Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Leonilde Machado"'
Autor:
Tânia B Cavaco, Marta Novo, Sara Soares, Inês Vaz Matos, Diana Gonzaga, Leonilde Machado, Teresa Borges, Catarina Prior
Publikováno v:
Gazeta Médica, Vol 1, Iss 1 (2024)
Externí odkaz:
https://doaj.org/article/89dc49988c9c4c308c256952c3258921
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 11, Iss 1, Pp e110115-e110115 (2022)
Mycoplasma pneumoniae (M. pneumoniae) is frequently associated with respiratory infections in pediatric patients, but can also cause mucosal and cutaneous lesions. It has a wide spectrum of manifestations, including Kawasaki disease, erythema multifo
Externí odkaz:
https://doaj.org/article/3b7df72e35c84c3fb632bec381b9fef1
Publikováno v:
Pediatric Oncall. 19
Autor:
Sofia Pimenta, Carolina Fraga, Manuel Ferreira, Leonilde Machado, Margarida Tavares, Joaquim Cunha
Publikováno v:
Pediatric Oncall. 19
Introduction Peroneal neuropathy is the most common mononeuropathy found in the lower extremities. It may be the result of habitual leg crossing or other prolonged posture, ankle orthoses, leg casting, inflammatory disease, surgery or trauma. Electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c0d62d5a3a2edb3c0a02c2a41dd9b9d
Introduction Coffin-Siris syndrome is a rare genetic disease, characterized by global developmental delay, typical facial dysmorphisms, hirsutism and bilateral aplasia or hypoplasia of the 5th distal phalange, although other malformations may be foun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37cb67ab9fc8f2708df17d7c197b5671
Publikováno v:
Portuguese Journal of Pediatrics, Vol 51, Iss 1 (2020)
Scombrotoxicosis or histamine poisoning is a common type of fish food poisoning, with an increasing prevalence due to changes in industry and food consumption. Histamine is a non-volatile amine that can be used in the action of bacterial decarboxylas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f236bcd70d62c38dda909e549a3a7563
Publikováno v:
International Journal of Medical Reviews and Case Reports. :1
Culler-Jones Syndrome (CJS) is a rare autosomal dominant disorder, caused by heterozygous mutation in the GLI2 gene on chromosome 2q14. The phenotype is highly variable due to incomplete penetrance and variable expressivity. It is characterized by hy
Autor:
Abílio Oliveira, Clara Alves Pereira, Sandra Pereira, Isabel Vale, Leonilde Machado, Sara Domingues, Ilidio Quelhas, Carla Fraga, Angela Machado
Publikováno v:
Archivos Argentinos de Pediatria. 112
Steinert myotonic dystrophy is a multisystemic disease, autosomal dominant, with a wide spectrum of severity and clinical manifestations. The most severe form is one that manifests in the neonatal period, called congenital myotonic dystrophy. This co
Autor:
Sara, Domingues, Clara, Alves Pereira, Angela, Machado, Sandra, Pereira, Leonilde, Machado, Carla, Fraga, Abílio, Oliveira, Isabel, Vale, Ilídio, Quelhas
Publikováno v:
Archivos argentinos de pediatria. 112(1)
Steinert myotonic dystrophy is a multisystemic disease, autosomal dominant, with a wide spectrum of severity and clinical manifestations. The most severe form is one that manifests in the neonatal period, called congenital myotonic dystrophy. This co