Detalhe da pesquisa
1.
Gestational Trophoblastic Disease with Coexisting Progressing Pregnancy: Personalised Treatment Modalities.
Int J Clin Pract;
2023: 5502317, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37927849
2.
Necrotizing Enterocolitis: The Role of Hypoxia, Gut Microbiome, and Microbial Metabolites.
Int J Mol Sci;
24(3)2023 Jan 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36768793
3.
Dysregulation of Notch signaling in cardiac mesenchymal cells of patients with tetralogy of Fallot.
Pediatr Res;
88(1): 38-47, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31952074
4.
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
Hum Mutat;
39(9): 1161-1172, 2018 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29858533
5.
Insights Image for "Dysregulation of Notch signaling in cardiac mesenchymal cells of patients with Tetralogy of Fallot".
Pediatr Res;
88(1): 139, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32170193
6.
SIGIRR gene variants in term newborns with congenital heart defects and necrotizing enterocolitis.
Ann Pediatr Cardiol;
16(5): 337-344, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38766461
7.
Severe Course of COVID-19 and Long-COVID-19 in Children: Difficulties in Diagnosis.
Life (Basel);
13(3)2023 Mar 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36983936
8.
The phenotypic and genetic features of arrhythmogenic cardiomyopathy in the pediatric population.
Front Cardiovasc Med;
10: 1216976, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37781308
9.
Trial protocol for the study of recommendation system DiaCompanion with personalized dietary recommendations for women with gestational diabetes mellitus (DiaCompanion I).
Front Endocrinol (Lausanne);
14: 1168688, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37361536
10.
Simplified Convolutional Neural Network Application for Cervix Type Classification via Colposcopic Images.
Bioengineering (Basel);
9(6)2022 May 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35735482
11.
Development of computer-aided model to differentiate COVID-19 from pulmonary edema in lung CT scan: EDECOVID-net.
Comput Biol Med;
141: 105172, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34973585
12.
Intestinal microbiome changes in an infant with right atrial isomerism and recurrent necrotizing enterocolitis: A case report and review of literature.
World J Clin Cases;
10(29): 10583-10599, 2022 Oct 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36312470
13.
Vitamin D Status and Gestational Diabetes in Russian Pregnant Women in the Period between 2012 and 2021: A Nested Case-Control Study.
Nutrients;
14(10)2022 May 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35631298
14.
Case Report: COVID-19-Associated ROHHAD-Like Syndrome.
Front Pediatr;
10: 854367, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35433531
15.
Case Report: A novel PHOX2B p.Ala248_Ala266dup variant causing congenital central hypoventilation syndrome.
Front Pediatr;
10: 1070303, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36874254
16.
Association of Common Genetic Risk Variants With Gestational Diabetes Mellitus and Their Role in GDM Prediction.
Front Endocrinol (Lausanne);
12: 628582, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33953693
17.
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children.
Front Cardiovasc Med;
8: 668231, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34026875
18.
Sodium current abnormalities and deregulation of Wnt/ß-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene.
Biochim Biophys Acta Mol Basis Dis;
1866(11): 165915, 2020 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32768677
19.
Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val.
Stem Cell Res;
43: 101719, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32062135
20.
A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
BMC Med Genomics;
13(1): 175, 2020 11 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33218365