Detalhe da pesquisa
1.
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Am J Hum Genet
; 110(11): 1919-1937, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37827158
2.
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications.
Brain
; 146(6): 2285-2297, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36477332
3.
A Need for a Novel Survival Risk Scoring System for Intensive Care Admissions Due to Sepsis in Pediatric Hematology/Oncology Patients.
J Intensive Care Med
; 39(5): 484-492, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37981801
4.
A rare unbalanced translocation (trisomy 5q33.3-qter, monosomy 13q34-qter) results in growth hormone deficiency and brain anomalies.
Mol Genet Genomic Med
; 9(11): e1821, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34623774
5.
Waste pickers organizations and municipal selective waste collection: Sustainability indicators.
Waste Manag
; 118: 219-231, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32898775
6.
Developmental fluoxetine exposure in zebrafish reduces offspring basal cortisol concentration via life stage-dependent maternal transmission.
PLoS One
; 14(2): e0212577, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30789953