Results 61 to 70 of about 107,454 (217)

Systematic Review of Nasal Endoscopy Scores in Cystic Fibrosis Patients Treated With Cystic Fibrosis Transmembrane Conductance Regulator Modulators

Pediatric Pulmonology, Volume 61, Issue 4, April 2026.
ABSTRACT Introduction Cystic fibrosis (CF) is a severe genetic disorder caused by pathogenic variants in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene, leading to multisystem complications including chronic rhinosinusitis and nasal polyposis. Recent advances in CFTR modulator therapies have revolutionized systemic disease control,
Rebecca Gallardo, Bruna Santos Silva, Lucas Sousa Salgado, José Dirceu Ribeiro, Eulalia Sakano   +4 more
wiley   +1 more source

Crescimento e puberdade na diabetes mellitus tipo 1 – experiência de uma unidade de endocrinologia pediátrica

Acta Médica Portuguesa, 2012
Introdução: a Diabetes Mellitus tipo 1 (DM1) é a doença crónica endócrino-metabólica mais frequente em idade pediátrica. Associa-se a complicações vasculares e neuropáticas, podendo afectar também o crescimento e desenvolvimento. Objectivo: relacionar
Catarina Timóteo, Susana Castanhinha, Carolina Constant, Brígida Robalo, Carla Pereira, Lurdes Sampaio   +5 more
doaj   +1 more source

Caracteristicas epidemiológicas e clínicas de crianças hospitalizadas com diagnóstico de coqueluche [PDF]

, 2009
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Philippi, Joyce Tolentino
core  

Angiogenic factors and fetal Doppler for predicting adverse pregnancy outcome in early‐onset small fetuses with and without pre‐eclampsia

Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 4, Page 482-491, -Not available-.
ABSTRACT Objectives To assess the predictive performance of angiogenic factors and fetal Doppler, alone and in combination, for composite adverse perinatal outcome (CAPO) in early‐onset small‐for‐gestational age (SGA) and fetal growth restriction (FGR), in cases both with and without pre‐eclampsia (PE), in order to evaluate the ability of these markers
E. Bonacina, M. Armengol‐Alsina, A. Casellas, M. Dalmau, P. Diaz, E. Roldán, J. Temprado, M. Duaso, Q. Ampurdanes, M. San José, T. Armengol, Z. Lizarraga, N. Maiz, M. Mendoza   +13 more
wiley   +1 more source

Perfil clínico-epidemiológico dos pacientes portadores de Diabetes Mellitus tipo 1 atendidos no ambulatório de endocrinologia pediátrica do Hospital Universitário Polydoro Ernani de São Thiago [PDF]

, 2009
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Pereira, Daniela Aline
core  

Spatial Distribution of Organochlorine Pesticide Serum Concentrations in Mexican Children and Adolescents Living in and Out the Polluted Atoyac Watershed Basin

GeoHealth, Volume 10, Issue 4, April 2026.
Abstract The Atoyac river basin is one of the most polluted watershed basins in Mexico. Recent studies have reported the presence of organochlorine pesticides (OCPs) in this highly urbanized region through environmental monitoring, raising concerns about potential health risks, particularly for children and adolescents.
Sailing Jane Tak Tang, Rodrigo Ugalde‐Resano, Ángel Mérida‐Ortega, Paola Rodriguez‐Montoyo, Adamarie Márquez‐Acevedo, Mariano E. Cebrián, Juan C. Núñez‐Enríquez, Janet Flores‐Lujano, Lizbeth López‐Carillo   +8 more
wiley   +1 more source

Perturbação de Hiperatividade e Défice de Atenção em Idade Pediátrica: Papel dos Cuidados de Saúde Primários

Gazeta Médica, 2018
A perturbação de hiperatividade/défice de atenção (PHDA) é uma das perturbações do desenvolvimento mais fre-quentes em idade pediátrica. Caracteriza-se por manifestações comportamentais que afetam o funcionamento e de-senvolvimento da criança/adolescente,
Maria Inês Marques, Joana Matias, Raquel Machado, Ana Duarte, Maria José Fonseca, José Paulo Monteiro   +5 more
doaj   +1 more source

Aderências intestinais pós-operatórias em crianças [PDF]

, 2009
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Santos, Luiz Carlos Mattos dos
core  

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Evolution of Neurological Complications in Spine Deformities Surgery in Children

Global Spine Journal, 2015
Study Design This study is a retrospective descriptive study, and Evidence Level IV. Objective This study aims to assess the evolution of neurological complications because of kyphosis or scoliosis surgery in children.
Miguel Angel Godoy, Carlos A. Tello, Ida Alejandra Francheri, Mariano A. Noel, Eduardo Galaretto, Rodrigo G. Remondino, Ernesto Bersusky   +6 more
doaj   +1 more source