Wang P, Jiang W, Lai T, Liu Q, Shen Y, Ye B
Haematologica. 2024; 109(9):2778-2789.
PMID: 38988263
PMC: 11367197.
DOI: 10.3324/haematol.2023.284312.
Veltra D, Marinakis N, Kotsios I, Delaporta P, Kekou K, Kosma K
Children (Basel). 2024; 11(6).
PMID: 38929284
PMC: 11201973.
DOI: 10.3390/children11060705.
Yamaguchi M, Sera Y, Toga-Yamaguchi H, Kanegane H, Iguchi Y, Fujimura K
Int J Hematol. 2024; 119(4):383-391.
PMID: 38240987
DOI: 10.1007/s12185-024-03709-z.
Oyarbide U, Shah A, Staton M, Snyderman M, Sapra A, Calo E
Life Sci Alliance. 2023; 6(12).
PMID: 37816584
PMC: 10565674.
DOI: 10.26508/lsa.202201856.
Parker M, Karbstein K
J Cell Biol. 2023; 222(4).
PMID: 36790396
PMC: 9960125.
DOI: 10.1083/jcb.202209115.
Case report: Venetoclax therapy in a boy with acute myeloid leukemia in Shwachman Diamond syndrome.
Naviglio S, Grasso A, Iacono C, Zanella G, Kiren V, Giurici N
Front Pediatr. 2023; 10:1059569.
PMID: 36699295
PMC: 9869240.
DOI: 10.3389/fped.2022.1059569.
Phenotypic Variation in Two Siblings Affected with Shwachman-Diamond Syndrome: The Use of Expert Variant Interpreter (eVai) Suggests Clinical Relevance of a Variant in the KMT2A Gene.
Taha I, De Paoli F, Foroni S, Zucca S, Limongelli I, Cipolli M
Genes (Basel). 2022; 13(8).
PMID: 35893049
PMC: 9394309.
DOI: 10.3390/genes13081314.
Lessons From Pediatric MDS: Approaches to Germline Predisposition to Hematologic Malignancies.
Avagyan S, Shimamura A
Front Oncol. 2022; 12:813149.
PMID: 35356204
PMC: 8959480.
DOI: 10.3389/fonc.2022.813149.
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome.
West R, Calvo K, Embree L, Wang W, Tuschong L, Bauer T
Blood Adv. 2021; 6(3):793-807.
PMID: 34529785
PMC: 8945308.
DOI: 10.1182/bloodadvances.2021005065.
Clonal hematopoiesis and bone marrow failure syndromes.
Pasca S, Gondek L
Best Pract Res Clin Haematol. 2021; 34(2):101273.
PMID: 34404525
PMC: 8374084.
DOI: 10.1016/j.beha.2021.101273.
Association of isochromosome (7)(q10) in Shwachman-Diamond syndrome with the severity of cytopenia.
Shimosato Y, Tanoshima R, Tsujimoto S, Takeuchi M, Sasaki K, Kajiwara R
Clin Case Rep. 2018; 6(1):125-128.
PMID: 29375851
PMC: 5771925.
DOI: 10.1002/ccr3.1249.
Mechanistic insight into eukaryotic 60S ribosomal subunit biogenesis by cryo-electron microscopy.
Greber B
RNA. 2016; 22(11):1643-1662.
PMID: 27875256
PMC: 5066618.
DOI: 10.1261/rna.057927.116.
Approach to the patient with neutropenia in childhood.
Celkan T, Koc B
Turk Pediatri Ars. 2015; 50(3):136-44.
PMID: 26568688
PMC: 4629920.
DOI: 10.5152/TurkPediatriArs.2015.2295.
Ribosomopathies: Global process, tissue specific defects.
Yelick P, Trainor P
Rare Dis. 2015; 3(1):e1025185.
PMID: 26442198
PMC: 4590025.
DOI: 10.1080/21675511.2015.1025185.
Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes.
Zambetti N, Bindels E, van Strien P, Valkhof M, Adisty M, Hoogenboezem R
Haematologica. 2015; 100(10):1285-93.
PMID: 26185170
PMC: 4591760.
DOI: 10.3324/haematol.2015.131573.
Current insights into inherited bone marrow failure syndromes.
Chung N, Kim M
Korean J Pediatr. 2014; 57(8):337-44.
PMID: 25210520
PMC: 4155177.
DOI: 10.3345/kjp.2014.57.8.337.
Spindle microtubule dysfunction and cancer predisposition.
Stumpff J, Ghule P, Shimamura A, Stein J, Greenblatt M
J Cell Physiol. 2014; 229(12):1881-3.
PMID: 24905602
PMC: 4149604.
DOI: 10.1002/jcp.24691.
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms.
Valli R, Pressato B, Marletta C, Mare L, Montalbano G, Lo Curto F
Mol Cytogenet. 2013; 6(1):56.
PMID: 24330778
PMC: 3914702.
DOI: 10.1186/1755-8166-6-56.
Cytokine production by bone marrow mononuclear cells in inherited bone marrow failure syndromes.
Matsui K, Giri N, Alter B, Pinto L
Br J Haematol. 2013; 163(1):81-92.
PMID: 23889587
PMC: 3930339.
DOI: 10.1111/bjh.12475.
Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.
Myers K, Davies S, Shimamura A
Hematol Oncol Clin North Am. 2013; 27(1):117-28, ix.
PMID: 23351992
PMC: 5693339.
DOI: 10.1016/j.hoc.2012.10.003.