Results 161 to 170 of about 2,034,014 (299)

Night work and cancer risk: results from the ELSA-Brasil worker cohort. [PDF]

Rev Saude Publica
Bernardino DCAM, Otero UB, Pimenta IT, Griep RH, Giatti L, Barreto SM, Fonseca MJMD.   +6 more
europepmc   +1 more source

O Brasil antes de Cabral : os índios e nações indígenas [gravação de som]

, 2000
Série de programas produzidos pela Rádio Senado FM em comemoração aos 500 anos do Brasil. Programa 4 (30'01'')Texto e roteiro - Cezar Motta ; Produção - Adele Heusi ; Coordenação de áudio – Agnaldo Scárdua ; Sonoplastia – Sílvio Hauagen, Marcos Coutinho

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First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa, Joana Rosa Marques Prota, Antonia Paula Marques‐de‐Faria, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source

Chegada ao Brasil e primeiro contato com os índios [gravação de som]

, 2000
Série de programas produzidos pela Rádio Senado FM em comemoração aos 500 anos do Brasil. Programa 3 (29'29'')Texto e roteiro - Cezar Motta ; Produção - Adele Heusi ; Coordenação de áudio – Agnaldo Scárdua ; Sonoplastia – Sílvio Hauagen, Marcos Coutinho

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Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos, Natasha Monte, Kaio Evandro Cardoso Aguiar, Rita de Cássia Calderaro, Aline Pasquini Santos, Juliana Carla Gomes Rodrigues, André Maurício Ribeiro‐Dos‐Santos, Sandro José De Souza, Ândrea Ribeiro‐Dos‐Santos, João Farias Guerreiro, Sidney Emanuel Batista Dos Santos, Ney Pereira Carneiro Dos Santos   +11 more
wiley   +1 more source

Editorial: Integrative approaches to acute brain injury: vascular, electrical, and metabolic interactions. [PDF]

Front Physiol
Brasil S, Solla DJF, Hoiland R.
europepmc   +1 more source

The Role of Glutamatergic and Dopaminergic Genes in Resistant Schizophrenia: A Systematic Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Psychosis is a heterogeneous disorder, with approximately one‐third of patients experiencing treatment resistance, predominantly among individuals diagnosed with Schizophrenia. Treatment‐resistant schizophrenia (TRS) may stem from a distinct biological signature, involving abnormalities in the dopaminergic and glutamatergic systems.
Maria Teresa Moreno‐Calle, Silvia Iñiguez‐Barrio, Maria Aurora Arrue, Leire Erkoreka   +3 more
wiley   +1 more source

SB Brasil Project: brief history and perspectives for the 2030 edition. [PDF]

Rev Bras Epidemiol
Narvai PC.
europepmc   +1 more source

Brasil. Lei n. 13.154, de 30 de julho de 2015

, 2015
Altera a Lei n. 9503, de 23 de setembro de 1997 (Código de Trânsito Brasileiro), a Consolidação das Leis do Trabalho (CLT), aprovada pelo Decreto-Lei n. 5452, de 1º de maio de 1943, e a Lei n. 13001, de 20 de junho de 2014;
Brasil
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Genetic Variants of Na+,K+‐ATPase Associated With Neurological Disorders: A Systematic Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Neurological disorders encompass a wide range of severe symptoms and manifestations, many of which are associated with genetic variants that affect ionic homeostasis. Na+,K+‐ATPase, a transmembrane enzyme responsible for maintaining electrochemical gradients in cells, plays a crucial role in neuronal excitability and brain function.
Giovana Kummer da Rosa, Leandro Rodrigo Ribeiro, Jéssica Lorena Bariviera, Mauro Schneider Oliveira   +3 more
wiley   +1 more source