Neurologic side effects in neuroleptic-naïve patients treated with haloperidol or risperidone

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Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease.

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Neuromuscular complications in cancer.

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Secondary myopathy due to systemic diseases.

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Endovascular stroke therapy in Austria: a nationwide 1-year experience.

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Effect of a ≥50% Reduction in Low-Density Lipoprotein Cholesterol From Baseline in Patients With Ischemic Stroke.

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Effect of Baseline ASPECTS on Tenecteplase Efficacy Before Thrombectomy in Acute Large-Vessel Occlusion Stroke: A Post Hoc Analysis of the BRIDGE-TNK Randomized Trial.

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Paternal Valproate Exposure and Offspring Neurodevelopmental Outcomes.

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Application of the 2024 McDonald Criteria: Earlier Diagnosis and Avoiding Misdiagnosis of Multiple Sclerosis in a Global Setting.

Neurology·2026

Epidemiological investigation and risk factor analysis of acute kidney injury in non-intensive care unit hospitalized patients following neurosurgery.

Frontiers in neurology·2026

The origin of non-specific effects of vaccines and the role of randomised clinical trials.

Human vaccines & immunotherapeutics·2026

Non-alcoholic Wernicke-Korsakoff Syndrome: A Narrative Review.

Saudi journal of medicine & medical sciences·2026

Circulating long non-coding RNAs as diagnostic markers of lupus nephritis and 5-year follow-up disease flares.

Frontiers in immunology·2026

Sellar region neurocytomas exhibit a CIMP and neuroendocrine-like epigenetic signature distinct from other intra-axial neurocytomas.

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Mechanistic insights into the transcription-mediated roles of non-coding RNAs in gene regulation.

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Neurologic side effects in neuroleptic-naïve patients treated with haloperidol or risperidone

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The World Federation of Neurology and the challenges in Environment Neurology.

Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease.

Neuromuscular complications in cancer.

Prostate cancer, Hu antibodies and paraneoplastic neurological syndromes.

Secondary myopathy due to systemic diseases.

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