• 180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa
• A case of pretibial dystrophic epidermolysis bullosa: decreased expression of the non-helical domain of type VII collagen molecule
• A Case of Pretibial Epidermolysis Bullosa with Novel Mutations of the <em>COL7A1</em> Gene
• A Case of Pretibial Epidermolysis Bullosa with Novel Mutations of the COL7A1 Gene
• A Japanese case of Kindler syndrome
• A Japanese family with dominant pretibial dystrophic epidermolysis bullosa: Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen
• A novel COL7A1 gene mutation causing pretibial epidermolysis bullosa: report of a Chinese family with intra-familial phenotypical diversity
• A novel mutation of COL7A1 in a Chinese DEB-Pt family and review of the literature
• An update on the RAPH blood group system
• CD151, the first member of the tetraspanin (TM4) superfamily detected on erythrocytes, is essential for the correct assembly of human basement membranes in kidney and skin
• Clinical variability in dystrophic epidermolysis bullosa and findings with scanning electron microscopy
• Coinheritance of 2 New Potentially Damaging Heterozygous COL7A1 Variants in a Family With Autosomal Dominant Epidermolysis Bullosa Pruriginosa
• Connective tissue diseases with cutaneous manifestation (author's transl)
• Dominant pretibial dystrophic epidermolysis bullosa in an Italian family
• Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family
• Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity
• Endoplasmic reticulum stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa
• Epidermolysis bullosa
• Exon 87 skipping of the COL7A1 gene in dominant dystrophic epidermolysis bullosa
• Genetic linkage between the collagen type VII gene COL7A1 and pretibial epidermolysis bullosa with lichenoid features
• Genotype-phenotype correlation in italian patients with dystrophic epidermolysis bullosa
• Hereditary epidermolysis bullosa. Epidemiology and clinical classification of 23 cases
• Late-onset pretibial recessive dystrophic epidermolysis bullosa
• Nephrotic syndrome: Pretibial epidermolysis bullosa in a patient with CD151 tetraspanin defect: A case report
• New Onset Mitral Regurgitation Caused by Mitral Valve Prolapse in a Male Patient with Dominant Pretibial Dystrophic Epidermolysis Bullosa
• Novel frameshift mutation in the noncollagenous region of the COL7A1 gene in pretibial epidermolysis bullosa
• Novel glycine substitution G2037R of <em>COL7A1</em> in a Chinese boy with pretibial epidermolysis bullosa treated with oral olopatadine hydrochloride and topical Vitamin E
• Novel glycine substitution G2037R of COL7A1 in a Chinese boy with pretibial epidermolysis bullosa treated with oral olopatadine hydrochloride and topical Vitamin E
• Novel glycine substitution mutations in COL7A1 reveal that the Pasini and Cockayne-Touraine variants of dominant dystrophic epidermolysis bullosa are allelic
• Novel missense mutation in a patient with recessive pretibial epidermolysis bullosa and a mild phenotype
• Occurrence of hereditary nephritis, pretibial epidermolysis bullosa and beta-thalassemia minor in two siblings with end-stage renal disease
• Pretibial dystrophic epidermolysis bullosa
• Pretibial dystrophic epidermolysis bullosa
• Pretibial dystrophic epidermolysis bullosa associated with aberrant exon splicing of type VII collagen
• Pretibial dystrophic epidermolysis bullosa with localized cutaneous amyloidosis: coincidental or secondary amyloidosis?
• Pretibial dystrophic epidermolysis bullosa: a recessively inherited COL7A1 splice site mutation affecting procollagen VII processing
• Pretibial epidermolysis bullosa
• Pretibial epidermolysis bullosa
• Pretibial epidermolysis bullosa
• Pretibial epidermolysis bullosa and hypothyroidism
• Pretibial epidermolysis bullosa mimicking hypertrophic lichen planus
• Pretibial epidermolysis bullosa with vulvar involvement
• Pretibial epidermolysis bullosa: a clinicopathologic study
• Pretibial epidermolysis bullosa: a study in a family with lichenoid lesions
• Pretibial epidermolysis bullosa: genetic linkage to COL7A1 and identification of a glycine-to-cysteine substitution in the triple-helical domain of type VII collagen
• Pretibial epidermolysis bullosa: is this case a new subtype with loss of types IV and VII collagen?
• Pretibial epidermolysis bullosa: report of a case
• Pretibial epidermolysis bullosa: report of two families and review of the literature
• Pretibial epidermolysis bullosa. A rare form of epidermolysis bullosa simplex
• Pretibial epidermolysis bullosa. Successful therapy with a skin graft
• Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy
• Solitary angiokeratoma seen in a patient with pretibial epidermolysis bullosa
• Splice site mutation in COL7A1 resulting in aberrant in-frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial
• Splicing mutation in the COL7A1 gene mRNA exon 71 in a female patient with pretibial epidermolysis bullosa
• Sporadic dystrophic epidermolysis bullosa with concomitant atopic dermatitis
• The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation
• Three Hong Kong Chinese cases of pretibial epidermolysis bullosa: a genodermatosis that can masquerade as an acquired inflammatory disease
• Ulcers in pretibial epidermolysis bullosa. Grafting with autologous meshed split-thickness skin and allogeneic cultured keratinocytes