about
Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndromeEpithelial inflammation resulting from an inherited loss-of-function mutation in EGFRCell therapy in dermatology.A systematic review of the literature on the treatment of pityriasis rubra pilaris type 1 with TNF-antagonists.Desmosomal genodermatoses.Infliximab for the treatment of psoriasis in the U.K.: 9 years' experience of infusion reactions at a single centre.Bone marrow transplantation in epidermolysis bullosa.Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial.Retrospective review of 18 British South Asian women with frontal fibrosing alopecia.Serum levels of high mobility group box 1 correlate with disease severity in recessive dystrophic epidermolysis bullosa.A case of unilateral leg ulcers secondary to Brown-Séquard syndromeTo what extent do disease severity and illness perceptions explain depression, anxiety and quality of life in hidradenitis suppurativa?Clinical features andWNT10Amutations in seven unrelated cases of Schöpf-Schulz-Passarge syndromeSchöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10ASelf-Assessment examination of the American Academy of Dermatology∗
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Gabriela Petrof
@ast
Gabriela Petrof
@en
Gabriela Petrof
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Gabriela Petrof
@nl
Gabriela Petrof
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type
label
Gabriela Petrof
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Gabriela Petrof
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Gabriela Petrof
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Gabriela Petrof
@nl
Gabriela Petrof
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prefLabel
Gabriela Petrof
@ast
Gabriela Petrof
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Gabriela Petrof
@es
Gabriela Petrof
@nl
Gabriela Petrof
@sl
P106
P21
P31
P496
0000-0001-8113-0373