Search Results - "BOGGIO, PAULA"

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  1. 1

    Early propranolol treatment of infantile hemangiomas improves outcome by Giachetti, Ana, Díaz, María Sol, Boggio, Paula, Posadas Martínez, María Lourdes

    Published in Anais brasileiros de dermatología (01-05-2023)
    “…Infantile hemangiomas (IH) are the most common soft tissue tumors of childhood. Although most of these tumors are not worrisome, some IH may be life or…”
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    Journal Article
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    Dermatologic Aspects of Fabry Disease by Luna, Paula C., Boggio, Paula, Larralde, Margarita

    “…Isolated angiokeratomas (AKs) are common cutaneous lesions, generally deemed unworthy of further investigation. In contrast, diffuse AKs should alert the…”
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  3. 3

    Recomendaciones para el tratamiento de la psoriasis en Pediatría by Luna, Paula Carolina, Abad, María Eugenia, Larralde, Margarita, Boggio, Paula, Ferrari, Bruno, Maccario, María Fernanda, Castro, Carla, Moreno, Silvia, Kaplan, Débora, Echeverría, Cristina

    “…Introducción: un tercio de los pacientes con psoriasis comienzan con sus síntomas en la niñez y la adolescencia, con fuerte impacto emocional y psicosocial…”
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    Lupus erythematosus: Clinical and histopathological study of oral manifestations and immunohistochemical profile of the inflammatory infiltrate by Lourenço, Silvia V., De Carvalho, Fabio R. G., Boggio, Paula, Sotto, Mirian N., Vilela, Maria A. C., Rivitti, Evandro A., Nico, Marcello M. S.

    Published in Journal of cutaneous pathology (01-07-2007)
    “…Background:  Lupus erythematosus (LE) is a multifactorial autoimmune disease, which may affect the oral mucosa in either its cutaneous and systemic forms, with…”
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    Eccrine Angiomatous Hamartoma: Report of Five Congenital Cases by Larralde, Margarita, Bazzolo, Eleonora, Boggio, Paula, Abad, María Eugenia, Santos Muñoz, Andrea

    Published in Pediatric dermatology (01-05-2009)
    “…:  Eccrine angiomatous hamartoma is a rare entity characterized histologically by the combination of proliferative eccrine and vascular elements. It generally…”
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    Dyskeratosis Congenita – Report of a Case with Emphasis on Gingival Aspects by Lourenço, Silvia V., Boggio, Paula A., Fezzi, Fernando A., Sebastião, Alexandre L., Nico, Marcello Menta S.

    Published in Pediatric dermatology (01-03-2009)
    “…:  A case of dyskeratosis congenita (DC) of an 11‐year‐old male is reported. He presented with the characteristic clinical triad of reticular pigmentation of…”
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  7. 7

    Retronychia in children: A case series by Díaz, María Sol, Boggio, Paula, Calvano, Roberta, Scacchi, María Florencia, Giachetti, Ana

    Published in Pediatric dermatology (01-05-2024)
    “…Retronychia is characterized by proximal ingrowing of the nail plate into the proximal nail fold. It is always associated with the presence of two or more…”
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  8. 8

    Idiopathic aseptic facial granuloma: A retrospective study of 43 cases by Kuperman Wilder, Lola, Lamberti, Antonela, Boggio, Paula, Abad, María Eugenia, Luna, Paula C, Larralde, Margarita

    Published in Pediatric dermatology (01-03-2024)
    “…Idiopathic aseptic facial granuloma (IAFG) is an underrecognized pediatric skin disease, currently considered within the spectrum of rosacea. It usually…”
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    Aplasia Cutis Congenita Associated with Fetus Papyraceus by Pieretti, María Lía, Alcalá, Rebeca, Boggio, Paula, Noguera‐Morel, Lucero, Porriño, María Librada, Luna, Paula C., Hernández‐Martín, Angela, Schroh, Roberto, Larralde, Margarita, Torrelo, Antonio

    Published in Pediatric dermatology (01-11-2015)
    “…Aplasia cutis congenita (ACC), or congenital absence of skin, is a heterogeneous condition that may be due to varied mechanisms. ACC has rarely been reported…”
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  11. 11

    Neonatal Kerion Celsi: Report of Three Cases by Larralde, Margarita, Gomar, Begoña, Boggio, Paula, Abad, María Eugenia, Pagotto, Betina

    Published in Pediatric dermatology (01-07-2010)
    “…:  Tinea capitis is a fungal infection caused by dermatophytes, frequent in children but uncommon in the neonatal period. Kerion Celsi is the inflammatory…”
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  12. 12

    Nevus Trichilemmocysticus: Report of a New Case of a Recently Recognized Entity by Larralde, Margarita, Boggio, Paula, Abad, María Eugenia, Corbella, Cristina, Happle, Rudolf

    Published in Pediatric dermatology (01-05-2011)
    “…:  A new type of organoid epidermal nevus, characterized by the presence of multiple trichilemmal cysts disposed in a linear arrangement, was recently…”
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  13. 13

    Infantile Myofibromatosis: Report of Nine Patients by Larralde, Margarita, Hoffner, Mariana V., Boggio, Paula, Abad, María Eugenia, Luna, Paula C., Correa, Noemí

    Published in Pediatric dermatology (01-01-2010)
    “…:  Infantile myofibromatosis is a rare fibrous tumor of infancy that can be solitary or multiple. Although most of the cases are limited to the skin, in some…”
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    Inflammatory myofibroblastic tumor of the tongue: report of an unusual case in a teenage patient by Lourenço, Silvia Vanessa, Boggio, Paula, Simonsen Nico, Marcello Menta

    Published in Dermatology online journal (15-05-2012)
    “…Inflammatory myofibroblastic tumor is a rare and distinctive lesion composed of myofibroblastic cells accompanied by an inflammatory infiltration of plasma…”
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    Scurvy in a 10‐month‐old boy by Larralde, Margarita, Santos Muñoz, Andrea, Boggio, Paula, Di Gruccio, Vanesa, Weis, Isaac, Schygiel, Adolfo

    Published in International journal of dermatology (01-02-2007)
    “…We report a 10‐month‐old boy with inflammatory and necrotic gingival lesions, fever, irritability, and pseudoparalysis of the legs. Laboratory examinations…”
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    Doença de Fabry by Boggio, Paula, Luna, Paula Carolina, Abad, María Eugenia, Larralde, Margarita

    Published in Anais brasileiros de dermatología (01-08-2009)
    “…A doença de Fabry é enfermidade de armazenamento lisossômico rara, ligada ao cromossomo-X, causada pela deficiência parcial ou completa da enzima…”
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    Doença de Fabry Fabry disease by Paula Boggio, Paula Carolina Luna, María Eugenia Abad, Margarita Larralde

    Published in Anais brasileiros de dermatología (01-08-2009)
    “…A doença de Fabry é enfermidade de armazenamento lisossômico rara, ligada ao cromossomo-X, causada pela deficiência parcial ou completa da enzima…”
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    Journal Article