المؤلفون: Warady, BA, Pergola, PE, Agarwal, R, Andreoli, S, Appel, GB, Bangalore, S, Block, GA, Chapman, AB, Chin, MP, Gibson, KL, Goldsberry, A, Iijima, K, Inker, LA, Kashtan, CE, Knebelmann, B, Mariani, LH, Meyer, CJ, Nozu, K, O'Grady, M, Rheault, MN, Silva, AL, Stenvinkel, P, Torra, R, Chertow, GM

المصدر: Clinical journal of the American Society of Nephrology : CJASN. 17(12):1763-1774

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:151386212

المؤلفون: Lenkkeri, U, Mannikko, M, McCready, P, Lamerdin, J, Gribouval, O, Niaudet, P, Antignac, C, Kashtan, CE, Holmberg, C, Olsen, A, Kestila, M, Tryggvason, K

المصدر: American journal of human genetics. 64(1):51-61

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:1931465

المؤلفون: Kestila, M, Lenkkeri, U, Mannikko, M, Lamerdin, J, McCready, P, Putaala, H, Ruotsalainen, V, Morita, T, Nissinen, M, Herva, R, Kashtan, CE, Peltonen, L, Holmberg, C, Olsen, A, Tryggvason, K

المصدر: Molecular cell. 1(4):575-582

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:1928681

المؤلفون: Kashtan CE

المصدر: International Journal of Nephrology and Renovascular Disease, Vol Volume 11, Pp 267-270 (2018)

مصطلحات موضوعية: Alport Syndrome, Kidney Transplantation, Collagen IV, Post-transplant anti-GBM nephritis, Diseases of the genitourinary system. Urology, RC870-923

وصف الملف: electronic resource

Relation: https://www.dovepress.com/renal-transplantation-in-patients-with-alport-syndrome-patient-selecti-peer-reviewed-article-IJNRD; https://doaj.org/toc/1178-7058

URL الوصول: https://doaj.org/article/9dd45d4d1ef948a5a0c6a4b2806a3a84

المؤلفون: Kashtan CE

المصدر: Pediatric Health, Medicine and Therapeutics, Vol 2013, Iss default, Pp 41-45 (2013)

مصطلحات موضوعية: Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: http://www.dovepress.com/long-term-management-of-alport-syndrome-in-pediatric-patients-a13233; https://doaj.org/toc/1179-9927

URL الوصول: https://doaj.org/article/c5adb0a4c9064f56ac4d90b54b91c0b0

المؤلفون: Gross, O, Kashtan, CE, Rheault, MN, Flinter, F, Savige, J, Miner, JH, 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, Ding, J, Zhang, Y, Gale, DP, Prunotto, M, Xue, Y, Schachter, AD, Morton, LCG, Blem, J, Huang, M, Liu, S, Vallee, S, Renault, D, Schifter, J, Skelding, J, Gear, S, Friede, T, Turner, AN, Lennon, R

Relation: pii: gfw095; 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. ,. Lennon, R. (2017). Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome. NEPHROLOGY DIALYSIS TRANSPLANTATION, 32 (6), pp.916-924. https://doi.org/10.1093/ndt/gfw095.; http://hdl.handle.net/11343/262434

الاتاحة: http://hdl.handle.net/11343/262434

المؤلفون: Mannikko, M, Lenkkeri, U, Kashtan, CE, Kestila, M, Holmberg, C, Tryggvason, K

المصدر: Journal of the American Society of Nephrology : JASN. 7(12):2700-2703

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:1927675

المؤلفون: Miner, JH, Baigent, C, Flinter, F, Gross, O, Judge, P, Kashtan, CE, Lagas, S, Savige, J, Blatt, D, Ding, J, Gale, DP, Midgley, JP, Povey, S, Prunotto, M, Renault, D, Skelding, J, Turner, AN, Gear, S

Relation: pii: S0085-2538(15)30392-6; Miner, J. H., Baigent, C., Flinter, F., Gross, O., Judge, P., Kashtan, C. E., Lagas, S., Savige, J., Blatt, D., Ding, J., Gale, D. P., Midgley, J. P., Povey, S., Prunotto, M., Renault, D., Skelding, J., Turner, A. N. & Gear, S. (2014). The 2014 International Workshop on Alport Syndrome. KIDNEY INTERNATIONAL, 86 (4), pp.679-684. https://doi.org/10.1038/ki.2014.229.; http://hdl.handle.net/11343/263310

الاتاحة: http://hdl.handle.net/11343/263310

المؤلفون: Miller, RB, Burke, BA, Schmidt, WJ, Gillingham, KJ, Matas, AJ, Mauer, M, Kashtan, CE

مصطلحات موضوعية: Original Articles

وصف الملف: text/html

Relation: http://ndt.oxfordjournals.org/cgi/content/short/12/7/1425; http://dx.doi.org/10.1093/ndt/12.7.1425

الاتاحة: http://ndt.oxfordjournals.org/cgi/content/short/12/7/1425
https://doi.org/10.1093/ndt/12.7.1425

المؤلفون: Gross, O, Kashtan, CE, Rheault, MN, Flinter, F, Savige, J, Miner, JH, 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, Ding, J, Zhang, Y, Gale, DP, Prunotto, M, Xue, Y, Schachter, AD, Morton, LC, Blem, J, Huang, M, Liu, S, Vallee, S, Renault, D, Schifter, J, Skelding, J, Gear, S, Friede, T, Turner, AN, Lennon, R

المصدر: Gross, O, Kashtan, C, Rheault, M, Flinter, F, Savige, J, Miner, J, 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, Ding, J, Zhang, Y, Gale, D, Prunotto, M, Xue, Y, Schachter, A, Morton, L, Blem, J, Huang, M, Liu, S, Vallee, S, Renault, D, Schifter, J, Skelding, J, Gear, S, Friede, T, Turner, A N & Lennon, R 2016, ' Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome ', Nephrology, Dialysis, Transplantation . https://doi.org/10.1093/ndt/gfw095
Nephrology Dialysis Transplantation
NEPHROLOGY DIALYSIS TRANSPLANTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

مصطلحات موضوعية: Collagen Type IV, nephroprotection, Podocytes, Reviews, Nephritis, Hereditary, Genetic Therapy, Quality Improvement, hereditary kidney disease, Mutation, Animals, Humans, Alport syndrome, chronic kidney disease, guidelines, Needs Assessment

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f92afe4fa2a7fc2cd57700c91bd39286
https://www.research.manchester.ac.uk/portal/en/publications/advances-and-unmet-needs-in-genetic-basic-and-clinical-science-in-alport-syndrome(09cb5a63-c7fa-4e27-8762-7a76040e0523).html

المؤلفون: Chertow, GM, Pergola, PE, Agarwal, R, Andreoli, SP, Appel, GB, Bangalore, S, Block, GA, Chin, M, Gibson, KL, Goldsberry, A, Iijima, K, Inker, LA, Kashtan, CE, Knebelmann, B, Mariani, LH, Meyer, CJ, Nozu, K, O'Grady, M, Silva, AL, Stenvinkel, P, Torra, R, Warady, BA

المصدر: JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. 32(10):418-418

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:159466804

المؤلفون: MELONI I., VITELLI F., PUCCI L., LOWRY RB., TONLORENZI R., ROSSI E., VENTURA M., RIZZONI G., KASHTAN CE., POBER B., RENIERI A.

المساهمون: Meloni, I., Vitelli, F., Pucci, L., Lowry, Rb., Tonlorenzi, R., Rossi, E., Ventura, M., Rizzoni, G., Kashtan, Ce., Pober, B., Renieri, A.

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/12011158; info:eu-repo/semantics/altIdentifier/wos/WOS:000175642900011; volume:39; issue:5; firstpage:359; lastpage:365; numberofpages:7; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11365/19048; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-18344377865; https://jmg.bmj.com/content/39/5/359

الاتاحة: http://hdl.handle.net/11365/19048
https://doi.org/10.1136/jmg.39.5.359
https://jmg.bmj.com/content/39/5/359

المؤلفون: MELONI I, VITELLI F, PUCCI L, LOWRY RB, TONLORENZI R, VENTURA M, RIZZONI G, KASHTAN CE, POBER B, RENIERI A., ROSSI, ELENA

المساهمون: Meloni, I, Vitelli, F, Pucci, L, Lowry, Rb, Tonlorenzi, R, Rossi, Elena, Ventura, M, Rizzoni, G, Kashtan, Ce, Pober, B, Renieri, A.

مصطلحات موضوعية: "ALPORT SYNDROME", "MENTAL RETARDATION", "GENE DELETION SYNDROME"

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/12011158; volume:39; issue:5; firstpage:359; lastpage:365; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11571/114744

الاتاحة: http://hdl.handle.net/11571/114744

المؤلفون: Kashtan, Clifford E., Ding, Jie, Gregory, Martin, Gross, Oliver, Heidet, Laurence, Knebelmann, Bertrand, Rheault, Michelle, Licht, Christoph

المساهمون: Kashtan, CE (reprint author), Univ Minnesota, Sch Med, Dept Pediat, Div Pediat Nephrol, Minneapolis, MN 55455 USA., Univ Minnesota, Sch Med, Dept Pediat, Div Pediat Nephrol, Minneapolis, MN 55455 USA., Peking Univ, Hosp 1, Dept Pediat, Beijing 100871, Peoples R China., Univ Utah, Hlth Sci Ctr, Div Nephrol, Salt Lake City, UT USA., Univ Med Goettingen, Dept Nephrol & Rheumatol, Gottingen, Germany., Hop Necker Enfants Malad, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France., Hop Necker Enfants Malad, Serv Nephrol Pediat, Paris, France., Hosp Sick Children, Div Nephrol, Toronto, ON M5G 1X8, Canada.

المصدر: SCI

مصطلحات موضوعية: Alport syndrome, Proteinuria, Angiotensin-converting enzyme inhibitor, Angiotensin receptor blocker, Aldosterone inhibitor, GENOTYPE-PHENOTYPE CORRELATIONS, DELAYS RENAL-FAILURE, HEREDITARY NEPHRITIS, PROLONGS SURVIVAL, NATURAL-HISTORY, KIDNEY-DISEASE, BLOOD-PRESSURE, ACE-INHIBITOR, 195 FAMILIES, CHILDREN

Relation: PEDIATRIC NEPHROLOGY.2013,28,(1),5-11.; 853900; http://hdl.handle.net/20.500.11897/228305; WOS:000311501500002

الاتاحة: https://hdl.handle.net/20.500.11897/228305
https://doi.org/10.1007/s00467-012-2138-4