Gene symbol: LMNA. Disease: EDMD2

Occupation and education level in functional motor disorders.

Parkinsonism & related disorders·2026

Bridging the global Parkinson's divide: Technology as a structural solution for equitable and brain health-integrated care.

Journal of Parkinson's disease·2026

Dopaminergic nigrostriatal vulnerability in Parkinson's Disease with diabetes: evidence from severity-matched cohorts.

European journal of nuclear medicine and molecular imaging·2026

Pain in Functional Motor Disorders: Clinical Correlates From the Italian Registry.

European journal of neurology·2026

Trazodone for management of depression in Parkinson's disease: expert opinion and proposal for a treatment algorithm.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology·2026

Wearable Inertial Sensor Analysis of Turning Performance Reveals Motor Reserve Effects in Drug-Naïve Parkinson's Disease.

Sensors (Basel, Switzerland)·2026

The NeuroWES project: lessons learned from comprehensive phenotyping and genetic analysis of neurodevelopmental disorders over a decade.

Human genetics·2026

Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project.

Human genetics·2026

A novel pathogenic synonymous DHCR7 variant unveiled by aberrant splicing in Smith-Lemli-Opitz syndrome.

Human genetics·2026

Blending borders: reconstructing the genetic history of the Sindhi population.

Human genetics·2026

Within-sibling attenuation of polygenic risk score accuracy: investigating the effects of principal component analysis, LD score regression, and mixed model association in the UK Biobank.

Human genetics·2026

Long-read genome sequencing resolves a de novo complex 18q12.1q21.2 triplication causing partial tetrasomy and reveals its underlying mechanism.

Human genetics·2026

Vascular Smooth Muscle Myosin 2 Filaments Dynamically Assemble and Stabilize During Induced Contractility.

Arteriosclerosis, thrombosis, and vascular biology·2026

CRISPR-mediated targeting of the <i>LMNA</i> c.745C>T mutation enhances survival and cardiac function in congenital muscular dystrophy.

Molecular therapy. Advances·2026

A Multicenter Cohort Study of 3805 RibXcar Cases: Safety and Efficacy in Incisionless Rib Remodeling.

Plastic and reconstructive surgery. Global open·2026

Structural Gains Without Symptomatic Benefit After Microfracture During High Tibial Osteotomy.

Orthopaedic journal of sports medicine·2026

Coexistence of Multiple Endocrine Neoplasia Type 2B and Centri-Acinar Emphysema With Alpha-1 Antitrypsin Deficiency: A Case Report.

Respirology case reports·2026

Inter-Observer Variability of Gerd-Related Metrics on High-Resolution Manometry and Calculation of the Milan Score.

Neurogastroenterology and motility·2026

Related Experiment Videos

Gene symbol: LMNA. Disease: EDMD2

Related Concept Videos

Occupation and education level in functional motor disorders.

Bridging the global Parkinson's divide: Technology as a structural solution for equitable and brain health-integrated care.

Dopaminergic nigrostriatal vulnerability in Parkinson's Disease with diabetes: evidence from severity-matched cohorts.

Pain in Functional Motor Disorders: Clinical Correlates From the Italian Registry.

Trazodone for management of depression in Parkinson's disease: expert opinion and proposal for a treatment algorithm.

Wearable Inertial Sensor Analysis of Turning Performance Reveals Motor Reserve Effects in Drug-Naïve Parkinson's Disease.

The NeuroWES project: lessons learned from comprehensive phenotyping and genetic analysis of neurodevelopmental disorders over a decade.

Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project.

A novel pathogenic synonymous DHCR7 variant unveiled by aberrant splicing in Smith-Lemli-Opitz syndrome.

Blending borders: reconstructing the genetic history of the Sindhi population.

Within-sibling attenuation of polygenic risk score accuracy: investigating the effects of principal component analysis, LD score regression, and mixed model association in the UK Biobank.

Long-read genome sequencing resolves a de novo complex 18q12.1q21.2 triplication causing partial tetrasomy and reveals its underlying mechanism.

Vascular Smooth Muscle Myosin 2 Filaments Dynamically Assemble and Stabilize During Induced Contractility.

CRISPR-mediated targeting of the <i>LMNA</i> c.745C>T mutation enhances survival and cardiac function in congenital muscular dystrophy.

A Multicenter Cohort Study of 3805 RibXcar Cases: Safety and Efficacy in Incisionless Rib Remodeling.

Structural Gains Without Symptomatic Benefit After Microfracture During High Tibial Osteotomy.

Coexistence of Multiple Endocrine Neoplasia Type 2B and Centri-Acinar Emphysema With Alpha-1 Antitrypsin Deficiency: A Case Report.

Inter-Observer Variability of Gerd-Related Metrics on High-Resolution Manometry and Calculation of the Milan Score.

Related Experiment Videos

Gene symbol: LMNA. Disease: EDMD2

Related Concept Videos

Related Articles