809 results on '"Bruckner‐Tuderman, L."'
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2. Epidermolysis bullosa
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Books, media, physical & digital resources
3. Binde- und Stützgewebe
4. Wound healing in epidermolysis bullosa
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. Neues über hereditäre, blasenbildende Hauterkrankungen
8. Necrobiosis lipoidica: Kasuistische Vielfalt einer Diagnose
9. Epidermolysis bullosa: Diagnostik und Therapie
10. Phased-array of microcoils allows MR microscopy of ex vivo human skin samples at 9.4 T
11. Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergies
12. ‘Double trouble’: diagnostic challenges in genetic skin disorders
13. Cell interactions with the extracellular matrix
14. Genetische Ursachen für epidermale Fragilität
15. “Double trouble”: Diagnostic challenges in genetic skin disorders: OY1
16. Extending the phenotypic spectrum associated with loss of desmoglein 1: O9
17. Genabelte Blasen auf lichtexponierter Haut
18. Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study
19. Epidermolysis Bullosa
20. Generalisiertes noduläres Exanthem mit Augenentzündung bei einer 34-Jährigen
21. 486 Systemic collagen VII protein therapy for treatment of advanced RDEB
22. Hereditäre Blasen bildende Hauterkrankungen
23. Expression of the sweat-derived innate defence antimicrobial peptide dermcidin is not impaired in Staphylococcus aureus colonization or recurrent skin infections
24. Guidelines on the use of extracorporeal photopheresis
25. Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations
26. Großflächige melanozytäre Nävi bei generalisierter atrophisierender benigner Epidermolysis bullosa (Epidermolysis-bullosa-Nävi)
27. Collagen XVII promotes integrin-mediated squamous cell carcinoma transmigration—A novel role for αII b integrin and tirofiban
28. Tissue-specific expression and long-term deposition of human collagen VII in the skin of transgenic mice: implications for gene therapy
29. Stable integration of large (>100 kb) PAC constructs in HaCaT keratinocytes using an integrin-targeting peptide delivery system
30. Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene
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. Epidemiology of rare diseases is important
40. Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma
41. Diagnose "Genodermatose" erst im Alter - ist dies möglich?: WS 19/05
42. Schmerzen - Relevanz in der konservativen Dermatologie: WS08/01
43. A study into growth and anaemia in children with epidermolysis bullosa
44. 大疱性表皮松解症患儿生长发育及贫血的研究
45. Grey spots in a patient with dystrophic epidermolysis bullosa
46. Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria
47. Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype
48. Basement membrane antibodies in sera of haematopoietic cell recipients are associated with graft-versus-host disease
49. A familial case of tricho-rhino-phalangeal syndrome type III with a novel missense mutation in exon 6 of the TRPS1 gene
50. Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort
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