26 Bilder zum Thema "lipid disorder" bei ClipDealer

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Cholesterol Disease Challenge
Tay-Sachs disease, 3D illustration. A genetic disorder that progressively destroys brain neurons, is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A
Hyperlipidemia with blood vessel isolated, 3d rendering
Cholesterol test (lipid panel) analysis result, test tubes with blood and a medical stethoscope lies on table. Concept of diagnosis atherosclerosis in patient with high level cholesterol in blood test
A cluster of Fat cells
A cluster of Fat cells
Fatty liver, liver steatosis
Eye retina in Tay-Sachs disease, 3D illustration with so-called cherry-red spot. A genetic disorder that progressively destroys brain neurons, is caused by a genetic mutation in the HEXA gene
Fatty liver, liver steatosis
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Young female wearing white underwear checking and squeeze her belly fat condition stomach healthy lifestyle isolated on white background
High Cholesterol Represents Ill Health And Affliction
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
cholesterol
High Cholesterol Represents Poor Health And Affliction
A Adipocyte aka Fat cell isolated on white
Eye retina in sphingolipid storage diseases, 3D illustration. Macular cherry red spot. Tay-Sachs disease and Niemann Pick disease
3D illustration of a cluster of Fat cells isolated on white.
A single Fat cell aka Adipocyte
High Cholesterol Means Poor Health And Hypercholesterolemia
Light micrograph of a fatty liver
Light micrograph of a fatty liver
A single Fat cell aka Adipocyte
Molecule of beta-hexosaminidase A enzyme, or HEXA, 3D illustration. Mutations in the gene encoding HEXA decrease the hydrolysis of GM2 gangliosides, which is the main cause of Tay-Sachs disease
Tay-Sachs disease, a lysosomal storage genetic disorder, 3D illustration. A child with macrocephaly, and close-up view of swollen neurons with lamellar inclusions due to accumulation of gangliosides
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes

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