Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Skin Health and Disease
|
June 6, 2022
Prevalence and treatment of vitamin K deficiency in paediatric patients with recessive dystrophic epidermolysis bullosa-severe subtype
N Yerlett, G Petrof, K Holsgrove, et al.
The British Journal of Dermatology
|
September 21, 2011
Desmosomal genodermatoses
G Petrof, J E Mellerio, J A McGrath
Clinical and Experimental Dermatology
|
June 26, 2021
Infantile haemangioma presenting in combination with a cerebriform naevus sebaceous on the scalp
S Chottianchaiwat, A E Martinez, L Solman, et al.
Clinical and Experimental Dermatology
|
June 28, 2008
Unusual presentation of cutaneous metastases in renal cell carcinoma
N Sheth, G Petrof, D Greenblatt, et al.
The British Journal of Dermatology
|
September 2, 2018
To what extent do disease severity and illness perceptions explain depression, anxiety and quality of life in hidradenitis suppurativa?
A Pavon Blanco, M A Turner, G Petrof, et al.
The British Journal of Dermatology
|
September 17, 2013
Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial
G Petrof, M Martinez-Queipo, J E Mellerio, et al.
Clinical and Experimental Dermatology
|
May 14, 2011
A case of unilateral leg ulcers secondary to Brown-Séquard syndrome
J S Wee, S M Langan, G Petrof, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 14, 2012
A systematic review of the literature on the treatment of pityriasis rubra pilaris type 1 with TNF-antagonists
G Petrof, N Almaani, C B Archer, et al.
The British Journal of Dermatology
|
March 13, 2012
Infliximab for the treatment of psoriasis in the U.K.: 9 years' experience of infusion reactions at a single centre
J S Wee, G Petrof, K Jackson, et al.
The British Journal of Dermatology
|
June 7, 2014
Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome
C Tziotzios, G Petrof, L Liu, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Skin Health and Disease
|
June 6, 2022
Prevalence and treatment of vitamin K deficiency in paediatric patients with recessive dystrophic epidermolysis bullosa-severe subtype
N Yerlett, G Petrof, K Holsgrove, et al.
The British Journal of Dermatology
|
September 21, 2011
Desmosomal genodermatoses
G Petrof, J E Mellerio, J A McGrath
Clinical and Experimental Dermatology
|
June 26, 2021
Infantile haemangioma presenting in combination with a cerebriform naevus sebaceous on the scalp
S Chottianchaiwat, A E Martinez, L Solman, et al.
Clinical and Experimental Dermatology
|
June 28, 2008
Unusual presentation of cutaneous metastases in renal cell carcinoma
N Sheth, G Petrof, D Greenblatt, et al.
The British Journal of Dermatology
|
September 2, 2018
To what extent do disease severity and illness perceptions explain depression, anxiety and quality of life in hidradenitis suppurativa?
A Pavon Blanco, M A Turner, G Petrof, et al.
The British Journal of Dermatology
|
September 17, 2013
Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial
G Petrof, M Martinez-Queipo, J E Mellerio, et al.
Clinical and Experimental Dermatology
|
May 14, 2011
A case of unilateral leg ulcers secondary to Brown-Séquard syndrome
J S Wee, S M Langan, G Petrof, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 14, 2012
A systematic review of the literature on the treatment of pityriasis rubra pilaris type 1 with TNF-antagonists
G Petrof, N Almaani, C B Archer, et al.
The British Journal of Dermatology
|
March 13, 2012
Infliximab for the treatment of psoriasis in the U.K.: 9 years' experience of infusion reactions at a single centre
J S Wee, G Petrof, K Jackson, et al.
The British Journal of Dermatology
|
June 7, 2014
Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome
C Tziotzios, G Petrof, L Liu, et al.
Page
of 2