[PDF][PDF] Episignatures stratifying Helsmoortel-Van Der Aa syndrome show modest correlation with phenotype

MS Breen, P Garg, L Tang, D Mendonca, T Levy… - The American Journal of …, 2020 - cell.com
Helsmoortel-Van der Aa syndrome (HVDAS) is a neurodevelopmental condition associated
with intellectual disability/developmental delay, autism spectrum disorder, and multiple …

[HTML][HTML] Developmental and behavioral phenotypes in a mouse model of DDX3X syndrome

…, M Garcia-Forn, DC Ung, K Niblo, D Mendonca… - Biological …, 2021 - Elsevier
Background Mutations in the X-linked gene DDX3X account for approximately 2% of intellectual
disability in females, often comorbid with behavioral problems, motor deficits, and brain …

[HTML][HTML] Common variable immunodeficiency patient fecal microbiota transplant recapitulates gut dysbiosis

…, A Swennes, S Fowler, C Calarge, D Mendonca… - Research …, 2023 - ncbi.nlm.nih.gov
Purpose Patients with non-infectious complications have worse clinical outcomes in
common variable immunodeficiency (CVID) than those with infections-only. Non-infectious …

Association of free amino acids with caries experience and mutans streptococci levels in whole saliva of children with early childhood caries

…, MH Guerra, TR Ribeiro, DN Mendonça… - archives of oral …, 2009 - Elsevier
OBJECTIVE: The aim of the present study was to identify the free amino acid content in
whole saliva of children with (CE) and without early childhood caries (CF) (ECC), correlating …

[HTML][HTML] Selected Abstracts from the 13 th Annual Meeting of the Clinical Immunology Society: 2022 Annual Meeting: Immune Deficiency and Dysregulation North …

J Hajjar, D Mendonca, M Conner, T Savidge… - Journal of Clinical …, 2022 - Springer
or NS 50μl, intraperitoneally (n= 4/group). D30 and D40 represent days 30 & 40 post-FMT,
respectively. Principal coordinate analysis plots of unweighted distances of fecal microbiota …

[HTML][HTML] Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome

D Mendonca, G Cappuccio, J Sheppard, M Delacruz… - Stem Cell Research, 2024 - Elsevier
MECP2 Duplication Syndrome (MDS) is a rare, severe neurodevelopmental disorder arising
from duplications in the Xq28 region containing the MECP2 gene that predominantly affects …

[HTML][HTML] Cross-cultural adaptation and content validity of the Adverse Events Associated with Nursing Practices instrument

…, SMO Pinto, FG Camerini, DH Mendonça… - Revista Gaúcha de …, 2023 - SciELO Brasil
SciELO - Brasil - Cross-cultural adaptation and content validity of the Adverse Events Associated
with Nursing Practices instrument Cross-cultural adaptation and content validity of the …

Episignatures stratifying ADNP syndrome show modest correlation with phenotype

MS Breen, P Garg, L Tang, D Mendonca, T Levy… - BioRxiv, 2020 - biorxiv.org
ADNP syndrome, also known as Helsmoortel-van Der Aa syndrome, is a neurodevelopmental
condition associated with intellectual disability/developmental delay, autism spectrum …

Developmental and behavioral phenotypes in a new mouse model of DDX3X syndrome

…, DC Ung, M Garcia-Forn, K Niblo, D Mendonca… - bioRxiv, 2021 - biorxiv.org
Background Mutations in the X-linked gene DDX3X account for ~2% of intellectual disability
in females, often co-morbid with behavioral problems, motor deficits, and brain …

Changes in NR2B-NMDA Receptor Expression Relate to Individual Differences in Adaptability to Food Restriction-Stress

D Mendonca, C Aoki, K Varela, YW Chen - 2018 - academiccommons.columbia.edu
The eating disorder Anorexia Nervosa has an extremely high mortality rate of 5.9%(Arcelus
et al. 2011) and a poorly understood neurobiology. Research indicates the animal model …