Results 291 to 300 of about 116,124 (316)
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Histochemistry of sarcoidotic-hyaline
Pneumonologie Pneumonology, 1976On account of its weaker reactions for tryptophan, tyrosine, proteolipids, and lipoproteins, sarcoidotic-hyaline (Sa. Hy.) is immediately distinguishable from caseosis. However, protein histochemistry fails to differentiate Sa. Hy. from normal (fixed and insoluble postfixed) and pericaseous collagen. Evidence of this is provided by the present study on
G. Barbolini, S. Battaglia
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British Journal of Dermatology, 1983
SUMMARY A 4-year-old boy with juvenile hyaline fibromatosis (systemic hyalinosis) is described. The clinical features, pathology and prognosis of this condition are discussed.
Andrew Yule Finlay +2 more
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SUMMARY A 4-year-old boy with juvenile hyaline fibromatosis (systemic hyalinosis) is described. The clinical features, pathology and prognosis of this condition are discussed.
Andrew Yule Finlay +2 more
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Pulmonary Hyalinizing Granuloma
American Journal of Clinical Pathology, 1987Pulmonary hyalinizing granulomas are distinct fibrosing lesions of lung, having central whorled deposits of lamellar collagen. Twenty-four cases of this unusual pulmonary lesion are reported herein. Hyalinizing granulomas occur in middle-aged persons and are frequently mistaken for metastatic carcinoma radiographically.
Liselotte Hochholzer, Samuel A. Yousem
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The Journal of Pediatrics, 1957
Summary A review of the literature relating to the possible causes, composition, and treatment of “hyaline membrane disease” has been presented.
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Summary A review of the literature relating to the possible causes, composition, and treatment of “hyaline membrane disease” has been presented.
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Revista Española de Cardiología (English Edition), 2016
Varon de 44 anos, con antecedentes de sindrome depresivo en tratamiento farmacologico, fallecio como consecuencia de suicidio por ahorcamiento. Durante la autopsia, ademas de los signos propios de la causa de fallecimiento, encontramos 3 nodulos perlados pediculados, de 0,5 cm de diametro en la cara posterior del ventriculo izquierdo (figura 1) y 2 con
Helena Martínez-Alcázar +2 more
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Varon de 44 anos, con antecedentes de sindrome depresivo en tratamiento farmacologico, fallecio como consecuencia de suicidio por ahorcamiento. Durante la autopsia, ademas de los signos propios de la causa de fallecimiento, encontramos 3 nodulos perlados pediculados, de 0,5 cm de diametro en la cara posterior del ventriculo izquierdo (figura 1) y 2 con
Helena Martínez-Alcázar +2 more
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Pediatric Dermatology, 2001
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with onset in infancy or early childhood. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints. The light and electron microscopic features are very distinctive. Here we report an 8‐month‐old boy
A. Santos‐Muñoz +3 more
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Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with onset in infancy or early childhood. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints. The light and electron microscopic features are very distinctive. Here we report an 8‐month‐old boy
A. Santos‐Muñoz +3 more
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Neuromuscular Disorders, 1994
Muscle biopsy from two unrelated patients, a male aged 40 and a female aged 3, with relatively non-progressive limb weakness since infancy, revealed numerous subsarcolemmal glassy, hyaline appearing bodies present in 20-30% of the fibres. Type 1 fibre predominance was present, and the hyaline bodies were exclusive to type 1 fibres.
Jerry R. Mendell +2 more
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Muscle biopsy from two unrelated patients, a male aged 40 and a female aged 3, with relatively non-progressive limb weakness since infancy, revealed numerous subsarcolemmal glassy, hyaline appearing bodies present in 20-30% of the fibres. Type 1 fibre predominance was present, and the hyaline bodies were exclusive to type 1 fibres.
Jerry R. Mendell +2 more
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PULMONARY CYTOPLASMIC HYALIN RESEMBLING MALLORY'S ALCOHOLIC HYALIN IN THE LIVER
Acta Pathologica Japonica, 1986Sixty‐three consecutive autopsy cases of interstitial fibrosis of the lung, 6 cases of organizing pneumonia, 14 of pneumocystis pneumonia, and 20 of acute bacterial pneumonia complicating as a terminal illness listed in our Department of Pathology during a period from 1978 to 1983 were surveyed for Mallory body‐like cytoplasmic hyalins in the alveolar ...
Naoko Kono +2 more
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Archives of Dermatology, 1976
A boy had multiple large tumors on the scalp, whitish nodules on the nape and both sides of the neck, hypertrophic gingiva, and severe flexural contractures of hip and knee joints. The histopathologic structure of the tumor was characteristic of juvenile hyalin fibromatosis.
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A boy had multiple large tumors on the scalp, whitish nodules on the nape and both sides of the neck, hypertrophic gingiva, and severe flexural contractures of hip and knee joints. The histopathologic structure of the tumor was characteristic of juvenile hyalin fibromatosis.
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Diagnosing Hyaline Membrane Disease
AJN, American Journal of Nursing, 1961OF THE BABIES WHO ARE born alive, about 2 percent die during the neonatal period. Around one third of the deaths of these infants result from hyaline membrane disease. In spite of this, the disease may not always be fatal. Estimates of the fatality rate vary from 20 percent to 60 percent.
James M. Sutherland, Doris S. Newman
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