Search Results - "Azaña, J M"

Capillary malformation−arteriovenous malformation syndrome: a multicentre study by Valdivielso‐Ramos, M., Martin‐Santiago, A., Azaña, J. M., Hernández‐Nuñez, A., Vera, A., Perez, B., Tercedor, J., Feito, M., Vicente, A., Prat, C., Lopez‐Gutierrez, J. C., Garnacho, G., Baselga, E., Roe, E., Palencia, S., Cordero, P., Moreno, R., Agudo, A., Cueva, P., Torrelo, A.

“…Summary Background Capillary malformation–arteriovenous malformation (CM‐AVM) syndrome is a rare syndrome with characteristic skin lesions that are associated…”
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Histopathological hallmarks of cutaneous lesions of capillary malformation–arteriovenous malformation syndrome by Valdivielso‐Ramos, M., Torrelo, A., Martin‐Santiago, A., Hernández‐Nuñez, A., Azaña, J.M., Campos, M., Berenguer, B., Garnacho, G., Moreno, R., Colmenero, I.

“…Importance Capillary malformation–arteriovenous malformation (CM‐AVM) syndrome is a recently described syndrome with distinctive cutaneous lesions. Very little…”
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Interobserver variability in the classification of childhood maculopapular cutaneous mastocytosis by Torrelo, A., Vergara‐de‐la‐Campa, L., Azaña, J.M., Greenberger, S., Lam, J.M., Lawley, L.P., Morren, M.‐A., Schaffer, J.V., García‐Doval, I., Matito, A., Alvarez‐Twose, I.

“…Background Maculopapular cutaneous mastocytosis (MPCM) in children is classified in two variants: (i) monomorphic variant, presenting with the small macules or…”
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Update on Mastocytosis (Part 2): Categories, Prognosis, and Treatment by Azaña, J M, Torrelo, A, Matito, A

“…Mastocytosis is a term used to describe a heterogeneous group of disorders characterized by clonal proliferation of mast cells in different organs. The organ…”
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Update on Mastocytosis (Part 1): Pathophysiology, Clinical Features, and Diagnosis by Azaña, J M, Torrelo, A, Matito, A

“…Mastocytosis is a term used to describe a heterogeneous group of disorders characterized by clonal proliferation of mast cells in various organs. The organ…”
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CD133 Expression in Normal Skin and in Epithelial Cutaneous Tumors by Poblet, E., Calero-Oliver, R., Azaña, J. M., Escario, E., Serrano-Vargas, R., Nam-Cha, S. H., Martín, A. G.

“…Background. Expression of human CD133 (human prominin-1) in cancer cells has been postulated to be a marker of stemness and is considered as a putative marker…”
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Chronic Lichenoid Folliculitis Decalvans by López Mateos, A, Plata Clemente, S, Guerrero Ramírez, C, Azaña Defez, J M

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Cutaneous leishmaniasis by Leishmania infantum: behind granulomatous lesions of unknown aetiology by Merino‐Espinosa, G., Corpas‐López, V., Díaz‐Sáez, V., Morillas‐Márquez, F., Tercedor‐Sánchez, J., Azaña‐Defez, J.M., López‐Hidalgo, J., Aneiros‐Fernández, J., Martín‐Sánchez, J.

“…Background Cutaneous leishmaniasis (CL) is underestimated in Spain as in other European countries due to the polymorphism of its clinical manifestations and…”
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Comparison of PCR‐based methods for the diagnosis of cutaneous leishmaniasis in two different epidemiological scenarios: Spain and Morocco by Merino‐Espinosa, G., Rodríguez‐Granger, J., Morillas‐Márquez, F., Tercedor, J., Corpas‐López, V., Chiheb, S., Alcalde‐Alonso, M., Azaña‐Defez, J.M., Riyad, M., Díaz‐Sáez, V., Martín‐Sánchez, J.

“…Background Cutaneous leishmaniasis (CL) is a disfiguring and stigmatising disease occurring in more than 70 countries across the world including Spain and…”
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Intralymphatic Histiocytosis: A Report of 2 Cases by Gómez-Sánchez, M E, Azaña-Defez, J M, Martínez-Martínez, M L, López-Villaescusa, M T

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Intralymphatic Histiocytosis: A Report of 2 Cases by Gómez-Sánchez, M.E., Azaña-Defez, J.M., Martínez-Martínez, M.L., López-Villaescusa, M.T.

“…Intralymphatic histiocytosis is a benign condition characterized by poorly defined erythematous plaques (sometimes forming a reticular pattern) as well as the…”
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Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership by Hernández-Martín, A., Dávila-Seijo, P., de Lucas, R., Baselga, E., Redondo, P., Martín-Santiago, A., Azaña-Defez, J.M., González-Viejo, I., Jiménez-Ferreres, L., González-Enseñat, M.A., Arroyo-Manzanal, M.I., Soria, J.M., Garcia-Doval, I.

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Urticaria pigmentosa: a review of 67 pediatric cases by Azaña, J M, Torrelo, A, Mediero, I G, Zambrano, A

“…Mastocytosis is a disorder of mast cell proliferation that may appear during infancy, childhood, or adulthood. We studied 67 consecutive patients (33 males, 34…”
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Topical cyclosporine for cicatricial pemphigoid by Azaña, J M, de Misa, R F, Boixeda, J P, Ledo, A

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Dermatology consultations in an emergency department prior to establishment of emergency dermatology cover by Martínez-Martínez, M L, Escario-Travesedo, E, Rodríguez-Vázquez, M, Azaña-Defez, J M, Martín de Hijas-Santos, M C, Juan-Pérez-García, L

“…BACKGROUND AND OBJECTIVEan increasing number of patients seek emergency treatment for dermatologic complaints. The aim of this study was to assess the…”
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Is ILVEN a misnomer? Proposal of MALID as a more accurate nomenclature by López Sanz, P, Azaña Defez, J M

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Plasma levels of 8-methoxypsoralen after bath-PUVA for psoriasis: relationship to disease severity by Gómez, M I, Azaña, J M, Arranz, I, Harto, A, Ledo, A

“…Plasma levels of 8-methoxypsoralen (8-MOP) were determined by high-pressure liquid chromatography in 19 patients with psoriasis who were receiving bath-PUVA…”
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Referrals to Dermatology: Proportion of Banal Disorders by Martínez-Martínez, M.L, Pérez-García, L.J, Escario-Travesedo, E, Rodríguez-Vázquez, M, Azaña-Defez, J.M, Martín de Hijas Santos, M.C

“…Abstract Background and objective Skin diseases account for a large number of consultations in primary care. The objective of this study was to determine the…”
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Update on Mastocytosis (Part 1): Pathophysiology, Clinical Features, and Diagnosis by Azaña, J.M, Torrelo, A, Matito, A

“…Abstract Mastocytosis is a term used to describe a heterogeneous group of disorders characterized by clonal proliferation of mast cells in various organs. The…”
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Update on Mastocytosis (Part 2): Categories, Prognosis, and Treatment by Azaña, J.M, Torrelo, A, Matito, A

“…Abstract Mastocytosis is a term used to describe a heterogeneous group of disorders characterized by clonal proliferation of mast cells in different organs…”
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