jackson. Brain 1874.

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.

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.

Astrocytic PDE7B Drives Blood-Brain Barrier Breakdown via Extracellular Vesicles in Demyelinating Disease.

miRNA-34b overexpression alleviates neuromyelitis optica spectrum disorders by regulating the TIA-1-stress granule pathway.

Validation and interpretation of the Persian Multiple Sclerosis Neuropsychological Screening Questionnaire.

Disease-Associated Mutations Impact DNA Methyltransferase 1 Function through Dynamic Allosteric Effects and Solvent Exposure.

Risk of radial nerve injury during deltoid intramuscular injection in shoulder internal rotation and abduction position-cadaveric anatomical study.

BetaII-spectrin gaps and patches emerge from the patterned assembly of the actin/spectrin membrane skeleton in human motor neuron axons.

Related Experiment Videos

[Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing...

Related Concept Videos

Related Articles

[Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing