An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

Generation of two LGMDR4 patients derived induced pluripotent stem cell line carrying the SGCB frameshift mutation (p.Gly129_Arg130insGlnTer).

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Proteomic Analysis of Corpora Amylacea Extracted From Post-mortem Brain of MAiD-end-of-life Sporadic ALS Patients.

Brain and behavior·2026

Utility of 18F-FDG PET/CT in the Surveillance of Patients With Neurofibromatosis Type 1.

Neurology. Genetics·2026

Multicenter evaluation of the Idylla IDH1-2 Mutation Assay Kit for detection of IDH mutational status in glioma.

Virchows Archiv : an international journal of pathology·2026

An Optimized Protocol for the Generation of iPSC Lines from Lymphoblastoid Cell Lines Using the Non-integrative Sendai Virus.

Current protocols·2026

Diverse Genetic Etiologies of Unilateral Polymicrogyria.

Annals of neurology·2026

Cofilin 1 Is an Extracellular Vesicle-Associated Plasma Biomarker of Parkinson's Disease in Humans.

Annals of neurology·2026

Effects of an Inpatient Program on Medication Errors in Hospitalized People with Parkinson's Disease.

Annals of neurology·2026

Multimodal Characterization of Glymphatic-Related Magnetic Resonance Imaging Markers in Huntington's Disease: A Multi-Cohort Retrospective Study.

Annals of neurology·2026

Therapeutic Prospects of Ketamine for Cataplexy in Narcolepsy Type 1: Evidence from a Human Case and a Murine Model.

Annals of neurology·2026

Cortical Thickness and White Matter Surface Morphology in Tourette Syndrome: A Cohort Study.

Annals of neurology·2026

Accelerated Brain Atrophy in Epilepsy: A Prospective Population-Based Study.

Annals of neurology·2026

Simple and robust aqueous sheet jets in vacuum.

IUCrJ·2026

Primary intradural extramedullary anaplastic ependymoma of the cauda equina: a rare and challenging case.

Folia medica·2026

Electron-Ion Covariance Reveals Geometry-Resolved Inner-Shell Spectra in CS2 Photodissociation.

The journal of physical chemistry letters·2026

Transient Receptor Potential (TRP) Channels and Calcium Signaling: A Structural Point of View.

Cold Spring Harbor perspectives in biology·2026

Dynamic NMR Relaxometry Highlights Drying-Induced Heterogeneity and Structural Reconfiguration in Colloidal Gels.

Langmuir : the ACS journal of surfaces and colloids·2026

Temporal Inflammatory Profile in Skin Surface after Oronasal Mask Application.

Acta dermato-venereologica·2026

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An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

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Generation of two LGMDR4 patients derived induced pluripotent stem cell line carrying the SGCB frameshift mutation (p.Gly129_Arg130insGlnTer).

Proteomic Analysis of Corpora Amylacea Extracted From Post-mortem Brain of MAiD-end-of-life Sporadic ALS Patients.

Utility of 18F-FDG PET/CT in the Surveillance of Patients With Neurofibromatosis Type 1.

Multicenter evaluation of the Idylla IDH1-2 Mutation Assay Kit for detection of IDH mutational status in glioma.

An Optimized Protocol for the Generation of iPSC Lines from Lymphoblastoid Cell Lines Using the Non-integrative Sendai Virus.

Diverse Genetic Etiologies of Unilateral Polymicrogyria.

Cofilin 1 Is an Extracellular Vesicle-Associated Plasma Biomarker of Parkinson's Disease in Humans.

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Multimodal Characterization of Glymphatic-Related Magnetic Resonance Imaging Markers in Huntington's Disease: A Multi-Cohort Retrospective Study.

Therapeutic Prospects of Ketamine for Cataplexy in Narcolepsy Type 1: Evidence from a Human Case and a Murine Model.

Cortical Thickness and White Matter Surface Morphology in Tourette Syndrome: A Cohort Study.

Accelerated Brain Atrophy in Epilepsy: A Prospective Population-Based Study.

Simple and robust aqueous sheet jets in vacuum.

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An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

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