L. Patzer

发表

Day- and night-time blood pressure elevation in children with higher grades of renal scarring.

T. Seeman, J. Janda, E. Wühl, 2003, The Journal of pediatrics.

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

B. Tönshoff, D. Haffner, L. Pape, 2022, Frontiers in Medicine.

Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a multicentre, international, prospective cohort study

Merin K Kurian, F. O. Kumolalo, A. S. Arar, 2021, The Lancet.

Treatment and long-term outcome in primary distal renal tubular acidosis.

F. Trepiccione, G. Gambaro, Z. Gucev, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)

M. Marlais, M. Litwin, L. Weber, 2020, Scientific Reports.

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

A. Anarat, S. Schmidt, S. Testa, 2018, The Journal of pediatrics.

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

A. Bakkaloğlu, F. Hildebrandt, J. Haas, 2004, Kidney international.

Renal function following hematological stem cell transplantation in childhood

K. Kentouche, J. Misselwitz, L. Patzer, 2003, Pediatric Nephrology.

Contrast-enhanced sonography of vesicoureterorenal reflux in children: preliminary results.

U. John, S. Vogt, J. Misselwitz, 1999, AJR. American journal of roentgenology.

Cluster of hemolytic-uremic syndrome caused by Shiga toxin-producing Escherichia coli O26:H11

H. Karch, U. John, J. Misselwitz, 2003, The Pediatric infectious disease journal.

Urinary supersaturation of calcium oxalate and phosphate in patients with X-linked hypophosphatemic rickets and in healthy schoolchildren.

T. Barratt, M. Dillon, G. Kasidas, 1999, The Journal of pediatrics.

X-linked hypophosphataemic rickets: Recognition, treatment and prognosis

W. Hoff, M. Dillon, L. Patzer, 1998 .

C. Eng, T. Fehr, K. Budde, 2011, Annals of human genetics.

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

T. Meitinger, V. Tasic, B. Tönshoff, 2022, Frontiers in Medicine.

Ifosfamide metabolites CAA, 4-OH-Ifo and Ifo-mustard reduce apical phosphate transport by changing NaPi-IIa in OK cells.

B. Beck-Schimmer, H. Murer, U. Ziegler, 2006, Kidney international.

Diagnosis of Alport syndrome—search for proteomic biomarkers in body fluids

M. Walther, O. Witzke, M. Feldkötter, 2013, Pediatric Nephrology.

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

M. Marlais, L. Weber, D. Mekahli, 2021, Scientific Reports.

Renal function after conditioning therapy for bone marrow transplantation in childhood.

M. Debroe, F. Zintl, M. Brandis, 1997, Medical and pediatric oncology.

Renal function in long-term survivors of stem cell transplantation in childhood. A prospective trial

F. Zintl, M. Brandis, K. Kentouche, 2001, Bone Marrow Transplantation.

Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndrome.

L. Weber, J. Dötsch, L. Pape, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Multicentre approach to epidemiological aspects of craniosynostosis in Germany.

S. Kropf, R. Haase, G. Jorch, 2018, The British journal of oral & maxillofacial surgery.

Growth impairment after ifosfamide‐induced nephrotoxicity in children

W. Stöhr, T. Langer, J. Beck, 2007, Pediatric blood & cancer.

Nephrotoxicity as a cause of acute kidney injury in children

L. Patzer, 2008, Pediatric Nephrology.

Epidemiological Approach to Identifying Genetic Predispositions for Atypical Hemolytic Uremic Syndrome

K. Budde, H. Neumann, M. Zeier, 2010, Annals of human genetics.

Blood Pressure, Renal Function, and Proteinuria in Children with Unilateral Renal Agenesis

T. Seeman, J. Janda, J. Dušek, 2006, Kidney and Blood Pressure Research.

Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathies

J. Gerss, B. Tönshoff, P. Pennekamp, 2020, Journal of Medical Genetics.

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.

M. Konrad, E. Levtchenko, C. Wagner, 2016, Journal of the American Society of Nephrology : JASN.

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease.

T. Friedrich, R. Thakker, T. Jentsch, 2000, Journal of the American Society of Nephrology : JASN.

Molecular Characteristics of German G8P[4] Rotavirus Strain GER1H-09 Suggest that a Genotyping and Subclassification Update Is Required for G8

U. Liebert, L. Petersen, C. Pietsch, 2009, Journal of Clinical Microbiology.

HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry

N. Ortiz-Brüchle, L. Weber, B. Tönshoff, 2019, Pediatric Nephrology.

Renal artery stenosis and aneurysmatic dilatation of arteria carotis interna in tuberous sclerosis complex

J. Misselwitz, L. Patzer, S. Basche, 2002, Pediatric Nephrology.

Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.

K. Zerres, L. Weber, D. Mekahli, 2021, Kidney international.

Oligohydramnios associated with sonographically normal kidneys.

A. Hübler, K. Amann, M. Zenker, 2012, Urology.

Potential Benefit of Probiotic E. Coli Nissle in Term Neonates

H. Proquitté, L. Patzer, D. Olbertz, 2022, Klinische Pädiatrie.

Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.

A. Boulesteix, W. Gahl, B. Tönshoff, 2022, Molecular genetics and metabolism.

Efforts to establish an animal model of Fanconi syndrome after ifosfamide administration to rats

A. Lupp, J. Misselwitz, L. Patzer, 2007, Journal of applied toxicology : JAT.

Alport syndrome associated with diffuse leiomyomatosis: COL4A5-COL4A6 deletion associated with a mild form of Alport nephropathy.

C. Antignac, M. Gubler, Y. Sado, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.