Fanconi syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

15nih.gov

4^th place

10doi.org

2^nd place

2web.archive.org

1^st place

1merckmanuals.com

3,097^th place

2,317^th place

1medscape.com

719^th place

636^th place

1ucl.ac.uk

1,306^th place

885^th place

1asnjournals.org

low place

1fda.gov

447^th place

338^th place

1the-medical-dictionary.com

low place

asnjournals.org

jasn.asnjournals.org

Lee JW, Chou CL, Knepper MA (November 2015). "Deep Sequencing in Microdissected Renal Tubules Identifies Nephron Segment-Specific Transcriptomes". Journal of the American Society of Nephrology. 26 (11): 2669–77. doi:10.1681/ASN.2014111067. PMC 4625681. PMID 25817355.

doi.org

Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K (March 2010). "A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome". The New England Journal of Medicine. 362 (12): 1102–9. doi:10.1056/NEJMoa0905647. PMID 20335586.
Cochat P, Pichault V, Bacchetta J, Dubourg L, Sabot JF, Saban C, Daudon M, Liutkus A (March 2010). "Nephrolithiasis related to inborn metabolic diseases". Pediatric Nephrology. 25 (3): 415–24. doi:10.1007/s00467-008-1085-6. PMC 2810370. PMID 19156444.
Vilasi A, Cutillas PR, Maher AD, Zirah SF, Capasso G, Norden AW, Holmes E, Nicholson JK, Unwin RJ (August 2007). "Combined proteomic and metabonomic studies in three genetic forms of the renal Fanconi syndrome". American Journal of Physiology. Renal Physiology. 293 (2): F456-67. doi:10.1152/ajprenal.00095.2007. PMID 17494094.
Assmann N, Dettmer K, Simbuerger JM, Broeker C, Nuernberger N, Renner K, Courtneidge H, Klootwijk ED, Duerkop A, Hall A, Kleta R, Oefner PJ, Reichold M, Reinders J (May 2016). "Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy" (PDF). Cell Reports. 15 (7): 1423–1429. doi:10.1016/j.celrep.2016.04.037. PMID 27160910.
Hamilton AJ, Bingham C, McDonald TJ, Cook PR, Caswell RC, Weedon MN, Oram RA, Shields BM, Shepherd M, Inward CD, Hamilton-Shield JP, Kohlhase J, Ellard S, Hattersley AT (March 2014). "The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype". Journal of Medical Genetics. 51 (3): 165–9. doi:10.1136/jmedgenet-2013-102066. PMC 3932761. PMID 24285859.
Lee JW, Chou CL, Knepper MA (November 2015). "Deep Sequencing in Microdissected Renal Tubules Identifies Nephron Segment-Specific Transcriptomes". Journal of the American Society of Nephrology. 26 (11): 2669–77. doi:10.1681/ASN.2014111067. PMC 4625681. PMID 25817355.
Marable SS, Chung E, Adam M, Potter SS, Park JS (July 2018). "Hnf4a deletion in the mouse kidney phenocopies Fanconi renotubular syndrome". JCI Insight. 3 (14). doi:10.1172/jci.insight.97497. PMC 6124415. PMID 30046000.
Barbier O, Jacquillet G, Tauc M, Cougnon M, Poujeol P (2005). "Effect of heavy metals on, and handling by, the kidney". Nephron Physiology. 99 (4): 105–10. doi:10.1159/000083981. PMID 15722646.
Hashimoto T, Arakawa K, Ohta Y, Suehiro T, Uesugi N, Nakayama M, Tsuchihashi T (2007). "Acquired fanconi syndrome with osteomalacia secondary to monoclonal gammopathy of undetermined significance". Internal Medicine. 46 (5): 241–5. doi:10.2169/internalmedicine.46.1882. PMID 17329920.
Kobayashi T, Muto S, Nemoto J, Miyata Y, Ishiharajima S, Hironaka M, Asano Y, Kusano E (June 2006). "Fanconi's syndrome and distal (type 1) renal tubular acidosis in a patient with primary Sjögren's syndrome with monoclonal gammopathy of undetermined significance". Clinical Nephrology. 65 (6): 427–32. doi:10.5414/CNP65427. PMID 16792139.

fda.gov

accessdata.fda.gov

Viread Label Information, U.S. Food and Drug Administration (FDA), 2008-04-11

medscape.com

emedicine.medscape.com

Fanconi Syndrome at eMedicine

merckmanuals.com

Fanconi Syndrome at Merck Manual Home Health Handbook

nih.gov

pubmed.ncbi.nlm.nih.gov

Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K (March 2010). "A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome". The New England Journal of Medicine. 362 (12): 1102–9. doi:10.1056/NEJMoa0905647. PMID 20335586.
Cochat P, Pichault V, Bacchetta J, Dubourg L, Sabot JF, Saban C, Daudon M, Liutkus A (March 2010). "Nephrolithiasis related to inborn metabolic diseases". Pediatric Nephrology. 25 (3): 415–24. doi:10.1007/s00467-008-1085-6. PMC 2810370. PMID 19156444.
Vilasi A, Cutillas PR, Maher AD, Zirah SF, Capasso G, Norden AW, Holmes E, Nicholson JK, Unwin RJ (August 2007). "Combined proteomic and metabonomic studies in three genetic forms of the renal Fanconi syndrome". American Journal of Physiology. Renal Physiology. 293 (2): F456-67. doi:10.1152/ajprenal.00095.2007. PMID 17494094.
Assmann N, Dettmer K, Simbuerger JM, Broeker C, Nuernberger N, Renner K, Courtneidge H, Klootwijk ED, Duerkop A, Hall A, Kleta R, Oefner PJ, Reichold M, Reinders J (May 2016). "Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy" (PDF). Cell Reports. 15 (7): 1423–1429. doi:10.1016/j.celrep.2016.04.037. PMID 27160910.
Hamilton AJ, Bingham C, McDonald TJ, Cook PR, Caswell RC, Weedon MN, Oram RA, Shields BM, Shepherd M, Inward CD, Hamilton-Shield JP, Kohlhase J, Ellard S, Hattersley AT (March 2014). "The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype". Journal of Medical Genetics. 51 (3): 165–9. doi:10.1136/jmedgenet-2013-102066. PMC 3932761. PMID 24285859.
Lee JW, Chou CL, Knepper MA (November 2015). "Deep Sequencing in Microdissected Renal Tubules Identifies Nephron Segment-Specific Transcriptomes". Journal of the American Society of Nephrology. 26 (11): 2669–77. doi:10.1681/ASN.2014111067. PMC 4625681. PMID 25817355.
Marable SS, Chung E, Adam M, Potter SS, Park JS (July 2018). "Hnf4a deletion in the mouse kidney phenocopies Fanconi renotubular syndrome". JCI Insight. 3 (14). doi:10.1172/jci.insight.97497. PMC 6124415. PMID 30046000.
Irizarry-Alvarado JM, Dwyer JP, Brumble LM, Alvarez S, Mendez JC (March 2009). "Proximal tubular dysfunction associated with tenofovir and didanosine causing Fanconi syndrome and diabetes insipidus: a report of 3 cases". The AIDS Reader. 19 (3): 114–21. PMID 19334328.
Barbier O, Jacquillet G, Tauc M, Cougnon M, Poujeol P (2005). "Effect of heavy metals on, and handling by, the kidney". Nephron Physiology. 99 (4): 105–10. doi:10.1159/000083981. PMID 15722646.
Hashimoto T, Arakawa K, Ohta Y, Suehiro T, Uesugi N, Nakayama M, Tsuchihashi T (2007). "Acquired fanconi syndrome with osteomalacia secondary to monoclonal gammopathy of undetermined significance". Internal Medicine. 46 (5): 241–5. doi:10.2169/internalmedicine.46.1882. PMID 17329920.
Kobayashi T, Muto S, Nemoto J, Miyata Y, Ishiharajima S, Hironaka M, Asano Y, Kusano E (June 2006). "Fanconi's syndrome and distal (type 1) renal tubular acidosis in a patient with primary Sjögren's syndrome with monoclonal gammopathy of undetermined significance". Clinical Nephrology. 65 (6): 427–32. doi:10.5414/CNP65427. PMID 16792139.

ncbi.nlm.nih.gov

Cochat P, Pichault V, Bacchetta J, Dubourg L, Sabot JF, Saban C, Daudon M, Liutkus A (March 2010). "Nephrolithiasis related to inborn metabolic diseases". Pediatric Nephrology. 25 (3): 415–24. doi:10.1007/s00467-008-1085-6. PMC 2810370. PMID 19156444.
Hamilton AJ, Bingham C, McDonald TJ, Cook PR, Caswell RC, Weedon MN, Oram RA, Shields BM, Shepherd M, Inward CD, Hamilton-Shield JP, Kohlhase J, Ellard S, Hattersley AT (March 2014). "The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype". Journal of Medical Genetics. 51 (3): 165–9. doi:10.1136/jmedgenet-2013-102066. PMC 3932761. PMID 24285859.
Lee JW, Chou CL, Knepper MA (November 2015). "Deep Sequencing in Microdissected Renal Tubules Identifies Nephron Segment-Specific Transcriptomes". Journal of the American Society of Nephrology. 26 (11): 2669–77. doi:10.1681/ASN.2014111067. PMC 4625681. PMID 25817355.
Marable SS, Chung E, Adam M, Potter SS, Park JS (July 2018). "Hnf4a deletion in the mouse kidney phenocopies Fanconi renotubular syndrome". JCI Insight. 3 (14). doi:10.1172/jci.insight.97497. PMC 6124415. PMID 30046000.

the-medical-dictionary.com

"Fanconi Syndrome". The Medical Dictionary.

ucl.ac.uk

discovery.ucl.ac.uk

Assmann N, Dettmer K, Simbuerger JM, Broeker C, Nuernberger N, Renner K, Courtneidge H, Klootwijk ED, Duerkop A, Hall A, Kleta R, Oefner PJ, Reichold M, Reinders J (May 2016). "Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy" (PDF). Cell Reports. 15 (7): 1423–1429. doi:10.1016/j.celrep.2016.04.037. PMID 27160910.

web.archive.org

"Fanconi syndrome" at Dorland's Medical Dictionary
Tenofovir (Viread) Associated with Mild Kidney Function Impairment, but not Clinically Relevant Renal Disease, hivandhepatitis.com, 2008-10-14