193 related articles for article (PubMed ID: 18326324)
21. Diamond Blackfan anemia: A paradigm for a ribosome-based disease.
Ellis SR; Massey AT
Med Hypotheses; 2006; 66(3):643-8. PubMed ID: 16239073
[TBL] [Abstract][Full Text] [Related]
22. Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromes.
Alter BP; Rosenberg PS; Day T; Menzel S; Giri N; Savage SA; Thein SL
Br J Haematol; 2013 Aug; 162(4):542-6. PubMed ID: 23713742
[TBL] [Abstract][Full Text] [Related]
23. Fanconi's anaemia and related bone marrow failure syndromes.
Dokal I
Br Med Bull; 2006; 77-78():37-53. PubMed ID: 16968690
[TBL] [Abstract][Full Text] [Related]
24. Bone marrow cells from patients with Shwachman-Diamond syndrome abnormally express genes involved in ribosome biogenesis and RNA processing.
Rujkijyanont P; Adams SL; Beyene J; Dror Y
Br J Haematol; 2009 Jun; 145(6):806-15. PubMed ID: 19438500
[TBL] [Abstract][Full Text] [Related]
25. The Czech National Diamond-Blackfan Anemia Registry: clinical data and ribosomal protein mutations update.
Pospisilova D; Cmejlova J; Ludikova B; Stary J; Cerna Z; Hak J; Timr P; Petrtylova K; Blatny J; Vokurka S; Cmejla R
Blood Cells Mol Dis; 2012 Apr; 48(4):209-18. PubMed ID: 22381658
[TBL] [Abstract][Full Text] [Related]
26. Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes.
Hamilton JG; Hutson SP; Frohnmayer AE; Han PK; Peters JA; Carr AG; Alter BP
J Genet Couns; 2015 Oct; 24(5):760-70. PubMed ID: 25540896
[TBL] [Abstract][Full Text] [Related]
27. Molecular mechanisms of pathology and treatment in Diamond Blackfan Anaemia.
Horos R; von Lindern M
Br J Haematol; 2012 Dec; 159(5):514-27. PubMed ID: 23016900
[TBL] [Abstract][Full Text] [Related]
28. A novel initiation codon mutation in the ribosomal protein S17 gene (RPS17) in a patient with Diamond-Blackfan anemia.
Song MJ; Yoo EH; Lee KO; Kim GN; Kim HJ; Kim SY; Kim SH
Pediatr Blood Cancer; 2010 Apr; 54(4):629-31. PubMed ID: 19953637
[TBL] [Abstract][Full Text] [Related]
29. How Altered Ribosome Production Can Cause or Contribute to Human Disease: The Spectrum of Ribosomopathies.
Venturi G; Montanaro L
Cells; 2020 Oct; 9(10):. PubMed ID: 33076379
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita.
Vulliamy TJ; Knight SW; Mason PJ; Dokal I
Blood Cells Mol Dis; 2001; 27(2):353-7. PubMed ID: 11259155
[TBL] [Abstract][Full Text] [Related]
32. Immune status of patients with inherited bone marrow failure syndromes.
Giri N; Alter BP; Penrose K; Falk RT; Pan Y; Savage SA; Williams M; Kemp TJ; Pinto LA
Am J Hematol; 2015 Aug; 90(8):702-8. PubMed ID: 25963299
[TBL] [Abstract][Full Text] [Related]
33. Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification.
Ruggero D; Grisendi S; Piazza F; Rego E; Mari F; Rao PH; Cordon-Cardo C; Pandolfi PP
Science; 2003 Jan; 299(5604):259-62. PubMed ID: 12522253
[TBL] [Abstract][Full Text] [Related]
34. [Ribosomal protein in impaired erythropoiesis: Diamond-Blackfan anemia and 5q- syndrome].
Ito E
Rinsho Ketsueki; 2009 Oct; 50(10):1539-47. PubMed ID: 19915364
[No Abstract] [Full Text] [Related]
35. [Impaired ribosomal protein and bone marrow failure].
Hamaguchi I
Rinsho Ketsueki; 2010 Aug; 51(8):638-45. PubMed ID: 20805670
[No Abstract] [Full Text] [Related]
36. Shwachman-Diamond syndrome.
Shimamura A
Semin Hematol; 2006 Jul; 43(3):178-88. PubMed ID: 16822460
[TBL] [Abstract][Full Text] [Related]
37. Identification of DKC1 gene mutations in Japanese patients with X-linked dyskeratosis congenita.
Kanegane H; Kasahara Y; Okamura J; Hongo T; Tanaka R; Nomura K; Kojima S; Miyawaki T
Br J Haematol; 2005 May; 129(3):432-4. PubMed ID: 15842668
[TBL] [Abstract][Full Text] [Related]
38. Aplastic Anemia, Pediatric Aspects.
Alter BP
Oncologist; 1996; 1(6):361-366. PubMed ID: 10388017
[TBL] [Abstract][Full Text] [Related]
39. Dyskeratosis congenita: molecular insights into telomerase function, ageing and cancer.
Marrone A; Dokal I
Expert Rev Mol Med; 2004 Dec; 6(26):1-23. PubMed ID: 15613268
[TBL] [Abstract][Full Text] [Related]
40. Dyskeratosis congenita: advances in the understanding of the telomerase defect and the role of stem cell transplantation.
de la Fuente J; Dokal I
Pediatr Transplant; 2007 Sep; 11(6):584-94. PubMed ID: 17663679
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
