急性間欠性ポルフィリン症 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "急性間欠性ポルフィリン症" in Japanese language version.

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2web.archive.org

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1porphyriafoundation.com

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bmj.com

jcp.bmj.com

Hift, Richard J.; Peters Timothy J., Meissner Peter N. (2012). “A review of the clinical presentation, natural history and inheritance of variegate porphyria: its implausibility as the source of the 'Royal Malady'”. Journal of Clinical Pathology 65: 200–605.

clinchem.org

Aarsand, AK; Petersen PH, Sandberg S (April 2006). “Estimation and application of biological variation of urinary delta-aminolevulinic acid and porphobilinogen in healthy individuals and in patients with acute intermittent porphyria”. Clinical Chemistry 52 (4): 650–656. doi:10.1373/clinchem.2005.060772. PMID 16595824.

doi.org

Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (2000). “Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Hum. Genet. 107 (3): 243–8. doi:10.1007/s004390000356. PMID 11071386. オリジナルの2002年1月13日時点におけるアーカイブ。.
Aarsand, AK; Petersen PH, Sandberg S (April 2006). “Estimation and application of biological variation of urinary delta-aminolevulinic acid and porphobilinogen in healthy individuals and in patients with acute intermittent porphyria”. Clinical Chemistry 52 (4): 650–656. doi:10.1373/clinchem.2005.060772. PMID 16595824.

nih.gov

pubmed.ncbi.nlm.nih.gov

Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (2000). “Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Hum. Genet. 107 (3): 243–8. doi:10.1007/s004390000356. PMID 11071386. オリジナルの2002年1月13日時点におけるアーカイブ。.
Aarsand, AK; Petersen PH, Sandberg S (April 2006). “Estimation and application of biological variation of urinary delta-aminolevulinic acid and porphobilinogen in healthy individuals and in patients with acute intermittent porphyria”. Clinical Chemistry 52 (4): 650–656. doi:10.1373/clinchem.2005.060772. PMID 16595824.

porphyriafoundation.com

*American Porphyria Foundation. "About Porphyria: Acute Intermittent Porhyria" Archived 2008年4月25日, at the Wayback Machine., 2007,

springer.de

link.springer.de

Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (2000). “Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Hum. Genet. 107 (3): 243–8. doi:10.1007/s004390000356. PMID 11071386. オリジナルの2002年1月13日時点におけるアーカイブ。.

web.archive.org

Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (2000). “Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Hum. Genet. 107 (3): 243–8. doi:10.1007/s004390000356. PMID 11071386. オリジナルの2002年1月13日時点におけるアーカイブ。.
*American Porphyria Foundation. "About Porphyria: Acute Intermittent Porhyria" Archived 2008年4月25日, at the Wayback Machine., 2007,