Published in Eur J Pediatr on April 01, 2002
Risk of long term renal impairment and duration of follow up recommended for Henoch-Schonlein purpura with normal or minimal urinary findings: a systematic review. Arch Dis Child (2005) 1.29
A randomized, placebo-controlled trial of prednisone in early Henoch Schönlein Purpura [ISRCTN85109383]. BMC Med (2004) 1.18
Treatment-based literature of Henoch-Schönlein purpura nephritis in childhood. Pediatr Nephrol (2008) 1.18
Differences in clinical manifestations and outcomes between adult and child patients with Henoch-Schönlein purpura. J Korean Med Sci (2014) 1.01
Prediction of total body water in infants and children. Arch Dis Child (2005) 0.97
Henoch Schonlein purpura in childhood: clinical analysis of 254 cases over a 3-year period. Clin Rheumatol (2008) 0.95
Henoch schonlein purpura--a 5-year review and proposed pathway. PLoS One (2012) 0.83
Henoch Schonlein Purpura in children: clinical analysis of 120 cases. Afr Health Sci (2013) 0.80
Construction of a scoring system for predicting the risk of severe gastrointestinal involvement in Henoch-Schönlein Purpura. Springerplus (2014) 0.76
Establishing hospital admission criteria of pediatric Henoch-Schonlein purpura. Rheumatol Int (2014) 0.76
Dapsone therapy for Henoch-Schonlein purpura. Arch Dis Child (2006) 0.75
Atopic Dermatitis and Association of Risk for Henoch-Schönlein Purpura (IgA Vasculitis) and Renal Involvement Among Children: Results From a Population-Based Cohort Study in Taiwan. Medicine (Baltimore) (2016) 0.75
Henoch-Schonlein Purpura in Children Hospitalized at a Tertiary Hospital during 2004-2015 in Korea: Epidemiology and Clinical Management. Pediatr Gastroenterol Hepatol Nutr (2016) 0.75
Adjuvant treatments for Henoch-Schönlein purpura nephritis in children: A systematic review. Curr Ther Res Clin Exp (2009) 0.75
Association between allergic diseases and risks of HSP and HSP nephritis: a population-based study. Pediatr Res (2015) 0.75
Henoch-Schonlein purpura presenting sequentially as nodular rash, erythema nodosum, and palpable purpura. J Family Community Med (2014) 0.75
Risk Factors Associated with Renal Involvement in Childhood Henoch-Schönlein Purpura: A Meta-Analysis. PLoS One (2016) 0.75
The association between genetic variation in interleukin-10 gene and susceptibility to Henoch-Schönlein purpura in Chinese children. Clin Rheumatol (2017) 0.75
Adult-Onset Henoch-Schonlein Purpura Duodenitis. J Clin Med Res (2017) 0.75
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB. J Am Acad Dermatol (2008) 3.72
Mesenchymal stem cells are recruited into wounded skin and contribute to wound repair by transdifferentiation into multiple skin cell type. J Immunol (2008) 3.67
Genotoxic stress abrogates renewal of melanocyte stem cells by triggering their differentiation. Cell (2009) 2.99
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. J Am Acad Dermatol (2010) 2.87
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet (2003) 2.73
Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer. J Clin Invest (2005) 1.92
Consensus statement on definitions of disease, end points, and therapeutic response for pemphigus. J Am Acad Dermatol (2008) 1.81
Elephantiasis nostras verrucosa successfully treated by surgical debridement. Dermatol Surg (2004) 1.70
Increased soluble Fas ligand levels in patients with Stevens-Johnson syndrome and toxic epidermal necrolysis preceding skin detachment. J Allergy Clin Immunol (2008) 1.69
Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation. J Invest Dermatol (2003) 1.67
Fibroblasts show more potential as target cells than keratinocytes in COL7A1 gene therapy of dystrophic epidermolysis bullosa. J Invest Dermatol (2006) 1.67
Consequences of two different amino-acid substitutions at the same codon in KRT14 indicate definitive roles of structural distortion in epidermolysis bullosa simplex pathogenesis. J Invest Dermatol (2011) 1.53
Comprehensive phenotypic analysis for identification of genes affecting growth under ethanol stress in Saccharomyces cerevisiae. FEMS Yeast Res (2008) 1.52
Hair follicle stem cells provide a functional niche for melanocyte stem cells. Cell Stem Cell (2011) 1.48
Humanization of autoantigen. Nat Med (2007) 1.47
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis. J Allergy Clin Immunol (2007) 1.45
Overview of infectious disease surveillance system in Japan, 1999-2005. J Epidemiol (2007) 1.42
Self-involution of giant keratoacanthoma on the tip of the nose. Plast Reconstr Surg (2003) 1.37
Epidemics of vector-borne diseases observed in infectious disease surveillance in Japan, 2000-2005. J Epidemiol (2007) 1.34
Identification of target genes conferring ethanol stress tolerance to Saccharomyces cerevisiae based on DNA microarray data analysis. J Biotechnol (2007) 1.33
Overexpression of pigment epithelium-derived factor decreases angiogenesis and inhibits the growth of human malignant melanoma cells in vivo. Am J Pathol (2004) 1.29
An improved physico-chemical model of hybridization on high-density oligonucleotide microarrays. Bioinformatics (2008) 1.21
Truncation of CGI-58 protein causes malformation of lamellar granules resulting in ichthyosis in Dorfman-Chanarin syndrome. J Invest Dermatol (2003) 1.16
Clinical severity correlates with impaired barrier in filaggrin-related eczema. J Invest Dermatol (2008) 1.16
Speciation of sulfate in size-fractionated aerosol particles using sulfur K-edge X-ray absorption near-edge structure. Environ Sci Technol (2006) 1.15
Novel duplication mutation in the patatin domain of adipose triglyceride lipase (PNPLA2) in neutral lipid storage disease with severe myopathy. Muscle Nerve (2007) 1.15
Lupus erythematosus panniculitis (lupus profundus): clinical, histopathological, and molecular analysis of nine cases. J Cutan Pathol (2005) 1.15
Toxic epidermal necrolysis and Stevens-Johnson syndrome are induced by soluble Fas ligand. Am J Pathol (2003) 1.14
Comprehensive phenotypic analysis of single-gene deletion and overexpression strains of Saccharomyces cerevisiae. Yeast (2011) 1.13
Transcriptome analysis of parallel-evolved Escherichia coli strains under ethanol stress. BMC Genomics (2010) 1.13
CTACK/CCL27 accelerates skin regeneration via accumulation of bone marrow-derived keratinocytes. Stem Cells (2006) 1.11
Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis. Am J Hum Genet (2008) 1.10
An update on molecular aspects of the non-syndromic ichthyoses. Exp Dermatol (2008) 1.10
Regulation of human melanoma growth and metastasis by AGE-AGE receptor interactions. J Invest Dermatol (2004) 1.09
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma. Nat Genet (2012) 1.08
Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan. Am J Hum Genet (2004) 1.07
Type XVII collagen is a key player in tooth enamel formation. Am J Pathol (2008) 1.07
Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects. Hum Mol Genet (2008) 1.07
A randomized double-blind trial of intravenous immunoglobulin for pemphigus. J Am Acad Dermatol (2009) 1.06
Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan. J Invest Dermatol (2008) 1.06
Localization of ABCA12 from Golgi apparatus to lamellar granules in human upper epidermal keratinocytes. Exp Dermatol (2007) 1.05
Definitions and outcome measures for bullous pemphigoid: recommendations by an international panel of experts. J Am Acad Dermatol (2011) 1.04
Hidradenoma papilliferum with mixed histopathologic features of syringocystadenoma papilliferum and anogenital mammary-like glands. J Cutan Pathol (2004) 1.04
Neurobehavioral changes associated with bilateral caudate nucleus infarctions. Psychiatry Clin Neurosci (2005) 1.04
Alterations in desmosome size and number coincide with the loss of keratinocyte cohesion in skin with homozygous and heterozygous defects in the desmosomal protein plakophilin 1. J Invest Dermatol (2003) 1.04
Bioinformatics research on inter-racial difference in drug metabolism I. Analysis on frequencies of mutant alleles and poor metabolizers on CYP2D6 and CYP2C19. Drug Metab Pharmacokinet (2003) 1.02
Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients. J Invest Dermatol (2003) 1.00
Impaired epidermal permeability barrier in mice lacking elovl1, the gene responsible for very-long-chain fatty acid production. Mol Cell Biol (2013) 1.00
Flux analysis and metabolomics for systematic metabolic engineering of microorganisms. Biotechnol Adv (2013) 1.00
Epidermal basement membrane zone components: ultrastructural distribution and molecular interactions. J Dermatol Sci (2003) 0.99
Ultraviolet A-induced production of matrix metalloproteinase-1 is mediated by macrophage migration inhibitory factor (MIF) in human dermal fibroblasts. J Biol Chem (2003) 0.99
Embryonic hair follicle fate change by augmented beta-catenin through Shh and Bmp signaling. Development (2009) 0.99
Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis. J Invest Dermatol (2005) 0.98
Squamous cell carcinoma in a chronic genital ulcer in Behçet's disease. Acta Derm Venereol (2010) 0.98
A novel N14Y mutation in Connexin26 in keratitis-ichthyosis-deafness syndrome: analyses of altered gap junctional communication and molecular structure of N terminus of mutated Connexin26. Am J Pathol (2006) 0.98
Development and experimental verification of a genome-scale metabolic model for Corynebacterium glutamicum. Microb Cell Fact (2009) 0.98
Bone marrow transplantation restores epidermal basement membrane protein expression and rescues epidermolysis bullosa model mice. Proc Natl Acad Sci U S A (2010) 0.98
Minodronate, a newly developed nitrogen-containing bisphosphonate, suppresses melanoma growth and improves survival in nude mice by blocking vascular endothelial growth factor signaling. Am J Pathol (2004) 0.97
Correlation of clinical severity and ELISA indices for the NC16A domain of BP180 measured using BP180 ELISA kit in bullous pemphigoid. J Dermatol Sci (2004) 0.97
Study on roles of anaplerotic pathways in glutamate overproduction of Corynebacterium glutamicum by metabolic flux analysis. Microb Cell Fact (2007) 0.96
Compound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity. J Invest Dermatol (2006) 0.96
Paper-based ELISA for the detection of autoimmune antibodies in body fluid-the case of bullous pemphigoid. Anal Chem (2014) 0.95
Reconstruction and verification of a genome-scale metabolic model for Synechocystis sp. PCC6803. Appl Microbiol Biotechnol (2011) 0.95
Spontaneous giant aneurysm of the superficial temporal artery: case report. Neurol Med Chir (Tokyo) (2009) 0.95
Stable disruption of ethanol production by deletion of the genes encoding alcohol dehydrogenase isozymes in Saccharomyces cerevisiae. J Biosci Bioeng (2011) 0.93
Targeted skipping of a single exon harboring a premature termination codon mutation: implications and potential for gene correction therapy for selective dystrophic epidermolysis bullosa patients. J Invest Dermatol (2006) 0.93
Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1). J Mol Diagn (2005) 0.93
Epithelioid sarcoma presenting as pulmonary cysts with cancer antigen 125 expression. Respirology (2006) 0.93
Neutral lipid storage leads to acylceramide deficiency, likely contributing to the pathogenesis of Dorfman-Chanarin syndrome. J Invest Dermatol (2010) 0.93
Characteristics of electrocardiographic repolarization in acute myocardial infarction complicated by ventricular fibrillation. J Electrocardiol (2012) 0.93
Macrophage migration inhibitory factor is essential for eosinophil recruitment in allergen-induced skin inflammation. J Invest Dermatol (2010) 0.93
Sequential reorganization of cornified cell keratin filaments involving filaggrin-mediated compaction and keratin 1 deimination. J Invest Dermatol (2002) 0.92
Induction of therapeutically relevant cytotoxic T lymphocytes in humans by percutaneous peptide immunization. Cancer Res (2006) 0.92
A denatured collagen microfiber scaffold seeded with human fibroblasts and keratinocytes for skin grafting. Biomaterials (2011) 0.92
Toughening of polylactide by melt blending with a biodegradable poly(ether)urethane elastomer. Macromol Biosci (2007) 0.92
Collagen XVII participates in keratinocyte adhesion to collagen IV, and in p38MAPK-dependent migration and cell signaling. J Invest Dermatol (2009) 0.92
Steroidogenic acute regulatory protein-binding protein cloned by a yeast two-hybrid system. J Biol Chem (2003) 0.92
What's new in bullous pemphigoid. J Dermatol (2010) 0.91
Mechanical properties of injection-molded thermoplastic denture base resins. Acta Odontol Scand (2010) 0.91
Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis. Hum Mutat (2010) 0.91
Response of intractable skin ulcers in recessive dystrophic epidermolysis bullosa patients to an allogeneic cultured dermal substitute. Acta Derm Venereol (2010) 0.91
Animal models of epidermolysis bullosa. Dermatol Clin (2010) 0.91
Differential importance of trehalose accumulation in Saccharomyces cerevisiae in response to various environmental stresses. J Biosci Bioeng (2009) 0.90
Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly. J Biol Chem (2002) 0.90
Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes. Pigment Cell Res (2006) 0.90
High expression of Ki-67 and cyclin D1 in invasive extramammary Paget's disease. J Dermatol Sci (2008) 0.90
Keratin 1 gene mutation detected in epidermal nevus with epidermolytic hyperkeratosis. J Invest Dermatol (2007) 0.90
Model-based analysis of non-specific binding for background correction of high-density oligonucleotide microarrays. Bioinformatics (2008) 0.90
Granulysin as a marker for early diagnosis of the Stevens-Johnson syndrome. Ann Intern Med (2009) 0.90
The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa. J Dermatol Sci (2004) 0.90
Lupus erythematosus profundus successfully treated with dapsone: review of the literature. Arch Dermatol (2006) 0.90
Interleukin-1beta and macrophage migration inhibitory factor (MIF) in dermal fibroblasts mediate UVA-induced matrix metalloproteinase-1 expression. J Dermatol Sci (2007) 0.90
Ultrastructural orientation of laminin 5 in the epidermal basement membrane: an updated model for basement membrane organization. J Histochem Cytochem (2003) 0.90
[Validation of the Japanese-translated version Multiple Sclerosis Quality of Life-54 instrument]. Rinsho Shinkeigaku (2004) 0.89
Surfactant therapy in neonates with respiratory failure due to haemorrhagic pulmonary oedema. Eur J Pediatr (2003) 0.89
Interactions between Lactobacillus kefiranofaciens and Saccharomyces cerevisiae in mixed culture for kefiran production. J Biosci Bioeng (2003) 0.89
Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias. Acta Derm Venereol (2011) 0.89
Changing pattern of deiminated proteins in developing human epidermis. J Invest Dermatol (2003) 0.89
Effect of trehalose accumulation on response to saline stress in Saccharomyces cerevisiae. Yeast (2009) 0.89