Results: 34

Avaliação e ensino de emoções com crianças e jovens adultos com autismo ou síndrome de down mediado pela família

Psicol. ciênc. prof; 44 (), 2024
Este estudo avaliou o reconhecimento (imitação, identidade e identificação) e a nomeação de estímulos emocionais de valência negativa (raiva e tristeza) e positiva (alegria e surpresa) em conjunto com a influência dos tipos de estímulos utilizados (social-feminino, social-masculino, familiar e ...
Psicología, Trastorno Autístico, Familia, Síndrome de Down, Emoción Expresada, Emociones, d0078580, d0136630, ddcs0296530, d0062400, d0007860, d0332420, d0087220, d0119300, d0000786020, d0018870, Adulto Joven, Niño, COVID-19, Pandemias, , d0057830, Imagen Corporal, Ego, Reconocimiento Facial, Delegación al Personal, Apoyo Familiar, Expresión Facial, , Conducta, Comunicación, , Análisis y Desempeño de Tareas, Interacción Social, Adaptación Psicológica, Actitud, Discapacidad Intelectual, , Manifestaciones Neurológicas, Trastornos de los Cromosomas, Trastornos Mentales, Competencia Cultural, Educación Especial, , Educación de las Personas con Discapacidad Intelectual, Trastorno del Espectro Autista, Pesar, Miedo, Comprensión, Terapia Cognitivo-Conductual, Prejuicio, Habilidades Sociales, Cognición, Procesos Mentales, Lenguaje, Memoria a Corto Plazo, Competencia Mental, Personalidad, Confianza, Optimismo, Respeto, Estereotipo, Ansiedad, Enfermedades del Sistema Nervioso, Cromosomas, Cara, Comunicación no Verbal, Manejo Psicológico, Conducta Exploratoria, Medio Social, Socialización, Percepción, Reconocimiento de Identidad, Ensayo Clínico, Distorsión de la Percepción, Inteligencia Artificial, Análisis Aplicado de la Conducta, Generalización Psicológica, Actividades Cotidianas, Acontecimientos que Cambian la Vida, Detección de Señal Psicológica, Educación, Relaciones Interpersonales, Ajuste Emocional, Normas Sociales, Valores Sociales, Intuición, Velocidad de Procesamiento, Imaginación, Autonomía Personal, Recursos Audiovisuales, Empatía, Inteligencia Emocional, Retroalimentación, Conciencia, Juego e Implementos de Juego, Trastorno de Movimiento Estereotipado, Entrenamiento Cognitivo, Deseabilidad Social, Estigma Social, Regulación Emocional, Genética, Pruebas Neuropsicológicas, Neurología, Signos y Síntomas, Observación, Percepción Visual, Atención, Automanejo, Compresión de Datos, Procesamiento de Imagen Asistido por Computador, Padres, Cuidadores, Hijos Adultos, Crianza del Niño, Relaciones Padres-Hijo, Psicología Social, Psiquiatría, Mujeres, Hombres, Metacognición, Gestos, Simbolismo

Alterações sistêmicas na assinatura do ciclo celular de pacientes com COVID-19

Com base nas perturbações fosfoproteômicas de moléculas associadas ao ciclo celular em células infectadas pelo coronavírus causador da síndrome respiratória aguda grave (SARSCoV)-2, a hipótese de inibidores do ciclo celular como uma terapia potencial para a doença de coronavírus 2019 (COVID-19...

Cherubism in Saudi population: a rare case report

Braz. dent. sci; 26 (2), 2023
Cherubism is a rare hereditary benign fibro-osseous disorder characterised by bilateral swelling of the mandible and/or maxilla with varying severity of involvement. It occurs because of dominant mutations in SH3BP2 gene on the chromosome 4p16.3. On radiography cherubic lesions appear as multilocular cys...

9p21 Locus Polymorphisms: Risk and Severity Factors of Coronary Artery Disease in Venezuelan Patients

Abstract Background: The 9p21 region is the most relevant locus associated with coronary heart disease in different populations. However, there are no studies that prove that this region is a risk factor in the Venezuelan population. Objectives: To analyze whether or not the 9p21 rs1333049 polymorphism...

Síndrome de insensibilidad completa a andrógenos
Complete androgen insensitivity syndrome

Alerta (San Salvador); 5 (2), 2022
El síndrome de insensibilidad a los andrógenos (SIA), conocido también como un síndrome de feminización testicular, incluye un grupo variado de mutaciones que se relacionan con la disfunción de los receptores de andrógenos y la resistencia de los tejidos diana a la acción de las hormonas masculin...

Tracking the evolutionary pathways among Brazilian Lebiasina species (Teleostei: Lebiasinidae): a chromosomal and genomic comparative investigation

Neotrop. ichthyol; 20 (1), 2022
Despite several difficulties in chromosomal analyses of small-sized fishes, the cytogenetics of the Lebiasinidae was largely improved in the last years, showing differential patterns in the chromosomal evolution inside the family. In this context, it has been shown that genus Lebiasina preserves its kary...

Searching chromosome mosaicisms in 45, X Turner syndrome: how relevant is it?

ABSTRACT Objective: To investigate the presence of chromosome mosaicism, especially for the presence of Y derived material in 45,X women with Turner syndrome (TS). Materials and methods: FISH and PCR were performed for the presence of chromosome mosaicism and Y-derived-material and genetic findings wer...

Cytogenetic and molecular characterization of an SRY-negative 46, XX ovotesticular DSD: a case report

Introduction: Ovotesticular disorder of sex development is a rare condition characterized by the concomitant presence of testicular and ovarian tissue, and usually presents genital ambiguity. They are chromosomally heterogeneous, and cytogenetic analyses is relevant. Objective: to report a patient from M...

Occurrence of euchromatic B chromosomes in natural populations of Moenkhausia bonita and M. forestii (Pisces: Characidae)

Neotrop. ichthyol; 19 (4), 2021
Moenkhausia is a highly specious genus among the Characidae, composed of 96 valid species. Only twelve species have a known karyotype. Thus, here are presented the first cytogenetic data of two allopatric populations of Moenkhausia bonita and one of M. forestii, both belonging to the upper Paraná River ...

Effects of trichostatin A on FHIT and WWOX genes expression, cell growth inhibition and apoptosis induction in hepatocellular carcinoma WCH 17 cell line

Previously, we evaluated the effect of trichostatin A (TSA) on the expression of DNA methyltransferase 1 (DNMT1) in Hepatocellular Carcinoma (HCC). Fragile histidine triad (FHIT) and WW domain-containing oxidoreductase (WWOX) are two of the most common down-regulated genes in many cancers located on chro...