Connective Tissue Pathology
Mostrando 1-12 de 18 artigos, teses e dissertações.
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1. Ultrasonographic, macroscopic and histological characterization of the proximal insertion of the suspensory ligament in Crioulo horses
RESUMO: Embora uma modalidade diagnóstica rotineira, a ultrassonografia ainda possui algumas limitações para o diagnóstico de lesões como as que afetam a inserção proximal do ligamento suspensório (IPLS). Uma dessas limitações é relacionada à composição desse ligamento que inclui fibras musculares e tecido adiposo intercalados entre as fibras l
Pesq. Vet. Bras.. Publicado em: 01/07/2019
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2. Estudo clinicopatologico e imunoistoquimico de prurigo actinico de labio / Clinicopathological and imunohistochemical study af actinic prurigo of lip
Actinic prurigo (AP) is a specific familial photodermatosis that affects mainly mestizos, who live in many parts of North, Central and South America. AP can be clinically evident at any age, but it starts in infancy, between 6 and 8 years of age. It is more frequent in women. AP affects mainly persons living in regions above one thousand meters sea level. Th
Publicado em: 2009
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3. Dermatomyositis: analysis of 109 patients surveyed at the CHSPU / Dermatomiosite: estudo de 109 pacientes avaliados no HCFMUSP
Dermatomyositis is a chronic idiopathic inflammatory disorder which affects the striated skeletal muscles, the skin, and other organs. This present study aims at characterizing the patients who have been affected by this disease and were under treatment at HCFMUSP from January, 1992 to December, 2002 Its classification, the cutaneous and systemical manifesta
Publicado em: 2005
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4. Biochemistry and Pathology of Connective Tissue
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5. A study of headaches and migraine in Sjögren's syndrome and other rheumatic disorders.
Migraine occurs with increased frequency in patients with systemic lupus erythematosus and in subjects suffering from Raynaud's phenomenon without any underlying connective tissue disorders. A possible link between migraine and Raynaud's phenomenon has been suggested. Two rheumatic conditions where Raynaud's phenomenon occurs very commonly are scleroderma an
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6. Glycosaminoglycans are a potential cause of rheumatoid arthritis
Rheumatoid arthritis (RA) is a chronic, systemic, and inflammatory disease of connective tissue with unknown etiology. We investigated whether aberrant immune responses to glycosaminoglycans (GAGs), a major component of joint cartilage, joint fluid, and other soft connective tissue, causes this disease. Here we show that injection of GAGs such as hyaluronic
National Academy of Sciences.
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7. Anticardiolipin antibodies: occurrence in Behçet's syndrome.
Anticardiolipin antibodies have recently been described in association with arterial and venous thrombosis, and with neurological symptoms, in connective tissue diseases. In a study of 70 patients with Behçet's syndrome 13 patients had these antibodies. Of these 13 patients eight had a history of either retinal vascular pathology, cerebral infarction, or th
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8. Experience with the sodium sulphate-Alcian Blue stain for amyloid in cardiac pathology.
The sodium sulphate-Alcian Blue (SAB) method, which stains amyloid green, was evaluated in 220 hearts from elderly patients. The technique proved superior to the Congo red, crystal violet, and thioflavine T methods used either singly or as a battery for the demonstration of cardiac amyloid. Amyloid was easily identified under the X3 objective, even in small
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9. Vasculitis and renal disease in nail-patella syndrome: case report and literature review.
A 57 year old man with nail-patella syndrome (NPS) and associated renal disease is described who developed an inflammatory polyarthropathy and polyarteritis-like vasculitis. Vasculitis and serum complement abnormalities have not previously been reported in NPS. NPS is a rare autosomal dominant connective tissue disorder affecting both mesenchymal and ectoder
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10. Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin gene leading to the absence of the corresponding RNA transcript and protein. Absence of dystrophin leads to disruption of the dystrophin-associated protein complex and substantial changes in skeletal muscle pathology. Although the histological pathology of dystrophic tissu
National Academy of Sciences.
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11. Immunohistochemical identification of tumours of adipocytic differentiation using an antibody to aP2 protein.
AIM--To determine whether aP2 expression is a useful diagnostic marker in soft tissue tumour pathology. METHODS--A polyclonal antibody to aP2 was used to investigate the immunohistochemical expression of this protein in benign and malignant tumours of adipocytic differentiation and a wide variety of other neoplasms. RESULTS--aP2 was only expressed by lipobla
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12. Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome.
We report studies that suggest enzyme replacement therapy will result in a significant reduction in disease progression and tissue pathology in patients with Maroteaux-Lamy syndrome (Mucopolysaccharidosis type VI, MPS VI). A feline model for MPS VI was used to evaluate tissue distribution and clinical efficacy of three forms of recombinant human N-acetylgala