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Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease—are patient-centered outcomes our blind spot?
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 12, p. 3841, doi. 10.1007/s00467-021-05192-8
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- Publication type:
- Article
Early clinical management of autosomal recessive polycystic kidney disease.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 11, p. 3561, doi. 10.1007/s00467-021-04970-8
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- Publication type:
- Article
Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoring.
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- Pediatric Nephrology, 2018, v. 33, n. 4, p. 619, doi. 10.1007/s00467-017-3846-6
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- Publication type:
- Article
Expanding the role of vasopressin antagonism in polycystic kidney diseases: From adults to children?
- Published in:
- Pediatric Nephrology, 2018, v. 33, n. 3, p. 395, doi. 10.1007/s00467-017-3672-x
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- Publication type:
- Article
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1269, doi. 10.1007/s00467-017-3648-x
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- Publication type:
- Article
Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 5, p. 791, doi. 10.1007/s00467-016-3556-5
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- Publication type:
- Article
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing.
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- Pediatric Nephrology, 2016, v. 31, n. 1, p. 73, doi. 10.1007/s00467-015-3167-6
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- Publication type:
- Article
Looking at the (w)hole: magnet resonance imaging in polycystic kidney disease.
- Published in:
- Pediatric Nephrology, 2013, v. 28, n. 9, p. 1771, doi. 10.1007/s00467-012-2370-y
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- Publication type:
- Article
Primary cilia contribute to the aggressiveness of atypical teratoid/rhabdoid tumors.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 9, p. 1, doi. 10.1038/s41419-022-05243-4
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- Publication type:
- Article
Bicarbonate buffered peritoneal dialysis fluid upregulates angiopoietin-1 and promotes vessel maturation.
- Published in:
- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189903
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- Publication type:
- Article
IL-6/Smad2 signaling mediates acute kidney injury and regeneration in a murine model of neonatal hyperoxia.
- Published in:
- FASEB Journal, 2019, v. 33, n. 5, p. 5887, doi. 10.1096/fj.201801875RR
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- Publication type:
- Article
Differential regulation of MYC expression by PKHD1/Pkhd1 in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease.
- Published in:
- Frontiers in Cell & Developmental Biology, 2023, p. 1, doi. 10.3389/fcell.2023.1270980
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- Publication type:
- Article
NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway.
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- Journal of Cell Biology, 2011, v. 193, n. 4, p. 633, doi. 10.1083/jcb.201009069
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- Publication type:
- Article
Translational research approaches to study pediatric polycystic kidney disease.
- Published in:
- Molecular & Cellular Pediatrics, 2021, v. 8, n. 9, p. 1, doi. 10.1186/s40348-021-00131-x
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- Publication type:
- Article
Toxigenic Corynebacterium diphtheriae-Associated Genital Ulceration.
- Published in:
- 2020
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- Publication type:
- journal article
Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4.
- Published in:
- Clinical Infectious Diseases, 2017, v. 64, n. 12, p. 1637, doi. 10.1093/cid/cix218
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- Publication type:
- Article
Erbliche Zystennierenerkrankungen: Autosomal-dominante und autosomal-rezessive polyzystische Nierenerkrankung (ADPKD und ARPKD).
- Published in:
- Medizinische Genetik, 2018, v. 30, n. 4, p. 422, doi. 10.1007/s11825-018-0224-0
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- Publication type:
- Article
Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic Treatment.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 17, p. 6093, doi. 10.3390/ijms21176093
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- Publication type:
- Article
TAPT1—at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta.
- Published in:
- EMBO Molecular Medicine, 2023, v. 15, n. 7, p. 1, doi. 10.15252/emmm.202317528
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- Publication type:
- Article
L1CAM mutation in a boy with hydrocephalus and duplex kidneys.
- Published in:
- 2007
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- Publication type:
- Report
Implications of early diagnosis of autosomal dominant polycystic kidney disease: A post hoc analysis of the TEMPO 3:4 trial.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-61303-9
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- Publication type:
- Article
Dysregulated Autophagy Contributes to Podocyte Damage in Fabry’s Disease
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0063506
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- Publication type:
- Article
The Centrosomal Kinase Plk1 Localizes to the Transition Zone of Primary Cilia and Induces Phosphorylation of Nephrocystin-1.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038838
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- Publication type:
- Article
Enzyme Replacement Therapy Clears Gb3 Deposits from a Podocyte Cell Culture Model of Fabry Disease but Fails to Restore Altered Cellular Signaling.
- Published in:
- Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2019, v. 52, n. 5, p. 1139, doi. 10.33594/000000077
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- Publication type:
- Article
Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT).
- Published in:
- Molecular & Cellular Pediatrics, 2021, v. 8, n. 1, p. 1, doi. 10.1186/s40348-021-00112-0
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- Publication type:
- Article
Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality.
- Published in:
- Molecular & Cellular Pediatrics, 2021, v. 8, n. 1, p. 1, doi. 10.1186/s40348-021-00111-1
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- Publication type:
- Article
Cilia-associated cellular function of the AAA ATPases RUVBL1 and RUVBL2.
- Published in:
- 2015
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- Publication type:
- Abstract
AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosis.
- Published in:
- EMBO Journal, 2012, v. 31, n. 20, p. 3961, doi. 10.1038/emboj.2012.236
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- Publication type:
- Article
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics.
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- 2011
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- Publication type:
- journal article
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.
- Published in:
- 2010
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- Publication type:
- journal article
A defect in molybdenum cofactor binding causes an attenuated form of sulfite oxidase deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2022, v. 45, n. 2, p. 169, doi. 10.1002/jimd.12454
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- Publication type:
- Article
Clinicians’ attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease.
- Published in:
- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0185779
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- Publication type:
- Article
Unmet needs and challenges for follow-up and treatment of autosomal dominant polycystic kidney disease: the paediatric perspective.
- Published in:
- Clinical Kidney Journal, 2018, v. 11, p. i14, doi. 10.1093/ckj/sfy088
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- Publication type:
- Article
Altered molecular signatures during kidney development after intrauterine growth restriction of different origins.
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- Journal of Molecular Medicine, 2020, v. 98, n. 3, p. 395, doi. 10.1007/s00109-020-01875-1
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- Publication type:
- Article
Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT).
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- Journal of Molecular Medicine, 2013, v. 91, n. 6, p. 739, doi. 10.1007/s00109-013-1000-x
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- Publication type:
- Article
Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature Reviews.
- Published in:
- JAMA Pediatrics, 2018, v. 172, n. 1, p. 74, doi. 10.1001/jamapediatrics.2017.3938
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- Publication type:
- Article
The carboxy‐terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC‐activation.
- Published in:
- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 24, p. 14633, doi. 10.1111/jcmm.16014
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- Publication type:
- Article
Shift from severe hypotension to salt-dependent hypertension in a child with autosomal recessive polycystic kidney disease after bilateral nephrectomies: a case report.
- Published in:
- 2023
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- Publication type:
- Case Study
Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease.
- Published in:
- BMC Nephrology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12882-023-03072-x
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- Publication type:
- Article
Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease.
- Published in:
- BMC Nephrology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12882-023-03072-x
- By:
- Publication type:
- Article
ATRT-07. TARGETING PRIMARY CILIOGENESIS IN ATYPICAL TERATOID/RHABDOID TUMORS.
- Published in:
- Neuro-Oncology, 2019, v. 21, p. ii64, doi. 10.1093/neuonc/noz036.006
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- Publication type:
- Article
Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases.
- Published in:
- 2022
- By:
- Publication type:
- journal article