Ornithine transcarbamylase deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ornithine transcarbamylase deficiency" in English language version.

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Global rank English rank

12nih.gov

4^th place

5doi.org

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2semanticscholar.org

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1medlineplus.gov

1,581^st place

1,299^th place

1omim.org

4,380^th place

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1worldcat.org

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doi.org

Wraith, J. E. (2001). "Ornithine carbamoyltransferase deficiency". Archives of Disease in Childhood. 84 (1): 84–88. doi:10.1136/adc.84.1.84. PMC 1718609. PMID 11124797.
Walker, V. (2009). "Ammonia toxicity and its prevention in inherited defects of the urea cycle". Diabetes, Obesity and Metabolism. 11 (9): 823–835. doi:10.1111/j.1463-1326.2009.01054.x. PMID 19531057. S2CID 25998574.
Deakin, C. T.; Alexander, I. E.; Kerridge, I. (2009). "Accepting Risk in Clinical Research: Is the Gene Therapy Field Becoming Too Risk-averse?". Molecular Therapy. 17 (11): 1842–1848. doi:10.1038/mt.2009.223. PMC 2835028. PMID 19773741.
Morioka, D.; Kasahara, M.; Takada, Y.; Shirouzu, Y.; Taira, K.; Sakamoto, S.; Uryuhara, K.; Egawa, H.; Shimada, H.; Tanaka, K. (2005). "Current role of liver transplantation for the treatment of urea cycle disorders: A review of the worldwide English literature and 13 cases at Kyoto University". Liver Transplantation. 11 (11): 1332–1342. doi:10.1002/lt.20587. PMID 16237708. S2CID 25787334.
Maestri, N. E.; Clissold, D.; Brusilow, S. W. (1999-03-01). "Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis". The Journal of Pediatrics. 134 (3): 268–272. doi:10.1016/s0022-3476(99)70448-8. ISSN 0022-3476. PMID 10064660.

medlineplus.gov

"Ornithine transcarbamylase deficiency: MedlinePlus Genetics". MedlinePlus. October 1, 2017. Retrieved October 22, 2023.

nih.gov

pubmed.ncbi.nlm.nih.gov

Donovan, Kathleen; Guzman, Nilmarie (August 8, 2022). "Ornithine Transcarbamylase Deficiency". StatPearls Publishing. PMID 30725942. Retrieved October 22, 2023.
Lichter-Konecki, Uta; Caldovic, Ljubica; Morizono, Hiroki; Simpson, Kara; Mew, Nicholas Ah; MacLeod, Erin (May 26, 2022). "Ornithine Transcarbamylase Deficiency". University of Washington, Seattle. PMID 24006547. Retrieved October 22, 2023.
Wraith, J. E. (2001). "Ornithine carbamoyltransferase deficiency". Archives of Disease in Childhood. 84 (1): 84–88. doi:10.1136/adc.84.1.84. PMC 1718609. PMID 11124797.
Walker, V. (2009). "Ammonia toxicity and its prevention in inherited defects of the urea cycle". Diabetes, Obesity and Metabolism. 11 (9): 823–835. doi:10.1111/j.1463-1326.2009.01054.x. PMID 19531057. S2CID 25998574.
Lichter-Konecki, U.; Caldovic, L.; Morizono, H.; Simpson, K.; Pagon, R. A.; Adam, M. P.; Bird, T. D.; Dolan, C. R.; Fong, C. T.; Stephens, K. (1993). "Ornithine Transcarbamylase Deficiency". PMID 24006547. {{cite journal}}: Cite journal requires |journal= (help)
Deakin, C. T.; Alexander, I. E.; Kerridge, I. (2009). "Accepting Risk in Clinical Research: Is the Gene Therapy Field Becoming Too Risk-averse?". Molecular Therapy. 17 (11): 1842–1848. doi:10.1038/mt.2009.223. PMC 2835028. PMID 19773741.
Morioka, D.; Kasahara, M.; Takada, Y.; Shirouzu, Y.; Taira, K.; Sakamoto, S.; Uryuhara, K.; Egawa, H.; Shimada, H.; Tanaka, K. (2005). "Current role of liver transplantation for the treatment of urea cycle disorders: A review of the worldwide English literature and 13 cases at Kyoto University". Liver Transplantation. 11 (11): 1332–1342. doi:10.1002/lt.20587. PMID 16237708. S2CID 25787334.
Maestri, N. E.; Clissold, D.; Brusilow, S. W. (1999-03-01). "Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis". The Journal of Pediatrics. 134 (3): 268–272. doi:10.1016/s0022-3476(99)70448-8. ISSN 0022-3476. PMID 10064660.

ncbi.nlm.nih.gov

Donovan, Kathleen; Guzman, Nilmarie (August 8, 2022). "Ornithine Transcarbamylase Deficiency". StatPearls Publishing. PMID 30725942. Retrieved October 22, 2023.
Lichter-Konecki, Uta; Caldovic, Ljubica; Morizono, Hiroki; Simpson, Kara; Mew, Nicholas Ah; MacLeod, Erin (May 26, 2022). "Ornithine Transcarbamylase Deficiency". University of Washington, Seattle. PMID 24006547. Retrieved October 22, 2023.
Wraith, J. E. (2001). "Ornithine carbamoyltransferase deficiency". Archives of Disease in Childhood. 84 (1): 84–88. doi:10.1136/adc.84.1.84. PMC 1718609. PMID 11124797.
Deakin, C. T.; Alexander, I. E.; Kerridge, I. (2009). "Accepting Risk in Clinical Research: Is the Gene Therapy Field Becoming Too Risk-averse?". Molecular Therapy. 17 (11): 1842–1848. doi:10.1038/mt.2009.223. PMC 2835028. PMID 19773741.

omim.org

"#311250 - Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To". Johns Hopkins University. Retrieved 2014-01-01.

semanticscholar.org

api.semanticscholar.org

Walker, V. (2009). "Ammonia toxicity and its prevention in inherited defects of the urea cycle". Diabetes, Obesity and Metabolism. 11 (9): 823–835. doi:10.1111/j.1463-1326.2009.01054.x. PMID 19531057. S2CID 25998574.
Morioka, D.; Kasahara, M.; Takada, Y.; Shirouzu, Y.; Taira, K.; Sakamoto, S.; Uryuhara, K.; Egawa, H.; Shimada, H.; Tanaka, K. (2005). "Current role of liver transplantation for the treatment of urea cycle disorders: A review of the worldwide English literature and 13 cases at Kyoto University". Liver Transplantation. 11 (11): 1332–1342. doi:10.1002/lt.20587. PMID 16237708. S2CID 25787334.

worldcat.org

search.worldcat.org

Maestri, N. E.; Clissold, D.; Brusilow, S. W. (1999-03-01). "Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis". The Journal of Pediatrics. 134 (3): 268–272. doi:10.1016/s0022-3476(99)70448-8. ISSN 0022-3476. PMID 10064660.