Maria Rita Passos Bueno
Overview
Explore the profile of Maria Rita Passos Bueno including associated specialties, affiliations and a list of published articles.
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5
Citations
64
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Recent Articles
1.
Garcia F, de Sousa V, Silva-Dos-Santos P, Fernandes I, Sarquis Serpa F, Paula F, et al.
Clin Rev Allergy Immunol
. 2025 Jan;
68(1):4.
PMID: 39755867
Asthma is a complex disease with varied clinical manifestations resulting from the interaction between environmental and genetic factors. While chronic airway inflammation and hyperresponsiveness are central features, the etiology of...
2.
Teles E Silva A, Yokota-Moreno B, Branquinho M, Salles G, de Souza T, de Carvalho R, et al.
Neurochem Int
. 2024 Sep;
180:105854.
PMID: 39241808
Cortical organoids derived from human induced pluripotent stem cells (hiPSCs) represent a powerful in vitro experimental system to investigate human brain development and disease, often inaccessible to direct experimentation. However,...
3.
Srivastava S, Sahin M, Buxbaum J, Berry-Kravis E, Soorya L, Thurm A, et al.
Am J Med Genet A
. 2023 Jul;
191(8):2015-2044.
PMID: 37392087
Phelan-McDermid syndrome (PMS) is a genetic condition caused by SHANK3 haploinsufficiency and characterized by a wide range of neurodevelopmental and systemic manifestations. The first practice parameters for assessment and monitoring...
4.
Dos Santos L, Pimassoni L, Sena G, Camporez D, Belcavello L, Trancozo M, et al.
J Mol Neurosci
. 2017 May;
62(2):215-221.
PMID: 28477215
Late-onset Alzheimer's disease (LOAD) is a multifactorial neurodegenerative disorder that corresponds to most Alzheimer's disease (AD) cases. Inflammation is frequently related to AD, whereas microglial cells are the major phagocytes...
5.
Doherty E, Lacbawan F, Hadley D, Brewer C, Zalewski C, Kim H, et al.
Am J Med Genet A
. 2007 Nov;
143A(24):3204-15.
PMID: 18000976
Muenke syndrome is an autosomal dominant disorder characterized by coronal suture craniosynostosis, hearing loss, developmental delay, carpal and tarsal fusions, and the presence of the Pro250Arg mutation in the FGFR3...