Alport syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alport syndrome" in English language version.

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25nih.gov

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11doi.org

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5web.archive.org

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3lecturio.com

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2medscape.com

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2edren.org

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1utah.edu

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1alportsyndrome.org

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1kidney.org

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1jstor.org

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1alportsyndromenews.com

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1rarerenal.org

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1medlineplus.gov

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1columbiaeye.org

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1omim.org

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1sjkdt.org

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1semanticscholar.org

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alportsyndrome.org

"What is Alport syndrome?". Alport syndrome. Archived from the original on 2019-01-06. Retrieved 2019-01-06.

alportsyndromenews.com

Zaunbrecher, Nicole. "Types of Alport Syndrome". Alport Syndrome News. Retrieved 2022-08-01.

columbiaeye.org

Columbia University, Department of Ophthalmology. Link https://www.columbiaeye.org/content/retinitis-pigmentosa

doi.org

Alport AC (March 1927). "Hereditary familial congenital haemorrhagic nephritis". British Medical Journal. 1 (3454): 504–6. doi:10.1136/bmj.1.3454.504. JSTOR 25322864. PMC 2454341. PMID 20773074.
Chugh KS, Sakhuja V, Agarwal A, Jha V, Joshi K, Datta BN, et al. (1993). "Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds". Nephrology, Dialysis, Transplantation. 8 (8): 690–5. doi:10.1093/ndt/8.8.690. PMID 8414153.
Hess K, Pfau M, Wintergerst MW, Loeffler KU, Holz FG, Herrmann P (February 2020). "Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome". Invest Ophthalmol Vis Sci. 61 (2): 5. doi:10.1167/iovs.61.2.5. PMC 7324255. PMID 32031577.
Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, et al. (February 2019). "A review of clinical characteristics and genetic backgrounds in Alport syndrome". Clinical and Experimental Nephrology. 23 (2): 158–168. doi:10.1007/s10157-018-1629-4. PMC 6510800. PMID 30128941.
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, et al. (October 2003). "X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study". Journal of the American Society of Nephrology. 14 (10): 2603–10. doi:10.1097/01.ASN.0000090034.71205.74. PMID 14514738.
Pescucci C, Mari F, Longo I, Vogiatzi P, Caselli R, Scala E, et al. (May 2004). "Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene". Kidney International. 65 (5): 1598–603. doi:10.1111/j.1523-1755.2004.00560.x. PMID 15086897.
Hertz JM, Thomassen M, Storey H, Flinter F (June 2012). "Clinical utility gene card for: Alport syndrome". European Journal of Human Genetics. 20 (6): 713. doi:10.1038/ejhg.2011.237. PMC 3355248. PMID 22166944.
Zhang KW, Colville D, Tan R, Jones C, Alexander SI, Fletcher J, Savige J (August 2008). "The use of ocular abnormalities to diagnose X-linked Alport syndrome in children". Pediatric Nephrology. 23 (8): 1245–50. doi:10.1007/s00467-008-0759-4. PMID 18343956. S2CID 28650514.
Tryggvason K, Heikkilä P, Pettersson E, Tibell A, Thorner P (May 1997). "Can Alport syndrome be treated by gene therapy?". Kidney International. 51 (5): 1493–9. doi:10.1038/ki.1997.205. PMID 9150464.
Temme J, Kramer A, Jager KJ, Lange K, Peters F, Müller GA, et al. (December 2012). "Outcomes of male patients with Alport syndrome undergoing renal replacement therapy". Clinical Journal of the American Society of Nephrology. 7 (12): 1969–76. doi:10.2215/CJN.02190312. PMC 3513741. PMID 22997344.
Chen D, Jefferson B, Harvey SJ, Zheng K, Gartley CJ, Jacobs RM, Thorner PS (March 2003). "Cyclosporine a slows the progressive renal disease of alport syndrome (X-linked hereditary nephritis): results from a canine model". Journal of the American Society of Nephrology. 14 (3): 690–8. doi:10.1097/01.ASN.0000046964.15831.16. PMID 12595505.

edren.org

"Alport syndrome". Renal Unit at the Royal Infirmary of Edinburgh, Scotland. Archived from the original on 2010-04-17. Retrieved 2010-03-24.
"EdRen - Edinburgh Royal Infirmary Renal Unit - Alport anti-GBM disease". www.edren.org. Archived from the original on 2016-02-10. Retrieved 2016-02-17.

jstor.org

Alport AC (March 1927). "Hereditary familial congenital haemorrhagic nephritis". British Medical Journal. 1 (3454): 504–6. doi:10.1136/bmj.1.3454.504. JSTOR 25322864. PMC 2454341. PMID 20773074.

kidney.org

"Alport Syndrome". National Kidney Foundation. 2015-12-24. Retrieved 2022-08-01.

lecturio.com

"Alport Syndrome". The Lecturio Medical Concept Library. Retrieved 28 June 2021.
"Alport Syndrome". The Lecturio Medical Concept Library. Retrieved 8 July 2021.
"Alport Syndrome". The Lecturio Medical Concept Library. Retrieved 28 June 2021.

medlineplus.gov

"Alport syndrome". MedlinePlus. Retrieved 28 June 2021.

medscape.com

emedicine.medscape.com

Alport Syndrome~clinical at eMedicine
Alport Syndrome~treatment at eMedicine

nih.gov

pubmed.ncbi.nlm.nih.gov

Lagona E, Tsartsali L, Kostaridou S, Skiathitou A, Georgaki E, Sotsiou F (April 2008). "Skin biopsy for the diagnosis of Alport syndrome". Hippokratia. 12 (2): 116–8. PMC 2464308. PMID 18923659.
Alport AC (March 1927). "Hereditary familial congenital haemorrhagic nephritis". British Medical Journal. 1 (3454): 504–6. doi:10.1136/bmj.1.3454.504. JSTOR 25322864. PMC 2454341. PMID 20773074.
Zhou J, Hertz JM, Tryggvason K (June 1992). "Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: detection by denaturing gradient gel electrophoresis of a PCR product". American Journal of Human Genetics. 50 (6): 1291–300. PMC 1682577. PMID 1598909.
Watson S, Padala SA, Bush JS (28 May 2020). "Alport Syndrome". StatPearls. PMID 29262041. Retrieved 30 May 2020. {{cite journal}}: Cite journal requires |journal= (help)
Chugh KS, Sakhuja V, Agarwal A, Jha V, Joshi K, Datta BN, et al. (1993). "Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds". Nephrology, Dialysis, Transplantation. 8 (8): 690–5. doi:10.1093/ndt/8.8.690. PMID 8414153.
Hess K, Pfau M, Wintergerst MW, Loeffler KU, Holz FG, Herrmann P (February 2020). "Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome". Invest Ophthalmol Vis Sci. 61 (2): 5. doi:10.1167/iovs.61.2.5. PMC 7324255. PMID 32031577.
Kashtan CE (February 2019). "Alport Syndrome". In Adam MP, Ardinger HH, Pagon RA, et al. (eds.). Gene Reviews. Seattle (WA): University of Washington, Seattle. PMID 20301386.
Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, et al. (February 2019). "A review of clinical characteristics and genetic backgrounds in Alport syndrome". Clinical and Experimental Nephrology. 23 (2): 158–168. doi:10.1007/s10157-018-1629-4. PMC 6510800. PMID 30128941.
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, et al. (October 2003). "X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study". Journal of the American Society of Nephrology. 14 (10): 2603–10. doi:10.1097/01.ASN.0000090034.71205.74. PMID 14514738.
Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, et al. (September 2006). "Autosomal dominant Alport's syndrome: study of a large Tunisian family". Saudi Journal of Kidney Diseases and Transplantation. 17 (3): 320–5. PMID 16970251.
Pescucci C, Mari F, Longo I, Vogiatzi P, Caselli R, Scala E, et al. (May 2004). "Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene". Kidney International. 65 (5): 1598–603. doi:10.1111/j.1523-1755.2004.00560.x. PMID 15086897.
Hertz JM, Thomassen M, Storey H, Flinter F (June 2012). "Clinical utility gene card for: Alport syndrome". European Journal of Human Genetics. 20 (6): 713. doi:10.1038/ejhg.2011.237. PMC 3355248. PMID 22166944.
Zhang KW, Colville D, Tan R, Jones C, Alexander SI, Fletcher J, Savige J (August 2008). "The use of ocular abnormalities to diagnose X-linked Alport syndrome in children". Pediatric Nephrology. 23 (8): 1245–50. doi:10.1007/s00467-008-0759-4. PMID 18343956. S2CID 28650514.
Tryggvason K, Heikkilä P, Pettersson E, Tibell A, Thorner P (May 1997). "Can Alport syndrome be treated by gene therapy?". Kidney International. 51 (5): 1493–9. doi:10.1038/ki.1997.205. PMID 9150464.
Temme J, Kramer A, Jager KJ, Lange K, Peters F, Müller GA, et al. (December 2012). "Outcomes of male patients with Alport syndrome undergoing renal replacement therapy". Clinical Journal of the American Society of Nephrology. 7 (12): 1969–76. doi:10.2215/CJN.02190312. PMC 3513741. PMID 22997344.
Chen D, Jefferson B, Harvey SJ, Zheng K, Gartley CJ, Jacobs RM, Thorner PS (March 2003). "Cyclosporine a slows the progressive renal disease of alport syndrome (X-linked hereditary nephritis): results from a canine model". Journal of the American Society of Nephrology. 14 (3): 690–8. doi:10.1097/01.ASN.0000046964.15831.16. PMID 12595505.

ncbi.nlm.nih.gov

Lagona E, Tsartsali L, Kostaridou S, Skiathitou A, Georgaki E, Sotsiou F (April 2008). "Skin biopsy for the diagnosis of Alport syndrome". Hippokratia. 12 (2): 116–8. PMC 2464308. PMID 18923659.
Alport AC (March 1927). "Hereditary familial congenital haemorrhagic nephritis". British Medical Journal. 1 (3454): 504–6. doi:10.1136/bmj.1.3454.504. JSTOR 25322864. PMC 2454341. PMID 20773074.
Zhou J, Hertz JM, Tryggvason K (June 1992). "Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: detection by denaturing gradient gel electrophoresis of a PCR product". American Journal of Human Genetics. 50 (6): 1291–300. PMC 1682577. PMID 1598909.
Watson S, Padala SA, Bush JS (28 May 2020). "Alport Syndrome". StatPearls. PMID 29262041. Retrieved 30 May 2020. {{cite journal}}: Cite journal requires |journal= (help)
Hess K, Pfau M, Wintergerst MW, Loeffler KU, Holz FG, Herrmann P (February 2020). "Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome". Invest Ophthalmol Vis Sci. 61 (2): 5. doi:10.1167/iovs.61.2.5. PMC 7324255. PMID 32031577.
Kashtan CE (February 2019). "Alport Syndrome". In Adam MP, Ardinger HH, Pagon RA, et al. (eds.). Gene Reviews. Seattle (WA): University of Washington, Seattle. PMID 20301386.
Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, et al. (February 2019). "A review of clinical characteristics and genetic backgrounds in Alport syndrome". Clinical and Experimental Nephrology. 23 (2): 158–168. doi:10.1007/s10157-018-1629-4. PMC 6510800. PMID 30128941.
Hertz JM, Thomassen M, Storey H, Flinter F (June 2012). "Clinical utility gene card for: Alport syndrome". European Journal of Human Genetics. 20 (6): 713. doi:10.1038/ejhg.2011.237. PMC 3355248. PMID 22166944.
Temme J, Kramer A, Jager KJ, Lange K, Peters F, Müller GA, et al. (December 2012). "Outcomes of male patients with Alport syndrome undergoing renal replacement therapy". Clinical Journal of the American Society of Nephrology. 7 (12): 1969–76. doi:10.2215/CJN.02190312. PMC 3513741. PMID 22997344.

omim.org

"Alport Syndrome, Autosomal Dominant". Online Mendelian Inheritance in Man (OMIM). Johns Hopkins University. Retrieved 2008-11-24.

rarerenal.org

UK Alport Group (2013-07-25). "Alport SyndromeL Clinician information". RareRenal. Renal Rare Diseases Registry. Retrieved 17 February 2016.

semanticscholar.org

api.semanticscholar.org

Zhang KW, Colville D, Tan R, Jones C, Alexander SI, Fletcher J, Savige J (August 2008). "The use of ocular abnormalities to diagnose X-linked Alport syndrome in children". Pediatric Nephrology. 23 (8): 1245–50. doi:10.1007/s00467-008-0759-4. PMID 18343956. S2CID 28650514.

sjkdt.org

Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, et al. (September 2006). "Autosomal dominant Alport's syndrome: study of a large Tunisian family". Saudi Journal of Kidney Diseases and Transplantation. 17 (3): 320–5. PMID 16970251.

utah.edu

cc.utah.edu

"Diseases of the Kidney: Alport Syndrome". Archived from the original on 2004-06-12. Retrieved 2004-06-16.

web.archive.org

"Diseases of the Kidney: Alport Syndrome". Archived from the original on 2004-06-12. Retrieved 2004-06-16.
"What is Alport syndrome?". Alport syndrome. Archived from the original on 2019-01-06. Retrieved 2019-01-06.
"Alport syndrome" at Dorland's Medical Dictionary
"Alport syndrome". Renal Unit at the Royal Infirmary of Edinburgh, Scotland. Archived from the original on 2010-04-17. Retrieved 2010-03-24.
"EdRen - Edinburgh Royal Infirmary Renal Unit - Alport anti-GBM disease". www.edren.org. Archived from the original on 2016-02-10. Retrieved 2016-02-17.