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1. Low rate of new‐onset primary biliary cholangitis in a cohort of anti‐mitochondrial antibody‐positive subjects over six years of follow‐up

2. New guidelines for the diagnosis of epidermolysis bullosa

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3. 大疱性表皮松解症诊断的新指南

4. Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa

5. Mapeo por inmunofluorescencia para el diagnóstico de epidermólisis ampollosa congénita

6. Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis Bullosa

7. Epidermolysis bullosa hereditaria

8. Zahnveranderung bei junktionaler Epidermolysis bullosa - Bericht uber eine Patientin mit einer Mutation im LAMB3-Gen. Dental alterations in junctional epidermolysis bullosa - report of a patient with a mutation in the LAMB3-gene

9. Telepathology using immunofluorescence/immunoperoxidase microscopy

10. Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

11. Pathogenic Mechanisms in Epidermolysis Bullosa Naevi

12. Unilaterale Blepharochalasis mit läsionalen IgA-Ablagerungen

13. Antinuclear antibodies (ANA) Diagnostic value of different methods for screening and differentiation

14. Transient Autoimmune Hepatitis Induced by a Thymoma

15. Ocular involvement in IgA-epidermolysis bullosa acquisita

16. Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab

17. Premature Termination Codons Are Present on Both Alleles of the Bullous Pemphigoid Antigen 2/Type XVII Collagen Gene in Five Austrian Families with Generalized Atrophic Benign Epidermolysis Bullosa

18. Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa

19. Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa

20. A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner

21. Contents, Vol. 189, Supplement 1, 1994

22. Role of immunofluorescence microscopy in dermatology

23. [Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa]

24. Diagnostic pitfalls in newborns and babies with blisters and erosions

25. [Hereditary blistering diseases. Symptoms, diagnosis and treatment of epidermolysis bullosa]

26. Ocular involvement in anti-epiligrin cicatricial pemphigoid

27. Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement

28. Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay

30. Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

31. A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner

32. Ungewöhnliche Manifestationen blasenbildender Dermatosen

33. [Unilateral blepharochalasis with IgA-deposits]

34. Histopathology of human corneas after amniotic membrane and limbal stem cell transplantation for severe chemical burn

35. A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency

37. [Quality control in the allergy laboratory--4 years 'Allergy Ring Trial' in Austria]

38. Perioperative immunoglobulin E response to coronary artery bypass grafting

39. Klinik und einfache Laborparameter bei Chlamydien-Infektionen

40. Diagnosis of Chlamydia trachomatis infection--culture versus serology

41. [Clinical aspects and simple laboratory parameters in Chlamydia infections]

43. Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significance.

44. Epidermolysis bullosa House Austria and Epidermolysis bullosa clinical network : Example of a centre of expertise implemented in a European reference network to face the burden of a rare disease.

45. Diffuse cutaneous mastocytosis masquerading as epidermolysis bullosa.

46. Autoimmune bullous diseases in Austria.

47. Direct and indirect immunofluorescence for the diagnosis of bullous autoimmune diseases.

48. Role of immunofluorescence microscopy in dermatology.

49. [Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa].

50. Immunofluorescence mapping for the diagnosis of epidermolysis bullosa.