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Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea

American journal of human genetics, 2016-09, Vol.99 (3), p.753-761

2016

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The Contributions of Fiber Atrophy, Fiber Loss, In Situ Specific Force, and Voluntary Activation to Weakness in Sarcopenia

The journals of gerontology. Series A, Biological sciences and medical sciences, 2018-09, Vol.73 (10), p.1287-1294

2018

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PPARs and Microbiota in Skeletal Muscle Health and Wasting

International journal of molecular sciences, 2020-10, Vol.21 (21), p.8056

2020

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Neuromuscular involvement in COVID-19 critically ill patients

Clinical neurophysiology, 2020-12, Vol.131 (12), p.2809-2816

2020

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Diaphragm muscle fiber weakness and ubiquitin-proteasome activation in critically ill patients

American journal of respiratory and critical care medicine, 2015-05, Vol.191 (10), p.1126-1138

2015

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IFN-β-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis

Acta neuropathologica, 2017-10, Vol.134 (4), p.655-666

2017

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The Roles of Vitamin D in Skeletal Muscle: Form, Function, and Metabolism

Endocrine reviews, 2013-02, Vol.34 (1), p.33-83

2013

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Advanced glycation end-products induce skeletal muscle atrophy and dysfunction in diabetic mice via a RAGE-mediated, AMPK-down-regulated, Akt pathway

The Journal of pathology, 2016-02, Vol.238 (3), p.470-482

2016

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Chronic muscle weakness and mitochondrial dysfunction in the absence of sustained atrophy in a preclinical sepsis model

eLife, 2019-12, Vol.8

2019

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AGE-RELATED CHANGES IN THE STRUCTURE AND FUNCTION OF SKELETAL MUSCLES

Clinical and experimental pharmacology & physiology, 2007-11, Vol.34 (11), p.1091-1096

2007

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Is REDD1 a metabolic double agent? Lessons from physiology and pathology

American Journal of Physiology: Cell Physiology, 2020-11, Vol.319 (5), p.C807-C824

2020

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Sarcopenia and Neuroscience: Learning to Communicate

The journals of gerontology. Series A, Biological sciences and medical sciences, 2021-10, Vol.76 (10), p.1882-1890

2021

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Rapidly Progressive Diaphragmatic Weakness and Injury during Mechanical Ventilation in Humans

American journal of respiratory and critical care medicine, 2011-02, Vol.183 (3), p.364-371

2011

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Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease

Journal of neurology, neurosurgery and psychiatry, 2022-12, Vol.93 (12), p.1289-1298

2022

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Effects of aging on human skeletal muscle after immobilization and retraining

Journal of applied physiology (1985), 2009-10, Vol.107 (4), p.1172-1180

2009

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Validation of the FNIH sarcopenia criteria and SOF frailty index as predictors of long-term mortality in ambulatory older men

Age and ageing, 2016-09, Vol.45 (5), p.602-608

2016

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Long-term observational study of sporadic inclusion body myositis

Brain (London, England : 1878), 2011-11, Vol.134 (11), p.3176-3184

2011

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Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice

Human molecular genetics, 2021-05, Vol.30 (11), p.1006-1019

2021

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Sarcopenia and obesity

Current opinion in clinical nutrition and metabolic care, 2019-01, Vol.22 (1), p.13-19

2019

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Leucyl-tRNA Synthetase Contributes to Muscle Weakness through Mammalian Target of Rapamycin Complex 1 Activation and Autophagy Suppression in a Mouse Model of Duchenne Muscular Dystrophy

The American journal of pathology, 2024-08, Vol.194 (8), p.1571-1580

2024

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Ultrasound measurement of rectus femoris cross-sectional area and the relationship with quadriceps strength in COPD

Thorax, 2009-05, Vol.64 (5), p.418-423

2009

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Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model

Human molecular genetics, 2024-07, Vol.33 (14), p.1195-1206

2024

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Involvement of Type I Interferon Signaling in Muscle Stem Cell Proliferation During Dermatomyositis

Neurology, 2022-05, Vol.98 (21), p.e2108

2022

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Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy

Human molecular genetics, 2015-09, Vol.24 (18), p.5219-5233

2015

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Cellular Consequences of Coenzyme Q10 Deficiency in Neurodegeneration of the Retina and Brain

International journal of molecular sciences, 2020-12, Vol.21 (23), p.9299

2020

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Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea

The Contributions of Fiber Atrophy, Fiber Loss, In Situ Specific Force, and Voluntary Activation to Weakness in Sarcopenia

PPARs and Microbiota in Skeletal Muscle Health and Wasting

Neuromuscular involvement in COVID-19 critically ill patients

Diaphragm muscle fiber weakness and ubiquitin-proteasome activation in critically ill patients

IFN-β-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis

The Roles of Vitamin D in Skeletal Muscle: Form, Function, and Metabolism

Advanced glycation end-products induce skeletal muscle atrophy and dysfunction in diabetic mice via a RAGE-mediated, AMPK-down-regulated, Akt pathway

Chronic muscle weakness and mitochondrial dysfunction in the absence of sustained atrophy in a preclinical sepsis model

AGE-RELATED CHANGES IN THE STRUCTURE AND FUNCTION OF SKELETAL MUSCLES

Is REDD1 a metabolic double agent? Lessons from physiology and pathology

Sarcopenia and Neuroscience: Learning to Communicate

Rapidly Progressive Diaphragmatic Weakness and Injury during Mechanical Ventilation in Humans

Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease

Effects of aging on human skeletal muscle after immobilization and retraining

Validation of the FNIH sarcopenia criteria and SOF frailty index as predictors of long-term mortality in ambulatory older men

Long-term observational study of sporadic inclusion body myositis

Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice

Sarcopenia and obesity

Leucyl-tRNA Synthetase Contributes to Muscle Weakness through Mammalian Target of Rapamycin Complex 1 Activation and Autophagy Suppression in a Mouse Model of Duchenne Muscular Dystrophy

Ultrasound measurement of rectus femoris cross-sectional area and the relationship with quadriceps strength in COPD

Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model

Involvement of Type I Interferon Signaling in Muscle Stem Cell Proliferation During Dermatomyositis

Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy

Cellular Consequences of Coenzyme Q10 Deficiency in Neurodegeneration of the Retina and Brain

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