Search Results - "Campos‐Domínguez, Minia"

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    Omeprazole‐induced hypertrichosis in two children by Elosua‐González, Marta, CamposDomínguez, Minia, Bancalari, Daniel, Noguera‐Morel, Lucero, Hernández‐Martín, Angela, Huerta‐Aragonés, Jorge, Torrelo, Antonio

    Published in Pediatric dermatology (01-07-2018)
    “…Omeprazole significantly increases duodenal prostaglandin E2 synthesis. Prostaglandins are involved in hair growth regulation: prostaglandin E2 and…”
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    Overlap between angiolymphoid hyperplasia with eosinophilia and Kimura's disease in a child with immune thrombocytopenic purpura by Bardon-Cancho, Eduardo, Garrido-Colino, Carmen, Hernández-García, Bárbara, Parra-Blanco, Verónica, García-Morín, Marina, Cela, Elena, Domínguez, Minia

    Published in Indian journal of dermatology (01-03-2019)
    “…Sir, Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon benign vasoproliferative disorder of unknown origin characterized by erythematous or…”
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    Adams-Oliver Syndrome with Unusual Central Nervous System Findings and an Extrahepatic Portosystemic Shunt by Pérez-García, Carlos, Martín, Yolanda Ruíz, Del Hoyo, Alejandra Aguado, Rodríguez, Carlos Marín, Domínguez, Minia Campos

    Published in Pediatric reports (26-06-2017)
    “…We report a case of a premature neonate girl with scalp and skull defects and brachydactyly of the feet consistent with an Adams-Oliver syndrome (AOS). The…”
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    A novel pathogenic variation of DOCK6 gene: the genotype-phenotype correlation in Adams-Oliver syndrome by Nieto-Benito, Lula Maria, Suárez-Fernández, Ricardo, Campos-Domínguez, Minia

    Published in Molecular biology reports (01-06-2023)
    “…Background Adams-Oliver syndrome (AOS) (#614,219) is a multiple malformation disorder characterized by the presence of aplasia cutis congenita (ACC) and…”
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    Ectodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia by Nieto‐Benito, Lula María, Molina‐López, Irene, Feito‐Rodríguez, Marta, Martínez‐González, Víctor, Suárez‐Fernández, Ricardo, CamposDominguez, Minia

    Published in Pediatric dermatology (01-03-2021)
    “…Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congenital acral bullae, congenital milia and adermatoglyphia…”
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    Langerhans cell histiocytosis mimicking lichen nitidus with bone involvement by Lozano Masdemont, Belén, Gómez‐Recuero Muñoz, Laura, Villanueva Álvarez‐Santullano, Ana, Parra Blanco, Verónica, Campos Domínguez, Minia

    Published in Australasian journal of dermatology (01-08-2017)
    “…We report the case of a 6‐month‐old Hispanic boy with a 4‐month history of widespread pruritic hypopigmented papules mimicking lichen nitidus. The final…”
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    Mammary hemangioma in an infant with apparent mastitis. Case report by Rodríguez Jiménez, Cristina, Míguez Navarro, Concepción, Campos Domínguez, Minia, Garrido Colino, Carmen

    Published in Archivos argentinos de pediatría (01-02-2018)
    “…Mammary pathology is infrequent during childhood. It is rare the probability of finding a breast mass in an infant. The most frequent possible diagnoses at…”
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