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Publikováno v:
Neonatology, surgery and perinatal medicine. 10:87-91
Summary. Hereditary bullous epidermolysis (BE) is a group of genetically and clinically heterogeneous diseases characterized by the formation of blisters and erosion due to injury on the skin and mucous membranes. Different forms of BE can be accompa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c208850b2337f2ea132afe477b59877c
https://doi.org/10.24061/2413-4260.x.4.38.2020.10
https://doi.org/10.24061/2413-4260.x.4.38.2020.10
Autor:
Luiza Monteavaro Mariath, Juliana Tosetto Santin, Lavínia Schuler-Faccini, Ana Elisa Kiszewski
Publikováno v:
Anais Brasileiros de Dermatologia v.95 n.5 2020
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Anais Brasileiros de Dermatologia, Volume: 95, Issue: 5, Pages: 551-569, Published: 16 NOV 2020
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 95, Iss 5, Pp 551-569 (2020)
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Anais Brasileiros de Dermatologia, Volume: 95, Issue: 5, Pages: 551-569, Published: 16 NOV 2020
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 95, Iss 5, Pp 551-569 (2020)
Inherited epidermolysis bullosa is a group of genetic diseases characterized by skin fragility and blistering on the skin and mucous membranes in response to minimal trauma. Epidermolysis bullosa is clinically and genetically very heterogeneous, bein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d97d8cacf961e6baf6cc82e23b5c9e5f
https://doi.org/10.1016/j.abd.2020.05.001
https://doi.org/10.1016/j.abd.2020.05.001
Autor:
Gobinda Chatterjee, Keya Basu, Raghavendra Rao, Abhishek De, Manimoy Bandopadhyay, Subhrajyoti Karmakar
Publikováno v:
International Journal of Clinical and Diagnostic Pathology. 3:461-468
Background: Epidermolysis Bullosa is a rare genetic mechanobullous skin and mucosal fragility with blistering. It is classified into: Epidermolysis (Simplex), lucidolytic (Junctional) and dermolytic (Dystrophic). The disease is extremely debilitating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90c94ace7f24693a13ce342c180699cf
https://doi.org/10.33545/pathol.2020.v3.i1g.212
https://doi.org/10.33545/pathol.2020.v3.i1g.212
Publikováno v:
Panminerva Medica. 63
Bullous pemphigoid (BP) is an autoimmune blistering disorder with substantial morbidity and mortality. BP is regarded as a disorder driven by IgG due to BP180 and BP230 IgG autoantibodies, yet, new advances highlight the function of eosinophils and I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3a3715db8eada7dbff4392657191114
https://doi.org/10.23736/s0031-0808.20.03997-x
https://doi.org/10.23736/s0031-0808.20.03997-x
Publikováno v:
The American Journal of Case Reports
Patient: Female, 77-year-old Final Diagnosis: Atypical bullous pemphigoid Symptoms: Bullous skin lesions Medication: — Clinical Procedure: — Specialty: Dermatology Objective: Unusual clinical course Background: Bullous pemphigoid is a common prur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d103cab79f1d083a09da815592c884a3
https://pubmed.ncbi.nlm.nih.gov/34584063
https://pubmed.ncbi.nlm.nih.gov/34584063
Autor:
M.A. de Laat, Christopher C. Pollitt
Publikováno v:
Domestic Animal Endocrinology. 69:30-34
The third phalanx of the equine digit is suspended within the hoof capsule by a specialized interdigitating dermoepidermal layer called the lamellae, which fails during laminitis. Pathology of the basement membrane (BM), which interfaces epidermis an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1220547947544394d3af5bdf348bf34b
https://doi.org/10.1016/j.domaniend.2019.04.004
https://doi.org/10.1016/j.domaniend.2019.04.004
Autor:
Luciane Donida Bartoli Miot, Daniela Carvalho dos Santos, Hélio Amante Miot, Ana Cláudia Cavalcante Espósito, Gabrielli Brianezi, Nathália Pereira de Souza
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2020-12-12T01:42:44Z (GMT). No. of bitstreams: 0 Previous issue date: 2020-04-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a29ff8153e98483d24c2d772c420382a
https://doi.org/10.1007/s00403-019-01979-w
https://doi.org/10.1007/s00403-019-01979-w
Autor:
Hassell, John R., Robey, Pamela Gehron, Barrach, Hans-Jurgen, Wilczek, Joseph, Rennard, Stephen I., Martin, George R.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1980 Aug 01. 77(8), 4494-4498.
Externí odkaz:
https://www.jstor.org/stable/9130
Autor:
Natasha J. Olby, Keith E. Linder, Steven G. Friedenberg, Kathryn M. Meurs, Jonah N. Cullen, Ina Herrmann, Petra Bizikova
Publikováno v:
Vet Dermatol
Junctional epidermolysis bullosa (JEB) is a group of congenital blistering skin diseases characterized by clefting through the lamina lucida of the basement membrane zone.To characterize the clinical and morphological features of a congenital mechano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed7999d547833a66c7f75a4eaf554d18
https://pubmed.ncbi.nlm.nih.gov/34250689
https://pubmed.ncbi.nlm.nih.gov/34250689