friedreich

navigate by keyword : friedreich ataxia genetic disorder neurology disease condition movement coordination inherited mutation diagnosis symptom nerve muscle therapy study patient treatment physiology anatomy disability care medicine health evaluation progressive damage cause medical explanation function body research science clinical term concept background healthcare rehabilitation degeneration system word pathology meaning

Friedreich`s ataxia. Text label for a medical diagnosis. Royalty Free Stock Photo
Frataxin (human) mitochondrial protein. Reduced expression causes Friedreich's ataxia. 3D render. Royalty Free Stock Photo
Frataxin (human) mitochondrial protein. Reduced expression causes Friedreich's ataxia. 3D render. Royalty Free Stock Photo
Neurological diagnosis of Friedreichs ataxia. Neurological hammer, shape of brain, pen and pencil the lying on medical report, lab Royalty Free Stock Photo
Friedreich's Ataxia is a rare, inherited, degenerative disease that damages the spinal cord, peripheral nerves Royalty Free Stock Photo
Idebenone drug molecule Royalty Free Stock Photo
Crystal structure of mature human frataxin Royalty Free Stock Photo
FRIEDREICH ATAXIA word on torn paper background. Genetic disorder term representing progressive nervous system damage and movement
Frataxin (human) mitochondrial protein. Reduced expression causes Friedreich\'s ataxia. 3D illustration Royalty Free Stock Photo
Idebenone drug molecule. Skeletal formula. Royalty Free Stock Photo
Idebenone drug molecule Royalty Free Stock Photo
Idebenone drug molecule. Skeletal formula. Royalty Free Stock Photo
Frataxin (human) mitochondrial protein. Reduced expression causes Friedreich\'s ataxia. 3D illustration Royalty Free Stock Photo
Frataxin (human) mitochondrial protein. Reduced expression causes Friedreich\'s ataxia. 3D illustration Royalty Free Stock Photo
Idebenone drug molecule Royalty Free Stock Photo
FRIEDREICH ATAXIA word on torn paper background. Genetic disorder term representing progressive nervous system damage and movement coordination loss caused by inherited mutation


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