G. Pohla‐Gubo

Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa

Cristina Has, L. Liu, Maria C. Bolling et al. · British Journal of Dermatology · 2019 · 150 citations · Full text

Medicine, Dermatology, Pathology +6

Novel KIND1 Gene Mutation in Kindler Syndrome With Severe Gastrointestinal Tract Involvement

Elke Sadler, Alfred Klausegger, Wolfgang Muss et al. · Archives of Dermatology · 2006 · 62 citations

Life Sciences, Genetics, Molecular Genetics +14

Ocular involvement in IgA-epidermolysis bullosa acquisita

Johann Bauer, Herwig Schaeppi, Dieter Metze et al. · British Journal of Dermatology · 1999 · 55 citations

Medicine, Dermatology, Immunology +17

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

Johann Bauer, Fatima Rouan, Barbara Kofler et al. · American Journal Of Pathology · 2001 · 54 citations · Full text

Medicine, Genetics, Molecular Genetics +7

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

Thomas N. Darling, John A. McGrath, Carole Yee et al. · Journal of Investigative Dermatology · 1997 · 51 citations · Full text

Medicine, Dermatology, Genetics +14