Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pereira, Isabel Ayres"'
Autor:
Pereira,Isabel Ayres, Teles-Silva,Cláudia, Gonçalves,Edite Serrano, Mota,Teresa Cunha da, Sequeira,Maria de Lurdes Lisboa, Ribeiro,António
Publikováno v:
Nascer e Crescer v.31 n.2 2022
Acute myocarditis is a potentially life-threatening disease in pediatric age, with risk of severe cardiac dysfunction and intracardiac thrombus formation. A previously healthy 16-year-old boy was admitted to the Pediatric Intensive Care Unit with sus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______616::fcc4c8f6b743ad9446cff1abf004a881
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542022000200166
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542022000200166
Autor:
Pinho, Joana, Lopes, Vilma, Pereira, Isabel Ayres, Silva, Joana Brandão, Rangel, Maria Adriana, Carvalho, Isabel
Publikováno v:
In Pulmonology September-October 2021 27(5):469-471
Autor:
Leitão, Cátia Vilas Boas, Pereira, Isabel Ayres, Tenente, Joana, Real, Marta Vila, Oliveira, Ana, Leite, Ana Luísa
Publikováno v:
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 30 No. 1 (2021); 61-63
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 30 N.º 1 (2021); 61-63
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 30 N.º 1 (2021); 61-63
ncontinentia pigmenti is an X-linked neuroectodermal dysplasia. It is a rare genetic disease with multiorgan involvement, and hence a multidisciplinary approach is of paramount importance. Although diagnosis is based on clinical findings, genetic mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=sarcservicod::5df4e89447e4637b0f4f7e6ee709f430
https://revistas.rcaap.pt/nascercrescer/article/view/18674
https://revistas.rcaap.pt/nascercrescer/article/view/18674
Autor:
Pereira, Isabel Ayres, Leite, Ana Luísa, Barbosa, Luciana, Duarte, Ana Luísa, Haneke, Eckart, Correia, Osvaldo
Publikováno v:
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; v. 24 (2015): Suplemento II: XVII Reunião Anual de Pediatria do CMIN; S26
Nascer e Crescer, Volume: 24 Supplement 2, Pages: 26-26, Published: 01 DEC 2015
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 24 (2015): Supplement II: XVII Reunião Anual de Pediatria do CMIN; S26
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 24 (2015): Suplemento II: XVII Reunião Anual de Pediatria do CMIN; S26
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nascer e Crescer, Vol 24, Iss 0 (2016)
Nascer e Crescer, Volume: 24 Supplement 2, Pages: 26-26, Published: 01 DEC 2015
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 24 (2015): Supplement II: XVII Reunião Anual de Pediatria do CMIN; S26
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol. 24 (2015): Suplemento II: XVII Reunião Anual de Pediatria do CMIN; S26
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nascer e Crescer, Vol 24, Iss 0 (2016)
Introdução: O Síndroma de Buschke Ollendorff (SBO) é uma entidade rara de transmissão autossómica dominante caracterizada por nevos de tecido conjuntivo e osteopoiquilose. Resulta de uma mutação com perda de função do gene LEMD3 que codific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a66f8b0bab17a7dcd290e03c622e0d9d
http://revistas.rcaap.pt/nascercrescer/article/view/9599
http://revistas.rcaap.pt/nascercrescer/article/view/9599
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.