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Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations.
Blood Adv. 2016 Nov 22;1(1):36-46. doi: 10.1182/bloodadvances.2016001313. eCollection 2016 Nov 29.
Blood Adv. 2016.
PMID: 29296694
Free PMC article.
The French paediatric cohort of Castleman disease: a retrospective report of 23 patients.
Borocco C, Ballot-Schmit C, Ackermann O, Aladjidi N, Delaleu J, Giacobbi-Milet V, Jannier S, Jeziorski E, Maurier F, Perel Y, Piguet C, Oksenhendler E, Koné-Paut I, Galeotti C.
Borocco C, et al. Among authors: giacobbi milet v.
Orphanet J Rare Dis. 2020 Apr 17;15(1):95. doi: 10.1186/s13023-020-1345-5.
Orphanet J Rare Dis. 2020.
PMID: 32303241
Free PMC article.
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The severe phenotype of Diamond-Blackfan anemia is modulated by heat shock protein 70.
Gastou M, Rio S, Dussiot M, Karboul N, Moniz H, Leblanc T, Sevin M, Gonin P, Larghéro J, Garrido C, Narla A, Mohandas N, Vainchenker W, Hermine O, Solary E, Da Costa L; French Society of Hematology (SFH); French Society of Immunology and Hematology (SHIP).
Gastou M, et al.
Blood Adv. 2017 Oct 10;1(22):1959-1976. doi: 10.1182/bloodadvances.2017008078. eCollection 2017 Oct 10.
Blood Adv. 2017.
PMID: 29296843
Free PMC article.
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