Results 81 to 90 of about 629 (153)

Impacto Psicossocial da Rinoplastia em pacientes com anomalias craniofaciais congênitas

open access: yes
Congenital craniofacial anomalies pose significant challenges not only physically, but also psychosocially for patients. Rhinoplasty, as an integral part of reconstructive surgery, aims to improve not only aesthetic function, but also the psychosocial ...
Pezato Bertolli, Larissa   +23 more
core   +1 more source

Rupture of sinus of Valsalva aneurysm to the right atrium resolved with interventionism. [PDF]

open access: yesArch Cardiol Mex, 2023
Jiménez-Garcés VG   +7 more
europepmc   +1 more source

Malformações congênitas no estado do Pará, Brasil: uma avaliação através do Sistema de Informação Sobre Nascidos Vivos (SINASC)

open access: yes, 2017
Introduction: Congenital malformations are characterized by structural abnormalities present at birth as a consequence of a factor originated during development, and may be genetic, environmental or unknown factors. It is estimated that, worldwide, 7.9
PARENTE, Angeline do Nascimento
core  

Clusters of rare disorders and congenital anomalies in South America. [PDF]

open access: yesRev Panam Salud Publica, 2023
Cardoso-Dos-Santos AC   +2 more
europepmc   +1 more source

Family Counseling after the Diagnosis of Congenital Heart Disease in the Fetus: Scoping Review. [PDF]

open access: yesHealthcare (Basel), 2023
Almeida SLM   +7 more
europepmc   +1 more source

[Copy number variation and parental consanguinity elevated in newborns of high altitude with major congenital anomalies in Perú]. [PDF]

open access: yesRev Fac Cien Med Univ Nac Cordoba, 2022
Abarca Barriga HH   +8 more
europepmc   +1 more source

“Malignant” origin of the left coronary artery, case report [PDF]

open access: yesArch Cardiol Mex, 2022
Martínez-Cano CA   +3 more
europepmc   +1 more source

Holoprosencephaly in Patau Syndrome. [PDF]

open access: yesRev Paul Pediatr, 2023
Schlosser AS   +6 more
europepmc   +1 more source

Revista de Ciências Médicas e Biológicas

open access: yes, 2013
A síndrome do triplo X (47,XXX), constitui distúrbio cromossômico frequente (1:1000 nascimentos femininos), com espectro clínico variável, de fenótipo normal a casos de malformações congênitas e incompetência reprodutiva.
Cabanelas, Iago Teles Dominguez   +4 more
core  

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