Published in Arch Dermatol Res on January 01, 1987
Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagen. J Clin Invest (2005) 1.38
Epidermolysis bullosa acquisita--successful treatment with colchicine. Arch Dermatol Res (1994) 0.81
Fixation by means of glutaraldehyde-hydrogen peroxide reaction products. J Cell Biol (1972) 2.18
Differentiating anti-lamina lucida and anti-sublamina densa anti-BMZ antibodies by indirect immunofluorescence on 1.0 M sodium chloride-separated skin. J Invest Dermatol (1984) 1.85
Identification of the skin basement-membrane autoantigen in epidermolysis bullosa acquisita. N Engl J Med (1984) 1.80
Epidermolysis bullosa acquisita. Report of three cases and review of all published cases. Arch Dermatol (1971) 1.57
Ultrastructural localization of immunoglobulins in bullous pemphigoid skin. Employment of a new peroxidase-antiperoxidase multistep method. J Invest Dermatol (1975) 1.57
Epidermolysis bullosa acquisita: ultrastructural and immunological studies. J Invest Dermatol (1981) 1.55
Epidermolysis bullosa acquisita with electron microscopical studies. Arch Dermatol (1975) 1.26
[Electron microscopic studies of the dynamics of blister formation in bullous pemphigoid]. Arch Klin Exp Dermatol (1967) 1.15
Unusual subepidermal bullous diseases with immunologic features of bullous pemphigoid. Arch Dermatol (1979) 1.12
Epidermolysis bullosa acquisita. Immunofluorescence, electron microscopic and immunoelectron microscopic studies in four patients. Br J Dermatol (1980) 1.05
IgA linear dermatosis of childhood (chronic bullous disease of childhood). Br J Dermatol (1979) 0.99
Dermatitis herpetiformis and bullous pemphigoid. Intermediate and mixed forms. Arch Dermatol (1976) 0.99
Oral lesions in bullous pemphigoid. Arch Dermatol (1969) 0.97
Histochemistry and fine structure of oral lesions of mucous membrane pemphigoid. Preliminary observations. Arch Dermatol (1971) 0.96
Cicatricial pemphigoid: direct and indirect immunofluorescent studies. Oral Surg Oral Med Oral Pathol (1981) 0.94
Immunofluorescence and immunoelectron microscopic studies in cicatricial pemphigoid. J Invest Dermatol (1984) 0.94
Benign pemphigold; a report of seven cases with chronic, scarring, herpetiform plaques about the head and neck. AMA Arch Derm (1957) 0.91
Epidermolysis bullosa acquisita: a clinical disorder of varied etiologies. Two cases and a review of immunologic and other reported findings. J Am Acad Dermatol (1980) 0.90
Epidermolysis bullosa acquisita antigen, a new major component of cutaneous basement membrane, is a glycoprotein with collagenous domains. J Invest Dermatol (1986) 0.88
Epidermolysis bullosa acquisita: a heterogeneous disease. J Am Acad Dermatol (1981) 0.86
Epidermolysis bullosa acquisita. The search for identity. Arch Dermatol (1986) 0.86
Epidermolysis bullosa acquisita with negative direct immunofluorescence. Arch Dermatol (1985) 0.85
An acquired form of epidermolysis bullosa without immunoreactants. Report of a case. J Am Acad Dermatol (1985) 0.84
Pathogenesis of the blister in cicatricial pemphigoid and in bullous pemphigoid. A comparative ultrastructural study. Arch Dermatol Forsch (1973) 0.82
The immunopathology of epidermolysis bullosa acquisita. Can Med Assoc J (1973) 0.82
Anatomical distribution and immunological characteristics of epidermolysis bullosa acquisita antigen and bullous pemphigoid antigen. Br J Dermatol (1986) 0.81
Epidermolysis bullosa acquisita--a sign of cicatricial pemphigoid? Br J Dermatol (1979) 0.81
Cicatricial pemphigoid. Immunofluorescent studies. Arch Dermatol (1972) 0.81
[Acquired epidermolysis bullosa in Crohn's disease]. Hautarzt (1975) 0.80
[Generalized cutaneous involvement during Lortat-Jacob disease (cicatricial pemphigoid)]. Ann Dermatol Venereol (1980) 0.77
[Epidermolysis bullosa acquisita? Cicatricial pemphigoid?]. Z Hautkr (1980) 0.77
Disseminated cicatricial pemphigoid. Dermatologica (1985) 0.77
[Pathomorphogenesis of blistering in epidermolysis bullosa acquisita and epidermolysis bullosa dystrophica (author's transl)]. Arch Dermatol Res (1975) 0.77
[Disseminated cicatricial pemphigoid]. Hautarzt (1981) 0.77
Epidermolysis bullosa acquisita and Crohn's disease. Acta Derm Venereol (1978) 0.77
[Hereditary bullous epidermolyses. Recent aspects of diagnosis and therapy]. Hautarzt (1986) 0.76
Benign mucous membrane pemphigoid. An unusual case with electron microscopic findings. Arch Dermatol (1972) 0.76
Epidermolysis bullosa acquisita in a patient with multiple endocrinopathies syndrome. Arch Dermatol (1986) 0.76
Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling. FASEB J (2000) 2.09
When should a substance be designated as sensitizing for the skin ('Sh') or for the airways ('Sa')? Hum Exp Toxicol (2002) 1.95
A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein. Genes Dev (1994) 1.65
Consequences of beta-glucocerebrosidase deficiency in epidermis. Ultrastructure and permeability barrier alterations in Gaucher disease. J Clin Invest (1994) 1.58
Prevention of latex allergy by selection of low-allergen gloves. Clin Exp Allergy (2000) 1.55
Ultrastructural connective tissue abnormalities in patients with spontaneous cervicocerebral artery dissections. Ann Neurol (1998) 1.42
[Epidermolysis bullosa dystrophica inversa: report on 2 sisters]. Hautarzt (1976) 1.39
Prenatal diagnosis of junctional epidermolysis bullosa Herlitz type. Lancet (1989) 1.38
Fibrillar protein deposits with tubular substructure in a systemic disease beginning as cutis laxa. Arch Dermatol (1993) 1.38
Painful stimuli evoke itch in patients with chronic pruritus: central sensitization for itch. Neurology (2004) 1.34
Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II. Am J Hum Genet (1997) 1.33
[Epidermolysis bullosa dystrophica dominans-a defect of the anchoring fibrils? (authors transl)]. Dermatologica (1973) 1.27
Epidermolysis bullosa herpetiformis Dowling-Meara. Report of a case and pathomorphogenesis. Dermatologica (1982) 1.27
[Ultrastructure of inborn erors of keratinization. I. Ichthyosis congenita]. Arch Dermatol Forsch (1972) 1.22
Microdialysis for the evaluation of penetration through the human skin barrier - a promising tool for future research? Eur J Pharm Sci (2001) 1.20
Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification. Hum Genet (1994) 1.17
Management of esophageal stenosis in recessive dystrophic epidermolysis bullosa. Gastroenterology (1984) 1.16
Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis. J Invest Dermatol (1983) 1.16
Ultrastructure of inborn errors of keratinization. VI. Inherited ichthyoses--a model system for heterogeneities in keratinization disturbances. Arch Dermatol Forsch (1974) 1.13
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis. J Med Genet (2007) 1.13
Epidermolysis bullosa hereditaria with junctional blistering in an adult. Dermatologica (1976) 1.09
The genetic basis of epidermolysis bullosa simplex with mottled pigmentation. Proc Natl Acad Sci U S A (1996) 1.08
Electron microscopical evidence of unusual structures in the cytoplasm of some plasmotypes of Epilobium hybrids. J Ultrastruct Res (1965) 1.05
Origin of the corneocyte lipid envelope (CLE): observations in harlequin ichthyosis and cultured human keratinocytes. J Invest Dermatol (2000) 1.04
[The "Stade éphélide" of precancerous melanosis. A comparative clinical, histopathological, and electron microscopical study]. Arch Dermatol Forsch (1970) 1.01
Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease. Pediatr Res (1996) 1.01
Multicentre study for the development of an in vivo model to evaluate the influence of topical formulations on irritation. Contact Dermatitis (2000) 1.00
Guidelines on sodium lauryl sulfate (SLS) exposure tests. A report from the Standardization Group of the European Society of Contact Dermatitis. Contact Dermatitis (1997) 0.99
Apolipoprotein E deficiency leads to cutaneous foam cell formation in mice. J Invest Dermatol (1995) 0.98
Ultrastructural studies in epidermolysis bullosa heriditaria. I. Dominant dystrophic type of Pasini. Arch Dermatol Forsch (1975) 0.98
[Ultrastructure of inborn errors of keratinization. 3. Autosomal dominant ichthyosis vulgaris (author's transl)]. Arch Dermatol Forsch (1973) 0.98
Early preclinical diagnosis of dominant pseudoxanthoma elasticum by specific ultrastructural changes of dermal elastic and collagen tissue in a family at risk. Hum Genet (1991) 0.97
Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type). Arch Dermatol Res (1976) 0.97
Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome. Pediatr Dermatol (1996) 0.97
[Comèl-Netherton syndrome]. Hautarzt (1998) 0.96
[Congenital reticular ichthyosiform erythroderma]. Hautarzt (1984) 0.95
[Dilatation treatment of esophageal stenoses in young patients with recessive epidermolysis bullosa dystrophica]. Z Gastroenterol (1990) 0.95
Ultrastructural distinction of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis. Humangenetik (1972) 0.95
Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway. Eur J Hum Genet (1999) 0.95
Evaluation and relevance of atopic basic and minor features in patients with atopic dermatitis and in the general population. Acta Derm Venereol Suppl (Stockh) (1989) 0.94
The spectrum of renal involvement in epidermolysis bullosa dystrophica hereditaria: report of two cases. Am J Kidney Dis (1988) 0.93
Round-headed human spermatozoa. Fertil Steril (1976) 0.92
Development and validation of diagnostic scores for atopic dermatitis incorporating criteria of data quality and practical usefulness. J Clin Epidemiol (1996) 0.91
Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy. Hum Genet (1981) 0.91
Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis. Am J Med Genet (1990) 0.91
Occupational skin cancer induced by ultraviolet radiation and its prevention. Br J Dermatol (2012) 0.91
[Ultrastructure of inborn errors of keratinization. IV. X-linked recessive ichthyosis (author's transl)]. Arch Dermatol Forsch (1974) 0.91
Ichthyosis congenita type III. Clinical and ultrastructural characteristics and distinction within the heterogeneous ichthyosis congenita group. Arch Dermatol Res (1988) 0.90
Brother and sister with trisomy 10p: a new syndrome. Humangenetik (1974) 0.90
A strikingly constant ratio exists between Langerhans cells and other epidermal cells in human skin. A stereologic study using the optical disector method and the confocal laser scanning microscope. J Invest Dermatol (2001) 0.88
Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: correlation between genotype and phenotype. J Invest Dermatol (1999) 0.88
[Origin and nature of fibrillar bodies (author's transl)]. Arch Dermatol Forsch (1973) 0.87
Follow-up of a family group suffering from ichthyosis hystrix type Curth-Macklin. Humangenetik (1972) 0.87
Normal ultrastructure, but altered stratum corneum lipid and protein composition in a mouse model for epidermolytic hyperkeratosis. J Invest Dermatol (1999) 0.86
Ultrastructure of blister formation in epidermolysis bullosa hereditaria: V. Epidermolysis bullosa simplex localisata type Weber-Cockayne. J Invest Dermatol (1982) 0.86
Zunich neuroectodermal syndrome: migratory ichthyosiform dermatosis, colobomas, and other abnormalities. Pediatr Dermatol (1997) 0.85
Problems in prenatal diagnosis of the ichthyosis congenita group. Hum Genet (1985) 0.85
[Ultrastructural distinctive features of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis]. Dermatologica (1972) 0.85
Prenatal diagnosis of inherited epidermolyses. Curr Probl Dermatol (1987) 0.85
Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis. Hum Genet (1995) 0.85
Epidermolysis bullosa dystrophica dominans (Pasini)-a primary structural defect of the anchoring fibrils. Hum Genet (1976) 0.85
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome. Hum Mutat (1998) 0.85
[Ultrastructure of inborn errors of keratinization. II. Ichthyosis hystrix type Curth-Macklin]. Arch Dermatol Forsch (1973) 0.84
Keratohyalin granules are heterogeneous in ridged and non-ridged human skin: evidence from anti-filaggrin immunogold labelling of normal skin and skin of autosomal dominant ichthyosis vulgaris patients. Arch Dermatol Res (1991) 0.84
Mal de Meleda keratoderma with pseudoainhum. Br J Dermatol (1993) 0.84
Pregnancy and delivery in a patient with mutilating dystrophic epidermolysis bullosa (Hallopeau-Siemens type). Obstet Gynecol (1997) 0.84
Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine. Arch Dermatol Res (1976) 0.84
Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features. Birth Defects Orig Artic Ser (1988) 0.84
Ultrastructural studies in epidermolysis bullosa hereditaria. IV. Recessive dystrophic types with junctional blistering. (Infantile or Herlitz-Pearson type and adult type). Arch Dermatol Res (1976) 0.83
Anchoring fibrils, collagen VII, and neutral metalloproteases in recessive dystrophic epidermolysis bullosa inversa. J Invest Dermatol (1992) 0.83
Incidence of work-related hand eczema during apprenticeship: first results of a prospective cohort study in the car industry. Contact Dermatitis (2001) 0.82
Prenatal diagnosis of epidermolysis bullosa dystrophica Hallopeau-Siemens with electron microscopy of fetal skin. Lancet (1981) 0.82
[Education programs on atopic eczema. Design and first results of the German Randomized Intervention Multicenter Study]. Hautarzt (2003) 0.82
[Intracellular cilia in human epidermal cells]. Arch Dermatol Forsch (1972) 0.82
Compound heterozygosity for COL7A1 mutations in twins with dystrophic epidermolysis bullosa: a recessive paternal deletion/insertion mutation and a dominant negative maternal glycine substitution result in a severe phenotype. Am J Hum Genet (1996) 0.82
Recent epidemiological and genetic studies in atopic dermatitis. Acta Derm Venereol Suppl (Stockh) (1992) 0.82
Bicomponent keratohyalin in normal human ridged skin. Arch Dermatol Res (1990) 0.82
Papular palmoplantar hyperkeratosis following chronic medical exposure to arsenic: human papillomavirus as a co-factor in the pathogenesis of arsenical keratosis? Acta Derm Venereol (2001) 0.81
A mother and two children with nonbullous congenital ichthyosiform erythroderma. Arch Dermatol (1986) 0.81
The European standard series in 9 European countries, 2002/2003 -- first results of the European Surveillance System on Contact Allergies. Contact Dermatitis (2005) 0.81
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skin. J Invest Dermatol (1997) 0.81
Monitoring of the disease progress in Sezary syndrome by cd7- cells using flow cytometry. Br J Dermatol (1996) 0.81
High molecular compounds (polysaccharides and proanthocyanidins) from Hamamelis virginiana bark: influence on human skin keratinocyte proliferation and differentiation and influence on irritated skin. Phytochemistry (2001) 0.80
Prenatal diagnosis of anhydrotic ectodermal dysplasia. Hum Genet (1982) 0.80
Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1. Hum Mol Genet (1994) 0.80
A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis. Hum Mol Genet (1993) 0.80
Direct detection of repetitive, whole chromosome paint and telomere DNA probes by immunogold electron microscopy. Chromosome Res (1993) 0.80
Epidermolysis bullosa hereditaria letalis: report of a case and probable ultrastructural defects. Helv Paediatr Acta (1976) 0.79
[Ultrastructure of inborn errors of keratinization. V. Ichthyosis in Refsum's syndrome (heredopathia atactica polyneuritiformis) (author's transl)]. Arch Dermatol Forsch (1974) 0.79
Netherton's syndrome: ultrastructure of the active lesion under retinoid therapy. Arch Dermatol Res (1989) 0.79
Occupational contact dermatitis in bakers, confectioners and cooks. A population-based study. Contact Dermatitis (1995) 0.79
Is filaggrin really a filament-aggregating protein in vivo? Arch Dermatol Res (1993) 0.79
Ultrastructure of inborm errors of keratinization. VII. Porokeratosis Mibelli and disseminated superficial actinic porokeratosis. Arch Dermatol Res (1976) 0.79
Hereditary palmoplantar keratosis of the Gamborg Nielsen type. Clinical and ultrastructural characteristics of a new type of autosomal recessive palmoplantar keratosis. Arch Dermatol Res (1990) 0.78
Prenatal diagnosis of anhidrotic ectodermal dysplasia. Prenat Diagn (1984) 0.78
[Deletion of the short arms of chromosome No. 18]. Humangenetik (1966) 0.78
Richner-Hanhart's syndrome: ultrastructural abnormalities of epidermal keratinization indicating a causal relationship to high intracellular tyrosine levels. J Invest Dermatol (1982) 0.78
Prenatal exclusion of Herlitz syndrome by electron microscopy of fetal skin biopsies obtained at fetoscopy. Acta Derm Venereol (1983) 0.78
Chromosome aberrations in mitoses and meioses in vivo. Arch Toxikol (1971) 0.78
[Clinical aspects of epidermolyses with junctional blister formation (author's transl)]. Dermatologica (1979) 0.78