Molybdenum cofactor deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Molybdenum cofactor deficiency" in English language version.

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2semanticscholar.org

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1childneurologyfoundation.org

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abc.net.au

Samantha Donovan (2009-11-05). "Dying baby cured in world first". abc.net.au/news. Australian Broadcasting Corporation. Archived from the original on November 6, 2009. Retrieved 2009-11-05.

childneurologyfoundation.org

Rathore, Geetanjali. "Molybdenum Cofactor Deficiency (MoCD) Type A". Child Neurology Foundation. Retrieved 20 January 2023.

doi.org

Reiss J, Johnson JL (June 2003). "Mutations in the molybdenum cofactor biosynthetic genes MOCS1, MOCS2, and GEPH". Human Mutation. 21 (6): 569–76. doi:10.1002/humu.10223. PMID 12754701. S2CID 41013043.
Ichida K, Aydin HI, Hosoyamada M, et al. (2006). "A Turkish case with molybdenum cofactor deficiency". Nucleosides, Nucleotides & Nucleic Acids. 25 (9–11): 1087–91. doi:10.1080/15257770600894022. PMID 17065069. S2CID 40601679.

fda.gov

"FDA Approves First Treatment for Molybdenum Cofactor Deficiency Type A". U.S. Food and Drug Administration (FDA) (Press release). 26 February 2021. Retrieved 26 February 2021. This article incorporates text from this source, which is in the public domain.

imoa.info

"Molybdenum cofactor deficiency in humans: Neurological consequences of sulfite oxidase deficiency". Archived from the original on 2008-10-11. Retrieved 2009-11-08.^{[full citation needed]}

news.com.au

McArthur, Grant (November 5, 2009). "Doctor cures 'Baby Z' of molybdenum cofactor deficiency in medical world first". news.com.au. Retrieved November 5, 2009.

nih.gov

pubmed.ncbi.nlm.nih.gov

Reiss J, Johnson JL (June 2003). "Mutations in the molybdenum cofactor biosynthetic genes MOCS1, MOCS2, and GEPH". Human Mutation. 21 (6): 569–76. doi:10.1002/humu.10223. PMID 12754701. S2CID 41013043.
Ichida K, Aydin HI, Hosoyamada M, et al. (2006). "A Turkish case with molybdenum cofactor deficiency". Nucleosides, Nucleotides & Nucleic Acids. 25 (9–11): 1087–91. doi:10.1080/15257770600894022. PMID 17065069. S2CID 40601679.

semanticscholar.org

api.semanticscholar.org

Reiss J, Johnson JL (June 2003). "Mutations in the molybdenum cofactor biosynthetic genes MOCS1, MOCS2, and GEPH". Human Mutation. 21 (6): 569–76. doi:10.1002/humu.10223. PMID 12754701. S2CID 41013043.
Ichida K, Aydin HI, Hosoyamada M, et al. (2006). "A Turkish case with molybdenum cofactor deficiency". Nucleosides, Nucleotides & Nucleic Acids. 25 (9–11): 1087–91. doi:10.1080/15257770600894022. PMID 17065069. S2CID 40601679.

timesonline.co.uk

Tedmanson, Sophie (November 5, 2009). "Doctors risk untried drug to stop baby's brain dissolving". The Times. London. Retrieved May 13, 2010.^{[dead link]}

web.archive.org

"Molybdenum cofactor deficiency in humans: Neurological consequences of sulfite oxidase deficiency". Archived from the original on 2008-10-11. Retrieved 2009-11-08.^{[full citation needed]}
Samantha Donovan (2009-11-05). "Dying baby cured in world first". abc.net.au/news. Australian Broadcasting Corporation. Archived from the original on November 6, 2009. Retrieved 2009-11-05.