Search Results - "Petrof, G."
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Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial
Published in British journal of dermatology (1951) (01-11-2013)“…Summary Background Fibroblast cell therapy can modify disease biology in recessive dystrophic epidermolysis bullosa (RDEB) although whether it improves wound…”
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British Association of Dermatologists guidelines for biologic therapy for psoriasis 2017
Published in British journal of dermatology (1951) (01-09-2017)“…Plain language summary available online…”
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British Association of Dermatologists guidelines for the management of hidradenitis suppurativa (acne inversa) 2018
Published in British journal of dermatology (1951) (01-05-2019)“…Linked Comment: Jemec. Br J Dermatol 2019; 180:975. Plain language summary available online…”
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4
To what extent do disease severity and illness perceptions explain depression, anxiety and quality of life in hidradenitis suppurativa?
Published in British journal of dermatology (1951) (01-02-2019)“…Summary Background Hidradenitis suppurativa (HS) can have significant psychological consequences and affect quality of life (QoL). This has been associated…”
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British Association of Dermatologists and U.K. Cutaneous Lymphoma Group guidelines for the management of primary cutaneous lymphomas 2018
Published in British journal of dermatology (1951) (01-03-2019)“…Linked Editorial: Wang and Bagot. Br J Dermatol 2019; 180:443–444…”
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6
Infantile haemangioma presenting in combination with a cerebriform naevus sebaceous on the scalp
Published in Clinical and experimental dermatology (01-01-2022)“…Click https://wileyhealthlearning.com/#/online-courses/a54fac75-89f4-4bf5-80a4-19e31765a7a4 for the corresponding questions to this CME article…”
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7
Illness perceptions and health outcomes in HS
Published in British journal of dermatology (1951) (01-02-2019)“…Summary Hidradenitis Suppurativa (HS) is a chronic skin condition that affects between 1 and 2% of the European population. It is caused by inflammation of the…”
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British Association of Dermatologists' guidelines for the management of Stevens–Johnson syndrome/toxic epidermal necrolysis in children and young people, 2018
Published in British journal of dermatology (1951) (01-07-2019)“…Linked Comment: Lee. Br J Dermatol 2019; 181:10–11. Plain language summary available online…”
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Desmosomal genodermatoses
Published in British journal of dermatology (1951) (01-01-2012)“…Summary Desmosomes are intercellular junctions that contribute to cell–cell adhesion, signalling, development and differentiation in various tissues, including…”
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Otological complications in inversa type recessive dystrophic epidermolysis bullosa
Published in Clinical and experimental dermatology (01-04-2022)“…Summary Background The rare inversa subtype of recessive dystrophic epidermolysis bullosa (RDEB‐I) is characterized by predominant intertriginous skin…”
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Prevalence and treatment of vitamin K deficiency in paediatric patients with recessive dystrophic epidermolysis bullosa‐severe subtype
Published in Skin health and disease (01-06-2021)“…Introduction Patients with recessive dystrophic epidermolysis bullosa‐severe subtype (RDEB‐S) are at risk of vitamin K deficiency, potentially causing abnormal…”
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Characteristics of children with Netherton syndrome: a review of 21 patients
Published in Journal of the European Academy of Dermatology and Venereology (01-07-2021)Get full text
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A systematic review of the literature on the treatment of pityriasis rubra pilaris type 1 with TNF-antagonists
Published in Journal of the European Academy of Dermatology and Venereology (01-01-2013)“…Background Adult pityriasis rubra pilaris (PRP) type 1 is a rare chronic papulosquamous disorder with clinical and histological parallels with psoriasis…”
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Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome
Published in British journal of dermatology (1951) (01-11-2014)“…Summary Background Schöpf‐Schulz‐Passarge syndrome (SSPS) is an autosomal recessive form of ectodermal dysplasia resulting from mutations in WNT10A. Objectives…”
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Optimal Management Of Chronic Wounds In Paediatric Junctional Epidermolysis Bullosa Patients
Published in Chronic wound care management and research (01-10-2019)“…Epidermolysis bullosa (EB) is a group of rare genetic mucocutaneous fragility disorders. Patients with EB can experience blister formation following minor skin…”
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化脓性汗腺炎患者的疾病感受和健康结局
Published in British journal of dermatology (1951) (01-02-2019)“…Summary 化脓性汗腺炎 (HS) 是一种慢性皮肤病,1% 到 2% 的欧洲人口受到累及。该病由毛囊和汗腺发炎所引起,可导致腋窝内、腹股沟、生殖器和乳房下方的皮肤下面发生有疼痛感并散发难闻气味的肿胀。HS 与抑郁、焦虑和生活质量 (QoL)…”
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Infliximab for the treatment of psoriasis in the U.K.: 9 years' experience of infusion reactions at a single centre
Published in British journal of dermatology (1951) (01-08-2012)“…Summary Background Infliximab is an antitumour necrosis factor‐α chimeric monoclonal antibody that is an established treatment for severe chronic plaque…”
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A case of unilateral leg ulcers secondary to Brown-Séquard syndrome
Published in Clinical and experimental dermatology (01-06-2011)Get full text
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Unusual presentation of cutaneous metastases in renal cell carcinoma
Published in Clinical and experimental dermatology (01-07-2008)Get full text
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British Association of Dermatologists guidelines for the management of lichen sclerosus, 2018
Published in British journal of dermatology (1951) (01-04-2018)“…Linked Comment: Akel and Fuller. Br J Dermatol 2018; 178:823–824. Plain language summary available online…”
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