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Mansoureh Tabatabaeifar

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Pediatric Nephrology (Berlin, Germany)|December 20, 2012
Animal models of nephrotic syndromeIvana Simic, Mansoureh Tabatabaeifar, Franz Schaefer
Stem Cell Research|September 17, 2025
iPSC line DHMCi019-A is generated from a patient with hereditary nephrotic syndrome harboring compound heterozygous NPHS2 variantsMansoureh Tabatabaeifar, Robert Matthes, Karin Burau, et al.
Stem Cell Research|September 20, 2025
iPSC line DHMCi010-A is derived from a hereditary nephrotic syndrome patient with an autosomal recessive NPHS2 mutationRobert Matthes, Mansoureh Tabatabaeifar, Karin Burau, et al.
Stem Cell Research|October 23, 2021
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 geneMansoureh Tabatabaeifar, Theresa Leonie Fluhr, Hanna Syring, et al.
Stem Cell Research|October 25, 2021
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 geneTheresa Leonie Fluhr, Mansoureh Tabatabaeifar, Hanna Syring, et al.
Journal of Pediatric Genetics|August 22, 2022
Molecular Study of Childhood Steroid-Resistant Nephrotic Syndrome: A Hospital-Based StudyAkanksha Singh, Ankur Singh, Om Prakash Mishra, et al.
Pediatric Nephrology (Berlin, Germany)|August 18, 2009
Functional analysis of BMP4 mutations identified in pediatric CAKUT patientsMansoureh Tabatabaeifar, Karl-Peter Schlingmann, Mieczyslaw Litwin, et al.
Plos One|October 20, 2017
An inducible mouse model of podocin-mutation-related nephrotic syndromeMansoureh Tabatabaeifar, Tanja Wlodkowski, Ivana Simic, et al.
Kidney International Reports|October 27, 2025
GDF-15 and uEGF Independently Associate With CKD Progression in ChildrenJulia Bartels, Mansoureh Tabatabaeifar, Marietta Kirchner, et al.
Kidney International|June 1, 2022
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyStefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatric Nephrology (Berlin, Germany)|December 20, 2012
Animal models of nephrotic syndromeIvana Simic, Mansoureh Tabatabaeifar, Franz Schaefer
Stem Cell Research|September 17, 2025
iPSC line DHMCi019-A is generated from a patient with hereditary nephrotic syndrome harboring compound heterozygous NPHS2 variantsMansoureh Tabatabaeifar, Robert Matthes, Karin Burau, et al.
Stem Cell Research|September 20, 2025
iPSC line DHMCi010-A is derived from a hereditary nephrotic syndrome patient with an autosomal recessive NPHS2 mutationRobert Matthes, Mansoureh Tabatabaeifar, Karin Burau, et al.
Stem Cell Research|October 23, 2021
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 geneMansoureh Tabatabaeifar, Theresa Leonie Fluhr, Hanna Syring, et al.
Stem Cell Research|October 25, 2021
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 geneTheresa Leonie Fluhr, Mansoureh Tabatabaeifar, Hanna Syring, et al.
Journal of Pediatric Genetics|August 22, 2022
Molecular Study of Childhood Steroid-Resistant Nephrotic Syndrome: A Hospital-Based StudyAkanksha Singh, Ankur Singh, Om Prakash Mishra, et al.
Pediatric Nephrology (Berlin, Germany)|August 18, 2009
Functional analysis of BMP4 mutations identified in pediatric CAKUT patientsMansoureh Tabatabaeifar, Karl-Peter Schlingmann, Mieczyslaw Litwin, et al.
Plos One|October 20, 2017
An inducible mouse model of podocin-mutation-related nephrotic syndromeMansoureh Tabatabaeifar, Tanja Wlodkowski, Ivana Simic, et al.
Kidney International Reports|October 27, 2025
GDF-15 and uEGF Independently Associate With CKD Progression in ChildrenJulia Bartels, Mansoureh Tabatabaeifar, Marietta Kirchner, et al.
Kidney International|June 1, 2022
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyStefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.
Pageof 2