Results 81 to 90 of about 347,599 (312)

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc   +7 more
wiley   +1 more source

El reconocimiento del agua como sujeto de derecho en Perú: una perspectiva en evolución

open access: yesRevista Catalana de Dret Ambiental
El presente artículo tiene como objetivo analizar la viabilidad de considerar al agua como sujeto de derecho dentro del ordenamiento jurídico peruano. El enfoque metodológico empleado es el análisis documental el cual consiste en examinar documentos que
Daniela Lucero Díaz López   +3 more
doaj   +1 more source

Neuroaprendizaje: Nuevas propuestas en la formación universitaria

open access: yes, 2018
In recent years, the vertiginous changes in all areas of human knowledge have modified the socioeconomic, political and educational structure; what forces to make use of new contributions, research products in different areas.
Rojas Anaya, Yanina, Rojas Anaya, Y.
core   +1 more source

Genetic Risk and High Burden of Depression and Suicide in the Maya‐Mestizo Population of Yucatán, México

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Major depression and suicide are critical public health concerns, particularly in underrepresented populations with unique genetic and sociocultural contexts. The Maya‐mestizo population presents the highest suicide rates in the country but remains understudied in psychiatric genetics. This study evaluated the association between three genetic
Marta Menjivar   +3 more
wiley   +1 more source

Plataforma Continental

open access: yes, 2017
El vídeo describe el contenido del curso de Centro de Idiomas Continental, además de describir las unidades didácticas a ...
Mendoza Balmaceda, Eva
core  

Satisfacción laboral de los docentes de la Universidad Continental, 2014

open access: yes, 2015
The purpose of this study was to describe the job satisfaction of teachers at the Continental University from their own perspective through a quantitative approach. The research was of descriptive and transversal type.
Carrillo Fernández, Armando
core   +1 more source

A Global Prospective Harmonization Framework for Suicidality, Anhedonia, and Obsessive‐Compulsive Symptoms in Psychiatric Genetic Studies: A Cross‐Continental Study Within the Ancestral Population Network

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT This study aims to prospectively collect harmonized, quantitative, and dimensional psychiatric phenotypes (suicidality, anhedonia, and obsessive‐compulsive symptoms) and information on discrimination, stigma, and unfair treatment in up to 27,500 individuals across diverse ancestries and clinical populations for genetic analysis within the NIMH
Ana M. Diaz‐Zuluaga   +36 more
wiley   +1 more source

Logro de emprendedores continental 2014 - 2015

open access: yes, 2015
- Alumno uc gana capital semilla en plei-up 2014.- Plan de negocio gana una categoría del concurso nacional para quitarse el sombrero.- Dos estudiantes de continental ganan beca de emprendedora.- Integrantes de la familia continental iniciarán sus ...
Emprender, Para
core  

Characteristics and work expectations of graduates of the Generation Y of the Universidad Continental, Huancayo

open access: yes, 2017
El objetivo fue determinar las características y expectativas laborales de los egresados de la Universidad Continental que pertenecen a la Generación “Y” desde la perspectiva de la Teoría de las Generaciones.
Gustavo Loayza, Loayza Acosta, Gustavo
core   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young   +6 more
wiley   +1 more source

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