Lista de obras - Thomas E. Lloyd - Dominio Público Uruguay

A Case of Morvan Syndrome Mimicking Amyotrophic Lateral Sclerosis With Frontotemporal Dementia.

artículo científico publicado en 2016

A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43.

artículo científico publicado en 2011

A TRPV channel in Drosophila motor neurons regulates presynaptic resting Ca2+ levels, synapse growth, and synaptic transmission

artículo científico

Antibody levels correlate with creatine kinase levels and strength in anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase-associated autoimmune myopathy.

artículo científico publicado en 2012

Axonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributions

artículo científico publicado en 2012

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

artículo científico publicado en 2014

Cytosolic 5'-Nucleotidase 1A As a Target of Circulating Autoantibodies in Autoimmune Diseases

artículo científico publicado en 2015

Drosophila models of neurologic disease.

artículo científico publicado en 2015

Endophilin mutations block clathrin-mediated endocytosis but not neurotransmitter release

artículo científico publicado en 2002

Evaluation and construction of diagnostic criteria for inclusion body myositis

artículo científico publicado en 2014

FIG4 regulates lysosome membrane homeostasis independent of phosphatase function

artículo científico publicado en 2015

Increased frequency of DRB1*11:01 in anti-hydroxymethylglutaryl-coenzyme A reductase-associated autoimmune myopathy.

artículo científico publicado en 2012

Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS

artículo científico publicado en 2021

Mutant Huntingtin Disrupts the Nuclear Pore Complex

artículo científico publicado en 2017

Myositis-specific autoantibodies are specific for myositis compared to genetic muscle disease.

artículo científico publicado en 2015

Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension

artículo científico publicado en 2021

Neuropeptide delivery to synapses by long-range vesicle circulation and sporadic capture.

artículo científico publicado en 2012

Novel therapeutic approaches for inclusion body myositis.

artículo científico publicado en 2010

Nucleocytoplasmic transport in C9orf72-mediated ALS/FTD.

artículo científico publicado en 2016

Overlapping features of polymyositis and inclusion body myositis in HIV-infected patients

artículo científico publicado en 2017

Peripheral neuropathy: clinical and electrophysiological considerations.

artículo científico publicado en 2014

Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis.

artículo científico publicado en 2016

Publisher Correction: Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS

artículo científico publicado en 2021

Sciatic nerve tumor and tumor-like lesions - uncommon pathologies.

artículo científico

Secondary Causes of Myositis

artículo científico publicado en 2020

Spectrum of Muscle Histopathologic Findings in Forty-Two Scleroderma Patients With Weakness

artículo científico publicado en 2015

Statin-Induced Anti-HMGCR-Associated Myopathy.

artículo científico publicado en 2016

Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy

artículo científico publicado en 2014

TFEB/Mitf links impaired nuclear import to autophagolysosomal dysfunction in C9-ALS

scientific article published on 10 December 2020

TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca2

artículo científico publicado en 2020

Tdp-43 cryptic exons are highly variable between cell types

artículo científico publicado en 2017

The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction.

artículo científico publicado en 2014

The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.

artículo científico publicado en 2015

The p150(Glued) CAP-Gly domain regulates initiation of retrograde transport at synaptic termini

artículo científico publicado en 2012

Thigh muscle MRI in immune-mediated necrotising myopathy: extensive oedema, early muscle damage and role of anti-SRP autoantibodies as a marker of severity

artículo científico publicado en 2016

Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation

artículo científico publicado en 2013

WIDE AWAKE mediates the circadian timing of sleep onset

artículo científico publicado en 2014

Whole-body MR neurography: Prospective feasibility study in polyneuropathy and Charcot-Marie-Tooth disease.

artículo científico publicado en 2016

Lista de obras de Thomas E. Lloyd

A Case of Morvan Syndrome Mimicking Amyotrophic Lateral Sclerosis With Frontotemporal Dementia.

A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43.

A TRPV channel in Drosophila motor neurons regulates presynaptic resting Ca2+ levels, synapse growth, and synaptic transmission

Antibody levels correlate with creatine kinase levels and strength in anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase-associated autoimmune myopathy.

Axonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributions

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis

Cytosolic 5'-Nucleotidase 1A As a Target of Circulating Autoantibodies in Autoimmune Diseases

Drosophila models of neurologic disease.

Endophilin mutations block clathrin-mediated endocytosis but not neurotransmitter release

Evaluation and construction of diagnostic criteria for inclusion body myositis

FIG4 regulates lysosome membrane homeostasis independent of phosphatase function

Increased frequency of DRB1*11:01 in anti-hydroxymethylglutaryl-coenzyme A reductase-associated autoimmune myopathy.

Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS

Mutant Huntingtin Disrupts the Nuclear Pore Complex

Myositis-specific autoantibodies are specific for myositis compared to genetic muscle disease.

Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension

Neuropeptide delivery to synapses by long-range vesicle circulation and sporadic capture.

Novel therapeutic approaches for inclusion body myositis.

Nucleocytoplasmic transport in C9orf72-mediated ALS/FTD.

Overlapping features of polymyositis and inclusion body myositis in HIV-infected patients

Peripheral neuropathy: clinical and electrophysiological considerations.

Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis.

Publisher Correction: Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS

Sciatic nerve tumor and tumor-like lesions - uncommon pathologies.

Secondary Causes of Myositis

Spectrum of Muscle Histopathologic Findings in Forty-Two Scleroderma Patients With Weakness

Statin-Induced Anti-HMGCR-Associated Myopathy.

Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy

TFEB/Mitf links impaired nuclear import to autophagolysosomal dysfunction in C9-ALS

TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca2

Tdp-43 cryptic exons are highly variable between cell types

The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction.

The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.

The p150(Glued) CAP-Gly domain regulates initiation of retrograde transport at synaptic termini

Thigh muscle MRI in immune-mediated necrotising myopathy: extensive oedema, early muscle damage and role of anti-SRP autoantibodies as a marker of severity

Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation

WIDE AWAKE mediates the circadian timing of sleep onset

Whole-body MR neurography: Prospective feasibility study in polyneuropathy and Charcot-Marie-Tooth disease.