Facial weakness in hereditary inclusion body myopathies

Life or death by NFκB, Losartan promotes survival in dy2J/dy2J mouse of MDC1A.

Cell death & disease·2015

Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.

Neuromuscular disorders : NMD·2013

MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation.

Cell death and differentiation·2013

Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2012

Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes.

Seizure·2009

Bilateral foot drop as a manifestation of myasthenia gravis.

Journal of clinical neuromuscular disease·2008

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy: Motor-Unit Reinnervation and Functional Recovery.

Neurology·2026

Centrally Acting Medications, Chronic Pain, and Orthopedic Surgical History Among Former American Football Players.

Neurology·2026

Bridging the Gap: Translating Microemboli-Induced Spreading Depolarization Into Clinical Practice.

Neurology·2026

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Neurology·2026

Child Neurology: Radiologic Evolution and Developmental Correlates in Fetal Cerebral Sinovenous Thrombosis: A Case Report.

Neurology·2026

De-Escalating and Discontinuing Immunotherapies in Patients With NMOSD and MOGAD.

Neurology·2026

Humidifier lung diagnosed by integrating environmental assessment and inhalation provocation testing: a case with Purpureocillium lilacinum as the most likely causative antigen.

Respiratory medicine case reports·2026

Invasive pulmonary aspergillosis as a sentinel manifestation of good syndrome in a patient with thymoma.

IDCases·2026

A case of autoimmune pulmonary alveolar proteinosis in a patient with chronic nicotine vaping exposure.

Respiratory medicine case reports·2026

Comparative analysis of microbiota in the ocular surface of patients with atopic keratoconjunctivitis and Stevens-Johnson Syndrome with severe ocular complications.

Frontiers in immunology·2026

Montelukast and Bilastine Combination Therapy in Allergic Rhinitis: A Narrative Review of Evidence.

Cureus·2026

The lung microbiome and asthma: from inflammatory phenotype differentiation to microbe-based immunomodulatory strategies.

Frontiers in immunology·2026

Related Experiment Videos

Facial weakness in hereditary inclusion body myopathies

Related Concept Videos

Life or death by NFκB, Losartan promotes survival in dy2J/dy2J mouse of MDC1A.

Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.

MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation.

Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene.

Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes.

Bilateral foot drop as a manifestation of myasthenia gravis.

Severe Parsonage-Turner Syndrome and Surgically Managed Traumatic Brachial Plexopathy: Motor-Unit Reinnervation and Functional Recovery.

Centrally Acting Medications, Chronic Pain, and Orthopedic Surgical History Among Former American Football Players.

Bridging the Gap: Translating Microemboli-Induced Spreading Depolarization Into Clinical Practice.

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Child Neurology: Radiologic Evolution and Developmental Correlates in Fetal Cerebral Sinovenous Thrombosis: A Case Report.

De-Escalating and Discontinuing Immunotherapies in Patients With NMOSD and MOGAD.

Humidifier lung diagnosed by integrating environmental assessment and inhalation provocation testing: a case with Purpureocillium lilacinum as the most likely causative antigen.

Invasive pulmonary aspergillosis as a sentinel manifestation of good syndrome in a patient with thymoma.

A case of autoimmune pulmonary alveolar proteinosis in a patient with chronic nicotine vaping exposure.

Comparative analysis of microbiota in the ocular surface of patients with atopic keratoconjunctivitis and Stevens-Johnson Syndrome with severe ocular complications.

Montelukast and Bilastine Combination Therapy in Allergic Rhinitis: A Narrative Review of Evidence.

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Related Experiment Videos

Facial weakness in hereditary inclusion body myopathies

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