Changes in policy for publishing manuscripts in Neurology

Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation.

Muscle & nerve. Supplement·2013

American Academy of Neurology policy on pharmaceutical and device industry support.

Neurology·2012

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype.

Neurology·2011

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Brain : a journal of neurology·2009

Primary episodic ataxias: diagnosis, pathogenesis and treatment.

Brain : a journal of neurology·2007

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

Brain : a journal of neurology·2005

Machine Learning Characterization of Readmissions After Chronic Subdural Hematoma Hospitalizations.

Neurology·2026

Acute Attack Treatment Escalation and Subsequent Relapse Risk in Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.

Neurology·2026

Pearls & Oy-sters: Bilateral Neuropathic Facial Pain With Autonomic Features and Neurovascular Contact.

Neurology·2026

Quantifying Disease Progression in Patients With Charcot-Marie-Tooth Neuropathy Type 1A Using Quantitative Muscle MRI and Clinical Outcomes.

Neurology·2026

Glucose and Methionine Metabolism in Disorders of Consciousness After Brain Injury: An Exploratory Longitudinal PET Study.

Neurology·2026

Nongenetic Factors Associated With Onset and Severity of Hereditary Ataxia.

Neurology·2026

The NIH Intramural Research Program: Opportunities for training and career development in neuroscience and beyond.

Annals of the Child Neurology Society·2026

Correction to Annals of the Child Neurology Society articles.

Annals of the Child Neurology Society·2026

[Late lyme neuroborreliosis with multifocal neurological symptoms and meningeal enhancement].

Ugeskrift for laeger·2026

Tumefactive parenchymal lesion of neurosarcoidosis responsive to infliximab.

Radiology case reports·2026

Altered neuronal start codon stringency favors cap-independent repeat-associated non-AUG translation.

bioRxiv : the preprint server for biology·2026

A single-cell cell-of-origin audit of the lncRNA RMST: bulk expression under-represents its broad neural expression and over-attributes a liver biomarker.

Functional & integrative genomics·2026

Related Experiment Videos

Changes in policy for publishing manuscripts in Neurology

Related Concept Videos

Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation.

American Academy of Neurology policy on pharmaceutical and device industry support.

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype.

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Primary episodic ataxias: diagnosis, pathogenesis and treatment.

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

Machine Learning Characterization of Readmissions After Chronic Subdural Hematoma Hospitalizations.

Acute Attack Treatment Escalation and Subsequent Relapse Risk in Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.

Pearls & Oy-sters: Bilateral Neuropathic Facial Pain With Autonomic Features and Neurovascular Contact.

Quantifying Disease Progression in Patients With Charcot-Marie-Tooth Neuropathy Type 1A Using Quantitative Muscle MRI and Clinical Outcomes.

Glucose and Methionine Metabolism in Disorders of Consciousness After Brain Injury: An Exploratory Longitudinal PET Study.

Nongenetic Factors Associated With Onset and Severity of Hereditary Ataxia.

The NIH Intramural Research Program: Opportunities for training and career development in neuroscience and beyond.

Correction to Annals of the Child Neurology Society articles.

[Late lyme neuroborreliosis with multifocal neurological symptoms and meningeal enhancement].

Tumefactive parenchymal lesion of neurosarcoidosis responsive to infliximab.

Altered neuronal start codon stringency favors cap-independent repeat-associated non-AUG translation.

A single-cell cell-of-origin audit of the lncRNA RMST: bulk expression under-represents its broad neural expression and over-attributes a liver biomarker.

Related Experiment Videos

Changes in policy for publishing manuscripts in Neurology

Related Concept Videos

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