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The British Journal of Dermatology
|
October 25, 2019
Severe early-onset manifestations of pseudoxanthoma elasticum resulting from the cumulative effects of several deleterious mutations in ENPP1, ABCC6 and HBB: transient improvement in ectopic calcification with sodium thiosulfate
L Omarjee, Y Nitschke, S Verschuere, et al.
The British Journal of Dermatology
|
December 24, 2018
Naevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal naevus) and mosaic FGFR3 and FGFR2 mutations
D Bessis, A Petit, M Battistella, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 25, 2014
[Superficial skin infections and bacterial dermohypodermitis]
M Lorrot, E Bourrat, C Doit, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 20, 2021
Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity
D Darbord, G Hickman, N Pironon, et al.
The British Journal of Dermatology
|
July 7, 2011
Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis
C Bodemer, E Bourrat, J Mazereeuw-Hautier, et al.
The British Journal of Dermatology
|
March 25, 2011
Palmoplantar keratodermas in black patients (Fitzpatrick skin phototype V-VI) of African descent: a multicentre comparative and descriptive series
E Bourrat, P-P Cabotin, M Baccard, et al.
The British Journal of Dermatology
|
January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C
S Hadj-Rabia, D Oriot, N Soufir, et al.
The British Journal of Dermatology
|
September 27, 2019
EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa
S Gaucher, S M Lwin, M Titeux, et al.
The British Journal of Dermatology
|
September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis
A Hotz, C Fagerberg, A Vahlquist, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 15, 2019
French expert opinion for the management of juvenile dermatomyositis
B Bader-Meunier, C Gitiaux, A Belot, et al.
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of 10
Search research articles
Search
Showing results (61-70 of 91) with videos related to
Sort By:
Page
of 10
The British Journal of Dermatology
|
October 25, 2019
Severe early-onset manifestations of pseudoxanthoma elasticum resulting from the cumulative effects of several deleterious mutations in ENPP1, ABCC6 and HBB: transient improvement in ectopic calcification with sodium thiosulfate
L Omarjee, Y Nitschke, S Verschuere, et al.
The British Journal of Dermatology
|
December 24, 2018
Naevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal naevus) and mosaic FGFR3 and FGFR2 mutations
D Bessis, A Petit, M Battistella, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 25, 2014
[Superficial skin infections and bacterial dermohypodermitis]
M Lorrot, E Bourrat, C Doit, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 20, 2021
Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity
D Darbord, G Hickman, N Pironon, et al.
The British Journal of Dermatology
|
July 7, 2011
Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis
C Bodemer, E Bourrat, J Mazereeuw-Hautier, et al.
The British Journal of Dermatology
|
March 25, 2011
Palmoplantar keratodermas in black patients (Fitzpatrick skin phototype V-VI) of African descent: a multicentre comparative and descriptive series
E Bourrat, P-P Cabotin, M Baccard, et al.
The British Journal of Dermatology
|
January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C
S Hadj-Rabia, D Oriot, N Soufir, et al.
The British Journal of Dermatology
|
September 27, 2019
EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa
S Gaucher, S M Lwin, M Titeux, et al.
The British Journal of Dermatology
|
September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis
A Hotz, C Fagerberg, A Vahlquist, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 15, 2019
French expert opinion for the management of juvenile dermatomyositis
B Bader-Meunier, C Gitiaux, A Belot, et al.
Page
of 10