Results 131 to 140 of about 3,245 (185)
A case of corneal opacity caused by atovaquone administration. [PDF]
Am J Ophthalmol Case RepAshizuka T +6 more
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Physiological Reviews, 1946
Gerhard Schmidt. Volume 26, page 275: Lipins and Lipidoses, by S. J. Thannhauser and The Sentence beginning on line 22 (page 301) should read as follows: They are all a part of the syndrome under discussion. The organs which may be involved singly or in various combinations in the syndrome (essential xanthomatosis of the normocholesteremic type ...
S J, THANNHAUSER, G, SCHMIDT
exaly +3 more sources
Gerhard Schmidt. Volume 26, page 275: Lipins and Lipidoses, by S. J. Thannhauser and The Sentence beginning on line 22 (page 301) should read as follows: They are all a part of the syndrome under discussion. The organs which may be involved singly or in various combinations in the syndrome (essential xanthomatosis of the normocholesteremic type ...
S J, THANNHAUSER, G, SCHMIDT
exaly +3 more sources
Pediatric Clinics of North America, 1976
The disorders presented consist of those clinical entities in which a reasonably well defined lipid storage material accumulated within nervous tissue. Many other progressive, degenerative disorders are suspected of being storage disorders, but their chemical pathology remains unclear.
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The disorders presented consist of those clinical entities in which a reasonably well defined lipid storage material accumulated within nervous tissue. Many other progressive, degenerative disorders are suspected of being storage disorders, but their chemical pathology remains unclear.
exaly +3 more sources
2019
Abstract Chapter 83 discusses lipidoses. The lipidoses are genetic diseases caused by enzyme deficiencies, which result in the cellular accumulation of lipids. These abnormal cells infiltrate tissues, including bone marrow, resulting in their dysfunction.
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Abstract Chapter 83 discusses lipidoses. The lipidoses are genetic diseases caused by enzyme deficiencies, which result in the cellular accumulation of lipids. These abnormal cells infiltrate tissues, including bone marrow, resulting in their dysfunction.
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Lipidoses detected in Poland through 1993
Pediatric Neurology, 1994It is estimated that 70-100 children suffering from a lysosomal storage disease are born in Poland every year. From 1975 to 1993, the activity of various lysosomal enzymes was determined in the leukocytes, cultured skin fibroblasts, or hair roots from 5,594 patients, mainly children, in whom the diagnosis of a lipidosis was suspected.
Anna Tylki-Szymanska
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