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1
Ulcero-necrotic monkeypox, a clue for an underlying immunosuppressive disease: Report of two cases
Ulcero-necrotic monkeypox, a clue for an underlying immunosuppressive disease: Report of two cases
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Ulcero-necrotic monkeypox, a clue for an underlying immunosuppressive disease: Report of two cases

Gonzalez-Rodriguez, B ; Calderon-Lozano, L ; Wang, A ; Gil-De la Cruz, E ; Tarin-Vicente, E J ; Fulgencio-Barbarin, J

Journal of the European Academy of Dermatology and Venereology : JEADV, 2023, Vol.37 (6), p.e754-e756

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2
Mogamulizumab combined with extracorporeal photopheresis for the treatment of refractory mycosis fungoides and Sézary syndrome. Report of seven cases
Mogamulizumab combined with extracorporeal photopheresis for the treatment of refractory mycosis fungoides and Sézary syndrome. Report of seven cases
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Mogamulizumab combined with extracorporeal photopheresis for the treatment of refractory mycosis fungoides and Sézary syndrome. Report of seven cases

Rubio-Muniz, C A ; Sánchez-Velázquez, A ; Arroyo-Andrés, J ; Agud-de Dios, M ; Tarín-Vicente, E J ; Falkenhain-López, D ; Ortiz-Romero, P L

Journal of the European Academy of Dermatology and Venereology : JEADV, 2024, Vol.38 (1), p.e102-e105

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3
Retinal arterial and venous occlusions in patients with ADPKD
Retinal arterial and venous occlusions in patients with ADPKD
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Retinal arterial and venous occlusions in patients with ADPKD

Qian, Qi ; Younge, Brian R. ; Torres, Vicente E.

Nephrology Dialysis Transplantation, 2007, Vol.22 (6), p.1769-1771

Oxford University Press

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4
Crohn's disease, relapsing polychondritis and epidermolysis bullosa acquisita: an immune-mediated inflammatory syndrome
Crohn's disease, relapsing polychondritis and epidermolysis bullosa acquisita: an immune-mediated inflammatory syndrome
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Crohn's disease, relapsing polychondritis and epidermolysis bullosa acquisita: an immune-mediated inflammatory syndrome

Vicente, E F ; Hernández-Núñez, A ; Aspa, J ; Aragües, M ; García-Vicuña, R

Rheumatology (Oxford, England), 2008, Vol.47 (3), p.380-381

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5
Duodenal diverticulosis in autosomal dominant polycystic kidney disease
Duodenal diverticulosis in autosomal dominant polycystic kidney disease
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Duodenal diverticulosis in autosomal dominant polycystic kidney disease

Kumar, Sumedha ; Adeva, Magdalena ; King, Bernard F. ; Kamath, Patrick S. ; Torres, Vicente E.

Nephrology Dialysis Transplantation, 2006, Vol.21 (12), p.3576-3578

Oxford University Press

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6
Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo
Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo
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Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo

Bravo-Pérez, C ; de la Morena-Barrio, M E ; Palomo, A ; Entrena, L ; de la Morena-Barrio, B ; Padilla, J ; Miñano, A ; Navarro, E ; Cifuentes, R ; Corral, J ; Vicente, V

British journal of haematology, 2020, Vol.191 (1), p.e32-e35

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7
Pediatric cryoglobulinemic vasculitis successfully managed with rituximab
Pediatric cryoglobulinemic vasculitis successfully managed with rituximab
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Pediatric cryoglobulinemic vasculitis successfully managed with rituximab

Giménez-Roca, C ; Iglesias, E ; Vicente, M A ; Bou, R ; Calzada-Hernández, J ; Prat, C ; García, M ; Antón, J

Dermatologic therapy, 2017, Vol.30 (2)

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8
Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome
Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome
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Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome

Bueno, E ; Cañueto, J ; García-Patos, V ; Vicente, M Asunción ; Bodet-Castillo, D ; Hernández-Ruíz, M Eugenia ; González-Sarmiento, R

Journal of the European Academy of Dermatology and Venereology : JEADV, 2017, Vol.31 (1), p.e11-e13

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9
Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia
Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia
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Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia

de la Morena-Barrio, M E ; Sevivas, T S ; Martinez-Martinez, I ; Miñano, A ; Vicente, V ; Jaeken, J ; Corral, J

Journal of thrombosis and haemostasis : JTH, 2012, Vol.10 (12), p.2625-2627

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10
Early-onset acral basal cell carcinomas in Gorlin syndrome
Early-onset acral basal cell carcinomas in Gorlin syndrome
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Early-onset acral basal cell carcinomas in Gorlin syndrome

Torrelo, A. ; Vicente, A. ; Navarro, L. ; Planaguma, M. ; Bueno, E. ; González-Sarmiento, R. ; Hernández-Martín, A. ; Noguera-Morel, L. ; Requena, L. ; Colmenero, I. ; Parareda, A. ; González-Enseñat, M.A. ; Happle, R.

British Journal of Dermatology, 2014, Vol.171 (5), p.1227-1229

Blackwell Publishing Ltd

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