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Autor:
Luis Puig, Jose Bernabeu-Wittel, Ignasi Gich, Monica Rios, María Teresa Montserrat-García, Eulalia Baselga, Fania Zamantta Muñoz-Garza, Esther Roé-Crespo
Publikováno v:
JAMA Dermatol
JAMA DERMATOLOGY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
JAMA Dermatology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
JAMA DERMATOLOGY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
JAMA Dermatology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
IMPORTANCE: Treatment of infantile hemangioma (IH) with topical timolol in the first 2 months of life (early proliferative phase) may prevent further growth and the need for treatment with oral propranolol. To our knowledge, no studies have determine
Publikováno v:
Archives of Neurology. 54:1026-1029
Background: Parkinsonism in a 42-year-old patient, which was presumably related to peripheral trauma, did not respond to levodopa therapy. Observation: We treated the patient with microelectrode-guided unilateral posteroventral medial pallidotomy and
Publikováno v:
JAMA: The Journal of the American Medical Association. 276:44-49
OBJECTIVE To compare the efficacy and safety of episodic patient-initiated oral famciclovir with placebo in recurrent genital herpes. DESIGN Randomized, double-blind, frequent-observation, dose-ranging study comparing twice-daily 125-mg, 250-mg, or 5
Publikováno v:
Archives of Otolaryngology - Head and Neck Surgery. 122:189-192
A destructive granulomatous lesion of the temporal bone caused byCoccidioides immitisdisseminated from a pulmonary lesion was found in a 4-year-old immunocompetent child. To our knowledge, it is the first case of coccidioidomycosis of the temporal bo
Publikováno v:
JAMA Oncology. 1:833
Publikováno v:
Archives of Dermatology. 129:343-346
• Background.— Familial cold urticaria is a rare cutaneous and systemic reaction to cold with autosomal dominant inheritance, distinctive clinical features, and unknown pathogenesis. Release of a chymotrypsinlike substance has been postulated. To
Autor:
Ludivine Gressier, Nicolas Ortonne, Martine Bagot, Jean-Daniel Lelièvre, Claire Hotz, Pierre Wolkenstein, Agnès Carlotti, Giovanna Melica, Marc Buffet
Publikováno v:
Archives of Dermatology. 146
Background Specific cutaneous lesions of Waldenstrom macroglobulinemia are rare and include neoplastic cell infiltrates, IgM bullous disease, and so-called IgM-storage papules, which characterize cutaneous macroglobulinosis (CM). Observations We repo
Autor:
Víctor M. Martínez-Taboada, Ignacio Villa, Mario Agudo, Marcos A. González-López, Héctor Fernández-Llaca, M. Carmen González-Vela, Ricardo Blanco
Publikováno v:
Archives of Dermatology. 145
Background Several studies report the use of tumor necrosis factor α (TNF-α) inhibitors in refractory hidradenitis suppurativa (HS), particularly infliximab and etanercept. However, very limited data have been reported for adalimumab, the newest fu
Publikováno v:
Archives of Dermatology. 143
A 59-year-old woman of Indian descent presented with a 6-month history of an increasing number of itchy hyperpigmented nodules on her trunk and limbs. The lesions were preceded by pruritus. Treatment with topical 0.05% clobetasone butyrate cream and
Publikováno v:
JAMA Otolaryngology–Head & Neck Surgery. 140:979
An adolescent male was referred to a pediatric otolaryngologist for a suspicious skin lesion. His medical history included T-cell acute lymphoblastic leukemia (ALL) diagnosed at age 6 years. He was initially treated with chemotherapeutic agents, incl