Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maria Eufémia Calmeiro"'
Publikováno v:
Acta Médica Portuguesa, Vol 30, Iss 7-8, Pp 581-585 (2017)
Maternally inherited diabetes and deafness is a rare form of diabetes caused by a mitochondrial DNA mutation. The index case is a 55-year-old woman who was admitted with hypertrophic cardiomyopathy. She had a history of diabetes mellitus and hearing
Externí odkaz:
https://doaj.org/article/9f8f1653d6694d698d3a3f1f1871f8f6
Autor:
Soraia Silva, Filipa Leitão, Paulina Mariano, Joana Carvalho, Maria Eugénia André, Isabel Antunes, Maria Eufémia Calmeiro
Publikováno v:
Gazeta Médica, Vol 8, Iss 1 (2021)
INTRODUÇÃO: A insuficiência cardíaca crónica é considerada, a nível mundial, a principal causa de internamento em doentes com idade superior a 65 anos. A Unidade de Hospitalização Domiciliária (UHD) foi criada com o objetivo de minimizar as
Publikováno v:
Dermatology Online Journal. 26
SAPHO syndrome is a rare entity, composed of dermatologic and osteoarticular manifestations. There are no validated diagnostic criteria and treatment is empirical, with a recent focus on biologics. Herein, we present a 50-year-old woman who developed
Publikováno v:
Acta Médica Portuguesa, Vol 30, Iss 7-8, Pp 581-585 (2017)
Maternally inherited diabetes and deafness is a rare form of diabetes caused by a mitochondrial DNA mutation. The index case is a 55-year-old woman who was admitted with hypertrophic cardiomyopathy. She had a history of diabetes mellitus and hearing
A 70-year-old man with a history of prostate cancer, previously submitted to surgical castration and trans-urethral resection of the prostate, was admitted to Accident and Emergency department. He had been suffering from osteoarticular and abdominal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57e3f5992f9e6df57f46322e333ff214
https://europepmc.org/articles/PMC5073671/
https://europepmc.org/articles/PMC5073671/