LIM/63 - Laboratório de Investigação Médica em Sono
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Apneia obstrutiva do sono
Dantas, Raíssa Karen Moraes; Lorenzi Filho, Geraldo. Apneia obstrutiva do sono. In: Favarato, Maria Helena Sampaio; Saad, Rafael; Ivanovic, Lígia Fidelis; Jorge, Maria Cecília Pavanel; Oliveira, Júlio César de; Santos, Valter Garcia; Morinaga, Christian Valle; Bricola, Solange Aparecida Petilo de Carvalho; Nunes, Maria do Patrocínio Tenório; Martins, Mílton de Arruda (eds); Soeiro, Alexandre de Matos; Silva, Bruno Caldin da; Filadelfo, Cesar Ribeiro; Andrade, Daniel Ciampi de; Carvalho, Daniel Fiordelisio de; Nakagawa, Daniel Makoto; Sitnik, Debora; Colombo, Elisabetta Sachsida; Fonseca, Fabricio Lopes da; Lauterbach, Gerhard da Paz; Maesaka, Jonathan Yugo; Oliveira, Júlio César de; Ivanovic, Lígia Fidelis; Fonseca, Luciana Mazoti Lopes da; Gil Junior, Luiz Antonio; Marzinotto, Maira Andrade Nacimbem; Aun, Marcelo Vivolo; Vieira, Marcio Eduardo Bergamini; Jorge, Maria Cecília Pavanel; Nunes, Maria do Patrocínio Tenório; Favarato, Maria Helena Sampaio; D´Alessandro, Maria Perez Soares; Cordeiro, Maurício Dener; Mak, Milena Perez; Lima, Moisés da Cunha; Guidi, Paula Machado; Saad, Rafael; Teixeira, Ralcyon Francis Azevedo; Bricola, Solange Aparecida Petilo de Carvalho; Takahashi, Tiago Kenji; Santos, Valter Garcia; Cesar, Wagner G. Galvão; Nahas, William (coords). Manual do residente de clínica médica [3.ed.]. SANTANA DE PARNAÍBA: Manole, 2023. p.530-534.
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BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening
BRAIN, v.146, n.7, p.3003-3013, 2023
There are few causes of treatable neurodevelopmental diseases described to date. Branched-chain ketoacid dehydrogenase kinase (BCKDK) deficiency causes branched-chain amino acid (BCAA) depletion and is linked to a neurodevelopmental disorder characterized by autism, intellectual disability and mi...
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Editorial: Melatonin and biological rhythms: from bench to bedside
FRONTIERS IN NEUROSCIENCE, v.17, article ID 1208878, 2p, 2023
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Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia
COLD SPRING HARBOR MOLECULAR CASE STUDIES, v.8, n.6, article ID a006232, 8p, 2022
Argininemia or arginase deficiency is a metabolic disorder caused by pathogenic variants in ARG1 and consists of a variable association of progressive spastic paraplegia, intellectual disability, and seizures. Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature...
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Post-COVID-19 Cardiopulmonary Symptoms: Predictors and Imaging Features in Patients after Hospital Discharge
ARQUIVOS BRASILEIROS DE CARDIOLOGIA, v.120, n.5, article ID e20220642, 9p, 2023
Background: Most of the evidence about the impact of the post-acute COVID-19 Syndrome (PACS) reports individual symptoms without correlations with related imaging. Objectives: To evaluate cardiopulmonary symptoms, their predictors and related images in COVID-19 patients discharged from hospital. ...
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Insomnia symptoms during the covid-19 a case-control
REVISTA DE SAUDE PUBLICA, v.57, suppl.1, article ID 8s, 11p, 2023
OBJECTIVE: To identify lifestyle-related, sociodemographic, and mental health characteristics of people with insomnia symptoms and people without insomnia during the pandemic. METHODS: A case-control study was conducted with data collected by snowball sampling using an online questionnaire. From ...
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Treatment of Sleep Disordered Breathing with Leptin Loaded Extracellular Vesicles
FASEB JOURNAL, v.36, suppl.1, 2022
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Task Accomplished Promising Effects of a New Antagonist in OSA
CHEST, v.163, n.4, p.749-750, 2023
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Intra-individual Variability of Serum Aldosterone and Implications for Primary Aldosteronism Screening
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, v.108, n.5, p.1143-1153, 2023
Context Primary aldosteronism (PA) screening relies on an elevated aldosterone to renin ratio with a minimum aldosterone level, which varies from 10 to 15 ng/dL (277-415.5 pmol/L) using immunoassay. Objective To evaluate intra-individual coefficient of variation (CV) of aldosterone and aldosteron...
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Intra-individual Variability of Serum Aldosterone and Implications for Primary Aldosteronism Screening (Nov, dgac679, 2022)
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, v.108, n.5, p.E204-E204, 2023
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