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Sensenbrenner syndrome: a further challenge in evaluating sagittal synostosis and a need for a multidisciplinary approach.
- Published in:
- Child's Nervous System, 2021, v. 37, n. 5, p. 1695, doi. 10.1007/s00381-021-05075-1
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- Article
Muscle and Bone Impairment in Infantile Nephropathic Cystinosis: New Concepts.
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- Cells (2073-4409), 2022, v. 11, n. 1, p. 170, doi. 10.3390/cells11010170
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- Article
Response to Cysteamine in Osteoclasts Obtained from Patients with Nephropathic Cystinosis: A Genotype/Phenotype Correlation.
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- Cells (2073-4409), 2021, v. 10, n. 9, p. 2498, doi. 10.3390/cells10092498
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- Article
Addressing the psychosocial aspects of transition to adult care in patients with cystinosis.
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- Pediatric Nephrology, 2024, v. 39, n. 10, p. 2861, doi. 10.1007/s00467-024-06345-1
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- Article
Creatinine-based formulas are not ideal to estimate glomerular filtration rate in selected pediatric patients: data from a tertiary pediatric nephrology center.
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- Pediatric Nephrology, 2024, v. 39, n. 10, p. 3023, doi. 10.1007/s00467-023-06275-4
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- Article
Nephrocalcinosis can disappear in infants receiving early lumasiran therapy.
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- Pediatric Nephrology, 2024, v. 39, n. 7, p. 2079, doi. 10.1007/s00467-023-06268-3
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- Article
Pediatric urogenital schistosomiasis diagnosed in France.
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- Pediatric Nephrology, 2024, v. 39, n. 6, p. 1893, doi. 10.1007/s00467-023-06260-x
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- Article
Worldwide disparities in access to treatment and investigations for nephropathic cystinosis: a 2023 perspective.
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- Pediatric Nephrology, 2024, v. 39, n. 4, p. 1113, doi. 10.1007/s00467-023-06179-3
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- Article
Kidney and urological involvement in Down syndrome: frequent, underestimated, but associated with impaired quality of life and risk of kidney failure.
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- Pediatric Nephrology, 2024, v. 39, n. 2, p. 347, doi. 10.1007/s00467-023-05986-y
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- Article
Daily practice evaluation of the paediatric set of a next-generation long-term haemodialysis machine.
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- Pediatric Nephrology, 2023, v. 38, n. 11, p. 3863, doi. 10.1007/s00467-023-05943-9
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- Article
Diagnosis and management of mineral and bone disorders in infants with CKD: clinical practice points from the ESPN CKD-MBD and Dialysis working groups and the Pediatric Renal Nutrition Taskforce.
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- Pediatric Nephrology, 2023, v. 38, n. 9, p. 3163, doi. 10.1007/s00467-022-05825-6
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- Article
CARPEDIEM® for continuous kidney replacement therapy in neonates and small infants: a French multicenter retrospective study.
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- Pediatric Nephrology, 2023, v. 38, n. 8, p. 2827, doi. 10.1007/s00467-022-05871-0
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- Article
X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study.
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- Pediatric Nephrology, 2023, v. 38, n. 3, p. 697, doi. 10.1007/s00467-022-05636-9
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- Article
Genetic assessment in primary hyperoxaluria: why it matters.
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- Pediatric Nephrology, 2023, v. 38, n. 3, p. 625, doi. 10.1007/s00467-022-05613-2
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- Article
Cardiac involvement in pediatric hemolytic uremic syndrome.
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- Pediatric Nephrology, 2022, v. 37, n. 12, p. 3215, doi. 10.1007/s00467-022-05427-2
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- Article
Nephrocalcinosis in very low birth weight infants: incidence, associated factors, and natural course.
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- Pediatric Nephrology, 2022, v. 37, n. 12, p. 3093, doi. 10.1007/s00467-021-05417-w
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- Article
Teenagers and young adults with a past of allogenic hematopoietic stem cell transplantation are at significant risk of chronic kidney disease.
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- Pediatric Nephrology, 2022, v. 37, n. 6, p. 1365, doi. 10.1007/s00467-021-05319-x
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- Article
The effect of lumasiran therapy for primary hyperoxaluria type 1 in small infants.
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- Pediatric Nephrology, 2022, v. 37, n. 4, p. 907, doi. 10.1007/s00467-021-05393-1
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- Article
To biopsy or not to biopsy: Henoch-Schönlein nephritis in children, a 5-year follow-up study.
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- Pediatric Nephrology, 2022, v. 37, n. 1, p. 147, doi. 10.1007/s00467-021-05086-9
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- Article
Pediatric atypical hemolytic–uremic syndrome due to auto-antibodies against factor H: is there an interest to combine eculizumab and mycophenolate mofetil?
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- Pediatric Nephrology, 2021, v. 36, n. 6, p. 1647, doi. 10.1007/s00467-021-05025-8
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- Article
Adherence to cysteamine in nephropathic cystinosis: A unique electronic monitoring experience for a better understanding. A prospective cohort study: CrYSTobs.
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- Pediatric Nephrology, 2021, v. 36, n. 3, p. 581, doi. 10.1007/s00467-020-04722-0
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- Article
Setting reasonable objectives for improving preemptive kidney transplantation rates in children.
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- Pediatric Nephrology, 2020, v. 35, n. 12, p. 2353, doi. 10.1007/s00467-020-04653-w
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- Article
The use of cinacalcet after pediatric renal transplantation: an international CERTAIN Registry analysis.
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- Pediatric Nephrology, 2020, v. 35, n. 9, p. 1707, doi. 10.1007/s00467-020-04558-8
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- Article
Cinacalcet studies in pediatric subjects with secondary hyperparathyroidism receiving dialysis.
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- Pediatric Nephrology, 2020, v. 35, n. 9, p. 1679, doi. 10.1007/s00467-020-04516-4
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- Article
Treatment of hyperphosphatemia: the dangers of high PTH levels.
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- Pediatric Nephrology, 2020, v. 35, n. 3, p. 493, doi. 10.1007/s00467-019-04400-w
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- Article
Towards adulthood with a solitary kidney.
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- Pediatric Nephrology, 2019, v. 34, n. 11, p. 2311, doi. 10.1007/s00467-018-4085-1
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- Article
Escherichia coli-associated hemolytic uremic syndrome and severe chronic hepatocellular cholestasis: complication or side effect of eculizumab?
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- Pediatric Nephrology, 2019, v. 34, n. 7, p. 1289, doi. 10.1007/s00467-019-04234-6
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- Article
Infants with congenital nephrotic syndrome have comparable outcomes to infants with other renal diseases.
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- Pediatric Nephrology, 2019, v. 34, n. 4, p. 649, doi. 10.1007/s00467-018-4122-0
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- Article
Skin microvascular dysfunction as an early cardiovascular marker in primary hyperoxaluria type I.
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- Pediatric Nephrology, 2019, v. 34, n. 2, p. 319, doi. 10.1007/s00467-018-4081-5
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- Article
The interplay between bone and vessels in pediatric CKD: lessons from a single-center study.
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- Pediatric Nephrology, 2018, v. 33, n. 9, p. 1565, doi. 10.1007/s00467-018-3978-3
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- Article
Hyperphosphatemic tumoral calcinosis caused by FGF23 compound heterozygous mutations: what are the therapeutic options for a better control of phosphatemia?
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- Pediatric Nephrology, 2018, v. 33, n. 7, p. 1263, doi. 10.1007/s00467-018-3945-z
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- Article
Teenagers and young adults with nephropathic cystinosis display significant bone disease and cortical impairment.
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- Pediatric Nephrology, 2018, v. 33, n. 7, p. 1165, doi. 10.1007/s00467-018-3902-x
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- Article
C3 glomerulopathy and eculizumab: a report on four paediatric cases.
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- Pediatric Nephrology, 2017, v. 32, n. 6, p. 1023, doi. 10.1007/s00467-017-3619-2
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- Article
Pediatric combined liver-kidney transplantation: a single-center experience of 18 cases.
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- Pediatric Nephrology, 2016, v. 31, n. 9, p. 1517, doi. 10.1007/s00467-016-3324-6
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- Article
Bone impairment in primary hyperoxaluria: a review.
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- Pediatric Nephrology, 2016, v. 31, n. 1, p. 1, doi. 10.1007/s00467-015-3048-z
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- Article
Renal function can be impaired in children with primary hyperoxaluria type 3.
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- Pediatric Nephrology, 2015, v. 30, n. 10, p. 1807, doi. 10.1007/s00467-015-3090-x
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- Article
Eculizumab in neonatal hemolytic uremic syndrome with homozygous factor H deficiency.
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- 2014
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- Publication type:
- Report
Fludrocortisone as a new tool for managing tubulopathy after pediatric renal transplantation: a series of cases.
- Published in:
- 2014
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- Publication type:
- Report
From bone abnormalities to mineral metabolism dysregulation in autosomal dominant polycystic kidney disease.
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- Pediatric Nephrology, 2013, v. 28, n. 11, p. 2089, doi. 10.1007/s00467-012-2384-5
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- Article
Beyond mineral metabolism, is there an interplay between FGF23 and vitamin D in innate immunity?
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- Pediatric Nephrology, 2013, v. 28, n. 4, p. 577, doi. 10.1007/s00467-012-2336-0
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- Article
Uric acid and IGF1 as possible determinants of FGF23 metabolism in children with normal renal function.
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- Pediatric Nephrology, 2012, v. 27, n. 7, p. 1131, doi. 10.1007/s00467-012-2110-3
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- Article
CKD-MBD after kidney transplantation.
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- Pediatric Nephrology, 2011, v. 26, n. 12, p. 2143, doi. 10.1007/s00467-011-1829-6
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- Article
Creatinine levels in French children with Down syndrome up to ten years old.
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- European Journal of Pediatrics, 2024, v. 183, n. 4, p. 1953, doi. 10.1007/s00431-024-05460-3
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- Article
Composition of urinary stones in children: clinical and metabolic determinants in a French tertiary care center.
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- European Journal of Pediatrics, 2021, v. 180, n. 12, p. 3555, doi. 10.1007/s00431-021-04151-7
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- Article
Is 25OH Vitamin D Excess before 36 Weeks Corrected Age an Independent Risk Factor for Bronchopulmonary Dysplasia or Death?
- Published in:
- Nutrients, 2023, v. 15, n. 20, p. 4423, doi. 10.3390/nu15204423
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- Article
Hydration and Nephrolithiasis in Pediatric Populations: Specificities and Current Recommendations.
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- Nutrients, 2023, v. 15, n. 3, p. 728, doi. 10.3390/nu15030728
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- Article
Young XLH Patients-Reported Experience with a Supportive Care Program.
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- Patient Preference & Adherence, 2023, v. 17, p. 1393, doi. 10.2147/PPA.S391025
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- Article
An Expert Perspective on Phosphate Dysregulation With a Focus on Chronic Hypophosphatemia.
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- Journal of Bone & Mineral Research, 2022, v. 37, n. 1, p. 12, doi. 10.1002/jbmr.4486
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- Article
Inhibition of Osteoclast Differentiation by 1.25‐D and the Calcimimetic KP2326 Reveals 1.25‐D Resistance in Advanced CKD.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 11, p. 2265, doi. 10.1002/jbmr.4122
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- Article
Maternal Transmission Ratio Distortion of GNAS Loss‐of‐Function Mutations.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 5, p. 913, doi. 10.1002/jbmr.3948
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- Article