Epidermolysis bullosa
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Publications (1054)
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Epidermolysis bullosa acquisita in association with mantle cell lymphoma. (2018/06/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Imaging findings in systemic childhood diseases presenting with dermatologic manifestations. (2018/05/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Bone Marrow-Derived Stem Cells Migrate into Intraepidermal Skin Defects of a Desmoglein-3 Knockout Mouse Model but Preserve their Mesodermal Differentiation. (2018/05/01) ♡
- Extracellular Vesicles as Biomarkers for the Detection of a Tumor Marker Gene in Epidermolysis Bullosa-Associated Squamous Cell Carcinoma. (2018/05/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. The Conundrum of Allogeneic Bone Marrow Transplantation for Epidermolysis Bullosa. (2018/05/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review. (2018/04/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Oral manifestations as the main feature of late-onset recessive dystrophic epidermolysis bullosa. (2018/04/01) ♡
- Serration pattern analysis for differentiating epidermolysis bullosa acquisita from other pemphigoid diseases. (2018/04/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Large Deletions Targeting the Triple-Helical Domain of Collagen VII Lead to Mild Acral Dominant Dystrophic Epidermolysis Bullosa. (2018/04/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Case of epidermolysis bullosa acquisita with concomitant anti-laminin-332 antibodies. (2018/04/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Functional therapies for cutaneous wound repair in epidermolysis bullosa. (2018/04/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [Renal Transplantation in a patient with Recessive Dystrophic Epidermolysis Bullosa: a case report]. (2018/03/26) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Erosive pustular dermatosis of the scalp and Kindler syndrome: a new association. (2018/03/01) ♡
- Threonine 150 Phosphorylation of Keratin 5 Is Linked to Epidermolysis Bullosa Simplex and Regulates Filament Assembly and Cell Viability. (2018/03/01) ♡
- Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. (2018/03/01) ♡
- Identification of tissue damage, extracellular matrix remodeling and bacterial challenge as common mechanisms associated with high-risk cutaneous squamous cell carcinomas. (2018/03/01) ♡
- Genetic diagnosis of epidermolysis bullosa: recommendations from an expert Spanish research group. (2018/03/01) ♡
- Activation of PKB/Akt and p44/42 by mechanical stretch utilizes desmosomal structures and the keratin filament. (2018/03/01) ♡
- Establishment of integration-free induced pluripotent stem cells from human recessive dystrophic epidermolysis bullosa keratinocytes. (2018/03/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Identical COL71A1 heterozygous mutations resulting in different dystrophic epidermolysis bullosa phenotypes. (2018/03/01) ♡
- Blistering diseases in the mature patient. (2018/03/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well-matched antibody panel. (2018/02/01) ♡
- Calcitriol Treatment Ameliorates Inflammation and Blistering in Mouse Models of Epidermolysis Bullosa Acquisita. (2018/02/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A Nonlethal Case of Junctional Epidermolysis Bullosa and Congenital Pyloric Atresia: Compound Heterozygosity in a Patient with a Novel Integrin Beta 4 Gene Mutation. (2018/02/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Anaesthetic management of children with epidermolysis bullosa. (2018/02/01) ♡
- Nutritional outcomes in children with epidermolysis bullosa: long-term follow-up. (2018/01/19) ♡
- Distinguishing Epidermolysis Bullosa Acquisita From Bullous Pemphigoid Without Direct Immunofluorescence. (2018/01/01) ♡
- Dimethyl fumarate modulates neutrophil extracellular trap formation in a glutathione- and superoxide-dependent manner. (2018/01/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Wound culture isolated antibiograms and caregiver-reported skin care practices in children with epidermolysis bullosa. (2018/01/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Inside out: regenerative medicine for recessive dystrophic epidermolysis bullosa. (2018/01/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Management of a granulomatous lesion in a patient with Kindler's Syndrome. (2018/01/01) ♡
- Expression of Laminin 332 in Vesicant Skin Injury and Wound Repair. (2018/01/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. [Inherited epidermolysis bullosa]. (2018/01/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Keratins and epidermolysis bullosa simplex. (2018/01/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Current Non-viral siRNA Delivery Systems as a Promising Treatment of Skin Diseases. (2018/01/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases. (2018/01/01) ♡
- Antisense-Mediated Splice Modulation to Reframe Transcripts. (2018/01/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Epidermolysis bullosa acquisita. (2017/12/15) ♡
- Interaction of Complement Defence Collagens C1q and Mannose-Binding Lectin with BMP-1/Tolloid-like Proteinases. (2017/12/05) ♡
- Health literacy in patients with epidermolysis bullosa in Iran. (2017/12/04) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis. (2017/12/01) ♡
- Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications. (2017/12/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. In vitro and in vivo models to investigate the pathomechanisms and novel treatments for pemphigoid diseases. (2017/12/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. CD11b-deficient mice exhibit an increased severity in the late phase of antibody transfer-induced experimental epidermolysis bullosa acquisita. (2017/12/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Structural proteins of the dermal-epidermal junction targeted by autoantibodies in pemphigoid diseases. (2017/12/01) ♡
- Evidence for a contributory role of a xenogeneic immune response in experimental epidermolysis bullosa acquisita. (2017/12/01) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Nanoparticles prepared from porcine cells support the healing of cutaneous inflammation in mice and wound re-epithelialization in human skin. (2017/12/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex. (2017/12/01) ♡
- [New developments in the management of congenital epidermolysis bullosa]. (2017/12/01) ♡
- Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. (2017/12/01) ♡
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