S. Blot

发表

Characterization of dystrophic muscle in golden retriever muscular dystrophy dogs by nuclear magnetic resonance imaging

P. Carlier, J. Thibaud, A. Monnet, 2007, Neuromuscular Disorders.

Tissue Doppler imaging detects early asymptomatic myocardial abnormalities in a dog model of Duchenne's cardiomyopathy.

F. Lallemand, V. Richard, G. Derumeaux, 2004, European heart journal.

Altered myofilament structure and function in dogs with Duchenne muscular dystrophy cardiomyopathy.

T. Irving, P. D. de Tombe, S. Blot, 2016, Journal of molecular and cellular cardiology.

Myostatin Is a Quantifiable Biomarker for Monitoring Pharmaco-gene Therapy in Duchenne Muscular Dystrophy

F. Muntoni, I. Barthélémy, S. Blot, 2020, Molecular therapy. Methods & clinical development.

Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy.

K. Patel, M. Schuelke, C. Hourde, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

Serum profiling identifies novel muscle miRNA and cardiomyopathy-related miRNA biomarkers in Golden Retriever muscular dystrophy dogs and Duchenne muscular dystrophy patients.

D. Israeli, L. Servais, I. Barthélémy, 2014, The American journal of pathology.

Serum Pro fi ling Identi fi es Novel Muscle miRNA and Cardiomyopathy-Related miRNA Biomarkers in Golden Retriever Muscular Dystrophy Dogs and Duchenne Muscular Dystrophy Patients

L. Servais, I. Barthélémy, S. Blot, 2014 .

Direct myocardial implantation of human embryonic stem cells in a dog model of Duchenne cardiomyopathy reveals poor cell survival in dystrophic tissue

M. Peschanski, C. Monville, M. Pucéat, 2011, Journal of stem cells & regenerative medicine.

Splitting of Pi and other 31P NMR anomalies of skeletal muscle metabolites in canine muscular dystrophy

P. Carlier, J. Thibaud, A. Monnet, 2012, NMR in biomedicine.

Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells

I. Barthélémy, S. Blot, M. Sampaolesi, 2015, Stem cells international.

iPSC–derived progenitor cells functionally regenerate cardiac and skeletal muscle

C. Verfaillie, G. Ceccarelli, S. Janssens, 2015 .

Mesodermal iPSC-derived progenitor cells functionally regenerate cardiac and skeletal muscle.

C. Verfaillie, G. Ceccarelli, S. Janssens, 2015, The Journal of clinical investigation.

Aldehyde dehydrogenases contribute to skeletal muscle homeostasis in healthy, aging, and Duchenne muscular dystrophy patients

S. Blot, O. Agbulut, J. Vilquin, 2020, Journal of cachexia, sarcopenia and muscle.

Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems.

F. Pilot-Storck, I. Barthélémy, S. Blot, 2017, The American journal of pathology.

1 PROGRESSIVE STRUCTURAL DEFECTS IN CANINE CENTRONUCLEAR MYOPATHY INDICATE A 1 ROLE FOR HACD 1 IN MAINTAINING SKELETAL MUSCLE MEMBRANE SYSTEMS 2 3

F. Pilot-Storck, Jordan, I. Barthélémy, 2016 .

HACD 1 in Maintaining Skeletal Muscle Membrane Systems

I. Barthélémy, S. Blot, C. Sewry, 2016 .

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis

S. Dréano, F. Pilot-Storck, J. Thibaud, 2010, Proceedings of the National Academy of Sciences.

A high-resolution genetic map of mouse Chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdfocd) region

J. Guénet, S. Blot, G. Carle, 1998, Mammalian Genome.

Centronuclear Myopathy in Labrador Retrievers: A Recent Founder Mutation in the PTPLA Gene Has Rapidly Disseminated Worldwide

J. Thibaud, I. Barthélémy, S. Blot, 2012, PloS one.

Vascular endothelial dysfunction in Duchenne muscular dystrophy is restored by bradykinin through upregulation of eNOS and nNOS

L. Hittinger, J. Thibaud, I. Barthélémy, 2011, Basic Research in Cardiology.

Cerebellar cortical degeneration in adult American Staffordshire Terriers.

J. Thibaud, S. Blot, M. Breen, 2004, Journal of veterinary internal medicine.

Bradykinin restores left ventricular function, sarcomeric protein phosphorylation, and e/nNOS levels in dogs with Duchenne muscular dystrophy cardiomyopathy.

L. Hittinger, J. Thibaud, I. Barthélémy, 2012, Cardiovascular research.

Diagnostic potential of natriuretic peptides in the occult phase of golden retriever muscular dystrophy cardiomyopathy.

G. Derumeaux, S. Blot, V. Chetboul, 2004, Journal of veterinary internal medicine.

Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

O. Pansarasa, G. D’Antona, I. Barthélémy, 2014, Nature.

Muscle function recovery in golden retriever muscular dystrophy after AAV1-U7 exon skipping.

A. Goyenvalle, A. Vulin, L. García, 2012, Molecular therapy : the journal of the American Society of Gene Therapy.

Nodo-paranodopathy, internodopathy and cleftopathy: Target-based reclassification of Guillain–Barré-like immune-mediated polyradiculoneuropathies in dogs and cats

S. Blot, K. Matiasek, A. Fischer, 2016, Neuromuscular Disorders.

Human Galectin 3 Binding Protein Interacts with Recombinant Adeno-Associated Virus Type 6

R. Kotin, R. Samulski, S. Blot, 2012, Journal of Virology.

A dog model for centronuclear myopathy carrying the most common DNM2 mutation

I. Barthélémy, S. Blot, J. Böhm, 2022, Disease models & mechanisms.

The authors reply: Comment on: "Aldehyde dehydrogenases contribute to skeletal muscle homeostasis in healthy, aging, and Duchenne muscular dystrophy patients" by Etienne et al.

S. Blot, O. Agbulut, J. Vilquin, 2020, Journal of cachexia, sarcopenia and muscle.

Spinal Cryptococcoma in an Immunocompetent Cat

M. Wyers, J. Thibaud, S. Blot, 2008, Journal of Comparative Pathology.

Fifth European Dirofilaria and Angiostrongylus Days (FiEDAD) 2016

H. Auer, L. Rinaldi, J. Votýpka, 2017, Parasites & Vectors.

Predictive markers of clinical outcome in the GRMD dog model of Duchenne muscular dystrophy

G. Butler-Browne, V. Mouly, A. Faussat, 2014, Disease Models & Mechanisms.

Title: Predictive markers of clinical outcome in the GRMD dog model of

G. Butler-Browne, V. Mouly, A. Faussat, 2014 .

J. Thibaud, I. Barthélémy, S. Blot, 2012, Veterinary radiology & ultrasound : the official journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association.

X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation

R. Weiss, K. Flanigan, C. Béroud, 2020, Skeletal Muscle.

Effects of an Immunosuppressive Treatment in the GRMD Dog Model of Duchenne Muscular Dystrophy

J. Thibaud, I. Barthélémy, S. Blot, 2012, PloS one.

The electroretinographic phenotype of dogs with Golden Retriever muscular dystrophy.

S. Blot, S. Chahory, B. Clerc, 2001, Veterinary ophthalmology.

Alteration in Left Ventricular Contractile Function Develops in Puppies With Duchenne Muscular Dystrophy.

L. Hittinger, I. Barthélémy, S. Blot, 2019, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

Cutaneous saphenous nerve graft for the treatment of sciatic neurotmesis in a dog.

S. Blot, N. Granger, A. Hidalgo, 2006, Journal of the American Veterinary Medical Association.

Tissue Doppler imaging for detection of radial and longitudinal myocardial dysfunction in a family of cats affected by dystrophin-deficient hypertrophic muscular dystrophy.

P. Bruneval, J. Thibaud, S. Blot, 2006, Journal of veterinary internal medicine.

Synaptic transmission blockade increases plasminogen activator activity in mouse skeletal muscle poisoned with botulinum toxin type A

S. Blot, B. Festoff, D. Hantaı̈, 1995, Synapse.

Suspected spontaneous early hemorrhagic transformation of multiple ischemic strokes secondary to primary splenic torsion in a German Shepherd dog

J. Thibaud, S. Blot, J. Mortier, 2022, Journal of veterinary internal medicine.

Progressive myelopathy due to a spontaneous intramedullary hematoma in a dog: pre- and postoperative clinical and magnetic resonance imaging follow-up.

J. Thibaud, S. Blot, F. Delisle, 2008, Journal of the American Animal Hospital Association.

Successful treatment of cervical spinal epidural empyema secondary to grass awn migration in a cat

J. Thibaud, S. Blot, F. Delisle, 2007, Journal of feline medicine and surgery.

Spinal subarachnoid cysts in 13 dogs.

S. Blot, F. Delisle, M. Colle, 2003, Veterinary radiology & ultrasound : the official journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association.

Nematode dermatitis due to Angiostrongylus vasorum infection in a dog.

S. Blot, B. Polack, E. Bensignor, 2015, Veterinary dermatology.

Fifth European Dirofilaria and Angiostrongylus Days (FiEDAD) 2016

H. Auer, L. Rinaldi, J. Votýpka, 2017, Parasites & Vectors.

First isolation of Mycobacterium microti (Llama-type) from a dog.

G Hewinson, J. Thibaud, S. Blot, 2004, Veterinary microbiology.

Surgical Treatment of Lumbosacral Discospondylitis with Gentamicin-Impregnated Polymethylmethacrylate Cement and Omentalization

S. Blot, P. Moissonnier, A. Jeandel, 2019, VCOT Open.

A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome

S. Blot, C. Hitte, L. Martignat, 2015, PloS one.

The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2

S. Blot, M. Breen, J. Kessler, 2003, Human Genetics.

SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs.

S. Blot, J. Kessler, J. Panthier, 2005, Human molecular genetics.

Protective effects of rimeporide on left ventricular function in golden retriever muscular dystrophy dogs.

J. Wojcik, L. Hittinger, I. Barthélémy, 2020, International journal of cardiology.

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

Giulio Cossu, Nicolas Granger, Sara Mantero, 2006, Nature.

Prevalence of neurological disorders in French bulldog: a retrospective study of 343 cases (2002–2016)

S. Blot, L. Desquilbet, A. Jeandel, 2017, BMC Veterinary Research.

Tissue Doppler assessment of diastolic and systolic alterations of radial and longitudinal left ventricular motions in Golden Retrievers during the preclinical phase of cardiomyopathy associated with muscular dystrophy.

J. Thibaud, S. Blot, V. Chetboul, 2004, American journal of veterinary research.

Gait analysis using accelerometry in dystrophin-deficient dogs

E. Barrey, J. Hogrel, J. Thibaud, 2009, Neuromuscular Disorders.

Alteration of cardiolipin-dependent mitochondrial coupling in muscle protects against obesity

S. Luquet, F. Pilot-Storck, A. Malgoyre, 2019, bioRxiv.

In Vivo Myoblasts Tracking Using the Sodium Iodide Symporter Gene Expression in Dogs

J. Thibaud, I. Barthélémy, S. Blot, 2020, Molecular therapy. Methods & clinical development.

Chronic traumatic brain injury in a dog.

J. Thibaud, S. Blot, F. Delisle, 2010, Journal of comparative pathology.

Surgical treatment and radiation therapy of frontal lobe meningiomas in 7 dogs.

J. Thibaud, S. Blot, P. Devauchelle, 2011, The Canadian veterinary journal = La revue veterinaire canadienne.

Juvenile‐onset polyneuropathy in American Staffordshire Terriers

J. Thibaud, S. Blot, K. Matiasek, 2018, Journal of veterinary internal medicine.

C8 cross transfer for the treatment of caudal brachial plexus avulsion in three dogs.

S. Blot, C. Carozzo, C. Escriou, 2017, Veterinary surgery : VS.

Restoration of elbow flexion by performing contralateral lateral thoracic and thoracodorsal nerve transfers after experimental musculocutaneous nerve transection.

S. Blot, C. Carozzo, C. Escriou, 2005, Journal of neurosurgery.

In vivo stem cell tracking using scintigraphy in a canine model of DMD

J. Thibaud, I. Barthélémy, S. Blot, 2020, Scientific Reports.

Electrophysiological features in dogs with peripheral nerve sheath tumors: 51 cases (1993-2010).

J. Thibaud, S. Blot, F. Delisle, 2012, Journal of the American Veterinary Medical Association.

Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy

Thomas Voit, Jean-Yves Hogrel, Laurent Servais, 2017, Nature Communications.

Alteration of Cardiac Progenitor Cell Potency in GRMD Dogs

I. Barthélémy, S. Blot, M. Sampaolesi, 2012, Cell transplantation.

Premature proliferative arrest of cricopharyngeal myoblasts in oculo-pharyngeal muscular dystrophy: Therapeutic perspectives of autologous myoblast transplantation

K. Mamchaoui, G. Butler-Browne, V. Mouly, 2006, Neuromuscular Disorders.

Myogenic Potential of Canine Craniofacial Satellite Cells

S. Fulle, I. Barthélémy, S. Blot, 2014, Front. Aging Neurosci..

HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth

F. Pilot-Storck, A. Kihara, A. Ferry, 2015, Journal of molecular cell biology.

Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

Giulio Cossu, Nicolas Granger, Sara Mantero, 2013, Nature.

Comprehensive longitudinal characterization of canine muscular dystrophy by serial NMR imaging of GRMD dogs

N. Azzabou, P. Carlier, N. Azzabou, 2012, Neuromuscular Disorders.

Minimally invasive video-assisted cervical ventral slot in dogs

J. Thibaud, S. Blot, V. Viateau, 2010, Veterinary and Comparative Orthopaedics and Traumatology.

Stereotactic CT-guided brain biopsy in the dog.

F. Beuvon, S. Blot, P. Devauchelle, 2002, The Journal of small animal practice.

Magnetic resonance imaging of a giant frontal hemorrhagic mucocele with intracranial extension in a cat.

J. Thibaud, S. Blot, P. Moissonnier, 2018, Veterinary radiology & ultrasound : the official journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association.

Current protocol of a research phase I clinical trial of full-length dystrophin plasmid DNA in Duchenne/Becker muscular dystrophies Part I: rationale

S. Blot, S. Braun, M. Fardeau, 2002, Neuromuscular Disorders.

Anatomical and mesoscopic characterization of the dystrophic diaphragm: An in vivo nuclear magnetic resonance imaging study in the Golden retriever muscular dystrophy dog

P. Carlier, J. Thibaud, I. Barthélémy, 2017, Neuromuscular Disorders.

Gait characterization in golden retriever muscular dystrophy dogs using linear discriminant analysis

E. Qannari, J. Hogrel, I. Barthélémy, 2017, BMC Musculoskeletal Disorders.

Sampaolesi et al. reply

S. Blot, M. Sampaolesi, G. Cossu, 2007, Nature.

Color discrimination in horses

S. Blot, B. Deputte, N. Kasbaoui, 2012 .

Botulism in 2 urban dogs.

J. Thibaud, S. Blot, A. Uriarte, 2010, The Canadian veterinary journal = La revue veterinaire canadienne.

miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy

P. Bénit, D. Israeli, L. Servais, 2020, Scientific Reports.

Erratum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs (Nature (2013) 494 (506) DOI: 10.1038/nature11976))

O. Pansarasa, G. D’Antona, I. Barthélémy, 2014 .

Evaluation of coexisting polymyositis in feline myasthenia gravis: A case series

S. Blot, G. Shelton, C. Escriou, 2017, Neuromuscular Disorders.

Stabilizing Ryanodine Receptors Improves Left Ventricular Function in Juvenile Dogs With Duchenne Muscular Dystrophy.

I. Barthélémy, S. Blot, A. Meli, 2021, Journal of the American College of Cardiology.

Epidemiological, clinical, and electrophysiological findings in dogs and cats with traumatic brachial plexus injury: A retrospective study of 226 cases

J. Thibaud, S. Blot, A. Nicolle, 2021, Journal of veterinary internal medicine.

Longitudinal ambulatory measurements of gait abnormality in dystrophin-deficient dogs

Eric Barrey, Thomas Voit, Jean-Yves Hogrel, 2011, BMC musculoskeletal disorders.

Facial and vestibular neuropathy of unknown origin in 16 dogs.

J. Thibaud, S. Blot, A. Jeandel, 2016, The Journal of small animal practice.

Transforming Growth Factor α Expression as a Response of Murine Motor Neurons to Axonal Injury and Mutation‐induced Degeneration

S. Blot, M. Junier, F. Lisovoski, 1997, Journal of neuropathology and experimental neurology.

miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy

P. Bénit, D. Israeli, M. Sanson, 2020, Scientific Reports.

Spatial and Temporal Non-Uniform Changes in Left Ventricular Myocardial Strain in Dogs with Duchenne Muscular Dystrophy

L. Hittinger, I. Barthélémy, S. Blot, 2023, Journal of cardiovascular development and disease.

Generalised idiopathic polymyositis mimicking masticatory myositis in a dog

S. Blot, N. Blanchard-Gutton, Nicolas Van Caenegem, 2022, Veterinary Record Case Reports.

The Mouse Mutation Muscle Deficient (mdf) is Characterized by a Progressive Motoneuron Disease

S. Blot, C. Poirier, P. Dreyfus, 1995, Journal of neuropathology and experimental neurology.

A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia

T. Leeb, S. Blot, V. Jagannathan, 2022, Animal Genetics.

Allogenic umbilical cord‐derived mesenchymal stromal cells improve motor function in prenatal surgical repair of myelomeningocele: An ovine model study

J. Larghero, S. Blot, C. Adam, 2023, BJOG : an international journal of obstetrics and gynaecology.

Immune‐mediated polyneuropathy in cats: Clinical description, electrodiagnostic assessment, and treatment

S. Blot, Nicolas Van Caenegem, K. Gnirs, 2023, Journal of veterinary internal medicine.

Acute idiopathic polyneuritis with spontaneous remission in an Abyssinian cat.

S. Blot, K. Matiasek, A. Jeandel, 2015, The Canadian veterinary journal = La revue veterinaire canadienne.

Improved survival in rats administered NG-nitro L-arginine methyl ester due to converting enzyme inhibition.

G. Chatellier, S. Blot, J. Michel, 1996, Journal of cardiovascular pharmacology.

Vascular endothelial dysfunction in Duchenne muscular dystrophy is restored by bradykinin through upregulation of eNOS and nNOS

L. Hittinger, J. Thibaud, I. Barthélémy, 2011, Basic Research in Cardiology.

Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy.

K. Patel, M. Schuelke, C. Hourde, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

Ambulatory electrocardiographic longitudinal monitoring in dystrophin-deficient dogs identifies decreased Very Low Frequency power as a hallmark of impaired Heart Rate Variability in Duchenne Muscular Dystrophy

I. Barthélémy, S. Blot, F. Relaix, 2023, bioRxiv.