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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 1
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2017 2
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48 results

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Page 1
Adenosine deaminase deficiency: a review.
Flinn AM, Gennery AR. Flinn AM, et al. Orphanet J Rare Dis. 2018 Apr 24;13(1):65. doi: 10.1186/s13023-018-0807-5. Orphanet J Rare Dis. 2018. PMID: 29690908 Free PMC article. Review.
Polyarteritis nodosa.
Bilginer Y, Ozen S. Bilginer Y, et al. Curr Opin Pediatr. 2022 Apr 1;34(2):229-233. doi: 10.1097/MOP.0000000000001106. Curr Opin Pediatr. 2022. PMID: 35081554 Review.
Severe combined immunodeficiency diagnosis and genetic defects.
Aranda CS, Gouveia-Pereira MP, da Silva CJM, Rizzo MCFV, Ishizuka E, de Oliveira EB, Condino-Neto A. Aranda CS, et al. Immunol Rev. 2024 Mar;322(1):138-147. doi: 10.1111/imr.13310. Epub 2024 Jan 29. Immunol Rev. 2024. PMID: 38287514 Review.
Genetic and biochemical consequences of adenosine deaminase deficiency in humans.
Bose R, Nandagopal K. Bose R, et al. Indian J Biochem Biophys. 2013 Oct;50(5):345-56. Indian J Biochem Biophys. 2013. PMID: 24772956 Review.
Due to underlying allelic heterogeneity, the disorder manifests as a spectrum, ranging from neonatal onset severe combined immunodeficiency to apparently normal partial adenosine deaminase deficiency. Tandem mass spectrometry coupled with high efficien …
Due to underlying allelic heterogeneity, the disorder manifests as a spectrum, ranging from neonatal onset severe combined immunodeficiency …
Deficiency of Adenosine Deaminase 2.
Coşkun Ç, Ünal Ş. Coşkun Ç, et al. Turk J Haematol. 2024 Aug 28;41(3):133-140. doi: 10.4274/tjh.galenos.2024.2024.0265. Epub 2024 Aug 9. Turk J Haematol. 2024. PMID: 39120005 Free PMC article. Review.
48 results