epidermolysis bullosa การใช้

• Mutations in this gene are associated with epidermolysis bullosa with pyloric atresia.
• Epidermolysis bullosa acquisita involves an autoimmune reaction to this form of collagen.
• The "'American Cream Draft "'is a rare draft horse junctional epidermolysis bullosa.
• Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa.
• Junctional epidermolysis bullosa is an inherited disease affecting laminin and collagen.
• Other autoimmune diseases include bullous pemphigoid and epidermolysis bullosa acquisita.
• Mutations in LAMB3 have been identified as the cause of various types of epidermolysis bullosa.
• Mutations in this gene have been identified as the cause of Herlitz type junctional epidermolysis bullosa.
• Victims of epidermolysis bullosa do not have the normal anchoring mechanisms that attach skin to flesh.
• Epidermolysis bullosa causes severe blistering that scars the internal organs and deforms the hands and feet.
• Epidermolysis bullosa simplex is a form of epidermolysis bullosa that causes blisters at the site of rubbing.
• The epidermolysis bullosa trial is still enrolling.
• The inherited disease is called epidermolysis bullosa.
• Epidermolysis Bullosa, Epidermolysis Bullosa Acquisita, Erythema Multiforme, Lichen Planus, pemphigus vulgaris, Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis.
• Epidermolysis Bullosa, Epidermolysis Bullosa Acquisita, Erythema Multiforme, Lichen Planus, pemphigus vulgaris, Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis.
• Dystrophic Epidermolysis Bullosa Research Association of America : http : / / www . debra . org
• Ari suffered from epidermolysis bullosa ( EB ), a rare disease in which the skin easily blisters.
• Epidermolysis bullosa simplex is a form of epidermolysis bullosa that causes blisters at the site of rubbing.
• Donations and proceeds from shops fund services for epidermolysis bullosa affected families and medical research into the condition.
• Epidermolysis bullosa simplex ( EBS ) is an inherited skin blistering disorder associated with mutations in either K5 or K14.