Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Prabha Senguttuvan"'
Autor:
Chen-Han Wilfred Wu, Tze Y. Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum, Sophia Schneider, Nina Mann, Dervla M. Connaughton, Makiko Nakayama, Amelie T. van der Ven, Rufeng Dai, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Natasa Stajic, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan M. Fathy, Danko Milosevic, Daniel Turudic, Muna Al Saffar, Hazem S. Awad, Loai A. Eid, Aravind Ramanathan, Prabha Senguttuvan, Shrikant M. Mane, Richard S. Lee, Stuart B. Bauer, Weining Lu, Alina C. Hilger, Velibor Tasic, Shirlee Shril, Simone Sanna-Cherchi, Friedhelm Hildebrandt
Publikováno v:
European Urology Open Science, Vol 44, Iss , Pp 106-112 (2022)
Background: Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease among children and adults younger than 30 yr. In our previous study, whole-exome sequencing (WES) identified a known monogen
Externí odkaz:
https://doaj.org/article/3efb0bd1ab7841249ffc6b6938766552
Autor:
Aravind S.K. Ramanathan, Prabha Senguttuvan, Vel Prakash, Appasamy Vengadesan, Rajendiran Padmaraj
Publikováno v:
Journal of Family and Community Medicine, Vol 23, Iss 1, Pp 38-42 (2016)
Background: Since the data of primary hypertension (HT) in children is scanty in India, this study attempted to evaluate HT by a multidimensional investigation of the various risk factors in children and adolescents. Materials and Methods: A total of
Externí odkaz:
https://doaj.org/article/1b6e20534560478a9666170f30c7975a
Autor:
Amelie T van der Ven, Birgit Kobbe, Stefan Kohl, Shirlee Shril, Hans-Martin Pogoda, Thomas Imhof, Hadas Ityel, Asaf Vivante, Jing Chen, Daw-Yang Hwang, Dervla M Connaughton, Nina Mann, Eugen Widmeier, Mary Taglienti, Johanna Magdalena Schmidt, Makiko Nakayama, Prabha Senguttuvan, Selvin Kumar, Velibor Tasic, Elijah O Kehinde, Shrikant M Mane, Richard P Lifton, Neveen Soliman, Weining Lu, Stuart B Bauer, Matthias Hammerschmidt, Raimund Wagener, Friedhelm Hildebrandt
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0191224 (2018)
Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause (40-50%) of chronic kidney disease (CKD) in children. About 40 monogenic causes of CAKUT have so far been discovered. To date less than 20% of CAKUT cases can be e
Externí odkaz:
https://doaj.org/article/2bc11b7231c74bacbf98e8696e293ebc
Autor:
Mahesh Kumar Kempanahalli Basappa, Prabha Senguttuvan, Ramprasad Elumalai, Bhaskar Lakkakula VKS, Soundararajan Periasamy
Publikováno v:
Journal of Nephropharmacology, Vol 4, Iss 2, Pp 52-56 (2015)
Introduction: Nephrotic syndrome (NS) is the most frequent cause of proteinuria in children and is emerging as a leading cause of uremia. Among idiopathic NS, 10% of children do not respond to steroids or to any other immunosuppressive therapy, and p
Externí odkaz:
https://doaj.org/article/d9602695e7784ed5a704dbc5186fef21
Autor:
Aravind Ramanathan, Prabha Senguttuvan, Vel Prakash, Appasamy Vengadesan, Rajendiran Padmaraj
Publikováno v:
Journal of Family and Community Medicine, Vol 24, Iss 1, Pp 56-56 (2017)
Externí odkaz:
https://doaj.org/article/0a203f053d4c41f086a71c736197e2f9
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 24, Iss 1, Pp 139-140 (2013)
Externí odkaz:
https://doaj.org/article/ce4c07deedcd4c97b5a3bc83cd28b08b
Autor:
Danielle J. Owen, David FitzPatrick, Nina Mann, Stuart B. Bauer, Ilona Krey, Heather C Mefford, Jacob Zyskind, Roger Fick, Ana C. Onuchic-Whitford, Floor A. M. Duijkers, Etienne Coyaud, Simon E. Fisher, Juliann M. Savatt, Richard P. Lifton, Isabel Ottlewski, Amelie T. van der Ven, Peter J. Hulick, Nancy Rodig, Michelle A. Baum, Marielle Alders, Elysa J. Marco, Konrad Platzer, Ghaleb Daouk, Hadas Ityel, Eva H. Brilstra, Ian A. Glass, Heiko Reutter, Adda L. Graham-Paquin, Makiko Nakayama, Michael A. J. Ferguson, Amy Kolb, Weining Lu, Florian Buerger, Prabha Senguttuvan, Marcia Ferguson, Ronen Schneider, Isabelle Thiffault, Hila Milo Rasouly, Verena Klämbt, Tobias Bartolomaeus, Evan Chen, Mao Youying, Amar J. Majmundar, Jia Rao, Carrie Costin, Dina Ahram, Ali G. Gharavi, Lot Snijders Blok, Avram Z. Traum, Franziska Kause, Konstantin Deutsch, Arianna Vino, Dervla M. Connaughton, Antonie D. Kline, Deborah R. Stein, Daanya Salmanullah, Maxime Bouchard, Estelle M.N. Laurent, Audrey Squire, Daniel G. MacArthur, Kristen M. Laricchia, Asaf Vivante, Thomas M. Kitzler, Jonathan St-Germain, Brian Raught, Heidi L. Rehm, Ellen van Binsbergen, Chen Han Wilfred Wu, Caroline M. Kolvenbach, Monkol Lek, Selvin Kumar, Jing Chen, Mustafa K. Khokha, Ankana Daga, Hong Xu, Andrew D. Sharrocks, N. V. Shcherbakova, Simone Sanna-Cherchi, Inna S. Povolotskaya, Tze Y Lim, Johanna M. Rieke, Katrina M. Dipple, Gabriel C. Dworschak, Michael J. Somers, Tobias Hermle, Stefan Kohl, Steve Seltzsam, Victoria Y. Voinova, Shirlee Shril, Ingrid M. Wentzensen, Daw Yang Hwang, Velibor Tasic, Shrikant Mane, Jonathan Marquez, Friedhelm Hildebrandt, Rufeng Dai, Paulien A Terhal, Loai A. Eid, Thomas D. Challman
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, 2020, 107 (4), pp.727-742. ⟨10.1016/j.ajhg.2020.08.013⟩
American journal of human genetics, 107(4), 727-742. Cell Press
Am J Hum Genet
American Journal of Human Genetics, 107, 4, pp. 727-742
American Journal of Human Genetics, Elsevier (Cell Press), 2020, 107 (4), pp.727-742. ⟨10.1016/j.ajhg.2020.08.013⟩
The American Journal of Human Genetics
American Journal of Human Genetics, 107, 727-742
American Journal of Human Genetics, 2020, 107 (4), pp.727-742. ⟨10.1016/j.ajhg.2020.08.013⟩
American journal of human genetics, 107(4), 727-742. Cell Press
Am J Hum Genet
American Journal of Human Genetics, 107, 4, pp. 727-742
American Journal of Human Genetics, Elsevier (Cell Press), 2020, 107 (4), pp.727-742. ⟨10.1016/j.ajhg.2020.08.013⟩
The American Journal of Human Genetics
American Journal of Human Genetics, 107, 727-742
International audience; Congenital anomalies of the kidney and urinary tract (CAKUT) constitute one of the most frequent birth defects and represent the most common cause of chronic kidney disease in the first three decades of life. Despite the disco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0bcf100f3cbcb4de0590d4409d43436
http://www.scopus.com/inward/record.url?scp=85091260805&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85091260805&partnerID=8YFLogxK
Autor:
Friedhelm Hildebrandt, Velibor Tasic, Shrikant Mane, Jameela A. Kari, Natasa Stajic, Nina Mann, Shirlee Shril, Richard P. Lifton, Zaheer Valivullah, Thomas M. Kitzler, Monkol Lek, Stefan Kohl, Sherif El Desoky, Ronen Schneider, Chen-Han W. Wu, Rufeng Dai, Amar J. Majmundar, Makiko Nakayama, Prabha Senguttuvan, Radovan Bogdanovic, Dervla M. Connaughton, Caroline M. Kolvenbach
Publikováno v:
Hum Genet
INTRODUCTION: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease (~45%) that manifests before 30 years of age. The genetic locus containing COL4A1 (13q33–34) has been implicated in vesic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8df72788d1165e3f56ef9ffe670e3647
https://doi.org/10.1007/s00439-019-02042-4
https://doi.org/10.1007/s00439-019-02042-4
Autor:
Kassaundra Amann, Richard P. Lifton, Shirlee Shril, Weizhen Tan, Aravind Selvin, Avram Z. Traum, Jameela A. Kari, Nancy Rodig, Rufeng Dai, Leslie Spaneas, David Schapiro, Daniela A. Braun, Jing Chen, Michelle A. Baum, Friedhelm Hildebrandt, Julian Schulz, Shazia Ashraf, Heiko Reutter, Ali Amar, Ronen Schneider, Prabha Senguttuvan, Michael A. J. Ferguson, Weining Lu, Thomas M. Kitzler, Hannah Hugo, Makiko Nakayama, Radovan Bogdanovic, Asaf Vivante, Daniel G. MacArthur, Hanan M. Fathy, Charlotte A. Hoogstraaten, Simone Sanna-Cherchi, Sherif El Desoky, Ghaleb Daouk, Natasa Stajic, Loai A. Eid, Deborah R. Stein, Amar J. Majmundar, Ankana Daga, Michael W. Wilson, Caroline M. Kolvenbach, Franziska Kause, Hazem S. Awad, Heidi L. Rehm, Velibor Tasic, Jillian K. Warejko, Shrikant Mane, Monkol Lek, Tobias Hermle, Richard S. Lee, Muna Al-Saffar, Neveen A. Soliman, Nina Mann, Stuart B. Bauer, Amelie T. van der Ven, Kristen M. Laricchia, Daw-Yang Hwang, Hadas Ityel, Danko Milosevic, Dervla M. Connaughton, Michael J. Somers, Eugen Widmeier, Tilman Jobst-Schwan, Johanna Magdalena Schmidt
Publikováno v:
Journal of the American Society of Nephrology, 29, 2348-2361
Journal of the American Society of Nephrology, 29, 9, pp. 2348-2361
Journal of the American Society of Nephrology, 29, 9, pp. 2348-2361
Item does not contain fulltext BACKGROUND: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most prevalent cause of kidney disease in the first three decades of life. Previous gene panel studies showed monogenic causation in up to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ee9b271c4fd4ef6df96cbcc3f821337
https://hdl.handle.net/2066/200746
https://hdl.handle.net/2066/200746
WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome
Autor:
Srilakshmi Rajagopal, Aravind Selvin Kumar Ramanathan, Prabha Senguttuvan, Padmaraj Rajendiran, Murali Vijayan
Publikováno v:
Molecular and Cellular Biochemistry. 426:177-181
Nephrotic syndrome (NS) is a kidney disease predominantly present in children with idiopathic condition; final stage of the disease progresses into end-stage renal disease. Generally, NS is treated using standard steroid therapy, however; most of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af35bfe690dc9e67cae5782e6a188ae6
https://doi.org/10.1007/s11010-016-2889-5
https://doi.org/10.1007/s11010-016-2889-5