Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Journal of Intellectual & Developmental Disability
|
January 16, 2025
Parents' tacit knowledge of their child with profound intellectual and multiple disabilities: A qualitative study
Kasper Kruithof, Maartje Hoogsteyns, Ilse Zaal-Schuller, et al.
Journal of Intellectual & Developmental Disability
|
January 17, 2025
Siblings' and parents' perspectives on the future care for their family member with profound intellectual and multiple disabilities: A qualitative study
Kasper Kruithof, Lisa IJzerman, Appolonia Nieuwenhuijse, et al.
European Journal of Medical Genetics
|
December 3, 2014
Building treasures for rare disorders
Melanie Baas, Sylvia Huisman, John van Heukelingen, et al.
Journal of Applied Research in Intellectual Disabilities : JARID
|
June 20, 2023
Tacit knowledge in dyads of persons with profound intellectual and multiple disabilities and their caregivers: An interpretative literature study
Maartje Hoogsteyns, Ilse Zaal-Schuller, Sylvia Huisman, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
October 9, 2018
Development, behaviour and autism in individuals with SMC1A variants
Paul A Mulder, Sylvia Huisman, Annemiek M Landlust, et al.
Neuroscience and Biobehavioral Reviews
|
July 12, 2017
Self-injurious behavior
Sylvia Huisman, Paul Mulder, Janneke Kuijk, et al.
American Journal of Medical Genetics. Part A
|
February 29, 2024
SMC1A epilepsy syndrome: clinical data from a large international cohort
Elisabetta Gibellato, Paola Cianci, Milena Mariani, et al.
European Journal of Human Genetics : EJHG
|
April 7, 2022
The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience
Sofia Douzgou, Janet Dell'Oro, Cristina Rodriguez Fonseca, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2021
Cornelia de Lange syndrome and the Cohesin complex: Abstracts from the 9th Biennial Scientific and Educational Virtual Symposium 2020
Chris Oliver, Laura Groves, Blake D Hansen, et al.
Clinical Genetics
|
January 25, 2019
Diagnosis and management in Pitt-Hopkins syndrome: First international consensus statement
Marcella Zollino, Christiane Zweier, Ingrid D Van Balkom, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Journal of Intellectual & Developmental Disability
|
January 16, 2025
Parents' tacit knowledge of their child with profound intellectual and multiple disabilities: A qualitative study
Kasper Kruithof, Maartje Hoogsteyns, Ilse Zaal-Schuller, et al.
Journal of Intellectual & Developmental Disability
|
January 17, 2025
Siblings' and parents' perspectives on the future care for their family member with profound intellectual and multiple disabilities: A qualitative study
Kasper Kruithof, Lisa IJzerman, Appolonia Nieuwenhuijse, et al.
European Journal of Medical Genetics
|
December 3, 2014
Building treasures for rare disorders
Melanie Baas, Sylvia Huisman, John van Heukelingen, et al.
Journal of Applied Research in Intellectual Disabilities : JARID
|
June 20, 2023
Tacit knowledge in dyads of persons with profound intellectual and multiple disabilities and their caregivers: An interpretative literature study
Maartje Hoogsteyns, Ilse Zaal-Schuller, Sylvia Huisman, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
October 9, 2018
Development, behaviour and autism in individuals with SMC1A variants
Paul A Mulder, Sylvia Huisman, Annemiek M Landlust, et al.
Neuroscience and Biobehavioral Reviews
|
July 12, 2017
Self-injurious behavior
Sylvia Huisman, Paul Mulder, Janneke Kuijk, et al.
American Journal of Medical Genetics. Part A
|
February 29, 2024
SMC1A epilepsy syndrome: clinical data from a large international cohort
Elisabetta Gibellato, Paola Cianci, Milena Mariani, et al.
European Journal of Human Genetics : EJHG
|
April 7, 2022
The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience
Sofia Douzgou, Janet Dell'Oro, Cristina Rodriguez Fonseca, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2021
Cornelia de Lange syndrome and the Cohesin complex: Abstracts from the 9th Biennial Scientific and Educational Virtual Symposium 2020
Chris Oliver, Laura Groves, Blake D Hansen, et al.
Clinical Genetics
|
January 25, 2019
Diagnosis and management in Pitt-Hopkins syndrome: First international consensus statement
Marcella Zollino, Christiane Zweier, Ingrid D Van Balkom, et al.
Page
of 2