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1 well as extended family members at risk for junctional epidermolysis bullosa.
2 al-epidermal junction, diagnostic of Herlitz junctional epidermolysis bullosa.
3 sal keratinocyte integrity and resilience in junctional epidermolysis bullosa.
4 tion of hemidesmosomes was also perturbed in junctional epidermolysis bullosa.
5 gene/protein for mutations in some forms of junctional epidermolysis bullosa.
6 the lethal skin blistering disorder Herlitz junctional epidermolysis bullosa.
8 understanding the role of alpha 6 beta 4 in junctional epidermolysis bullosa, an often lethal human
9 the U.S. population carrier risk for Herlitz junctional epidermolysis bullosa and all variants of jun
10 treatment of hemophilia, tyrosinemia type I, junctional epidermolysis bullosa and type 1 diabetes.
11 the epidermis, similar to that seen in human junctional epidermolysis bullosa, and death occurs withi
12 lex, epidermolytic palmoplantar keratoderma, junctional epidermolysis bullosa, and dystrophic forms o
13 abnormalities underlying different forms of junctional epidermolysis bullosa appear to affect certai
14 ively in 76 patients with severe generalized junctional epidermolysis bullosa born in the years 2000-
15 ese patients did not have the lethal form of junctional epidermolysis bullosa but, as adults, display
17 d the LAMB3 gene for mutations in 22 Herlitz junctional epidermolysis bullosa families, and identifie
20 molysis bullosa, a usually nonlethal form of junctional epidermolysis bullosa, have generalized blist
23 type in some cases of the nonlethal forms of junctional epidermolysis bullosa involving abnormalities
24 type in some cases of the nonlethal forms of junctional epidermolysis bullosa involving abnormalities
35 ringing the total number of distinct Herlitz junctional epidermolysis bullosa mutations in LAMB3 to 3
37 ncidence of 1 of 150,000, severe generalized junctional epidermolysis bullosa occurred more often tha
39 utosomal recessive blistering skin disorder, junctional epidermolysis bullosa, particularly in the le
40 COL7A1 in the cDNA were detected, and in the junctional epidermolysis bullosa patients transcripts wi
42 ecessive dystrophic epidermolysis bullosa or junctional epidermolysis bullosa phenotypes but in whom
43 cessive dystrophic epidermolysis bullosa and junctional epidermolysis bullosa phenotypes in these fam
45 port on two patients with severe generalized junctional epidermolysis bullosa treated with allogeneic
46 enes in two patients with nonlethal forms of junctional epidermolysis bullosa using polymerase chain
47 enes in two patients with nonlethal forms of junctional epidermolysis bullosa using polymerase chain
48 olysis bullosa, a distinct nonlethal form of junctional epidermolysis bullosa, using polymerase chain
49 al epidermolysis bullosa and all variants of junctional epidermolysis bullosa was calculated to be on
53 from a syndrome resembling the human disease junctional epidermolysis bullosa with pyloric atresia (P
54 is study, we report a patient with a form of junctional epidermolysis bullosa with skin fragility and
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