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Select item 88266401.

Clinical, histopathologic and molecular features of idiopathic and diabetic nodular mesangial sclerosis in humans

Michael T Eadon, Sam Lampe, Mirza M Baig, Kimberly S Collins, Ricardo Melo Ferreira, Henry Mang, Ying-Hua Cheng, Daria Barwinska, Tarek M El-Achkar, Tae-Hwi Schwantes-An, Seth Winfree, Constance J Temm, Michael J Ferkowicz, Kenneth W Dunn, Katherine J Kelly, Timothy A Sutton, Sharon M Moe, Ranjani N Moorthi, Carrie L Phillips, Pierre C Dagher, for the Kidney Precision Medicine Project

Nephrol Dial Transplant. 2022 Jan; 37(1): 72–84. Published online 2021 Feb 4. doi: 10.1093/ndt/gfaa331

PMCID:: PMC8826640

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Select item 86660292.

Mesangial sclerosis in a patient with type 1 diabetes following simultaneous pancreas-kidney transplantation despite maintenance of normoglycemia: a case report

Boonphiphop Boonpheng, Jonathan E. Zuckerman, Gerald S. Lipshutz, Gabriel M. Danovitch, Angela Phelps, Michele Pena, Julie M. Yabu

BMC Nephrol. 2021; 22: 412. Published online 2021 Dec 11. doi: 10.1186/s12882-021-02620-7

PMCID:: PMC8666029

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Select item 34595283.

Diffuse mesangial sclerosis – Report of two cases

M. Vankalakunti, P. K. Jha, R. M. Madraki, V. Siddini, K. Babu, S. H. Ballal

Indian J Nephrol. 2012 May-Jun; 22(3): 213–216. doi: 10.4103/0971-4065.98764

PMCID:: PMC3459528

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Select item 33299664.

RESPIRATORY CHAIN DEFICIENCY PRESENTING AS DIFFUSE MESANGIAL SCLEROSIS WITH NPHS3 MUTATION

Esra Baskin, Umut Selda Bayrakci, Füsun Alehan, Handan Ozdemir, Ayse Oner, Rita Horvath, Friedhelm Hildebrandt, V Vega-Varner, Fatih Ozaltın

Pediatr Nephrol. Author manuscript; available in PMC 2012 Apr 19.

Published in final edited form as: Pediatr Nephrol. 2011 Jul; 26(7): 1157–1161. Published online 2011 Mar 2. doi: 10.1007/s00467-011-1814-0

PMCID:: PMC3329966

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Select item 27339675.

Two Cases of Isolated Diffuse Mesangial Sclerosis with WT1 Mutations

Hyewon Hahn, Young Mi Cho, Young Seo Park, Han Wook You, Hae Il Cheong

J Korean Med Sci. 2006 Feb; 21(1): 160–164. Published online 2006 Feb 20. doi: 10.3346/jkms.2006.21.1.160

PMCID:: PMC2733967

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Select item 18775156.

Glomerular lesions in mice transgenic for growth hormone and insulinlike growth factor-I. I. Relationship between increased glomerular size and mesangial sclerosis.

T. Doi, L. J. Striker, C. C. Gibson, L. Y. Agodoa, R. L. Brinster, G. E. Striker

Am J Pathol. 1990 Sep; 137(3): 541–552.

PMCID:: PMC1877515

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Select item 18534397.

WT1 and PAX-2 Podocyte Expression in Denys-Drash Syndrome and Isolated Diffuse Mesangial Sclerosis

Youxin Yang, Cécile Jeanpierre, Gregory R. Dressler, Mireille Lacoste, Patrick Niaudet, Marie-Claire Gubler

Am J Pathol. 1999 Jan; 154(1): 181–192. doi: 10.1016/S0002-9440(10)65264-9

PMCID:: PMC1853439

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Select item 13770458.

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.

C Jeanpierre, E Denamur, I Henry, M O Cabanis, S Luce, A Cécille, J Elion, M Peuchmaur, C Loirat, P Niaudet, M C Gubler, C Junien

Am J Hum Genet. 1998 Apr; 62(4): 824–833. doi: 10.1086/301806

PMCID:: PMC1377045

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Select item 10496729.

Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

B Z Garty, B Eisenstein, J Sandbank, S Kaffe, R Dagan, N Gadoth

J Med Genet. 1994 Feb; 31(2): 121–125. doi: 10.1136/jmg.31.2.121

PMCID:: PMC1049672

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Select item 853139410.

Creation of X-linked Alport syndrome rat model with Col4a5 deficiency

Masumi Namba, Tomoe Kobayashi, Mayumi Kohno, Takayuki Koyano, Takuo Hirose, Masaki Fukushima, Makoto Matsuyama

Sci Rep. 2021; 11: 20836. Published online 2021 Oct 21. doi: 10.1038/s41598-021-00354-y

Correction in:: Sci Rep. 2021; 11: 22137.

PMCID:: PMC8531394

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Select item 747641411.

Clinical utility of ultra-rapid whole-genome sequencing in an infant with atypical presentation of WT1-associated nephrotic syndrome type 4

Erica Sanford, Terence Wong, Katarzyna A. Ellsworth, Elizabeth Ingulli, Stephen F. Kingsmore

Cold Spring Harb Mol Case Stud. 2020 Aug; 6(4): a005470. doi: 10.1101/mcs.a005470

PMCID:: PMC7476414

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Select item 744618712.

Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature

Daisuke Matsuoka, Shunsuke Noda, Motoko Kamiya, Yoshihiko Hidaka, Hisashi Shimojo, Yasushi Yamada, Tsutomu Miyamoto, Kandai Nozu, Kazumoto Iijima, Hiroyasu Tsukaguchi

BMC Nephrol. 2020; 21: 362. Published online 2020 Aug 24. doi: 10.1186/s12882-020-02007-0

PMCID:: PMC7446187

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Select item 599046113.

COQ2 nephropathy: A treatable cause of nephrotic syndrome in children

Michelle C. Starr, Irene J. Chang, Laura S. Finn, Angela Sun, Austin A. Larson, Jens Goebel, Coral Hanevold, Jenny Thies, Johan L.K. Van Hove, Sangeeta R. Hingorani, Christina Lam

Pediatr Nephrol. Author manuscript; available in PMC 2019 Jul 1.

Published in final edited form as: Pediatr Nephrol. 2018 Jul; 33(7): 1257–1261. Published online 2018 Apr 10. doi: 10.1007/s00467-018-3937-z

PMCID:: PMC5990461

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Select item 551638514.

Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report

Joseph L. Alge, Scott E. Wenderfer, John Hicks, Mir Reza Bekheirnia, Deborah A. Schady, Jamey S. Kain, Michael C. Braun

BMC Nephrol. 2017; 18: 243. Published online 2017 Jul 18. doi: 10.1186/s12882-017-0643-1

PMCID:: PMC5516385

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Select item 502767515.

Expansion of phenotype and genotypic data in CRB2-related syndrome

Ryan E Lamont, Wen-Hann Tan, A Micheil Innes, Jillian S Parboosingh, Dina Schneidman-Duhovny, Aleksandar Rajkovic, John Pappas, Pablo Altschwager, Stephanie DeWard, Anne Fulton, Kathryn J Gray, Max Krall, Lakshmi Mehta, Lance H Rodan, Devereux N Saller, Jr, Deanna Steele, Deborah Stein, Svetlana A Yatsenko, François P Bernier, Anne M Slavotinek

Eur J Hum Genet. 2016 Oct; 24(10): 1436–1444. Published online 2016 Mar 23. doi: 10.1038/ejhg.2016.24

PMCID:: PMC5027675

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Select item 469656616.

Podocyte-Specific Deletion of Yes-Associated Protein Causes FSGS and Progressive Renal Failure

Monica Schwartzman, Antoine Reginensi, Jenny S. Wong, John M. Basgen, Kristin Meliambro, Susanne B. Nicholas, Vivette D'Agati, Helen McNeill, Kirk N. Campbell

J Am Soc Nephrol. 2016 Jan; 27(1): 216–226. Published online 2015 May 26. doi: 10.1681/ASN.2014090916

PMCID:: PMC4696566

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Select item 442224717.

Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

Anja Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, Kerstin Benz, Marcus R. Benz, Klemens Budde, Anja K. Büscher, Thomas Fehr, Markus Feldkötter, Norbert Graf, Britta Höcker, Therese Jungraithmayr, Günter Klaus, Birgit Koehler, Martin Konrad, Birgitta Kranz, Carmen R. Montoya, Dominik Müller, Thomas J. Neuhaus, Jun Oh, Lars Pape, Martin Pohl, Brigitte Royer-Pokora, Uwe Querfeld, Reinhard Schneppenheim, Hagen Staude, Giuseppina Spartà, Kirsten Timmermann, Frauke Wilkening, Simone Wygoda, Carsten Bergmann, Markus J. Kemper

Clin J Am Soc Nephrol. 2015 May 7; 10(5): 825–831. Published online 2015 Mar 27. doi: 10.2215/CJN.10141014

PMCID:: PMC4422247

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Select item 417694918.

Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years

Jameela A. Kari, Giovanni Montini, Detlef Bockenhauer, Eileen Brennan, Lesley Rees, Richard S. Trompeter, Kjell Tullus, William van’t Hoff, Aoife Waters, Emma Ashton, Nicholas Lench, Neil J. Sebire, Stephen D. Marks

Pediatr Nephrol. 2014; 29(11): 2173–2180. Published online 2014 Jun 6. doi: 10.1007/s00467-014-2856-x

PMCID:: PMC4176949

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Select item 313757419.

Parietal Epithelial Cells Participate in the Formation of Sclerotic Lesions in Focal Segmental Glomerulosclerosis

Bart Smeets, Christoph Kuppe, Eva-Maria Sicking, Astrid Fuss, Peggy Jirak, Toin H. van Kuppevelt, Karlhans Endlich, Jack F.M. Wetzels, Hermann-Josef Gröne, Jürgen Floege, Marcus J. Moeller

J Am Soc Nephrol. 2011 Jul; 22(7): 1262–1274. doi: 10.1681/ASN.2010090970

PMCID:: PMC3137574

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Select item 311884020.

Advances in the Biology and Genetics of the Podocytopathies: Implications for Diagnosis and Therapy

Laura Barisoni, H. William Schnaper, Jeffrey B. Kopp

Arch Pathol Lab Med. Author manuscript; available in PMC 2011 Jun 21.

Published in final edited form as: Arch Pathol Lab Med. 2009 Feb; 133(2): 201–216. doi: 10.1043/1543-2165-133.2.201

PMCID:: PMC3118840

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