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Mato Nagel

Showing results (11-20 of 28) with videos related to

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Clinical Nephrology|June 27, 2012
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patientsAnja K Büscher, Martin Konrad, Mato Nagel, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|August 27, 2015
A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 geneWojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, et al.
Hypertension (Dallas, Tex. : 1979)|April 8, 2009
Gitelman syndromeMattias Roser, Nermin Eibl, Birgit Eisenhaber, et al.
Kidney International|July 2, 2015
Mutation in the V2 vasopressin receptor gene, AVPR2, causes nephrogenic syndrome of inappropriate diuresisLászló S Erdélyi, W Alexander Mann, Deborah J Morris-Rosendahl, et al.
Pediatric Nephrology (Berlin, Germany)|February 24, 2010
Novel heterozygous COL4A3 mutation in a family with late-onset ESRDJulia Hoefele, Bärbel Lange-Sperandio, Despina Ruessmann, et al.
Clinical and Experimental Dermatology|May 12, 2023
A 21-year-old woman with progressive asymptomatic skin laxity in flexural regionsThilo Gambichler, Sabine Hoffjan, Mato Nagel, et al.
Translational Vision Science & Technology|March 21, 2022
Characterization of Choriocapillaris and Choroidal Abnormalities in Alport SyndromeMaria Vittoria Cicinelli, Markus Ritter, Hassan Tausif, et al.
International Journal of Molecular Sciences|January 30, 2019
Kidney Injury by Variants in the <i>COL4A5</i> Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental GlomerulosclerosisJenny Frese, Matthias Kettwig, Hildegard Zappel, et al.
Clinical Nephrology|May 16, 2017
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome
Kathrin Ebner, Nadine Reintjes, Markus Feldkötter, et al.
Retina (Philadelphia, Pa.)|September 6, 2021
THE SPECTRUM OF INTERNAL LIMITING MEMBRANE DISEASE IN ALPORT SYNDROME: A Multimodal Imaging StudyMaria Vittoria Cicinelli, Markus Ritter, Cybele Ghossein, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Clinical Nephrology|June 27, 2012
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patientsAnja K Büscher, Martin Konrad, Mato Nagel, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|August 27, 2015
A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 geneWojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, et al.
Hypertension (Dallas, Tex. : 1979)|April 8, 2009
Gitelman syndromeMattias Roser, Nermin Eibl, Birgit Eisenhaber, et al.
Kidney International|July 2, 2015
Mutation in the V2 vasopressin receptor gene, AVPR2, causes nephrogenic syndrome of inappropriate diuresisLászló S Erdélyi, W Alexander Mann, Deborah J Morris-Rosendahl, et al.
Pediatric Nephrology (Berlin, Germany)|February 24, 2010
Novel heterozygous COL4A3 mutation in a family with late-onset ESRDJulia Hoefele, Bärbel Lange-Sperandio, Despina Ruessmann, et al.
Clinical and Experimental Dermatology|May 12, 2023
A 21-year-old woman with progressive asymptomatic skin laxity in flexural regionsThilo Gambichler, Sabine Hoffjan, Mato Nagel, et al.
Translational Vision Science & Technology|March 21, 2022
Characterization of Choriocapillaris and Choroidal Abnormalities in Alport SyndromeMaria Vittoria Cicinelli, Markus Ritter, Hassan Tausif, et al.
International Journal of Molecular Sciences|January 30, 2019
Kidney Injury by Variants in the <i>COL4A5</i> Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental GlomerulosclerosisJenny Frese, Matthias Kettwig, Hildegard Zappel, et al.
Clinical Nephrology|May 16, 2017
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome
Kathrin Ebner, Nadine Reintjes, Markus Feldkötter, et al.
Retina (Philadelphia, Pa.)|September 6, 2021
THE SPECTRUM OF INTERNAL LIMITING MEMBRANE DISEASE IN ALPORT SYNDROME: A Multimodal Imaging StudyMaria Vittoria Cicinelli, Markus Ritter, Cybele Ghossein, et al.
Pageof 3