[HTML][HTML] Epidermólisis bullosa en España: Estudio observacional de una cohorte de pacientes atendidos en un centro de referencia nacional
RM Pedrero, LQ Castanedo, IP Conde… - Actas Dermo …, 2021 - Elsevier
Antecedentes y objetivo: La epidermólisis bullosa (EB) es un grupo heterogéneo de
trastornos hereditarios caracterizado por un aumento de la fragilidad mucocutánea. El …
trastornos hereditarios caracterizado por un aumento de la fragilidad mucocutánea. El …
Épidermolyses bulleuses héréditaires: protocole national de diagnostic et de soins (PNDS)
C Chiaverini, E Bourrat, J Mazereeuw-Hautier… - … de Dermatologie et de …, 2017 - Elsevier
Résumé Les épidermolyses bulleuses héréditaires (EBH) sont un groupe hétérogène de
maladies génétiques rares caractérisées par une fragilité cutanée et/ou muqueuse …
maladies génétiques rares caractérisées par une fragilité cutanée et/ou muqueuse …
[图书][B] Therapy development for epidermolysis bullosa
Although rare genodermatoses such as Epidermolysis bullosa have received more attention
over the last years, no approved treatment options targeting causal mutations are currently …
over the last years, no approved treatment options targeting causal mutations are currently …
Allogeneic fibroblast cell therapy in the treatment of recessive dystrophic epidermolysis bullosa
A Kubanov, A Karamova, V Albanova, V Smoliannikova… - Wound medicine, 2018 - Elsevier
Background The non-healing wound is a characteristic clinical sign in recessive dystrophic
epidermolysis bullosa (RDEB). Methods Six patients with recessive dystrophic …
epidermolysis bullosa (RDEB). Methods Six patients with recessive dystrophic …
Epidermolysis Bullosa-Why Does a Multidisciplinary Team Approach Matter?/Epidermolysis Bullosa-Multidisipliner Ekip Yaklasimi Neden Önemlidir?
M Kim, A Yang, DF Murrell - Turk Dermatoloji Dergisi, 2016 - search.proquest.com
Epidermolysis bullosa (EB) is a rare inherited group of mechanobullous genodermatoses. It
is known to be one of the most devastating chronic conditions due to its frequent and …
is known to be one of the most devastating chronic conditions due to its frequent and …
[PDF][PDF] Врожденный буллезный эпидермолиз: особенности регенерации эпидермиса и методы терапии
АА Кубанов, АЭ Карамова… - Вестник …, 2017 - pdfs.semanticscholar.org
Врожденный буллезный эпидермолиз—группа наследственных заболеваний кожи,
обусловленных мутациями в генах структурных белков дермо-эпидермального …
обусловленных мутациями в генах структурных белков дермо-эпидермального …
Congenital epidermolysis bullosa: peculiarities of epidermis regeneration and methods of treatment
АA Kubanov, AEH Karamova, VI Al'banova… - Vestnik dermatologii i …, 2017 - vestnikdv.ru
Congenital epidermolysis bullosa is a group of hereditary skin diseases caused by
mutations in the genes of structural proteins of the dermoepidermal junction of the skin …
mutations in the genes of structural proteins of the dermoepidermal junction of the skin …
[HTML][HTML] Recent Trends in the Integrated Management of Cutaneous Squamous Cell Carcinoma
PP Naik - Dermato, 2022 - mdpi.com
Cutaneous squamous cell carcinoma (cSCC) is one of the most prevalent neoplasms
worldwide. Important risk factors for cSCC include sun exposure, immunosuppression, pale …
worldwide. Important risk factors for cSCC include sun exposure, immunosuppression, pale …
Epidermolysis bullosa
C Has - Braun-Falco´ s Dermatology, 2022 - Springer
The term “hereditary epidermolysis bullosa”(EB) covers clinically and genetically
heterogeneous diseases associated with blisters of the skin and mucous membranes after …
heterogeneous diseases associated with blisters of the skin and mucous membranes after …
Genetic blistering diseases
JA McGrath - Rook's Textbook of Dermatology, Ninth Edition, 2016 - Wiley Online Library
Resilient in health, the structural integrity of skin can become impaired or break down in a
collection of inherited skin diseases, referred to as the blistering genodermatoses. Most …
collection of inherited skin diseases, referred to as the blistering genodermatoses. Most …