These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
142 related articles for article (PubMed ID: 21501768)
1. [Shwachman-Bodian-Diamond syndrome (SBDS). Answer to January e-quid]. Iannessi A; Novellas S J Radiol; 2011 Mar; 92(3):262-5. PubMed ID: 21501768 [No Abstract] [Full Text] [Related]
2. Two cases of Shwachman-Diamond syndrome in adolescents confirmed by genetic analysis. Cho WK; Jung IA; Kim J; Chae H; Kim M; Chung NG; Suh BK Ann Lab Med; 2015 Mar; 35(2):269-71. PubMed ID: 25729736 [No Abstract] [Full Text] [Related]
3. Endocrine evaluation of children with and without Shwachman-Bodian-Diamond syndrome gene mutations and Shwachman-Diamond syndrome. Myers KC; Rose SR; Rutter MM; Mehta PA; Khoury JC; Cole T; Harris RE J Pediatr; 2013 Jun; 162(6):1235-40, 1240.e1. PubMed ID: 23305959 [TBL] [Abstract][Full Text] [Related]
4. Deficiency of Sbds in the mouse pancreas leads to features of Shwachman-Diamond syndrome, with loss of zymogen granules. Tourlakis ME; Zhong J; Gandhi R; Zhang S; Chen L; Durie PR; Rommens JM Gastroenterology; 2012 Aug; 143(2):481-92. PubMed ID: 22510201 [TBL] [Abstract][Full Text] [Related]
5. Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features. Carapito R; Konantz M; Paillard C; Miao Z; Pichot A; Leduc MS; Yang Y; Bergstrom KL; Mahoney DH; Shardy DL; Alsaleh G; Naegely L; Kolmer A; Paul N; Hanauer A; Rolli V; Müller JS; Alghisi E; Sauteur L; Macquin C; Morlon A; Sancho CS; Amati-Bonneau P; Procaccio V; Mosca-Boidron AL; Marle N; Osmani N; Lefebvre O; Goetz JG; Unal S; Akarsu NA; Radosavljevic M; Chenard MP; Rialland F; Grain A; Béné MC; Eveillard M; Vincent M; Guy J; Faivre L; Thauvin-Robinet C; Thevenon J; Myers K; Fleming MD; Shimamura A; Bottollier-Lemallaz E; Westhof E; Lengerke C; Isidor B; Bahram S J Clin Invest; 2017 Nov; 127(11):4090-4103. PubMed ID: 28972538 [TBL] [Abstract][Full Text] [Related]
6. Breast cancer in a case of Shwachman Diamond syndrome. Singh SA; Vlachos A; Morgenstern NJ; Ouansafi I; Ip W; Rommens JM; Durie P; Shimamura A; Lipton JM Pediatr Blood Cancer; 2012 Nov; 59(5):945-6. PubMed ID: 22213587 [TBL] [Abstract][Full Text] [Related]
7. Diagnosis, Treatment, and Molecular Pathology of Shwachman-Diamond Syndrome. Nelson AS; Myers KC Hematol Oncol Clin North Am; 2018 Aug; 32(4):687-700. PubMed ID: 30047420 [TBL] [Abstract][Full Text] [Related]
8. Immunophenotypic analysis of hematopoiesis in patients suffering from Shwachman-Bodian-Diamond Syndrome. Mercuri A; Cannata E; Perbellini O; Cugno C; Balter R; Zaccaron A; Tridello G; Pizzolo G; De Bortoli M; Krampera M; Cipolli M; Cesaro S Eur J Haematol; 2015 Oct; 95(4):308-15. PubMed ID: 25402872 [TBL] [Abstract][Full Text] [Related]
9. Shwachman-Bodian-Diamond syndrome: metaphyseal chondrodysplasia in children with pancreatic insufficiency and neutropenia. Levin TL; Mäkitie O; Berdon WE; Lachman RS Pediatr Radiol; 2015 Jul; 45(7):1066-71. PubMed ID: 25416932 [TBL] [Abstract][Full Text] [Related]
10. The Greek Registry of Shwachman Diamond-Syndrome: Molecular and clinical data. Delaporta P; Sofocleous C; Economou M; Makis A; Kostaridou S; Kattamis A Pediatr Blood Cancer; 2017 Nov; 64(11):. PubMed ID: 28509441 [TBL] [Abstract][Full Text] [Related]
11. Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients. Minelli A; Nacci L; Valli R; Pietrocola G; Ramenghi U; Locatelli F; Brescia L; Nicolis E; Cipolli M; Danesino C Blood Cells Mol Dis; 2016 Sep; 60():33-5. PubMed ID: 27519942 [No Abstract] [Full Text] [Related]
13. Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome. Nacci L; Danesino C; Sainati L; Longoni D; Poli F; Cipolli M; Perobelli S; Nicolis E; Cannioto Z; Morini J; Valli R; Pasquali F; Minelli A Br J Haematol; 2014 May; 165(4):573-5. PubMed ID: 24484588 [No Abstract] [Full Text] [Related]
14. Shwachman-Bodian-Diamond syndrome (SBDS) protein deficiency impairs translation re-initiation from C/EBPα and C/EBPβ mRNAs. In K; Zaini MA; Müller C; Warren AJ; von Lindern M; Calkhoven CF Nucleic Acids Res; 2016 May; 44(9):4134-46. PubMed ID: 26762974 [TBL] [Abstract][Full Text] [Related]
15. Novel myopathy in a newborn with Shwachman-Diamond syndrome and review of neonatal presentation. Topa A; Tulinius M; Oldfors A; Hedberg-Oldfors C Am J Med Genet A; 2016 May; 170A(5):1155-64. PubMed ID: 26866830 [TBL] [Abstract][Full Text] [Related]
16. Of blood, bones, and ribosomes: is Swachman-Diamond syndrome a ribosomopathy? Johnson AW; Ellis SR Genes Dev; 2011 May; 25(9):898-900. PubMed ID: 21536731 [TBL] [Abstract][Full Text] [Related]
17. [Two cases of Shwachman-Diamond syndrome with genetic confirmation and literature review]. Shen J; Lin K; An Y; Wu YM; Qiao ZW; Yu H; Zhu QR; Zhang T Zhonghua Er Ke Za Zhi; 2013 Sep; 51(9):679-83. PubMed ID: 24330988 [TBL] [Abstract][Full Text] [Related]
18. Mislocalization or low expression of mutated Shwachman-Bodian-Diamond syndrome protein. Yamaguchi M; Fujimura K; Kanegane H; Toga-Yamaguchi H; Chopra R; Okamura N Int J Hematol; 2011 Jul; 94(1):54-62. PubMed ID: 21660439 [TBL] [Abstract][Full Text] [Related]
19. Shwachman-Diamond Syndrome: Molecular Mechanisms and Current Perspectives. Bezzerri V; Cipolli M Mol Diagn Ther; 2019 Apr; 23(2):281-290. PubMed ID: 30413969 [TBL] [Abstract][Full Text] [Related]
20. Hematologically important mutations: Shwachman-Diamond syndrome. Costa E; Santos R Blood Cells Mol Dis; 2008; 40(2):183-4. PubMed ID: 17916435 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]