نشانگان نارپ (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "نشانگان نارپ" in Persian language version.

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9nih.gov

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6doi.org

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3web.archive.org

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2archive.org

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1archive.today

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1rarediseases.org

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1jle.com

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1metagene.de

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1athenadiagnostics.com

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1knightdxlabs.com

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archive.org

Chowers, I; Lerman-Sagie, T; Elpeleg, ON; Shaag, A; Merin, S (Feb 1999). "Cone and rod dysfunction in the NARP syndrome". The British journal of ophthalmology. 83 (2): 190–3. doi:10.1136/bjo.83.2.190. PMID 10396197.
Rak, M; Tetaud, E; Duvezin-Caubet, S; Ezkurdia, N; Bietenhader, M; Rytka, J; di Rago, JP (Nov 23, 2007). "A yeast model of the neurogenic ataxia retinitis pigmentosa (NARP) T8993G mutation in the mitochondrial ATP synthase-6 gene". The Journal of Biological Chemistry. 282 (47): 34039–47. doi:10.1074/jbc.M703053200. PMID 17855363.

archive.today

"Maternally inherited Leigh syndrome and NARP syndrome". rarediseases.org. NORD's Rare Disease Information Database. Archived from the original on 27 September 2014. Retrieved 27 September 2014.

athenadiagnostics.com

"ARP mtDNA Evaluation". athenadiagnostics.com. Athena Diagnostics, Inc. Archived from the original on 7 November 2014. Retrieved 27 September 2014.

doi.org

Kerrison, JB; Biousse, V; Newman, NJ (Feb 2000). "Retinopathy of NARP syndrome". Archives of ophthalmology. 118 (2): 298–9. doi:10.1001/archopht.118.2.298. PMID 10676807.
Chowers, I; Lerman-Sagie, T; Elpeleg, ON; Shaag, A; Merin, S (Feb 1999). "Cone and rod dysfunction in the NARP syndrome". The British journal of ophthalmology. 83 (2): 190–3. doi:10.1136/bjo.83.2.190. PMID 10396197.
Rak, M; Tetaud, E; Duvezin-Caubet, S; Ezkurdia, N; Bietenhader, M; Rytka, J; di Rago, JP (Nov 23, 2007). "A yeast model of the neurogenic ataxia retinitis pigmentosa (NARP) T8993G mutation in the mitochondrial ATP synthase-6 gene". The Journal of Biological Chemistry. 282 (47): 34039–47. doi:10.1074/jbc.M703053200. PMID 17855363.
Parfait, B; de Lonlay, P; von Kleist-Retzow, JC; Cormier-Daire, V; Chrétien, D; Rötig, A; Rabier, D; Saudubray, JM; Rustin, P; Munnich, A (Jan 1999). "The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia". European journal of pediatrics. 158 (1): 55–8. doi:10.1007/s004310051009. PMID 9950309.
Mattiazzi, M; Vijayvergiya, C; Gajewski, CD; DeVivo, DC; Lenaz, G; Wiedmann, M; Manfredi, G (Apr 15, 2004). "The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants". Human Molecular Genetics. 13 (8): 869–79. doi:10.1093/hmg/ddh103. PMID 14998933.
Debray, FG; Lambert, M; Lortie, A; Vanasse, M; Mitchell, GA (Sep 1, 2007). "Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation". American Journal of Medical Genetics Part A. 143A (17): 2046–51. doi:10.1002/ajmg.a.31880. PMID 17663470.

jle.com

Keränen, T; Kuusisto, H (Sep 2006). "NARP syndrome and adult-onset generalised seizures". Epileptic disorders: international epilepsy journal with videotape. 8 (3): 200–3. PMID 16987741.

knightdxlabs.com

"Mitochondrial Studies: NARP - Neuropathy, Ataxia and Retinitis Pigmentosa". knightdxlabs.com. Archived from the original on 4 March 2016. Retrieved 27 September 2014.

metagene.de

"NARP syndrome". metagene.de. MIC - Metabolic Information Centre. Archived from the original on 4 March 2016. Retrieved 27 September 2014.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kerrison, JB; Biousse, V; Newman, NJ (Feb 2000). "Retinopathy of NARP syndrome". Archives of ophthalmology. 118 (2): 298–9. doi:10.1001/archopht.118.2.298. PMID 10676807.
Chowers, I; Lerman-Sagie, T; Elpeleg, ON; Shaag, A; Merin, S (Feb 1999). "Cone and rod dysfunction in the NARP syndrome". The British journal of ophthalmology. 83 (2): 190–3. doi:10.1136/bjo.83.2.190. PMID 10396197.
Keränen, T; Kuusisto, H (Sep 2006). "NARP syndrome and adult-onset generalised seizures". Epileptic disorders: international epilepsy journal with videotape. 8 (3): 200–3. PMID 16987741.
Thorburn, DR; Rahman, S; Pagon, RA; Adam, MP; Ardinger, HH; Bird, TD; Dolan, CR; Fong, CT; Smith, RJH; Stephens, K (1993). Mitochondrial DNA-Associated Leigh Syndrome and NARP. PMID 20301352.
Rak, M; Tetaud, E; Duvezin-Caubet, S; Ezkurdia, N; Bietenhader, M; Rytka, J; di Rago, JP (Nov 23, 2007). "A yeast model of the neurogenic ataxia retinitis pigmentosa (NARP) T8993G mutation in the mitochondrial ATP synthase-6 gene". The Journal of Biological Chemistry. 282 (47): 34039–47. doi:10.1074/jbc.M703053200. PMID 17855363.
Parfait, B; de Lonlay, P; von Kleist-Retzow, JC; Cormier-Daire, V; Chrétien, D; Rötig, A; Rabier, D; Saudubray, JM; Rustin, P; Munnich, A (Jan 1999). "The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia". European journal of pediatrics. 158 (1): 55–8. doi:10.1007/s004310051009. PMID 9950309.
Mattiazzi, M; Vijayvergiya, C; Gajewski, CD; DeVivo, DC; Lenaz, G; Wiedmann, M; Manfredi, G (Apr 15, 2004). "The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants". Human Molecular Genetics. 13 (8): 869–79. doi:10.1093/hmg/ddh103. PMID 14998933.
Debray, FG; Lambert, M; Lortie, A; Vanasse, M; Mitchell, GA (Sep 1, 2007). "Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation". American Journal of Medical Genetics Part A. 143A (17): 2046–51. doi:10.1002/ajmg.a.31880. PMID 17663470.

ncbi.nlm.nih.gov

Thorburn, DR; Rahman, S; Pagon, RA; Adam, MP; Ardinger, HH; Bird, TD; Dolan, CR; Fong, CT; Smith, RJH; Stephens, K (1993). Mitochondrial DNA-Associated Leigh Syndrome and NARP. PMID 20301352.

rarediseases.org

"Maternally inherited Leigh syndrome and NARP syndrome". rarediseases.org. NORD's Rare Disease Information Database. Archived from the original on 27 September 2014. Retrieved 27 September 2014.

web.archive.org

"NARP syndrome". metagene.de. MIC - Metabolic Information Centre. Archived from the original on 4 March 2016. Retrieved 27 September 2014.
"ARP mtDNA Evaluation". athenadiagnostics.com. Athena Diagnostics, Inc. Archived from the original on 7 November 2014. Retrieved 27 September 2014.
"Mitochondrial Studies: NARP - Neuropathy, Ataxia and Retinitis Pigmentosa". knightdxlabs.com. Archived from the original on 4 March 2016. Retrieved 27 September 2014.