AMIR HOSSEIN SAEIDIAN to Epidermolysis Bullosa
This is a "connection" page, showing publications AMIR HOSSEIN SAEIDIAN has written about Epidermolysis Bullosa.
Connection Strength
1.358
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Pathomechanisms of epidermolysis bullosa: Beyond structural proteins. Matrix Biol. 2022 06; 110:91-105.
Score: 0.184
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Homozygous ITGA3 Missense Mutation in Adults in a Family with Syndromic Epidermolysis Bullosa (ILNEB) without Pulmonary Involvement. J Invest Dermatol. 2021 11; 141(11):2752-2756.
Score: 0.172
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Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation. Matrix Biol. 2021 05; 99:43-57.
Score: 0.172
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Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency. Matrix Biol. 2019 08; 81:91-106.
Score: 0.145
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Phenotypic Spectrum of Epidermolysis Bullosa: The Paradigm of Syndromic versus Non-Syndromic Skin Fragility Disorders. J Invest Dermatol. 2019 03; 139(3):522-527.
Score: 0.144
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Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zone. Matrix Biol. 2018 10; 71-72:313-329.
Score: 0.138
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Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Exp Dermatol. 2019 10; 28(10):1118-1121.
Score: 0.137
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Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biol. 2018 03; 66:22-33.
Score: 0.135
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Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications. J Invest Dermatol. 2017 12; 137(12):2649-2652.
Score: 0.133