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Identification of a Novel HLA Class II Association with DQB1*0502 in an Italian Myasthenic Population.
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- Annals of the New York Academy of Sciences, 1998, v. 841, n. 1, p. 355, doi. 10.1111/j.1749-6632.1998.tb10946.x
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- Article
Anti-titin and Antiryanodine Receptor Antibodies in Myasthenia Gravis Patients with Thymoma.
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- Annals of the New York Academy of Sciences, 1998, v. 841, n. 1, p. 538, doi. 10.1111/j.1749-6632.1998.tb10978.x
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- Article
T-Cell Receptor-CDR3 Sequences of Polymyositis Muscle-Infiltrating T-Lymphocytes Indicate a Conventional Antigen as Target<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1995, v. 756, n. 1, p. 414, doi. 10.1111/j.1749-6632.1995.tb44549.x
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- Article
T-Cell Infiltration in Polymyositis Is Characterized by Coexpression of Cytotoxic and T-Cell-Activating Cytokine Transcripts<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1995, v. 756, n. 1, p. 418, doi. 10.1111/j.1749-6632.1995.tb44550.x
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- Article
Immunization with Rat-, but Not Torpedo-Derived 97-116 Peptide of the AChR α-Subunit Induces Experimental Myasthenia Gravis in Lewis Rat.
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- Annals of the New York Academy of Sciences, 2003, v. 998, n. 1, p. 391, doi. 10.1196/annals.1254.048
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- Article
Analysis of SjTREC Levels in Thymus from MG Patients and Normal Children.
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- Annals of the New York Academy of Sciences, 2003, v. 998, n. 1, p. 270, doi. 10.1196/annals.1254.029
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- Article
Effect on T Cell Recognition and Immunogenicity of Alanine-Substituted Peptides Corresponding to 97-116 Sequence of the Rat AChR α-Subunit.
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- Annals of the New York Academy of Sciences, 2003, v. 998, n. 1, p. 395, doi. 10.1196/annals.1254.049
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- Article
Myasthenia Gravis (MG): Epidemiological Data and Prognostic Factors.
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- Annals of the New York Academy of Sciences, 2003, v. 998, n. 1, p. 413, doi. 10.1196/annals.1254.054
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- Article
Expression of Transforming Growth Factor-β1 in Thymus of Myasthenia Gravis Patients.
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- Annals of the New York Academy of Sciences, 2003, v. 998, n. 1, p. 278, doi. 10.1196/annals.1254.031
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- Article
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
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- Human Molecular Genetics, 2012, v. 21, n. 10, p. 2205, doi. 10.1093/hmg/dds035
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- Article
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathies.
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- 1994
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- journal article
Chloroquine myopathy and myasthenia-like syndrome.
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- Muscle & Nerve, 1988, v. 11, n. 2, p. 114, doi. 10.1002/mus.880110205
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- Article
Fetal myosin immunoreactivity in human dystrophic muscle.
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- Muscle & Nerve, 1986, v. 9, n. 1, p. 51, doi. 10.1002/mus.880090108
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- Publication type:
- Article
Increased myofibrillar protein catabolism in duchenne muscular dystrophy measured by 3-methylhistidine excretion in the urine.
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- 1984
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- Publication type:
- journal article
Content of methylhistidines in normal and pathological human skeletal muscles.
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- 1983
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- Publication type:
- journal article
Concordance between severity of disease, disability and health-related quality of life in Myasthenia gravis.
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- Neurological Sciences, 2010, v. 31, n. 1, p. 41, doi. 10.1007/s10072-009-0167-y
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- Article
Anti-MOG autoantibodies in Italian multiple sclerosis patients: specificity, sensitivity and clinical association.
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- International Immunology, 2004, v. 16, n. 4, p. 559, doi. 10.1093/intimm/dxh056
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- Article
Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenita.
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- Human Mutation, 1999, v. 14, n. 5, p. 447, doi. 10.1002/(SICI)1098-1004(199911)14:5<447::AID-HUMU13>3.0.CO;2-Z
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- Article
On the personal facets of quality of life in chronic neurological disorders.
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- Behavioural Neurology, 2009, v. 21, n. 3/4, p. 155, doi. 10.1155/2009/879576
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- Publication type:
- Article
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN.
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- Brain: A Journal of Neurology, 2014, v. 137, n. 6, p. 1643, doi. 10.1093/brain/awu069
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- Article
Identification of previously unreported mutations in CHRNA1, CHRNE and RAPSN genes in three unrelated Italian patients with congenital myasthenic syndromes.
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- Journal of Neurology, 2010, v. 257, n. 7, p. 1119, doi. 10.1007/s00415-010-5472-0
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- Article
The relationship between health, disability and quality of life in Myasthenia Gravis: results from an Italian study.
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- Journal of Neurology, 2010, v. 257, n. 1, p. 98, doi. 10.1007/s00415-009-5279-z
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- Article
Risk factors for tumor occurrence in patients with myasthenia gravis.
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- Journal of Neurology, 2009, v. 256, n. 8, p. 1221, doi. 10.1007/s00415-009-5091-9
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- Publication type:
- Article
Immunosuppressive Treatments: Their Efficacy on Myasthenia Gravis Patients' Outcome and on the Natural Course of the Diseasea.
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- Annals of the New York Academy of Sciences, 1993, v. 681, n. 1, p. 594, doi. 10.1111/j.1749-6632.1993.tb22951.x
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- Article
Development of muscle pathology in canine X-linked muscular dystrophy. II. Quantitative characterization of histopathological progression during postnatal skeletal muscle development.
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- Acta Neuropathologica, 2001, v. 101, n. 5, p. 469, doi. 10.1007/s004010000308
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- Publication type:
- Article
Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression.
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- Acta Neuropathologica, 1999, v. 97, n. 2, p. 127, doi. 10.1007/s004010050965
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- Publication type:
- Article
Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects.
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- Acta Neuropathologica, 1997, v. 94, n. 1, p. 28, doi. 10.1007/s004010050668
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- Publication type:
- Article
Abnormal lysosomal and ubiquitin‐proteasome pathways in 19p13.3 distal myopathy.
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- Annals of Neurology, 2004, v. 56, n. 1, p. 133
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- Article
Partial laminin α2 chain deficiency in a patient with myopathy resembling inclusion body myositis.
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- Annals of Neurology, 2000, v. 47, n. 6, p. 811, doi. 10.1002/1531-8249(200006)47:6<811::AID-ANA16>3.0.CO;2-9
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- Article
Clinical heterogeneity of adhalin deficiency.
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- 1996
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- Publication type:
- journal article
Promotion of ambulation of patients with spinal muscular atrophy by early fitting of knee-ankle-foot orthoses.
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- 1987
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- Publication type:
- journal article
Heart-Specific Localization of Emerin: New Insights Into Emery-Dreifuss Muscular Dystrophy.
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- Human Molecular Genetics, 1997, v. 6, n. 13, p. 2257, doi. 10.1093/hmg/6.13.2257
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- Publication type:
- Article