L‐Cysteine and N‐Acetylcysteine Supplementation Improves Clinical Outcome in a Patient With COXPD10
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT MTO1 is a nuclear gene that encodes a mitochondrial protein essential for modifying mitochondrial transfer RNAs (tRNAs) and stabilizing codon‐anticodon interactions to ensure accurate and efficient mitochondrial protein synthesis and oxidative phosphorylation.
Nishitha R. Pillai +5 more
wiley +1 more source
A análise de atividade e a construção do olhar do terapeuta ocupacional
Revista de Terapia Ocupacional da Universidade de São Paulo, 2004 This paper focuses on the discussion about the activity analyses in the occupational therapy's field and its role in the process of structuring the occupational therapist´s perception of the human action and people in activity.
Elizabeth M. F. Araújo Lima
doaj +1 more source
Consistency between two subjective assessments of activities of daily living: Patient- and occupational therapist-reported judgments. [PDF]
Hong Kong J Occup Ther, 2023 Lien HP +6 more
europepmc +1 more source
The Role of Glutamatergic and Dopaminergic Genes in Resistant Schizophrenia: A Systematic Review
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT Psychosis is a heterogeneous disorder, with approximately one‐third of patients experiencing treatment resistance, predominantly among individuals diagnosed with Schizophrenia. Treatment‐resistant schizophrenia (TRS) may stem from a distinct biological signature, involving abnormalities in the dopaminergic and glutamatergic systems.
Maria Teresa Moreno‐Calle +3 more
wiley +1 more source
Potential Role of Occupational Therapist Intervention in Elementary School for Children with Additional Support Needs: A Systematic Review. [PDF]
Children (Basel), 2023 Seoane-Martín ME +1 more
europepmc +1 more source
Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert +4 more
wiley +1 more source
Management of Chronic Pain by Occupational Therapist: A Description of Practice Profile. [PDF]
Can J Occup Ther, 2023 Lagueux É +4 more
europepmc +1 more source
, 2021 Wendy talks about moving to Central Newfoundland with her husband; raising 2 small chldren; working as a teacher in a special needs classroom; first occupational therapist working in a local Senior Citizens Home; creating and developing the outreach ...
Manojlovich, Mary
core
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan +13 more
wiley +1 more source
Wheeled and Seated Mobility Devices Provision: Quantitative Findings and SWOT Thematic Analysis of a Global Occupational Therapist Survey. [PDF]
Healthcare (Basel), 2023 Sarsak HI +3 more
europepmc +1 more source