Results 291 to 300 of about 405,511 (346)
Characterization of biomass based novel microcrystalline cellulose from Eucalyptus teriticornis leaf. [PDF]
Sci RepSenthamaraikannan P +5 more
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A- and B-Type Crystalline Forms in Aggregates and Solidified Materials Prepared from Short Linear Maltodextrin. [PDF]
J Appl Glycosci (1999)Kawano A +5 more
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Different Varieties of Water Caltrop (<i>Trapa bispinosa</i>) Starch: Physicochemical Properties and Digestibility Modulated by Its Multi-Scale Structure. [PDF]
FoodsMa T +7 more
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Enhanced UV resistance of polypropylene via copper nanoparticle incorporation for outdoor applications. [PDF]
Sci RepBaafif M, Abdo HS, Albedah A.
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Retina, 1984
A 52-year-old Japanese woman had retinal crystalline deposits with atrophy of the pigment epithelium and choriocapillaris and pigment clumps in the periphery. The patient did not have corneal crystals. The crystals were seen biomicroscopically in all layers of the retina and on the retinal vessels. The diagnosis of crystalline retinopathy was made. The
S, Hayasaka, S, Okuyama
openaire +2 more sources
A 52-year-old Japanese woman had retinal crystalline deposits with atrophy of the pigment epithelium and choriocapillaris and pigment clumps in the periphery. The patient did not have corneal crystals. The crystals were seen biomicroscopically in all layers of the retina and on the retinal vessels. The diagnosis of crystalline retinopathy was made. The
S, Hayasaka, S, Okuyama
openaire +2 more sources
American Journal of Ophthalmology, 1978
A 34-year-old woman had crystalline dystrophy of the retina associated with atrophy of the choriocapillaris and pigment epithelium, and pigment clumping in the fundus periphery. Consanguinity of her parents suggested an autosomal recessive inheritance pattern for this type of crystalline retinal dystrophy. The patient did not have corneal crystals. Her
W S, Grizzard +3 more
openaire +2 more sources
A 34-year-old woman had crystalline dystrophy of the retina associated with atrophy of the choriocapillaris and pigment epithelium, and pigment clumping in the fundus periphery. Consanguinity of her parents suggested an autosomal recessive inheritance pattern for this type of crystalline retinal dystrophy. The patient did not have corneal crystals. Her
W S, Grizzard +3 more
openaire +2 more sources