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CALR-mutated patients with low allele burden represent a specific subtype of essential thrombocythemia: A study on behalf of FIM and GBMHM.
Am J Hematol. 2024 May;99(5):1001-1004. doi: 10.1002/ajh.27265. Epub 2024 Feb 25.
Am J Hematol. 2024.
PMID: 38404143
How to diagnose acid sphingomyelinase deficiency (ASMD) and Niemann-Pick disease type C from bone marrow and peripheral blood smears.
Girard S, Pettazzoni M, Froissart R, Pagan C, Boyer T, Dulucq S, Gonçalves Monteiro V, Lechevalier N, Loosveld M, Lours C, Mayeur-Rousse C, Pannetier M, Peillon C, Rosenthal MA, Sep Hieng S, Trichet C, Baseggio L; on behalf the French‐Speaking Cellular Haematology Group (GFHC).
Girard S, et al. Among authors: goncalves monteiro v.
Hemasphere. 2024 Nov 5;8(11):e70042. doi: 10.1002/hem3.70042. eCollection 2024 Nov.
Hemasphere. 2024.
PMID: 39507854
Free PMC article.
No abstract available.
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