Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa

Gedde-Dahl, 1971, Epidermolysis bullosa, 1

Anton-Lamprecht, 1982, Epidermolysis bullosa herpetiformis Dowling-Meara: a report of a case and pathomorphogenesis, Dermatologica, 164, 221, 10.1159/000250096

Briggaman, 1983, Hereditary epidermolysis bullosa with special emphasis on newly recognized syndromes and complications, Dermatol Clin, 1, 263, 10.1016/S0733-8635(18)31044-1

Buchbinder, 1986, Severe infantile epidermolysis bullosa simplex: Dowling-Meara type, Arch Dermatol, 122, 190, 10.1001/archderm.1986.01660140080023

Cooper, 1987, The mechano-bullous diseases (epidermolysis bullosa), 610

Fine, 1986, Epidermolysis bullosa: clinical aspects, pathology, and recent advances in research, Int J Dermatol, 25, 143, 10.1111/j.1365-4362.1986.tb02206.x

Fine, 1987, Clinical and diagnostic aspects of inherited epidermolysis bullosa, Curr Concepts Skin Dis, 8, 5

Fine, 1988, Changing clinical and laboratory concepts in inherited epidermolysis bullosa, Arch Dermatol, 124, 523, 10.1001/archderm.1988.01670040025015

Fine, 1989, Autosomal recessive epidermolysis bullosa simplex: generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases, Arch Dermatol, 125, 931, 10.1001/archderm.1989.01670190065007

Fine, 1989, Epidermolysis bullosa simplex superficialis: a new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome, Arch Dermatol, 125, 633, 10.1001/archderm.1989.01670170047006

Fine, 1989, Epidermolysis bullosa simplex: identification of a kindred with autosomal recessive transmission of the Weber-Cockayne variety, Pediatr Dermatol, 6, 1, 10.1111/j.1525-1470.1989.tb00256.x

Gedde-Dahl, 1981, Sixteen types of epidermolysis. On the clinical discrimination, therapy, and prenatal diagnosis, Acta Derm Venereol [Suppl] (Stockh), 95, 74

Gedde-Dahl, 1987, Epidermolysis bullosa syndromes, Curr Probl Dermatol, 16, 129, 10.1159/000413461

Haber, 1985, Cicatricial junctional epidermolysis bullosa, J Am Acad Dermatol, 12, 836, 10.1016/S0190-9622(85)70105-3

Hashimoto, 1985, Transient bullous dermolysis of the newborn, Arch Dermatol, 121, 1429, 10.1001/archderm.1985.01660110077020

Hashimoto, 1989, Transient bullous dermolysis of the newborn: two additional cases, J Am Acad Dermatol, 21, 708, 10.1016/S0190-9622(89)70241-3

Hintner, 1982, Generalized atrophic benign epidermolysis bullosa, Arch Dermatol, 118, 375, 10.1001/archderm.1982.01650180009008

Medenica-Mojsilovic, 1986, Epidermolysis bullosa herpetiformis with mottled pigmentation and an unusual punctate keratoderma, Arch Dermatol, 122, 900, 10.1001/archderm.1986.01660200072019

Nielsen, 1985, Epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders: a new syndrome, Acta Derm Venereol (Stockh), 65, 526, 10.2340/0001555565526530

Niemi, 1988, Epidermolysis bullosa simplex associated with muscular dystrophy with recessive inheritance, Arch Dermatol, 124, 551, 10.1001/archderm.1988.01670040053022

Paller, 1986, The generalized atrophic benign form of junctional epidermolysis bullosa: experience with four patients in the United States, Arch Dermatol, 122, 704, 10.1001/archderm.1986.01660180110027

Pearson, 1988, Clinicopathologic types of epidermolysis bullosa and their nondermatological complications, Arch Dermatol, 124, 718, 10.1001/archderm.1988.01670050062023

Salih, 1985, Lethal epider-molytic epidermolysis bullosa: a new autosomal recessive type of epidermolysis bullosa, Br J Dermatol, 113, 135, 10.1111/j.1365-2133.1985.tb02055.x

Schachner, 1977, Epidermolysis bullosa hereditaria letalis: pathology, natural history, and therapy, Br J Dermatol, 96, 51, 10.1111/j.1365-2133.1977.tb05185.x

Tabas, 1987, The mechanobullous diseases, Dermatol Clin, 5, 123, 10.1016/S0733-8635(18)30770-8

Wright, 1988, Oral and ultra-structural dental manifestations of epidermolysis bullosa [Abstract], J Dental Res, 67, 249

Fine, 1990, Intraepidermal type VII collagen, J Am Acad Dermatol, 22, 188, 10.1016/0190-9622(90)70021-9

Eady, 1987, Approaches to the study of epidermolysis bullosa, Curr Probl Dermatol, 17, 127, 10.1159/000413479

Holbrook, 1988, Extracutaneous epithelial involvement in inherited epidermolysis bullosa, Arch Dermatol, 124, 726, 10.1001/archderm.1988.01670050070024

Pearson, 1962, Studies on the pathogenesis of epidermolysis bullosa, J Invest Dermatol, 39, 551, 10.1038/jid.1962.156

Pearson, 1985, Histopathologic and ultrastructural findings in certain genodermatoses, Clin Dermatol, 3, 143, 10.1016/0738-081X(85)90099-9

Tidman, 1985, Evaluation of anchoring fibrils and other components of the dermal-epidermal junction in dystrophic epidermolysis by a quantitative ultrastructural technique, J Invest Dermatol, 84, 374, 10.1111/1523-1747.ep12265460

Tidman, 1986, Hemidesmosomes heterogeneity in junctional epidermolysis bullosa revealed by morphometric analysis, J Invest Dermatol, 86, 51, 10.1111/1523-1747.ep12283807

Fine, 1987, Immunofluorescence studies in epidermolysis bullosa utilizing polyclonal and monoclonal antibodies, 399

Hintner, 1981, Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in mechanobullous diseases, J Invest Dermatol, 76, 113, 10.1111/1523-1747.ep12525447

Kero, 1982, Immunohistological localization of three basement membrane components in various forms of epidermolysis bullosa, J Cutan Pathol, 9, 316, 10.1111/j.1600-0560.1982.tb01068.x

Weber, 1982, Immunofluorescent localization of type IV collagen and laminin in human skin and its application in junctional zone pathology, Br J Dermatol, 106, 267, 10.1111/j.1365-2133.1982.tb01722.x

Fine, 1984, KF-1 monoclonal antibody defines a specific basement membrane antigenic defect in dystrophic forms of epidermolysis bullosa, J Invest Dermatol, 82, 35, 10.1111/1523-1747.ep12259063

Fine, 1987, Altered skin basement membrane antigenicity in epidermolysis bullosa, 111

Fine, 1988, Antigenic features and structural correlates of basement membranes: relationship to epidermolysis bullosa, Arch Dermatol, 124, 713, 10.1001/archderm.1988.01670050057022

Fine, 1989, Chondroitin 6-sulfate proteoglycan but not heparan sulfate proteoglycan is abnormally expressed in skin basement membrane from patients with dominant and recessive dystrophic epidermolysis bullosa, J Invest Dermatol, 92, 611, 10.1111/1523-1747.ep12712151

Fine, 1990, GB3 antigen is an accurate marker of only the Herlitz subset of junctional epidermolysis bullosa [Abstract], Clin Res, 38, 72A

Fine, 1989, 19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosa, Arch Dermatol, 125, 520, 10.1001/archderm.1989.01670160068010

Goldsmith, 1983, Monoclonal antibodies to anchoring fibrils for the diagnosis of epidermolysis bullosa, J Invest Dermatol, 81, 464, 10.1111/1523-1747.ep12522669

Heagerty, 1986, Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosis, Br J Dermatol, 115, 125, 10.1111/j.1365-2133.1986.tb05707.x

Heagerty, 1986, GB3 monoclonal antibody for diagnosis of junctional epidermolysis bullosa, Lancet, 1, 860, 10.1016/S0140-6736(86)90972-4

Kennedy, 1985, Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa, Br J Dermatol, 113, 651, 10.1111/j.1365-2133.1985.tb02400.x

Rusenko, 1989, The carboxyl-terminal domain of type VII collagen is present at the basement membrane in recessive dystrophic epidermolysis bullosa, J Invest Dermatol, 92, 623, 10.1111/1523-1747.ep12712167

Fine, 1988, Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping, J Invest Dermatol, 91, 465, 10.1111/1523-1747.ep12476604

Heagerty, 1986, Rapid prenatal diagnosis and exclusion of epidermolysis bullosa using novel antibody probes, J Invest Dermatol, 86, 603, 10.1111/1523-1747.ep12355579

Heagerty, 1987, Rapid prenatal diagnosis of epidermolysis bullosa letalis using GB3 monoclonal antibody, Br JDermatol, 117, 215, 10.1111/j.1365-2133.1987.tb04132.x

Bauer, 1977, The role of human skin collagenase in epidermolysis bullosa, J Invest Dermatol, 68, 119, 10.1111/1523-1747.ep12492226

Bauer, 1977, Recessive dystrophic epidermolysis bullosa: evidence for altered collagenase in fibroblast cultures, Proc Natl Acad Sci USA, 74, 4646, 10.1073/pnas.74.10.4646

Bauer, 1978, Recessive dystrophic epidermolysis bullosa: evidence for increased collagenase as a genetic characteristic in cell culture, J Exp Med, 148, 1378, 10.1084/jem.148.5.1378

Bauer, 1982, Abnormalities in collagenase expression as in vitro markers for recessive dystrophic epidermolysis bullosa, J Invest Dermatol, 79, 105s, 10.1111/1523-1747.ep12545885

Bauer, 1988, A perspective on the role of collagenase in recessive dystrophic epidermolysis bullosa, Arch Dermatol, 124, 734, 10.1001/archderm.1988.01670050078026

Eisen, 1969, Human skin collagenase: relationship to the pathogenesis of epidermolysis bullosa dystrophica, J Invest Dermatol, 52, 449, 10.1038/jid.1969.77

Stricklin, 1982, Human skin collagenase in recessive dystrophic epidermolysis bullosa: purification of a mutant enzyme from fibroblast cultures, J Clin Invest, 69, 1373, 10.1172/JCI110577

Valle, 1980, Enhanced biosynthesis of human skin collagenase in fibroblast cultures from recessive dystrophic epidermolysis bullosa, J Clin Invest, 66, 176, 10.1172/JCI109842

Welgus, 1986, Elevated levels of human collagenase inhibitor in blister fluids of diverse etiology, J Invest Dermatol, 87, 592, 10.1111/1523-1747.ep12455837

Kero, 1984, Collagen metabolism in two rare forms of epidermolysis bullosa, Br J Dermatol, 110, 177, 10.1111/j.1365-2133.1984.tb07464.x

Briggaman, 1977, Suction blister studies in epidermolysis bullosa [Abstract], J Invest Dermatol, 68, 231

Tidman, 1984, Evidence for a functional defect of the lamina lucida in recessive dystrophic epidermolysis bullosa demonstrated by suction blisters, Br J Dermatol, 111, 379, 10.1111/j.1365-2133.1984.tb06599.x

Carter, 1987, Treatment of junctional epidermolysis bullosa with epidermal autografts, J Am Acad Dermatol, 17, 246, 10.1016/S0190-9622(87)70199-6

Woodley, 1988, Epidermolysis bullosa acquisita antigen is the globular carboxyl terminus of type VII collagen, J Clin Invest, 81, 683, 10.1172/JCI113373