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The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study.
- Published in:
- Nephron, 2024, v. 148, n. 5, p. 319, doi. 10.1159/000528258
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- Publication type:
- Article
Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone.
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- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 1, p. 69, doi. 10.4274/jcrpe.galenos.2022.2022-8-19
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- Publication type:
- Article
Pediatric kidney care experience after the 2023 Türkiye earthquake.
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- Nephrology Dialysis Transplantation, 2024, v. 39, n. 9, p. 1514, doi. 10.1093/ndt/gfae033
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- Article
Evaluating renin and aldosterone levels in children with organic acidemia—therapeutic experience with fludrocortisone.
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- European Journal of Pediatrics, 2023, v. 182, n. 12, p. 5447, doi. 10.1007/s00431-023-05221-8
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- Publication type:
- Article
Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic.
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- Telemedicine & e-Health, 2021, v. 27, n. 10, p. 1180, doi. 10.1089/tmj.2020.0381
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- Publication type:
- Article
Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil?
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- Pediatric Nephrology, 2024, v. 39, n. 5, p. 1435, doi. 10.1007/s00467-023-06231-2
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- Publication type:
- Article
Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children.
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- Pediatric Nephrology, 2023, v. 38, n. 7, p. 2199, doi. 10.1007/s00467-022-05813-w
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- Article
HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract.
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- Pediatric Nephrology, 2023, v. 38, n. 3, p. 933, doi. 10.1007/s00467-022-05756-2
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- Publication type:
- Article
A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature.
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- Pediatric Nephrology, 2023, v. 38, n. 3, p. 711, doi. 10.1007/s00467-022-05656-5
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- Publication type:
- Article
Management of pediatric dialysis and kidney transplant patients after natural or man-made disasters.
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- Pediatric Nephrology, 2023, v. 38, n. 2, p. 315, doi. 10.1007/s00467-022-05734-8
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- Publication type:
- Article
Evaluation of the Claria sharesource system from the perspectives of patient/caregiver, physician, and nurse in children undergoing automated peritoneal dialysis.
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- Pediatric Nephrology, 2023, v. 38, n. 2, p. 471, doi. 10.1007/s00467-022-05563-9
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- Article
Increased risk for kidney sequelae surrogates in survivors of Wilms tumor.
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- Pediatric Nephrology, 2022, v. 37, n. 10, p. 2415, doi. 10.1007/s00467-022-05460-1
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- Publication type:
- Article
A broad clinical spectrum of PLCε1-related kidney disease and intrafamilial variability.
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- Pediatric Nephrology, 2022, v. 37, n. 8, p. 1855, doi. 10.1007/s00467-021-05371-7
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- Publication type:
- Article
Strong mesangial IgA staining—does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Answers.
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- 2021
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- Publication type:
- Test/Instrument
Strong mesangial IgA staining—does it always refer to IgA nephropathy in a patient with proteinuria and hematuria? Questions.
- Published in:
- 2021
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- Publication type:
- Test/Instrument
Predictors of poor kidney outcome in children with C3 glomerulopathy.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 5, p. 1195, doi. 10.1007/s00467-020-04799-7
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- Publication type:
- Article
Natural history of patients with infantile nephrolithiasis: what are the predictors of surgical intervention?
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- Pediatric Nephrology, 2021, v. 36, n. 4, p. 939, doi. 10.1007/s00467-020-04781-3
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- Publication type:
- Article
Treatment of ichthyosis and hypernatremia in a patient with Netherton syndrome with a SPINK5 c.153delT mutation using kallikrein inhibiting ointment.
- Published in:
- International Journal of Dermatology, 2017, v. 56, n. 1, p. 106, doi. 10.1111/ijd.13248
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- Article
Artificial Intelligence in Pediatrics: Learning to Walk Together.
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- Turkish Archives of Pediatrics, 2024, v. 59, n. 2, p. 121, doi. 10.5152/TurkArchPediatr.2024.24002
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- Publication type:
- Article
The Ebb and Flow of Social Media for Researchers.
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- Turkish Archives of Pediatrics, 2023, v. 58, n. 5, p. 456, doi. 10.5152/TurkArchPediatr.2023.232208
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- Publication type:
- Article
Cardiometabolic Risk Factors in Pediatric Kidney Transplant Recipients.
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- Turkish Archives of Pediatrics, 2023, v. 58, n. 2, p. 220, doi. 10.5152/TurkArchPediatr.2023.22310
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- Publication type:
- Article
Earthquake in Turkey: Disasters and Children.
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- Turkish Archives of Pediatrics, 2023, v. 58, n. 2, p. 119, doi. 10.5152/TurkArchPediatr.2023.160222
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- Publication type:
- Article
A Challenging Diagnosis of Hematuria.
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- Turkish Archives of Pediatrics, 2022, v. 57, n. 6, p. 668, doi. 10.5152/TurkArchPediatr.2022.22074
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- Publication type:
- Article
Rituximab treatment for difficult-to-treat nephrotic syndrome in children: a multicenter, retrospective study.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 4, p. 1781, doi. 10.3906/sag-2012-297
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- Publication type:
- Article
Growth in Children After Kidney Transplantation.
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- Cerrahpaşa Medical Journal, 2023, v. 47, n. 2, p. 182, doi. 10.5152/cjm.2023.23002
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- Publication type:
- Article
A case of crescentic glomerulonephritis with exacerbation of pre-existing IgA nephropathy after COVID-19.
- Published in:
- 2024
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- Publication type:
- Case Study
The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome.
- Published in:
- Turkish Journal of Pediatrics, 2023, v. 65, n. 3, p. 456, doi. 10.24953/turkjped.2022.735
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- Publication type:
- Article
Comprehensive evaluation of patients with primary hyperoxaluria type 1: A nationwide study.
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- Nephrology, 2024, v. 29, n. 4, p. 201, doi. 10.1111/nep.14273
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- Publication type:
- Article
COVID‐19 associated thrombotic microangiopathy.
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- Nephrology, 2023, v. 28, n. 10, p. 557, doi. 10.1111/nep.14225
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- Publication type:
- Article
A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT).
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- Clinical Genetics, 2023, v. 104, n. 6, p. 679, doi. 10.1111/cge.14406
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- Publication type:
- Article
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.
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- Clinical Genetics, 2022, v. 101, n. 3, p. 346, doi. 10.1111/cge.14105
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- Publication type:
- Article
A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract.
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- Clinical Genetics, 2020, v. 98, n. 4, p. 390, doi. 10.1111/cge.13813
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- Publication type:
- Article
DARBEPOETIN TREATMENT AFTER ETHANOL TOXICITY: AN EXPERIMENTAL STUDY IN RATS.
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- FASEB Journal, 2007, v. 21, n. 6, p. A1278, doi. 10.1096/fasebj.21.6.a1278-a
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- Publication type:
- Article
Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease.
- Published in:
- Frontiers in Pediatrics, 2024, p. 1, doi. 10.3389/fped.2024.1357365
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- Publication type:
- Article
Evaluation of non-infectious complications of peritoneal dialysis in children: a multicenter study.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 2, p. 417, doi. 10.1007/s00467-020-04719-9
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- Publication type:
- Article
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
- Published in:
- Pediatric Nephrology, 2020, v. 35, n. 10, p. 1941, doi. 10.1007/s00467-020-04574-8
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- Publication type:
- Article
Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar?
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- Pediatric Nephrology, 2020, v. 35, n. 7, p. 1267, doi. 10.1007/s00467-020-04526-2
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- Publication type:
- Article
A rare cause of proteinuria after kidney transplantation: Questions.
- Published in:
- 2019
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- Publication type:
- Case Study
A rare cause of proteinuria after kidney transplantation: Answers.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 11, p. 2333, doi. 10.1007/s00467-019-04263-1
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- Publication type:
- Article
Proteinuria in a patient with Graves' disease: Answers.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 8, p. 1383, doi. 10.1007/s00467-019-04221-x
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- Publication type:
- Article
Proteinuria in a patient with Graves' disease: Questions.
- Published in:
- 2019
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- Publication type:
- Case Study
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 1, p. 77, doi. 10.1007/s00467-018-3982-7
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- Publication type:
- Article
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Elevated Urinary VEGF-A, Transferrin, and Angiotensinogen Levels in Normoalbuminuric Children and Adolescents with Type 1 Diabetes: Can They Be Early Markers of Diabetic Kidney Disease?
- Published in:
- Hormone Research in Paediatrics, 2022, v. 94, n. 11/12, p. 426, doi. 10.1159/000521447
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- Publication type:
- Article