Detalhe da pesquisa
1.
Comparative Treatment of Mucocutaneous Lesions in Hereditary Haemorrhagic Telangiectasia Patients With Dual Sequential Pulsed Dye Laser and Neodymium: Yttrium-Aluminium-Garnet Versus Neodymium: Yttrium-Aluminium-Garnet Laser Alone: A Double-Blind Randomized Controlled Study With Quality-of-Life Evaluation.
Actas Dermosifiliogr
; 115(3): 246-257, 2024 Mar.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-37913989
2.
Comparative Treatment of Mucocutaneous Lesions in Hereditary Haemorrhagic Telangiectasia Patients With Dual Sequential Pulsed Dye Laser and Neodymium: Yttrium-Aluminium-Garnet Versus Neodymium: Yttrium-Aluminium-Garnet Laser Alone: A Double-Blind Randomized Controlled Study With Quality-of-Life Evaluation. / [Artículo traducido] Tratamiento comparativo de lesiones mucocutáneas en pacientes con telangiectasia hemorrágica hereditaria con láser dual secuencial de colorante pulsado y neodimio: itrio-aluminio-granate versus neodimio: itrio-aluminio-granate solo: un estudio controlado aleatorizado doble ciego con evaluación de la calidad de vida.
Actas Dermosifiliogr
; 115(3): T246-T257, 2024 Mar.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-38185205
3.
Capillary malformation-arteriovenous malformation syndrome: a multicentre study.
Clin Exp Dermatol
; 46(2): 300-305, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32840927
4.
TREatment of ATopic eczema (TREAT) Registry Taskforce: protocol for a European safety study of dupilumab and other systemic therapies in patients with atopic eczema.
Br J Dermatol
; 182(6): 1423-1429, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31444799
5.
Interventions for infantile haemangiomas of the skin: abridged Cochrane systematic review and GRADE assessments.
Br J Dermatol
; 180(3): 527-533, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30414269
6.
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses.
Br J Dermatol
; 181(3): 512-522, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30693469
7.
Sturge-Weber Syndrome: A Review. / Síndrome de Sturge-Weber: revisión.
Actas Dermosifiliogr
; 108(5): 407-417, 2017 Jun.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-28126187
8.
Propranolol in the treatment of infantile haemangiomas: lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce survey.
Br J Dermatol
; 174(3): 594-601, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26473312
9.
A novel vascular tumour characterized by coexisting HRAS and GNAQ activating mutations.
Br J Dermatol
; 180(4): 927-928, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30387498
10.
Capillary malformation-arteriovenous malformation syndrome: a report of 2 cases, diagnostic criteria, and management.
Actas Dermosifiliogr
; 104(8): 710-3, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23933248
11.
Prevalence of dystrophic epidermolysis bullosa in Spain: a population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care.
Actas Dermosifiliogr
; 104(10): 890-6, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23809583
12.
Congenital Plaque-type Glomuvenous Malformation: 11 Years of Follow-up and Response to Treatment With the Combined Pulsed-Dye and Neodymium:Yttrium-Aluminum-Garnet Laser. / Malformación glomovenosa congénita en placas: 11 años de seguimiento y respuesta al tratamiento con láser combinado PDL/Nd: YAG.
Actas Dermosifiliogr
; 108(1): 72-74, 2017.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-27555518
13.
Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership.
Br J Dermatol
; 173(5): 1280-3, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25996448
14.
Rapidly involuting congenital haemangioma associated with transient thrombocytopenia and coagulopathy: a case series.
Br J Dermatol
; 158(6): 1363-70, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18410425
15.
Reference centers for epidermolysis bullosa and ichthyosis: an urgent need in Spain.
Actas Dermosifiliogr
; 104(5): 363-6, 2013 Jun.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-23665435
16.
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect.
J Med Genet
; 42(2): e13, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15689436
17.
[Past, present, and future of propranolol for hemangiomas of infancy]. / Hemangiomas de la infancia: pasado, presente y futuro del tratamiento con propranolol.
Actas Dermosifiliogr
; 102(7): 484-6, 2011 Sep.
Artigo
em Espanhol
| MEDLINE | ID: mdl-21616473
18.
Chilblain and Acral Purpuric Lesions in Spain during Covid Confinement: Retrospective Analysis of 12 Cases. / Lesiones pernióticas y acrales en España durante el confinamiento por COVID: análisis retrospectivo de 12 casos.
Actas Dermosifiliogr (Engl Ed)
; 111(5): 426-429, 2020 Jun.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-32402369
19.
Dyskeratosis congenita with linear areas of severe cutaneous involvement.
Am J Med Genet
; 75(5): 492-6, 1998 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-9489792
20.
Preauricular skin defects. A consequence of a persistent ectodermal groove.
Arch Dermatol
; 133(12): 1551-4, 1997 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-9420540