Zobrazeno 1 - 10 of 26 pro vyhledávání: '"María Eugenia Abad"'
1
Akademický článek
Recomendaciones para el tratamiento de la psoriasis en Pediatría
Autor: Paula Carolina Luna, María Eugenia Abad, Margarita Larralde, Paula Boggio, Bruno Ferrari, María Fernanda Maccario, Carla Castro, Silvia Moreno, Débora Kaplan, Cristina Echeverría
Publikováno v: Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 80, Iss 4 (2023)
Introducción: un tercio de los pacientes con psoriasis comienzan con sus síntomas en la niñez y la adolescencia, con fuerte impacto emocional y psicosocial. Objetivo: elaborar una guía de tratamiento sistémico de la psoriasis en pacientes pediá
Externí odkaz: https://doaj.org/article/601f9376695b4a74b99819bb95e30983
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2
Akademický článek
Kaposi′s varicelliform eruption: A case series
Autor: Bruno Ferrari, Vanina Taliercio, Paula Luna, María Eugenia Abad, Margarita Larralde
Publikováno v: Indian Dermatology Online Journal, Vol 6, Iss 6, Pp 399-402 (2015)
Kaposi's varicelliform eruption is a rare and potentially fatal viral infection caused mainly by reactivation of herpes simplex virus. It concomitantly occurs with pre-existing skin conditions, mostly atopic dermatitis, so it is predominately found i
Externí odkaz: https://doaj.org/article/e7b27b031f6f433bb8b94e78aa356685
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3
Akademický článek
Doença de Fabry Fabry disease
Autor: Paula Boggio, Paula Carolina Luna, María Eugenia Abad, Margarita Larralde
Publikováno v: Anais Brasileiros de Dermatologia, Vol 84, Iss 4, Pp 367-376 (2009)
A doença de Fabry é enfermidade de armazenamento lisossômico rara, ligada ao cromossomo-X, causada pela deficiência parcial ou completa da enzima alfagalactosidase A. O defeito resulta no acúmulo de globotriaosilceramida no endotélio vascular e
Externí odkaz: https://doaj.org/article/50c560cb0d744ea1a092a4f0f371ecec
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6
Erythrosis Pigmentosa Peribuccalis in an Adolescent: Dermoscopic Description and Management
Autor: María Eugenia Abad, Margarita Larralde, Virginia M. González, José G. Casas, Felix Vigovich, Paula Carolina Luna
Publikováno v: Pediatric Dermatology. 33:e65-e68
Erythrosis pigmentosa peribuccalis is an infrequent condition, with fewer than 35 cases reported in the literature, that affects mainly women. It presents as small papules that form a hyperpigmented plaque around the mouth and nose. Little is known a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b72b0d58458271ee2450134d9039febb
https://doi.org/10.1111/pde.12756
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7
Onicomadesis asociada a la enfermedad de boca, mano y pie
Autor: Paula Carolina Luna, Bruno Ferrari, Lorena Hornos, Margarita Larralde, María Eugenia Abad, Vanina Taliercio
Publikováno v: Archivos Argentinos de Pediatria. 111:e148-e151
Onychomadesis is the spontaneous, complete shedding of the nail from its proximal side, without pain or inflammation, following nail matrix arrest. This disorder is uncommon in children and it can occur in fingernails, toenails or both. It may be sec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1ab5c08b3f04471a401f20f1caeb572a
https://doi.org/10.5546/aap.2013.e148
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8
Nevus Trichilemmocysticus: Report of a New Case of a Recently Recognized Entity
Autor: María Eugenia Abad, Rudolf Happle, Margarita Larralde, Cristina Corbella, Paula Boggio
Publikováno v: Pediatric Dermatology. 28:286-289
A new type of organoid epidermal nevus, characterized by the presence of multiple trichilemmal cysts disposed in a linear arrangement, was recently recognized and named nevus trichilemmocysticus. We report a 10-year-old girl with a congenital linear
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1351b232b1f020035e9ee06f4cacf5ae
https://doi.org/10.1111/j.1525-1470.2010.01246.x
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9
Infantile Myofibromatosis: Report of Nine Patients
Autor: Mariana V. Hoffner, Noemí Correa, María Eugenia Abad, Paula C. Luna, Paula Boggio, Margarita Larralde
Publikováno v: Pediatric Dermatology. 27:29-33
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 instances systemic involvement can be present. Solitary tumors limited to the skin usually pres
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91ccbeb486da79d599241aebdd5324ed
https://doi.org/10.1111/j.1525-1470.2009.01073.x
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10
Doença de Fabry
Autor: Margarita Larralde, Paula Boggio, Paula Carolina Luna, María Eugenia Abad
Publikováno v: Anais Brasileiros de Dermatologia v.84 n.4 2009
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Anais Brasileiros de Dermatologia, Volume: 84, Issue: 4, Pages: 367-376, Published: AUG 2009
A doença de Fabry é enfermidade de armazenamento lisossômico rara, ligada ao cromossomo-X, causada pela deficiência parcial ou completa da enzima alfagalactosidase A. O defeito resulta no acúmulo de globotriaosilceramida no endotélio vascular e
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f505a3cbd2a544bbc7d272cfb2ec33f
https://doi.org/10.1590/s0365-05962009000400008
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