Detalhe da pesquisa
1.
Racial and Ethnic Disparities in Acute Care Utilization Among Patients With Glomerular Disease.
Am J Kidney Dis
; 81(3): 318-328.e1, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36191724
2.
Association of infections and venous thromboembolism in hospitalized children with nephrotic syndrome.
Pediatr Nephrol
; 34(2): 261-267, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30194664
3.
Obesity in prematurely born children and adolescents: follow up in pediatric clinic.
Nutr J
; 12(1): 150, 2013 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24252330
4.
Restorative yoga therapy for third-year medical students in pediatrics rotation: Working to improve medical student well-being.
J Educ Health Promot
; 12: 76, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37288410
5.
Novel enhancer mediates the RPL36A-HNRNPH2 readthrough loci and GLA gene expressions associated with fabry disease.
Front Genet
; 14: 1229088, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38155709
6.
Change in Urinary Inflammatory Biomarkers and Psychological Health with Gut Microbiome Modulation after Six Months of a Lifestyle Modification Program in Children.
Nutrients
; 15(19)2023 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37836527
7.
Pregnancy History and Kidney Disease Progression Among Women Enrolled in Cure Glomerulonephropathy.
Kidney Int Rep
; 8(4): 805-817, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37069979
8.
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.
Nat Genet
; 55(7): 1091-1105, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37337107
9.
The potential consequences of bidirectional promoter methylation on GLA and HNRNPH2 expression in Fabry disease phenotypes in a family of patients carrying a GLA deletion variant.
Biomed Rep
; 17(2): 71, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35910704
10.
A Case of Pediatric Posterior Reversible Encephalopathy Syndrome (PRES) Secondary to Post-streptococcal Glomerulonephritis: A Literature Review and Assessment of Treatment Modalities.
Cureus
; 14(5): e25113, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35733462
11.
Congenital nephrotic syndrome in a Hispanic Guatemalan newborn associated with a NPHS1 variant: A case report.
Biomed Rep
; 16(1): 4, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34900253
12.
Clinical presentation and management of nephrotic syndrome in the first year of life: A report from the Pediatric Nephrology Research Consortium.
Front Pediatr
; 10: 988945, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36210940
13.
Unexplored regulatory sequences of divergently paired GLA and HNRNPH2 loci pertinent to Fabry disease in human kidney and skin cells: Presence of an active bidirectional promoter.
Exp Ther Med
; 21(2): 154, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33456521
14.
Racial-ethnic differences in health-related quality of life among adults and children with glomerular disease.
Glomerular Dis
; 1(3): 105-117, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34723246
15.
GANAB and PKD1 Variations in a 12 Years Old Female Patient With Early Onset of Autosomal Dominant Polycystic Kidney Disease.
Front Genet
; 10: 44, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30792735
16.
Dysbiosis of Gram-negative gut microbiota and the associated serum lipopolysaccharide exacerbates inflammation in type 2 diabetic patients with chronic kidney disease.
Exp Ther Med
; 18(5): 3461-3469, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31602221
17.
National Trends in the Epidemiology and Resource Use for Henoch-Schönlein Purpura (IgA Vasculitis) Hospitalizations in the United States From 2006 to 2014.
Hosp Pediatr
; 9(11): 888-896, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31575605
18.
Developing a Research Mentorship Program: The American Society of Pediatric Nephrology's Experience.
Front Pediatr
; 7: 155, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31069203
19.
Prevalence of Cardiovascular Disease Risk Factors in Childhood Glomerular Diseases.
J Am Heart Assoc
; 8(14): e012143, 2019 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31286821
20.
Possible Correlation between Hypomelanosis of Ito and Wilms' Tumor.
Case Rep Pediatr
; 2018: 5938120, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30123603