Bärbel Lange-Sperandio

Author

Ludwig-Maximilians-Universität München ORCID

Also Known As

B. Lange-Sperandio, Baerbel Lange-Sperandio, Barbel Lange-Sperandio, Bärbel Lange-Sperandio, Bärbel Lange-Sperandio, Felix Lechner, L BARBEL, Lange-Sperandio, Bärbel

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Heidelberg University Medizinische Hochschule Hannover University Hospital Cologne University Hospital Heidelberg

About

Bärbel Lange-Sperandio is an author at Ludwig-Maximilians-Universität München specializing in medicine, nephrology, and chronic kidney disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	653
2	Cellular Physiology	4	4	274
3	Cell Biology	3	3	155
4	Engineering	1	1	18
5	Public Health	1	1	81

Bärbel Lange-Sperandio

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid–Resistant Nephrotic Syndrome Anja Büscher, Bodo B. Beck, Anette Melk, Clinical Journal of the American Society of Nephrology	2015	138
Ureteral obstruction in neonatal mice elicits segment-specific tubular cell responses leading to nephron loss11See Editorial by Woolf, p. 761. François Cachat, Bärbel Lange-Sperandio, Alice Y. Chang, Kidney International Urological ResearchUrologyDevelopmental BiologyLoss11see EditorialRenal Function	2003	119
Leukocytes Induce Epithelial to Mesenchymal Transition after Unilateral Ureteral Obstruction in Neonatal Mice Bärbel Lange-Sperandio, Agnes Trautmann, Oliver Eickelberg, American Journal Of Pathology Regenerative MedicineUrologyTissue DevelopmentDevelopmental BiologyOrgan Development	2007	100
Selectins mediate macrophage infiltration in obstructive nephropathy in newborn mice11See Editorial by Kipari and Hughes, p. 760. Bärbel Lange-Sperandio, François Cachat, Barbara A. Thornhill, Kidney International InflammationGlomerulonephritisRenal FunctionMedicineKidney Failure	2002	88
Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants Kathrin Burgmaier, Leonie Violetta Brinker, Florian Erger, Kidney International UrologyGenetic DisorderMedicineGeneticsGenotype–phenotype Correlations	2021	81
Sialyltransferase ST3Gal-IV controls CXCR2-mediated firm leukocyte arrest during inflammation David Frommhold, Andreas Ludwig, M. Gabriele Bixel, The Journal of Experimental Medicine	2008	80
The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε Karolis Ažukaitis, Eva Šimková, Mohammad Abdul Majid, Journal of the American Society of Nephrology	2017	59
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, The Journal of Pediatrics GlomerulonephritisHemodialysisUrologyRenal DiseaseRenal Function	2018	58
The mitochondrial thioredoxin reductase system (TrxR2) in vascular endothelium controls peroxynitrite levels and tissue integrity Petra Kameritsch, Miriam Singer, Christoph Nuernbergk, Proceedings of the National Academy of Sciences	2021	57
Transitional Care and Adherence of Adolescents and Young Adults After Kidney Transplantation in Germany and Austria Martin Kreuzer, Jenny Prüfe, Martina Oldhafer, Medicine	2015	44

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