Results 251 to 260 of about 1,038,034 (386)

Including disabled children in learning: some challenges for inclusive pedagogy

, 2009
Alison Croft
openalex  

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

American 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, Jacey L. Anderberg, Ana M. Ramirez‐Diaz, Andrea Horvath Marques, Catherine E. Rast, Daniel Bustamante, Deborah Jonker, Johanna Valencia‐Echeverry, Joseph Kyebuzibwa, Josselyn S. Muñoz, Kristien van der Walt, Mauricio Castaño Ramirez, Olivia Wootton, Renee M. Frederick, Rocky E. Stroud II, Ruben Gur, Sang Jin Rhee, Shaili C. Jha, Stella Gichuru, Susan Service, Victor I. Reus, Akena Dickens, Carlos Lopez‐Jaramillo, Carrie E. Bearden, Dan J. Stein, Ezra S. Susser, James J. Crowley, Jonathan Flint, Kenneth S. Kendler, Lukoye Atwoli, Michele T. Pato, Nelson B. Freimer, Roel A. Ophoff, Yong Min Ahn, Loes Olde Loohuis, Eric A. Storch, Bizu Gelaye   +36 more
wiley   +1 more source

Maximizing the Value of Learning Assistants for Students' Belonging, Mattering, and Confidence in Gateway STEM Courses. [PDF]

CBE Life Sci Educ
Zepeda CD, Rosemond SN, Johnson HJ, Clements TP, Albarran M, Lee G, Watson M, Brame CJ.   +7 more
europepmc   +1 more source

(IM)PERTINENCE OF VYGOTSKY’S STUDIES IN DEFECTOLOGY (1924-1935) FOR CONTEMPORARY RESEARCH ABOUT PEDAGOGY AND CLINICS FROM AN INCLUSIVE PERSPECTIVE

Daniele Nunes Henrique Silva, Ana Paula de Freitas, Fabrício Santos Dias de Abreu   +2 more
openalex   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Creating safe spaces: fostering inclusion in animal science classrooms through DEI initiatives. [PDF]

Anim Front
Tillquist NM.
europepmc   +1 more source

SKILLS AND PEDAGOGICAL INNOVATIONS OF FUTURE TEACHERS IN INCLUSIVE EDUCATION

Rakhmonova Gullola Shavkatovna
openalex   +1 more source

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen, Kristin Ørstavik, Unni Steen, Mathias Toft, Cathrine Brunborg, Lena Lande Wekre   +5 more
wiley   +1 more source

Inclusive and effective teaching of Nature-Based Social Prescribing for allied health professional students within digital environments. [PDF]

Front Public Health
Pywell S, Wallace C, Wallace S, Davies M.   +3 more
europepmc   +1 more source

Social Justice Education: Using Communication Activism Pedagogy to Help University Cultural Centers Increase Campus Diversity & Inclusivity

, 2015
Sophia T Vu
openalex   +1 more source