இரெட் நோய்த்தொகை (Tamil Wikipedia)

Analysis of information sources in references of the Wikipedia article "இரெட் நோய்த்தொகை" in Tamil language version.

refsWebsite

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4web.archive.org

1^st place

4nih.gov

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2doi.org

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1books.google.com

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1rarediseases.org

5,181^st place

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1worldcat.org

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1elsevier.com

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1pubmedcentral.gov

low place

131^st place

books.google.com

Davis, Andrew S. (25 October 2010). Handbook of Pediatric Neuropsychology. Springer Publishing Company. பன்னாட்டுத் தரப்புத்தக எண் 082615736X. Archived from the original on 5 November 2017. Rett initially called this syndrome cerebroaatrophic hyperammonemia, but the elevated ammonia levels in the bloodstream were later found to be only rarely associated with this condition (can Acker, Loncola, & Can Acker, 2005).

doi.org

dx.doi.org

Percy, Alan (January 2014). "The American History of Rett Syndrome". Pediatric Neurology 50 (1): 1–3. doi:10.1016/j.pediatrneurol.2013.08.018. பப்மெட் சென்ட்ரல்:3874243. http://linkinghub.elsevier.com/retrieve/pii/S0887899413005432.
Amir, Ruthie; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda (1999). "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2". Nature Genetics 23 (2): 185–8. doi:10.1038/13810. பப்மெட்:10508514.

elsevier.com

linkinghub.elsevier.com

Percy, Alan (January 2014). "The American History of Rett Syndrome". Pediatric Neurology 50 (1): 1–3. doi:10.1016/j.pediatrneurol.2013.08.018. பப்மெட் சென்ட்ரல்:3874243. http://linkinghub.elsevier.com/retrieve/pii/S0887899413005432.

nih.gov

ncbi.nlm.nih.gov

Andreas Rett (1966-09-10). "[On a unusual brain atrophy syndrome in hyperammonemia in childhood]" (in de). Wiener Medizinische Wochenschrift 116 (37): 723–726. பன்னாட்டுத் தர தொடர் எண்:0043-5341. பப்மெட்:5300597.
Amir, Ruthie; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda (1999). "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2". Nature Genetics 23 (2): 185–8. doi:10.1038/13810. பப்மெட்:10508514.

ghr.nlm.nih.gov

"Rett syndrome". Genetics Home Reference (in ஆங்கிலம்). December 2013. Archived from the original on 14 October 2017. பார்க்கப்பட்ட நாள் 14 October 2017.

ninds.nih.gov

"Rett Syndrome Fact Sheet". National Institute of Neurological Disorders and Stroke. Archived from the original on 14 October 2017. பார்க்கப்பட்ட நாள் 14 October 2017.

pubmedcentral.gov

Percy, Alan (January 2014). "The American History of Rett Syndrome". Pediatric Neurology 50 (1): 1–3. doi:10.1016/j.pediatrneurol.2013.08.018. பப்மெட் சென்ட்ரல்:3874243. http://linkinghub.elsevier.com/retrieve/pii/S0887899413005432.

rarediseases.org

"Rett Syndrome". NORD (National Organization for Rare Disorders). 2015. Archived from the original on 19 February 2017. பார்க்கப்பட்ட நாள் 14 October 2017.

web.archive.org

Davis, Andrew S. (25 October 2010). Handbook of Pediatric Neuropsychology. Springer Publishing Company. பன்னாட்டுத் தரப்புத்தக எண் 082615736X. Archived from the original on 5 November 2017. Rett initially called this syndrome cerebroaatrophic hyperammonemia, but the elevated ammonia levels in the bloodstream were later found to be only rarely associated with this condition (can Acker, Loncola, & Can Acker, 2005).
"Rett syndrome". Genetics Home Reference (in ஆங்கிலம்). December 2013. Archived from the original on 14 October 2017. பார்க்கப்பட்ட நாள் 14 October 2017.
"Rett Syndrome Fact Sheet". National Institute of Neurological Disorders and Stroke. Archived from the original on 14 October 2017. பார்க்கப்பட்ட நாள் 14 October 2017.
"Rett Syndrome". NORD (National Organization for Rare Disorders). 2015. Archived from the original on 19 February 2017. பார்க்கப்பட்ட நாள் 14 October 2017.

worldcat.org

Andreas Rett (1966-09-10). "[On a unusual brain atrophy syndrome in hyperammonemia in childhood]" (in de). Wiener Medizinische Wochenschrift 116 (37): 723–726. பன்னாட்டுத் தர தொடர் எண்:0043-5341. பப்மெட்:5300597.