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Profound Changes in Functional Structure and Dynamics of Serum Albumin in Children with Nephrotic Syndrome: An Exploratory Research Study

Journal of medicinal chemistry, 2023-09, Vol.66 (17), p.12115-12129

2023

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Single Extracellular Vesicle Analysis Performed by Imaging Flow Cytometry and Nanoparticle Tracking Analysis Evaluate the Accuracy of Urinary Extracellular Vesicle Preparation Techniques Differently

International journal of molecular sciences, 2021-11, Vol.22 (22), p.12436

2021

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Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome

Clinical journal of the American Society of Nephrology, 2016-02, Vol.11 (2), p.245-253

2016

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Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome

Clinical journal of the American Society of Nephrology, 2010-11, Vol.5 (11), p.2075-2084

2010

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TRPC6 G757D Loss-of-Function Mutation Associates with FSGS

Journal of the American Society of Nephrology, 2016-09, Vol.27 (9), p.2771-2783

2016

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Examination of the eye and retinal alterations in primary hyperoxaluria type 1

Nephrology, dialysis, transplantation, 2022-01, Vol.37 (2), p.255-257

2022

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Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Scientific reports, 2019-05, Vol.9 (1), p.7919-7919, Article 7919

2019

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Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1

Clinical journal of the American Society of Nephrology, 2015-05, Vol.10 (5), p.825-831

2015

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Growth in Very Young Children Undergoing Chronic Peritoneal Dialysis

Journal of the American Society of Nephrology, 2011-12, Vol.22 (12), p.2303-2312

2011

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Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients

Clinical nephrology, 2012-07, Vol.78 (1), p.47-53

2012

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Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD

Scientific reports, 2021-11, Vol.11 (1), p.21677-21677, Article 21677

2021

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Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age

Frontiers in medicine, 2022-10, Vol.9, p.953643-953643

2022

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A multi-center interventional study to assess pharmacokinetics, effectiveness, and tolerability of prolonged-release tacrolimus after pediatric kidney transplantation: study protocol for a prospective, open-label, randomized, two-phase, two-sequence, single dose, crossover, phase III b trial

Frontiers in Nephrology (Online), 2024-02, Vol.4

2024

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Patients With Infantile Nephropathic Cystinosis in Germany and Austria: A Retrospective Cohort Study

Frontiers in medicine, 2022-04, Vol.9, p.864554-864554

2022

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COL4A5-associated X-linked Alport syndrome in a female patient with early inner ear deafness due to a mutation in MYH9

Nephrology, dialysis, transplantation, 2012-11, Vol.27 (11), p.4236-4240

2012

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Bone and Mineral Metabolism in Children with Nephropathic Cystinosis Compared with other CKD Entities

The journal of clinical endocrinology and metabolism, 2020-08, Vol.105 (8), p.e2738-e2752

2020

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Characteristic Alterations of Bone and Mineral Metabolism in Children and Adults with Nephropathic Cystinosis: SA-PO298

Journal of the American Society of Nephrology, 2023-11, Vol.34 (11S), p.805-805

2023

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1443 Bone and mineral metabolism in patients with nephropathic cystinosis as a function of age and eGFR

Nephrology, dialysis, transplantation, 2024-05, Vol.39 (Supplement_1)

2024

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Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies

Clinical journal of the American Society of Nephrology, 2017-12, Vol.12 (12), p.1974-1983

2017

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Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study

Transplantation, 2019-06, Vol.103 (6), p.1224-1233

2019

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5036 THE OUTCOME OF LUMASIRAN TREATMENT IN 10 PAEDIATRIC PATIENTS WITH PRIMARY HYPEROXALURIA TYPE 1

Nephrology, dialysis, transplantation, 2023-06, Vol.38 (Supplement_1)

2023

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Cystinosis-Associated Metabolic Bone Disease Across Ages and CKD Stages 1 to 5D/T

The journal of clinical endocrinology and metabolism, 2024-07

2024

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Hämaturiediagnostik bei Kindern

Der Nephrologe, 2022-05, Vol.17 (3), p.141-147

Büscher, Anja K.

2022

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Clinical Outcome After Combined Liver and Kidney Transplantation in Children in Europe: A CERTAIN Registry Analysis: PO2143

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.655-656

2021

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Profound Changes in Functional Structure and Dynamics of Serum Albumin in Children with Nephrotic Syndrome: An Exploratory Research Study

Single Extracellular Vesicle Analysis Performed by Imaging Flow Cytometry and Nanoparticle Tracking Analysis Evaluate the Accuracy of Urinary Extracellular Vesicle Preparation Techniques Differently

Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome

Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome

TRPC6 G757D Loss-of-Function Mutation Associates with FSGS

Examination of the eye and retinal alterations in primary hyperoxaluria type 1

Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1

Growth in Very Young Children Undergoing Chronic Peritoneal Dialysis

Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients

Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD

Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age

A multi-center interventional study to assess pharmacokinetics, effectiveness, and tolerability of prolonged-release tacrolimus after pediatric kidney transplantation: study protocol for a prospective, open-label, randomized, two-phase, two-sequence, single dose, crossover, phase III b trial

Patients With Infantile Nephropathic Cystinosis in Germany and Austria: A Retrospective Cohort Study

COL4A5-associated X-linked Alport syndrome in a female patient with early inner ear deafness due to a mutation in MYH9

Bone and Mineral Metabolism in Children with Nephropathic Cystinosis Compared with other CKD Entities

Characteristic Alterations of Bone and Mineral Metabolism in Children and Adults with Nephropathic Cystinosis: SA-PO298

1443 Bone and mineral metabolism in patients with nephropathic cystinosis as a function of age and eGFR

Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies

Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study

5036 THE OUTCOME OF LUMASIRAN TREATMENT IN 10 PAEDIATRIC PATIENTS WITH PRIMARY HYPEROXALURIA TYPE 1

Cystinosis-Associated Metabolic Bone Disease Across Ages and CKD Stages 1 to 5D/T

Isolated nocturnal and isolated daytime hypertension associate with altered cardiovascular morphology and function in children with chronic kidney disease: findings from the Cardiovascular Comorbidity in Children with Chronic Kidney Disease study

Hämaturiediagnostik bei Kindern

Clinical Outcome After Combined Liver and Kidney Transplantation in Children in Europe: A CERTAIN Registry Analysis: PO2143

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