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LIM/03 - Laboratório de Medicina Laboratorial

O Laboratório de Medicina Laboratorial é ligado ao Departamento de Patologia da Faculdade de Medicina da Universidade de São Paulo (FMUSP).

Linhas de pesquisa: epidemiologia; morfometria; defesa respiratória; poluição em plantas; patologia pulmonar e mutagênese ambiental.

Site oficial: http://limhc.fm.usp.br/portal/lim03-laboratorio-de-medicina-laboratorial/

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Recent Submissions

  1. Data-driven, cross-disciplinary collaboration: lessons learned at the largest academic health center in Latin America during the COVID-19 pandemic

    FRONTIERS IN PUBLIC HEALTH, v.12, article ID 1369129, 15p, 2024

    Introduction The COVID-19 pandemic has prompted global research efforts to reduce infection impact, highlighting the potential of cross-disciplinary collaboration to enhance research quality and efficiency.Methods At the FMUSP-HC academic health system, we implemented innovative flow management r...

  2. Pineal region high grade neuroepithelial tumors with NTRK fusions belonging to the novel methylation class ""diffuse high grade glioma, IDH-wildtype, subtype E"" (HGG_E)-A distinct clinicopathological and molecular presentation

    BRAIN PATHOLOGY, v.33, suppl.1, Special Issue, 2023

  3. Capelozzi's necrosis is a novel histological biomarker for the diagnosis of chronic microaspiration in fibrosing interstitial lung diseases

    EUROPEAN RESPIRATORY JOURNAL, v.62, suppl.67, article ID PA1152, 3p, 2023

  4. Lung ECM composition, its influence factors and transcriptomics in the lungs of severe COVID-19.

    EUROPEAN RESPIRATORY JOURNAL, v.62, suppl.67, article ID PA5250, 2p, 2023

  5. Rapid HIV progression in patients with increased prevalence of unstable HLA-C variants

    HIV MEDICINE, v.24, suppl.3, p.34-35, 2023

  6. Buccal cell whole exome sequencing improves the diagnostic yield in a Cornelia de Lange Syndrome Brazilian cohort

    EUROPEAN JOURNAL OF HUMAN GENETICS, v.32, suppl.1, p.539-540, 2024

  7. Investigation of copy number variations as possible genetic modifiers in patients with the 22q11.2 deletion syndrome

    EUROPEAN JOURNAL OF HUMAN GENETICS, v.31, suppl.1, p.239-239, 2023

  8. A 43 years-old patient with Cornelia de Lange Syndrome with NIPBL gene mutation and a mild phenotype

    EUROPEAN JOURNAL OF HUMAN GENETICS, v.32, suppl.1, p.235-235, 2024

  9. LONGITUDINAL ASSESSMENT OF HAND AND WRIST BONE DESTRUCTION BY ULTRASOUND, AND ITS ASSOCIATION WITH DISEASE ACTIVITY IN PRIMARY SJOGREN'S SYNDROME

    ANNALS OF THE RHEUMATIC DISEASES, v.82, suppl.1, p.1538-1538, 2023

  10. microRNAs associated with metastatic potential in salivary gland mucoepidermoid carcinoma

    CANCER RESEARCH, v.83, n.7, suppl.S, 2023