Articles

Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics

• Thien A. Nguyen
• Alexander W. Lehr
• Katherine W. Roche

Experiences of the Molecular Diagnosis of Fragile X Syndrome in Ecuador

in Child and Adolescent Psychiatry

• Juan Pozo-Palacios
• Arianne Llamos-Paneque
• Christian Rivas
• Emily Onofre
• Andrea López-Cáceres
• Jenniffer Villareal

Differences in pragmatic communication skills of adults with intellectual disabilities and dual diagnoses

in Intellectual Disabilities

• Mirjana Djordjevic
• Nenad Glumbić
• Branislav Brojčin
• Slobodan Banković
• Vesna Žunić Pavlović

Students' Problem Behaviors as Sources of Teacher Stress in Special Needs Schools for Individuals With Intellectual Disabilities

in Special Educational Needs

• Meta Amstad
• Christoph M. Müller

Identifying the genetic causes of developmental disorders and intellectual disability in Africa: a systematic literature review

in Genetics of Common and Rare Diseases

• Fiona Baine-Savanhu
• Shelley Macaulay
• Nadja Louw
• Alanna Bollweg
• Kaitlyn Flynn
• Mhlekazi Molatoli
• Patracia Nevondwe
• Heather Seymour
• Nadia Carstens
• Amanda Krause

How Can We Provide Better Healthcare for People With An Intellectual Disability?

in Human Health

• Simone Reppermund
• Janelle Weise
• Rachael Cvejic
• Julian Trollor

New arenas of inclusion: experiences of individuals with intellectual disability employed in higher education

in Intellectual Disabilities

• Gro H. Ramsdal
• Silje Mevold
• Leif Inge Johansen
• Rolf Wynn

How Older Adults Learn ICT—Guided and Self-Regulated Learning in Individuals With and Without Disabilities

in Human-Media Interaction

• Anna Schlomann
• Christiane Even
• Torsten Hammann

Trofinetide—a new chapter in rett syndrome’s treatment

in Neuropharmacology

• Muhammad Furqan

Benefits and challenges of a personal budget for people with mental health conditions or intellectual disability: A systematic review

in Public Mental Health

• Martina Micai
• Letizia Gila
• Angela Caruso
• Francesca Fulceri
• Elisa Fontecedro
• Giulio Castelpietra
• Giovanna Romano
• Mila Ferri
• Maria Luisa Scattoni

Clinical analysis in patients with SPG11 hereditary spastic paraplegia

in Neuromuscular Disorders and Peripheral Neuropathies

• You-Ri Kang
• Tai-Seung Nam
• Jae-Myung Kim
• Kyung Wook Kang
• Seong-Min Choi
• Seung-Han Lee
• Byeong C. Kim
• Myeong-Kyu Kim

Social Cognition in Children With Non-specific Intellectual Disabilities: An Exploratory Study

in Human Developmental Psychology

• Emilie Jacobs
• Poline Simon
• Nathalie Nader-Grosbois

Case Report: Clinical delineation of CACNA1D mutation: New cases and literature review

in Pediatric Neurology

• Alshaimaa Alzahrani
• Maha Alshalan
• Mohammed Alfurayh
• Abdulaziz Bin Akrish
• Najlaa A. Alsubeeh
• Fuad Al Mutairi

Spectrum of Mutations in NDP Resulting in Ocular Disease; a Systematic Review

in Genetics of Common and Rare Diseases

• James Wawrzynski
• Aara Patel
• Abdul Badran
• Isaac Dowell
• Robert Henderson
• Jane C. Sowden

Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases

in Epigenomics and Epigenetics

• Mojgan Rastegar
• Dag H. Yasui