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.
To evaluate the safety and effectiveness of middle meningeal artery embolization (MMAE) with the TRUFILL n-butyl cyanoacrylate (n-BCA) liquid embolic system plus standard of care versus standard of care alone in patients with symptomatic chronic subdural hematoma.
Primary effectiveness end point (residual/re-accumulation of hematoma >10 mm at 6 months or surgery on the cSDH within 6 months) occurred in 11.6% (17/146) with MMAE plus SOC vs 22.1% (29/131) with SOC alone β common OR 0.53 (90% CI, 0.31-0.91); P = .04, a 47% reduction in odds
View Summary →To evaluate the safety, tolerability, and efficacy of alixorexton (ALKS 2680), an oral orexin 2 receptor (OX2R) agonist, in adults with narcolepsy type 1.
Alixorexton dramatically improved wakefulness at week 6: placebo-corrected LSM change in mean sleep latency on the MWT was +22.2 min (95% CI 17.2β27.2, adjusted p=0.0099) for 4 mg, +24.1 min (19.0β29.1, p<0.0001) for 6 mg, and +26.0 min (21.0β31.0, p<0.0001) for 8 mg; observed MSL reached the normative range (β₯20 min) in all dose groups
View Summary →To evaluate the long-term safety, tolerability, and immunological memory of ABvac40 active immunotherapy (anti-AΞ²40 vaccine) in an 18-month extension (Part B) of a phase 2 trial in amnestic MCI and very mild Alzheimer's disease, including a delayed booster in previously vaccinated participants and first-time vaccination of prior placebo participants.
TEAEs occurred in 75.0% of the placebo + booster group and 81.1% of the ABvac40 group during Part B; serious TEAEs in 5.0% vs 16.2%, with no deaths and no TEAEs leading to discontinuation
View Summary →To systematically identify factors associated with an increased likelihood of a multiple sclerosis (MS) diagnosis after a clinically isolated syndrome (CIS), via systematic review and meta-analysis of observational studies.
Younger age at CIS onset (OR 1.60, 95% CI 1.30β2.00, p=0.0001) and multifocal presentation (OR 1.55, 95% CI 1.10β2.19, p=0.022) predicted subsequent MS diagnosis
View Summary →To determine whether plasma p-tau217 can reliably detect treatment-related amyloid clearance (TRAC, <24.1 Centiloids on amyloid PET) after donanemab treatment in early symptomatic Alzheimer's disease, using data from the phase 3 TRAILBLAZER-ALZ 2 trial.
Plasma p-tau217 (mass spectrometry) showed low diagnostic performance for detecting TRAC (<24.1 CL on PET): AUROC 0.61 at 52 weeks, 0.64 at 24 weeks, 0.63 at 76 weeks; immunoassay similar (AUROC 0.67 at 24 weeks, 0.64 at 52 and 76 weeks)
View Summary →In patients with acute ischaemic stroke due to large vessel occlusion undergoing endovascular thrombectomy, does a single IV dose of nerinetide (2.6 mg/kg) improve 90-day functional outcomes compared with placebo.
Primary outcome (mRS 0β2 at 90 days) was not met: 337/549 (61.4%) nerinetide vs 329/556 (59.2%) placebo; adjusted RR 1.04 (95% CI 0.96β1.14), p=0.35.
View Summary →Determine whether lying-flat vs sitting-up head positioning for 24 hours after acute stroke reduces 90-day disability.
No significant difference in 90-day disability distribution on modified Rankin scale: unadjusted OR 1.01 (95% CI 0.92β1.10), P=0.84.
View Summary →Determine whether mechanical thrombectomy added to intravenous alteplase improves functional independence at 3 months in patients with acute ischaemic stroke and proximal anterior-circulation large-vessel occlusion.
Primary: mRS 0-2 at 3 months achieved by 106/200 (53%) with IVT+thrombectomy vs 85/202 (42%) with IVT alone (OR 1.55, 95% CI 1.05-2.30; p=0.028; NNT=9).
View Summary →High-yield new articles from JAMA Neurology, Stroke, Neurology, and Lancet Neurology β distilled into 5-minute summaries.
The FDA's August 19 acceptance and priority review of ecopipam's NDA sets up the first genuinely new mechanism for pediatric Tourette syndrome since haloperidol β selective D1 receptor antagonism withoutβ¦
FDA approval of oveporexton (Orzeyful), the first drug to directly restore orexin signaling, marks a shift from symptomatic stimulants and oxybates to disease-mechanism therapy in NT1 β the article reviewsβ¦
The near-simultaneous FDA clearances of the Elecsys pTau217 plasma test (first rule-in/rule-out), PrecivityAD2 (down to age 40), and approval of the Tauklarify tau PET tracer create a practical diagnostic algorithmβ¦
With Novartis and BMS pausing CAR T-cell trials in myasthenia gravis and MS after three deaths from immune effector cell-associated hemophagocytic syndrome, the article reviews the mechanism, risk-benefit relative toβ¦
A rigorous walkthrough of the August 31, 2026 AAN/AHS joint guideline β the first update since 2012 β covering how CGRP monoclonals and gepants are now positioned against legacy oralβ¦
Two 2026 meta-analyses and a wave of positive trials - TRACE III, HOPE, OPTION, TRACE-5 - have made imaging-selected thrombolysis beyond 4.5 hours the emerging standard. What the evidence shows,β¦
PACAP is the most clinically advanced new migraine pathway since CGRP. After the failure of receptor blockade β and one anti-PACAP antibody β bocunebart has two positive phase 2 trials.β¦
A rotating set of reference pages across specialties β pathophysiology, diagnostic frameworks, and management. New picks every week.
Transcranial Direct Current Stimulation for Stroke Recovery Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that delivers weak electrical currents (typically 1β2 mA) through scalp electrodes to modulate corticalβ¦
Read Full Article →Autoimmune encephalitis antibodies are now identified by phenotype-driven Mayo panels rather than a single legacy reflexive test. This page is the lab-side reference: what to order, what assay, what sample, titer interpretation,β¦
Read Full Article →Facial weakness is one of the most common findings in clinical neurology, and one of the most useful for localization. The simple but critical distinction is central (supranuclear) vs peripheral (nuclear orβ¦
Read Full Article →EHDN International Guidelines for the Treatment of Huntington's Disease (2019) This is a condensed summary of the European Huntington's Disease Network (EHDN) international guidelines (Bachoud-Lévi et al., 2019). The task force reviewedβ¦
Read Full Article →The motor system is the brain's output to the world. Every voluntary movement, every postural adjustment, every reflexive response, every modulation of muscle tone passes through a hierarchical, parallel set of circuitsβ¦
Read Full Article →CT vs MRI: Choosing the Right Tool Few decisions shape a neurologic workup more than which scanner the patient enters first. CT and MRI are not competitors but complementary instruments, each tunedβ¦
Read Full Article →Progressive Multiple Sclerosis Progressive MS encompasses both primary progressive MS (PPMS) and secondary progressive MS (SPMS), accounting for the phase of the disease in which neurodegeneration predominates over acute inflammation. Approximately 10–15%β¦
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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