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Year | Number of Results |
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2006 | 1 |
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[Omenn Syndrome and DNA recombination defects].
Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(3):179-189. doi: 10.2177/jsci.40.179.
Nihon Rinsho Meneki Gakkai Kaishi. 2017.
PMID: 28747605
Free article.
Review.
Japanese.
Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan.
Kato M, Kimura H, Seki M, Shimada A, Hayashi Y, Morio T, Kumaki S, Ishida Y, Kamachi Y, Yachie A.
Kato M, et al.
Allergol Int. 2006 Jun;55(2):115-9. doi: 10.2332/allergolint.55.115.
Allergol Int. 2006.
PMID: 17075247
Free article.
Review.
Item in Clipboard
Omenn syndrome in the context of other B cell-negative severe combined immunodeficiencies.
Villa A, Sobacchi C, Vezzoni P.
Villa A, et al.
Isr Med Assoc J. 2002 Mar;4(3):218-21.
Isr Med Assoc J. 2002.
PMID: 11908269
Free article.
Review.
Item in Clipboard
Murine models of Omenn syndrome.
Wong SY, Roth DB.
Wong SY, et al.
J Clin Invest. 2007 May;117(5):1213-6. doi: 10.1172/JCI32214.
J Clin Invest. 2007.
PMID: 17476351
Free PMC article.
Review.
Item in Clipboard
Proposal of Slovenian guidelines for the diagnosis of neonatal erythroderma with a case report of Omenn syndrome.
Starbek Zorko M, Štublar Krašovec A, Dragoš V.
Starbek Zorko M, et al.
Acta Dermatovenerol Alp Pannonica Adriat. 2023 Jun;32(2):57-61.
Acta Dermatovenerol Alp Pannonica Adriat. 2023.
PMID: 37365893
Free article.
Review.
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