1986 …2020
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Fingerprint The Fingerprint is created by mining the titles and abstracts of the person's research outputs and projects/funding awards to create an index of weighted terms from discipline-specific thesauri.

  • 4 Similar Profiles
Hereditary Nephritis Medicine & Life Sciences
Kidney Medicine & Life Sciences
Glomerular Basement Membrane Medicine & Life Sciences
Collagen Type IV Medicine & Life Sciences
Basement Membrane Medicine & Life Sciences
Kidney Transplantation Medicine & Life Sciences
Collagen Medicine & Life Sciences
Mutation Medicine & Life Sciences

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Projects 1995 2020

Hereditary Nephritis
Sensorineural Hearing Loss
Hereditary Nephritis
Standard of Care
Natural History
Disease Progression
Hereditary Nephritis
Controlled Clinical Trials
Feasibility Studies
Hereditary Nephritis
Validation Studies

Research Output 1986 2019

Somatic Mosaicism in a Male Patient With X-linked Alport Syndrome

Bu, L., Chen, J., Nelson, A. C., Katz, A., Kashtan, C., Kim, Y. & Pierpont, M. E. M., Jul 1 2019, In : Kidney International Reports. 4, 7, p. 1031-1035 5 p.

Research output: Contribution to journalArticle

Open Access
Hereditary Nephritis
25 Citations (Scopus)

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group

Kashtan, C. E., Ding, J., Garosi, G., Heidet, L., Massella, L., Nakanishi, K., Nozu, K., Renieri, A., Rheault, M., Wang, F. & Gross, O., May 2018, In : Kidney international. 93, 5, p. 1045-1051 7 p.

Research output: Contribution to journalArticle

Hereditary Nephritis
Inborn Genetic Diseases
Glomerular Basement Membrane
1 Citation (Scopus)

BK nephropathy with glomerular involvement

Ravindran, A., Kashtan, C. E. & Sethi, S., Aug 2018, In : Kidney international. 94, 2, 1 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)
Open Access
Hereditary Nephritis
Kidney Transplantation
Patient Selection
Tissue Donors
Basement Membrane
23 Citations (Scopus)

Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: Report from the 2015 International Workshop on Alport Syndrome

Gross, O., Kashtan, C. E., Rheault, M. N., Flinter, F., Savige, J., Miner, J. H., Torra, R., Ars, E., Deltas, C., Savva, I., Perin, L., Renieri, A., Ariani, F., Mari, F., Baigent, C., Judge, P., Knebelman, B., Heidet, L., Lagas, S., Blatt, D. & 18 others, Ding, J., Zhang, Y., Gale, D. P., Prunotto, M., Xue, Y., Schachter, A. D., Morton, L. C. G., Blem, J., Huang, M., Liu, S., Vallee, S., Renault, D., Schifter, J., Skelding, J., Gear, S., Friede, T., Turner, A. N. & Lennon, R., Jan 1 2017, In : Nephrology Dialysis Transplantation. 32, 6, p. 916-924 9 p.

Research output: Contribution to journalReview article

Open Access
Hereditary Nephritis
Hearing Loss