782 results on '"Bruckner-Tuderman L"'
Search Results
2. Wound healing in epidermolysis bullosa
3. Epidermolysis bullosa
4. Binde- und Stützgewebe
5. Investigation of Components of the Dermal-Epidermal Junction Zone In Vitro: Effect of Transforming Growth Factor-beta on Collagen VII Expression
6. FERMT1 promoter mutations in patients with Kindler syndrome
7. Phased-array of microcoils allows MR microscopy of ex vivo human skin samples at 9.4 T
8. Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergies
9. ‘Double trouble’: diagnostic challenges in genetic skin disorders
10. Neues über hereditäre, blasenbildende Hauterkrankungen
11. Epidermolysis Bullosa
12. 486 Systemic collagen VII protein therapy for treatment of advanced RDEB
13. Necrobiosis lipoidica: Kasuistische Vielfalt einer Diagnose
14. Epidermolysis bullosa: Diagnostik und Therapie
15. Cell interactions with the extracellular matrix
16. Genetische Ursachen für epidermale Fragilität
17. “Double trouble”: Diagnostic challenges in genetic skin disorders: OY1
18. Extending the phenotypic spectrum associated with loss of desmoglein 1: O9
19. Expression of the sweat-derived innate defence antimicrobial peptide dermcidin is not impaired in Staphylococcus aureus colonization or recurrent skin infections
20. Guidelines on the use of extracorporeal photopheresis
21. Epidemiology of rare diseases is important
22. Genabelte Blasen auf lichtexponierter Haut
23. Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study
24. Generalisiertes noduläres Exanthem mit Augenentzündung bei einer 34-Jährigen
25. Hereditäre Blasen bildende Hauterkrankungen
26. Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations
27. Großflächige melanozytäre Nävi bei generalisierter atrophisierender benigner Epidermolysis bullosa (Epidermolysis-bullosa-Nävi)
28. Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene
29. Tissue-specific expression and long-term deposition of human collagen VII in the skin of transgenic mice: implications for gene therapy
30. Stable integration of large (>100 kb) PAC constructs in HaCaT keratinocytes using an integrin-targeting peptide delivery system
31. Deciphering keratinocyte-fibroblast communication in the human skin: who is talking?: P24-18
32. Conradi–Hünermann–Happle syndrome in males vs. MEND syndrome (male EBP disorder with neurological defects)
33. The flavonoid luteolin inhibits the autoantibody-induced granulocyte activation and tissue damage in experimental bullous pemphigoid: P188
34. Spleen tyrosine kinase (Syk) promotes granulocyte-mediated skin blistering induced by autoantibodies: P160 (V19)
35. Mapping of pathogenic epitopes in experimental epidermolysis bullosa acquisita: P163
36. Sensitive and specific detection of collagen VII-specific autoantibodies by novel immunoassay using chimeric recombinant antigen: P071
37. Mesenchymal stromal cells for the treatment of inherited skin fragility disorders: P060
38. Non-inflammatory pathogenic effects of collagen VII-specific autoantibodies: P039
39. Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma
40. Diagnose "Genodermatose" erst im Alter - ist dies möglich?: WS 19/05
41. Schmerzen - Relevanz in der konservativen Dermatologie: WS08/01
42. A study into growth and anaemia in children with epidermolysis bullosa
43. 大疱性表皮松解症患儿生长发育及贫血的研究
44. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
45. Skin Fragility: Perspectives on Evidence-based Therapies
46. Grey spots in a patient with dystrophic epidermolysis bullosa
47. Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria
48. STAT3 targeting in dystrophic epidermolysis bullosa
49. Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study*
50. Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype
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