Landmark trials with structured baseline tables. Real-world cases with discussion. Specialty references, board prep, and a journal-club reading list β built and maintained by clinicians, free for the community.
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Search 850+ landmark trials with structured baseline tables, exclusion criteria, and AI-assisted summaries.
Search trials →Specialty reference pages β pathophysiology, diagnostic frameworks, and evidence-based management, curated by clinicians.
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NeuroResidents
On-call templates, neuro-exam frameworks, summaries, and clinical pearls organised by rotation.
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NeuroJournal
Curated reading list. New articles from JAMA Neurology, Stroke, Neurology, and Lancet Neurology β distilled into 5-minute summaries.
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NeuroBoards
Practice questions, flashcards, study notes, and progress tracking β for RITE, boards, and continuing education.
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NeuroCasesNEW
Members share real-world cases with images, polls, and discussion. Vote on next steps, learn from outcomes, build the community.
Browse cases →The most recent landmark trials reviewed across all 9 specialties β structured summaries, baseline tables, and exclusion criteria.
Test whether an integrative polygenic score (iPGS) for ischemic stroke can identify older adults who derive net benefit from low-dose aspirin for the primary prevention of ischemic stroke.
In the highest iPGS quintile (Q5), aspirin reduced ischemic stroke by 51% (HR 0.49 [95% CI, 0.28β0.85]; P=0.011) with no increase in major bleeding (HR 1.15 [0.71β1.88]).
View Summary →Evaluate whether ultra-early remote ischemic postconditioning (RIPC) added to guideline-based therapy improves 90-day functional independence in patients with acute ischemic stroke (AIS) due to large vessel occlusion who underwent endovascular thrombectomy (EVT) with successful recanalization.
Primary outcome (mRS 0β2 at 90 days) not met: 60.9% RIPC vs 57.8% control (adjusted RR 1.07, 95% CI 0.89β1.30; P=0.46).
View Summary →Test whether combining clopidogrel-aspirin dual antiplatelet therapy with immediate intensive statin further reduces 90-day new stroke risk in acute mild ischemic stroke or high-risk TIA of presumed atherosclerotic cause, using a 2x2 factorial design.
Combination of clopidogrel-aspirin + immediate intensive statin lowered 90-day new stroke vs aspirin + delayed statin: 7.6% vs 9.9% (HR 0.76, 95% CI 0.60-0.97; ARR 2.2%, NNT 45)
View Summary →Test whether intensive blood pressure lowering (SBP <140 mm Hg) for 24 hours after successful endovascular thrombectomy in acute ischemic stroke has durable effects on functional outcome and mortality at 1 year, compared with conventional management (SBP 140β180 mm Hg).
Functional independence (mRS 0β2) at 1 year was lower with intensive vs conventional BP management: 40.5% vs 52.7% (ITT adj OR 0.59, 95% CI 0.34β1.00, P=0.051; per-protocol 41.1% vs 54.7%, adj OR 0.56, 95% CI 0.32β0.97, P=0.040)
View Summary →Determine the safety and optimal dose of rapid local ischemic postconditioning (RL-IPostC) delivered via a balloon-guiding catheter immediately after successful mechanical thrombectomy in acute anterior-circulation large-vessel occlusion stroke.
The 2 min inflation / 2 min deflation Γ 4 cycles regimen met prespecified safety and efficacy thresholds and was selected as the optimal dose (posterior probability true toxicity >15% β 0.16; efficacy <60% β 0.15).
View Summary →Assess whether baseline CT markers of cerebral small vessel disease (cSVD), as a surrogate for brain frailty, explain the reduced benefit of mechanical thrombectomy observed in elderly patients enrolled in the RESILIENT trial in Brazil.
Mechanical thrombectomy benefit was concentrated in patients <70 years with low cSVD burden (OR 4.16, 95% CI 1.6-10.4, p<0.01)
View Summary →Assess the safety and efficacy of long-term antiplatelet treatment after spontaneous intracerebral hemorrhage (ICH) in patients with vascular disease.
Trial terminated early due to slow recruitment (69 of 500 planned patients enrolled).
View Summary →In minor ischemic stroke (NIHSS 0β5) with proven intracranial occlusion enrolled in TEMPO-2, evaluate whether successful early recanalization on 4β8 hour follow-up CTA is associated with better 90-day functional outcomes, and identify predictors of successful recanalization.
Successful early recanalization (rAOL 2b/3) was independently associated with better 90-day functional outcome: 80.3% vs 66.4% return to baseline mRS (adjusted RR 1.21, 95% CI 1.09β1.34).
View Summary →High-yield new articles from JAMA Neurology, Stroke, Neurology, and Lancet Neurology β distilled into 5-minute summaries.
The first randomized head-to-head trial finds rituximab noninferior to IV ocrelizumab for MRI disease control in newly diagnosed relapsing MS β at roughly one-sixth the price. Where each anti-CD20 antibodyβ¦
The EU approved tolebrutinib (Cenrifki) as the first drug to slow disability in non-relapsing secondary progressive MS while the FDA rejected it over severe liver injury β a look atβ¦
A staged, evidence-based framework for Parkinson's treatment: when to start levodopa, how to manage motor fluctuations and dyskinesia, and when and how to choose among the three advanced modalities ββ¦
More than a dozen disease-modifying therapies, five mechanistic classes, and few head-to-head trials. A structured framework for choosing in MS: efficacy tiers and the limits of cross-trial comparison, the differencesβ¦
After two decades stuck against epilepsy's drug-resistance ceiling, the modern era delivered genuinely better molecules, mechanisms beyond ion channels, and the first epilepsy gene-regulation therapy with disease-modifying signals. From cenobamate'sβ¦
Six FDA-approved biologics now compete for the same generalized myasthenia gravis patient β three complement inhibitors, three FcRn antagonists, and not a single head-to-head trial to guide us. The "refractoryβ¦
For two decades, Alzheimer therapy meant cholinesterase inhibitors and memantine. Two FDA-approved anti-amyloid antibodies β lecanemab and donanemab β now slow cognitive decline by 27β35% over 18 months, and brexpiprazoleβ¦
A rotating set of reference pages across specialties β pathophysiology, diagnostic frameworks, and management. New picks every week.
Nystagmus Classification & Localization Nystagmus — involuntary, rhythmic oscillation of the eyes — is one of the most localizing signs in clinical neurology. Careful observation of the direction, waveform, conjugacy, and behaviorβ¦
Read Full Article →Behavioral Variant Frontotemporal Dementia Behavioral variant frontotemporal dementia (bvFTD) is the most common clinical syndrome within the frontotemporal dementia (FTD) spectrum, accounting for approximately 60% of FTD cases. Unlike Alzheimer disease (AD),β¦
Read Full Article →Semiology & Seizure Localization Seizure semiology — the detailed characterization of signs and symptoms during a seizure — remains the cornerstone of seizure localization and presurgical evaluation. The semiologic sequence of aβ¦
Read Full Article →The pattern of sensory loss is, in many cases, the single most localizing finding in clinical neurology. A patient with numbness from the umbilicus down has a cord lesion at T10. Aβ¦
Read Full Article →Leukodystrophies are inherited disorders of myelin (formation, maintenance, or degeneration). MRI pattern recognition narrows the differential dramatically before testing β adrenoleukodystrophy targets corticospinal tracts; metachromatic leukodystrophy spares the U-fibers; Alexander disease prefersβ¦
Read Full Article →Medication Overuse Headache Medication overuse headache (MOH) is the third most common headache disorder and the most common secondary cause of chronic daily headache. It develops when acute headache medications are usedβ¦
Read Full Article →Antithrombotic Therapy After ICH Survivors of intracerebral hemorrhage (ICH) face a fundamental therapeutic dilemma: many have compelling indications for antithrombotic therapy β atrial fibrillation (AF), coronary artery disease, prior stents, venous thromboembolismβ¦
Read Full Article →Cases shared by members β discuss, vote, learn from outcomes.
76F, baseline mRS 1, AF on sub-therapeutic warfarin, global aphasia with R-sided hemiplegia. NCCT ASPECTS 3, left M1 occlusion, LKW 15 h ago. Late window β pull straight to angio or get CTP first?
62F on apixaban, aphasia LKW Tuesday 6 PM, worsened Wednesday noon (18h). NIHSS 16, M3 anterior division occlusion, favorable mismatch. Late window β what do you do?
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