Lara Lourenço

ORCID: 0000-0002-5737-982X
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About
Contact & Profiles
Research Areas
  • Traumatic Ocular and Foreign Body Injuries
  • Child Abuse and Related Trauma
  • Attention Deficit Hyperactivity Disorder
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Genetics and Neurodevelopmental Disorders
  • Infant Development and Preterm Care
  • Congenital Heart Disease Studies
  • Nutritional Studies and Diet
  • Male Breast Health Studies
  • Pericarditis and Cardiac Tamponade
  • Intestinal Malrotation and Obstruction Disorders
  • Cerebral Palsy and Movement Disorders
  • Genomics and Rare Diseases
  • Autism Spectrum Disorder Research
  • Burn Injury Management and Outcomes
  • Spinal Cord Injury Research
  • International Relations and Autism
  • Breast Lesions and Carcinomas
  • Obesity, Physical Activity, Diet
  • Pediatric Hepatobiliary Diseases and Treatments
  • Breastfeeding Practices and Influences
  • Cardiovascular Syncope and Autonomic Disorders
  • Congenital Diaphragmatic Hernia Studies
  • Venous Thromboembolism Diagnosis and Management
  • Restraint-Related Deaths

Hospital de São João
2010-2023

Pediatrics and Genetics
2022

Universidade Federal de São Paulo
2014-2015

Coordenação de Aperfeicoamento de Pessoal de Nível Superior
2014

Universidade do Vale do Sapucaí
2014

Objective: To evaluate health-related quality of life (HRQoL) and self-esteem in patients with traumatic spinal cord injury (SCI) pressure ulcers. Method: This study was a controlled cross-sectional study. HRQoL assessed using the generic Medical Outcomes Study 36-Item Short Form Health Survey (SF-36) questionnaire Rosenberg Self-Esteem/UNIFESP-EPM Scale. A total 120 SCI were included sample, which 60 had ulcers assigned to group, no control group. Statistical analysis performed chi-square...

10.12968/jowc.2014.23.6.331 article EN Journal of Wound Care 2014-06-02

Objetivo: Discutir a atuação de profissionais da saúde no acompanhamento crianças com Transtorno do Espectro Autista. Metodologia: pesquisa descritivo-exploratória abordagem qualitativa. Participaram 5 que realizam terapia/tratamento pessoas TEA na Associação Pais e Amigos dos Excepcionais (APAE) Centro Reabilitação em Terapia Ocupacional (CERETO). A coleta dados ocorreu período setembro 2018 março 2019, por meio realização Entrevistas. Quanto as Entrevista informações colhidas foram...

10.36489/nursing.2025v29i319p10309-10316 article PT cc-by Nursing Edição Brasileira 2025-02-12

Few studies about food consumption of athletes have assessed the quality their choices, and factors that influence these choices. The aim this study was to assess diet team sports through a revised version Healthy Eating Index (HEI-R) in order identify nutritional knowledge stage intention change eating behavior (SICEB) possible association with demographic anthropometric variables. Seventy-two (35 men) were evaluated for following variables: body mass, height, Body Mass (BMI), fat...

10.5007/1980-0037.2015v17n3p280 article EN cc-by Brazilian Journal of Kinanthropometry and Human Performance 2015-05-18

Chest pain in children and adolescents is a common complaint the emergency department (ED), being mostly benign. A thorough patient history physical examination should be enough most cases for its proper management. Regarding non-cardiac chest pain, anxiety plays an important role.Retrospective analysis of all admissions pediatric ED Portuguese third-level hospital with chief between January December 2018. Chi-square test was used to compare different etiologies, considering significance...

10.1097/j.pbj.0000000000000150 article EN cc-by-nc-nd Porto Biomedical Journal 2022-05-01

Abstract Background The pathogenesis of autism spectrum disorder (ASD) is not fully clarified. Next-generation sequencing technologies have greatly enhanced the identification new genes associated with ASD. Variants in ANK2 gene are known to correlate a broad clinical cardiac phenotypes, but, more recently, it has also been pointed out as candidate for etiology Case presentation We report case female patient ASD and epilepsy whom exome was performed etiological enlightenment. A heterozygous...

10.1186/s43042-023-00389-y article EN cc-by Egyptian Journal of Medical Human Genetics 2023-01-21

Chiari Malformation Type 1 is a congenital, condition characterized by abnormally shaped cerebellar tonsils that are displaced below the level of foramen magnum. NKX2-1 gene encodes transcription factor expressed during early development thyroid, lung, and forebrain, germline mutations can lead to dysfunction in any these three organs, resulting brain-lung-thyroid syndrome. There have been few reports structural brain anomalies patients with an NKX2-1-related disorder. We report first case...

10.4103/jpn.jpn_108_18 article EN Journal of Pediatric Neurosciences 2019-01-01

Introduccion. El retraso general del desarrollo (RGD) constituye un trastorno intelectual y comportamiento adaptativo que aparece en los ninos menores de 5 anos no consiguen alcanzar hitos normal. La discapacidad se caracteriza por la limitacion el funcionamiento adaptativo, surgida infancia. Entre las causas frecuentes reconocibles RGD encuentran desequilibrios cromosomicos. Los arrays hibridacion genomica comparada (aCGH) han contribuido a mejorar tasa deteccion anomalias geneticas ya...

10.33588/rn.7105.2020211 article ES Revista de Neurología 2020-01-01

INTRODUÇÃO: Diversos estudos têm demonstrado existir uma perturbação do processamento emocional em crian-ças com hiperatividade/ défice de atenção (PHDA). No entanto, existem poucos relativos à as-sociação entre alexitimia e PHDA tanto adultos como crianças, nenhum na população portuguesa.
 MÉTODOS: A amostra acidental inclui 50 crianças previamente diagnosticadas sob tratamento 51 saudáveis sem PHDA, idades compreendidas os 8 17 anos. Com o intuito avaliar a alexiti-mia foi aplicada...

10.29315/gm.v6i2.240 article PT cc-by-nc-nd Gazeta Médica 2019-06-28

Tradicionalmente a nutricao parenterica nos Servicos de Cuidados Intensivos Neonatais e prescrita forma individualizada, obrigando uma preparacao morosa na Farmacia Hospitalar. As bolsas padronizadas, alem da economia recursos, trazem mais-valia muito importante: disponibilidade imediata. No entanto, utilizacao padronizadas que respondam as diferentes necessidades nutricionais dos doentes um Servico terciario, permanece em discussao. Objectivos: Avaliar retrospectivamente eficacia seguranca...

10.25754/pjp.2012.1278 article PT Portuguese Journal of Pediatrics 2012-01-01

Introduction: Shaken baby syndrome is one of the causes non-accidental injury most difficult to diagnose.Objectives: To characterize patients hospitalized in intensive care unit with shaken syndrome.Material and Methods: Retrospective study admitted at Paediatric Intensive Care Unit from 1 January 1999 31 December 2009.Results: There were eight children syndrome. The mean age was 4.1 months five male. One patient had a history trauma. frequent cause admission epileptic seizures...

10.25753/birthgrowthmj.v22.i2.10751 article EN 2013-04-01

A ginecomastia e definida pelo aumento do tecido glandular mamario no sexo masculino. E comum na adolescencia, sendo, maioria dos casos, fisiologica resulta normalmente de um desequilibrio entre a producao estrogenios androgenios. Na muitas vezes subvalorizada pediatra. Apresenta-se uma revisao da literatura mais recente sobre o tema, incidindo etiopatogenese avaliacao semiologica laboratorial, sentido elaborar orientacoes praticas abordagem desta anomalia.

10.25754/pjp.2012.646 article PT DOAJ (DOAJ: Directory of Open Access Journals) 2012-05-01

INTRODUÇÃO: A perturbação da hiperatividade - défice de atenção (PHDA) é a doença neurocomportamental mais comum em idade pediátrica, sendo frequentemente necessário na sua abordagem terapêutica o uso medidas farmacológicas. atomoxetina, inibidor seletivo recaptação pré-sináptica noradrenalina, um fármaco não estimulante aprovado desde 2002 para tratamento PHDA criança e no adolescente. O objetivo deste trabalho foi avaliar, num hospital terciário, perfil prescrição incluindo motivo...

10.29315/gm.v5i3.185 article PT cc-by-nc-nd Gazeta Médica 2018-09-28
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