Found: 109
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Presumptive motor neuron degeneration in an adult cat.
- Published in:
- Canadian Veterinary Journal / Revue Vétérinaire Canadienne, 2024, v. 65, n. 10, p. 1034
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- Publication type:
- Article
Pathologic Changes in and Immunophenotyping of Polymyositis in the Dutch Kooiker Dog.
- Published in:
- Animals (2076-2615), 2024, v. 14, n. 17, p. 2519, doi. 10.3390/ani14172519
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- Publication type:
- Article
Analysis of Risk Factors for Acquired Myasthenia in Dogs.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 841, n. 1, p. 587, doi. 10.1111/j.1749-6632.1998.tb10990.x
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- Publication type:
- Article
Acquired motor neuron loss causing severe pelvic limb contractures in a young cat
- Published in:
- Journal of Feline Medicine & Surgery, 2010, v. 12, n. 3, p. 237, doi. 10.1016/j.jfms.2010.01.007
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- Publication type:
- Article
Axonal neuropathy with unusual clinical course in young Snowshoe cats
- Published in:
- Journal of Feline Medicine & Surgery, 2009, v. 11, n. 12, p. 1005, doi. 10.1016/j.jfms.2009.02.011
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- Publication type:
- Article
Clinical and genetic characterisation of dystrophin-deficient muscular dystrophy in a family of Miniature Poodle dogs.
- Published in:
- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0193372
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- Publication type:
- Article
Routine and specialized laboratory testing for the diagnosis of neuromuscular diseases in dogs and cats.
- Published in:
- Veterinary Clinical Pathology, 2010, v. 39, n. 3, p. 278, doi. 10.1111/j.1939-165X.2010.00244.x
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- Publication type:
- Article
Main Immunogenic Region Structure Promotes Binding of Conformation-Dependent Myasthenia Gravis Autoantibodies, Nicotinic Acetylcholine Receptor Conformation Maturation, and Agonist Sensitivity.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 44, p. 13898, doi. 10.1523/JNEUROSCI.2833-09.2009
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- Publication type:
- Article
Loss of Modifier of Cell Adhesion Reveals a Pathway Leading to Axonal Degeneration.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 1, p. 118, doi. 10.1523/JNEUROSCI.3985-08.2009
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- Publication type:
- Article
Disruption of both nesprin 1 and desmin results in nuclear anchorage defects and fibrosis in skeletal muscle.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 22, p. 5879, doi. 10.1093/hmg/ddu310
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- Publication type:
- Article
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 1, p. 209, doi. 10.1093/hmg/ddt412
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- Publication type:
- Article
Nesprin 1 is critical for nuclear positioning and anchorage.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 2, p. 329, doi. 10.1093/hmg/ddp499
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- Publication type:
- Article
Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis.
- Published in:
- Journal of Neuroscience Research, 2014, v. 92, n. 4, p. 531, doi. 10.1002/jnr.23332
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- Publication type:
- Article
Vacuolar myopathy in a dog resembling human sporadic inclusion body myositis.
- Published in:
- 2009
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- Publication type:
- Report
Myopathy with tubulin-reactive inclusions in two cats.
- Published in:
- 2007
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- Publication type:
- Report
Comparable myelinated nerve pathology in feline and human diabetes mellitus.
- Published in:
- Acta Neuropathologica, 2007, v. 113, n. 4, p. 431, doi. 10.1007/s00401-006-0163-8
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- Publication type:
- Article
An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed.
- Published in:
- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 9, p. 2687, doi. 10.1534/g3.116.027896
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- Publication type:
- Article
A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1).
- Published in:
- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 2, p. 255, doi. 10.1534/g3.115.022707
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- Publication type:
- Article
Current Classification of Canine Muscular Dystrophies and Identification of New Variants.
- Published in:
- Genes, 2023, v. 14, n. 8, p. 1557, doi. 10.3390/genes14081557
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- Publication type:
- Article
An EHPB1L1 Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever Littermates.
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- 2022
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- Publication type:
- Case Study
LAMA2 Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy.
- Published in:
- 2021
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- Publication type:
- Case Study
A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy.
- Published in:
- Genes, 2020, v. 11, n. 12, p. 1426, doi. 10.3390/genes11121426
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- Publication type:
- Article
A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog.
- Published in:
- Genes, 2020, v. 11, n. 9, p. 1033, doi. 10.3390/genes11091033
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- Publication type:
- Article
Analysis of organic acids, amino acids, and carnitine in dogs with lipid storage myopathy.
- Published in:
- 1998
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- Publication type:
- journal article
Expression of fiber type specific proteins during ontogeny of canine temporalis muscle.
- Published in:
- Muscle & Nerve, 1988, v. 11, n. 2, p. 124, doi. 10.1002/mus.880110207
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- Publication type:
- Article
Canine masticatory muscle disorders: A study of 29 cases.
- Published in:
- Muscle & Nerve, 1987, v. 10, n. 8, p. 753, doi. 10.1002/mus.880100812
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- Publication type:
- Article
Fiber type-specific autoantibodies in a dog with eosinophilic myositis.
- Published in:
- Muscle & Nerve, 1985, v. 8, n. 9, p. 783, doi. 10.1002/mus.880080907
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- Publication type:
- Article
A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse.
- Published in:
- Nature Genetics, 2008, v. 40, n. 10, p. 1235, doi. 10.1038/ng.224
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- Publication type:
- Article
An ARHGEF10 Deletion Is Highly Associated with a Juvenile-Onset Inherited Polyneuropathy in Leonberger and Saint Bernard Dogs.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004635
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- Publication type:
- Article
Altered Splicing of the BIN1 Muscle-Specific Exon in Humans and Dogs with Highly Progressive Centronuclear Myopathy.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003430
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- Publication type:
- Article
Clinical presentation, MRI, histopathology and outcome in a cat with immune-mediated masticatory myositis.
- Published in:
- Journal of Feline Medicine & Surgery Open Reports, 2021, v. 7, n. 2, p. 1, doi. 10.1177/20551169211050037
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- Publication type:
- Article
Progressive increases in creatine kinase activity in an anorexic cat with necrotising myopathy.
- Published in:
- Journal of Feline Medicine & Surgery Open Reports, 2021, v. 7, n. 2, p. 1, doi. 10.1177/20551169211031790
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- Publication type:
- Article
Beta-sarcoglycan-deficient muscular dystrophy presenting as chronic bronchopneumonia in a young cat.
- Published in:
- Journal of Feline Medicine & Surgery Open Reports, 2019, v. 5, n. 2, p. N.PAG, doi. 10.1177/2055116919856457
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- Publication type:
- Article
Distal polyneuropathy in an adult Birman cat with toxoplasmosis.
- Published in:
- Journal of Feline Medicine & Surgery Open Reports, 2016, v. 2, n. 1, p. 1, doi. 10.1177/2055116916630335
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- Publication type:
- Article
Use of mycophenolate mofetil as a rescue agent in the treatment of severe generalized myasthenia gravis in three dogs.
- Published in:
- Journal of Veterinary Emergency & Critical Care, 2009, v. 19, n. 4, p. 369, doi. 10.1111/j.1476-4431.2009.00433.x
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- Publication type:
- Article
Organic acidemia in a young cat associated with cobalamin deficiency.
- Published in:
- Journal of Veterinary Emergency & Critical Care, 2007, v. 17, n. 3, p. 299, doi. 10.1111/j.1476-4431.2007.00234.x
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- Publication type:
- Article
Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D.
- Published in:
- Skeletal Muscle, 2021, v. 11, n. 1, p. 1, doi. 10.1186/s13395-020-00257-y
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- Publication type:
- Article
A QIL1 Variant Associated with Ventricular Arrhythmias and Sudden Cardiac Death in the Juvenile Rhodesian Ridgeback Dog.
- Published in:
- Genes, 2019, v. 10, n. 2, p. 168, doi. 10.3390/genes10020168
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- Publication type:
- Article
Identification of the mutation causing centronuclear myopathy in a border collie.
- Published in:
- 2014
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- Publication type:
- Letter to the Editor
IMAGING DIAGNOSIS—MASTICATORY MUSCLE MYOSITIS IN A YOUNG DOG.
- Published in:
- Veterinary Radiology & Ultrasound, 2008, v. 49, n. 3, p. 270, doi. 10.1111/j.1740-8261.2008.00364.x
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- Publication type:
- Article
MAGNETIC RESONANCE IMAGING IN THE DIAGNOSIS OF CANINE INFLAMMATORY MYOPATHIES IN THREE DOGS.
- Published in:
- Veterinary Radiology & Ultrasound, 2006, v. 47, n. 6, p. 532, doi. 10.1111/j.1740-8261.2006.00181.x
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- Publication type:
- Article
A Nonsense Variant in the DMD Gene Causes X-Linked Muscular Dystrophy in the Maine Coon Cat.
- Published in:
- Animals (2076-2615), 2022, v. 12, n. 21, p. 2928, doi. 10.3390/ani12212928
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- Publication type:
- Article
A Novel Mutation in CLCN1 Associated with Feline Myotonia Congenita.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109926
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- Publication type:
- Article
A <i>COLQ</i> Missense Mutation in Labrador Retrievers Having Congenital Myasthenic Syndrome.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0106425
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- Publication type:
- Article
Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 <i>(SLC19A3)</i> Gene Associated with Alaskan Husky Encephalopathy.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0057195
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- Publication type:
- Article
A <i>Gly98Val</i> Mutation in the N-Myc Downstream Regulated Gene 1 (<i>NDRG1</i>) in Alaskan Malamutes with Polyneuropathy.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0054547
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- Publication type:
- Article
Centronuclear Myopathy in Labrador Retrievers: A Recent Founder Mutation in the PTPLA Gene Has Rapidly Disseminated Worldwide.
- Published in:
- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046408
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- Publication type:
- Article
An ADAMTSL2 Founder Mutation Causes Musladin-Lueke Syndrome, a Heritable Disorder of Beagle Dogs, Featuring Stiff Skin and Joint Contractures.
- Published in:
- PLoS ONE, 2010, v. 5, n. 9, p. 1, doi. 10.1371/journal.pone.0012817
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- Publication type:
- Article
A Duchenne Muscular Dystrophy Gene Hot Spot Mutation in Dystrophin-Deficient Cavalier King Charles Spaniels Is Amenable to Exon 51 Skipping.
- Published in:
- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008647
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- Publication type:
- Article
The ER-Bound RING Finger Protein 5 (RNF5/RMA1) Causes Degenerative Myopathy in Transgenic Mice and Is Deregulated in Inclusion Body Myositis.
- Published in:
- PLoS ONE, 2008, v. 3, n. 2, p. 1, doi. 10.1371/journal.pone.0001609
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- Publication type:
- Article