Detalhe da pesquisa
1.
The expanding clinical and genetic spectrum of DYNC1H1-related disorders.
Brain
; 2024 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38848546
2.
Implementing the Lolli-Method and pooled RT-qPCR testing for SARS-CoV-2 surveillance in schools: a pilot project.
Infection
; 51(2): 459-464, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35759174
3.
Humoral immune response and live-virus neutralization of the SARS-CoV-2 omicron (BA.1) variant after COVID-19 mRNA vaccination in children and young adults with chronic kidney disease.
Pediatr Nephrol
; 38(6): 1935-1948, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36409368
4.
Perinatal Obesity Sensitizes for Premature Kidney Aging Signaling.
Int J Mol Sci
; 24(3)2023 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36768831
5.
Elevated n-3/n-6 PUFA ratio in early life diet reverses adverse intrauterine kidney programming in female rats.
J Lipid Res
; 63(11): 100283, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36152882
6.
Infection and transmission risks of COVID-19 in schools and their contribution to population infections in Germany: A retrospective observational study using nationwide and regional health and education agency notification data.
PLoS Med
; 19(12): e1003913, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36538517
7.
Macrophage-derived IL-6 trans-signalling as a novel target in the pathogenesis of bronchopulmonary dysplasia.
Eur Respir J
; 59(2)2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34446466
8.
Perinatal Obesity Induces Hepatic Growth Restriction with Increased DNA Damage Response, Senescence, and Dysregulated Igf-1-Akt-Foxo1 Signaling in Male Offspring of Obese Mice.
Int J Mol Sci
; 23(10)2022 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35628414
9.
Vascular tone regulation in renal interlobar arteries of male rats is dysfunctional after intrauterine growth restriction.
Am J Physiol Renal Physiol
; 321(1): F93-F105, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34056927
10.
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Kidney Int
; 100(3): 650-659, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33940108
11.
Ultra-rapid emergency genomic diagnosis of Donahue syndrome in a preterm infant within 17 hours.
Am J Med Genet A
; 185(1): 90-96, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33048476
12.
Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy -short version of the updated German best practice guideline (S2e) - AWMF register no. 166-001, 6/2020.
Pediatr Nephrol
; 36(10): 2971-2985, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34091756
13.
The carboxy-terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC-activation.
J Cell Mol Med
; 24(24): 14633-14638, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33112055
14.
Maternal high fat diet-induced obesity affects trophoblast differentiation and placental function in mice.
Biol Reprod
; 103(6): 1260-1274, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32915209
15.
Maternal high-fat diet induces long-term obesity with sex-dependent metabolic programming of adipocyte differentiation, hypertrophy and dysfunction in the offspring.
Clin Sci (Lond)
; 134(7): 921-939, 2020 04 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32239178
16.
IL-6/Smad2 signaling mediates acute kidney injury and regeneration in a murine model of neonatal hyperoxia.
FASEB J
; 33(5): 5887-5902, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30721632
17.
Strain-dependent effects on lung structure, matrix remodeling, and Stat3/Smad2 signaling in C57BL/6N and C57BL/6J mice after neonatal hyperoxia.
Am J Physiol Regul Integr Comp Physiol
; 317(1): R169-R181, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31067073
18.
Cleft Palate as Distinguishing Feature in a Patient with GABRB3 Epileptic Encephalopathy.
Neuropediatrics
; 50(6): 378-381, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31319422
19.
Glomerular disease patients have higher odds not to reach quality targets in chronic dialysis compared with CAKUT patients: analyses from a nationwide German paediatric dialysis registry.
Pediatr Nephrol
; 34(7): 1229-1236, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30843113
20.
Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathy.
J Med Genet
; 55(9): 637-640, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29661969