Adenosine deaminase deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Adenosine deaminase deficiency" in English language version.

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11nih.gov

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7doi.org

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2uptodate.com

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1semanticscholar.org

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1web.archive.org

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1utah.edu

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1nytimes.com

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1seekingalpha.com

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1europa.eu

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1nasonline.org

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doi.org

Flinn AM, Gennery AR (April 2018). "Adenosine deaminase deficiency: a review". Orphanet Journal of Rare Diseases. 13 (1): 65. doi:10.1186/s13023-018-0807-5. PMC 5916829. PMID 29690908.
Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS (October 1998). "Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles". American Journal of Human Genetics. 63 (4): 1049–1059. doi:10.1086/302054. PMC 1377486. PMID 9758612.
Whitmore KV, Gaspar HB (2016-08-16). "Adenosine Deaminase Deficiency - More Than Just an Immunodeficiency". Frontiers in Immunology. 7: 314. doi:10.3389/fimmu.2016.00314. PMC 4985714. PMID 27579027.
Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JM, Lechler RI, et al. (September 1994). "Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency". Journal of Immunology. 153 (5): 2331–2339. doi:10.4049/jimmunol.153.5.2331. PMID 8051429. S2CID 43108821.
Liebowitz J, Hellmann DB, Schnappauf O (August 2019). "Thirty Years of Followup in 3 Patients with Familial Polyarteritis Nodosa due to Adenosine Deaminase 2 Deficiency". The Journal of Rheumatology. 46 (8): 1059–1060. doi:10.3899/jrheum.180820. PMID 31092714.
Sanchez JJ, Monaghan G, Børsting C, Norbury G, Morling N, Gaspar HB (May 2007). "Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry". Annals of Human Genetics. 71 (Pt 3): 336–347. doi:10.1111/j.1469-1809.2006.00338.x. PMID 17181544.
Kohn DB, Hershfield MS, Puck JM, Aiuti A, Blincoe A, Gaspar HB, et al. (March 2019). "Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency". The Journal of Allergy and Clinical Immunology. 143 (3): 852–863. doi:10.1016/j.jaci.2018.08.024. PMC 6688493. PMID 30194989.

europa.eu

ema.europa.eu

"Summary of opinion1 (initial authorisation) Strimvelis" (PDF). European Medicines Agency. 1 April 2016. pp. 1–2. Retrieved 13 April 2016.

nasonline.org

Motulsky A, Gartler S (2009). "Biographical Memoirs: Eloise R. Giblett" (PDF). National Academy of Sciences.

nih.gov

pubmed.ncbi.nlm.nih.gov

Flinn AM, Gennery AR (April 2018). "Adenosine deaminase deficiency: a review". Orphanet Journal of Rare Diseases. 13 (1): 65. doi:10.1186/s13023-018-0807-5. PMC 5916829. PMID 29690908.
Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS (October 1998). "Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles". American Journal of Human Genetics. 63 (4): 1049–1059. doi:10.1086/302054. PMC 1377486. PMID 9758612.
Whitmore KV, Gaspar HB (2016-08-16). "Adenosine Deaminase Deficiency - More Than Just an Immunodeficiency". Frontiers in Immunology. 7: 314. doi:10.3389/fimmu.2016.00314. PMC 4985714. PMID 27579027.
Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JM, Lechler RI, et al. (September 1994). "Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency". Journal of Immunology. 153 (5): 2331–2339. doi:10.4049/jimmunol.153.5.2331. PMID 8051429. S2CID 43108821.
Liebowitz J, Hellmann DB, Schnappauf O (August 2019). "Thirty Years of Followup in 3 Patients with Familial Polyarteritis Nodosa due to Adenosine Deaminase 2 Deficiency". The Journal of Rheumatology. 46 (8): 1059–1060. doi:10.3899/jrheum.180820. PMID 31092714.
Sanchez JJ, Monaghan G, Børsting C, Norbury G, Morling N, Gaspar HB (May 2007). "Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry". Annals of Human Genetics. 71 (Pt 3): 336–347. doi:10.1111/j.1469-1809.2006.00338.x. PMID 17181544.
Kohn DB, Hershfield MS, Puck JM, Aiuti A, Blincoe A, Gaspar HB, et al. (March 2019). "Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency". The Journal of Allergy and Clinical Immunology. 143 (3): 852–863. doi:10.1016/j.jaci.2018.08.024. PMC 6688493. PMID 30194989.

ncbi.nlm.nih.gov

Flinn AM, Gennery AR (April 2018). "Adenosine deaminase deficiency: a review". Orphanet Journal of Rare Diseases. 13 (1): 65. doi:10.1186/s13023-018-0807-5. PMC 5916829. PMID 29690908.
Arredondo-Vega FX, Santisteban I, Daniels S, Toutain S, Hershfield MS (October 1998). "Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles". American Journal of Human Genetics. 63 (4): 1049–1059. doi:10.1086/302054. PMC 1377486. PMID 9758612.
Whitmore KV, Gaspar HB (2016-08-16). "Adenosine Deaminase Deficiency - More Than Just an Immunodeficiency". Frontiers in Immunology. 7: 314. doi:10.3389/fimmu.2016.00314. PMC 4985714. PMID 27579027.
Kohn DB, Hershfield MS, Puck JM, Aiuti A, Blincoe A, Gaspar HB, et al. (March 2019). "Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency". The Journal of Allergy and Clinical Immunology. 143 (3): 852–863. doi:10.1016/j.jaci.2018.08.024. PMC 6688493. PMID 30194989.

nytimes.com

Naam R (2005-07-03). "'More Than Human' - New York Times". The New York Times. Retrieved 2008-02-28.

seekingalpha.com

House DW (1 April 2016). "European Ad Comm backs Glaxo's stem cell therapy Strimvelis for rare autoimmune disorder". Seeking Alpha. Retrieved 13 April 2016.

semanticscholar.org

api.semanticscholar.org

Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JM, Lechler RI, et al. (September 1994). "Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency". Journal of Immunology. 153 (5): 2331–2339. doi:10.4049/jimmunol.153.5.2331. PMID 8051429. S2CID 43108821.

uptodate.com

Grunebaum E, Kohn DB (September 2023). "Adenosine deaminase deficiency: Pathogenesis, clinical manifestations, and diagnosis". UpToDate. Wolters Kluwer. Retrieved 2023-12-20.
Grunebaum E, Kohn DB (July 2023). "Adenosine deaminase deficiency: Treatment and prognosis". UpToDate. Wolters Kluwer. Retrieved 21 Dec 2023.

utah.edu

learn.genetics.utah.edu

"Adenosine Deaminase (ADA) Deficiency". Genetic Science Learning Center. The University of Utah. Archived from the original on 2008-02-12. Retrieved 2008-02-28.

web.archive.org

"Adenosine Deaminase (ADA) Deficiency". Genetic Science Learning Center. The University of Utah. Archived from the original on 2008-02-12. Retrieved 2008-02-28.