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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 2019

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

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
Mosaicism
10 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., Ding, J., Garosi, G., Heidet, L., Massella, L., Nakanishi, K., Nozu, K., Renieri, A., Rheault, M. N., Wang, F. & Gross, O., May 1 2018, In : Kidney international. 93, 5, p. 1045-1051 7 p.

Research output: Contribution to journalArticle

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

BK nephropathy with glomerular involvement

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

Research output: Contribution to journalArticle

Open Access
Hereditary Nephritis
Kidney Transplantation
Patient Selection
Tissue Donors
Basement Membrane
19 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 othersDing, 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
Education
Hearing Loss
Mutation
Research