Results 271 to 280 of about 5,720 (299)
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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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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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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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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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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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Journal of the American Medical Association, 1958
The clinical signs of hyaline membrane syndrome can simulate the respiratory difficulties seen in any one of a variety of abnormal states. If one could give a "characteristic" feature of this abnormal respiratory situation, it might be said that the infant is born well.
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The clinical signs of hyaline membrane syndrome can simulate the respiratory difficulties seen in any one of a variety of abnormal states. If one could give a "characteristic" feature of this abnormal respiratory situation, it might be said that the infant is born well.
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Journal of Craniofacial Surgery, 2013
Hyaline ring granuloma is a rare oral lesion with an unclear and controversial etiology, characterized by the presence of rings of palely eosinophilic structureless material (the so-called hyaline rings) with multinucleated giant cells around and within the very same rings.Various theories have been proposed about the pathogenesis of hyaline ring ...
Boffano P +4 more
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Hyaline ring granuloma is a rare oral lesion with an unclear and controversial etiology, characterized by the presence of rings of palely eosinophilic structureless material (the so-called hyaline rings) with multinucleated giant cells around and within the very same rings.Various theories have been proposed about the pathogenesis of hyaline ring ...
Boffano P +4 more
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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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Pediatrics, 1961
Pulmonary hyaline membranes were studied by observations on their dissolution in vitro by proteolytic enzymes, by streptokinase and by urea with and without added thioglycollic acid. Pepsin, trypsin and chymotrypsin dissolved the hyaline membranes both in sections of human lungs as well as in sections of mouse lung with the experimentally produced ...
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Pulmonary hyaline membranes were studied by observations on their dissolution in vitro by proteolytic enzymes, by streptokinase and by urea with and without added thioglycollic acid. Pepsin, trypsin and chymotrypsin dissolved the hyaline membranes both in sections of human lungs as well as in sections of mouse lung with the experimentally produced ...
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