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Items: 1 to 20 of 777

1.

Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes.

Dunn DE, Tanawattanacharoen P, Boccuni P, Nagakura S, Green SW, Kirby MR, Kumar MS, Rosenfeld S, Young NS.

Ann Intern Med. 1999 Sep 21;131(6):401-8.

PMID:
10498555
3.

Relationship between bone marrow failure syndromes and the presence of glycophosphatidyl inositol-anchored protein-deficient clones.

Maciejewski JP, Rivera C, Kook H, Dunn D, Young NS.

Br J Haematol. 2001 Dec;115(4):1015-22.

PMID:
11843844
4.

Increased frequency of HLA-DR2 in patients with paroxysmal nocturnal hemoglobinuria and the PNH/aplastic anemia syndrome.

Maciejewski JP, Follmann D, Nakamura R, Saunthararajah Y, Rivera CE, Simonis T, Brown KE, Barrett JA, Young NS.

Blood. 2001 Dec 15;98(13):3513-9.

5.

Special Education: Aplastic Anemia.

Teramura M, Mizoguchi H.

Oncologist. 1996;1(3):187-189.

6.

A cohort study of the nature of paroxysmal nocturnal hemoglobinuria clones and PIG-A mutations in patients with aplastic anemia.

Wanachiwanawin W, Siripanyaphinyo U, Piyawattanasakul N, Kinoshita T.

Eur J Haematol. 2006 Jun;76(6):502-9. Epub 2006 Mar 9.

PMID:
16529603
7.
8.

Paroxysmal nocturnal hemoglobinuria: the price for a chance.

Bessler M.

Schweiz Med Wochenschr. 1996 Nov 9;126(45):1912-21. Review.

PMID:
8946596
9.

Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anaemia patients: the high prevalence at diagnosis.

Wang H, Chuhjo T, Yamazaki H, Shiobara S, Teramura M, Mizoguchi H, Nakao S.

Eur J Haematol. 2001 Mar;66(3):200-5.

PMID:
11350489
10.

Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link.

Griscelli-Bennaceur A, Gluckman E, Scrobohaci ML, Jonveaux P, Vu T, Bazarbachi A, Carosella ED, Sigaux F, SociƩ G.

Blood. 1995 Mar 1;85(5):1354-63.

11.

Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay.

van der Schoot CE, Huizinga TW, van 't Veer-Korthof ET, Wijmans R, Pinkster J, von dem Borne AE.

Blood. 1990 Nov 1;76(9):1853-9.

12.

Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes.

Ware RE, Pickens CV, DeCastro CM, Howard TA.

Exp Hematol. 2001 Dec;29(12):1403-9.

PMID:
11750098
13.

Detection of paroxysmal nocturnal hemoglobinuria clones in patients with myelodysplastic syndromes and related bone marrow diseases, with emphasis on diagnostic pitfalls and caveats.

Wang SA, Pozdnyakova O, Jorgensen JL, Medeiros LJ, Stachurski D, Anderson M, Raza A, Woda BA.

Haematologica. 2009 Jan;94(1):29-37. doi: 10.3324/haematol.13601. Epub 2008 Nov 10.

14.

PNH revisited: Clinical profile, laboratory diagnosis and follow-up.

Gupta PK, Charan VD, Kumar H.

Indian J Pathol Microbiol. 2009 Jan-Mar;52(1):38-41.

15.
16.

Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia.

Mukhina GL, Buckley JT, Barber JP, Jones RJ, Brodsky RA.

Br J Haematol. 2001 Nov;115(2):476-82.

PMID:
11703352
17.

Screening for paroxysmal nocturnal hemoglobinuria (PNH) clone in Egyptian children with aplastic anemia.

Rizk S, Ibrahim IY, Mansour IM, Kandil D.

J Trop Pediatr. 2002 Jun;48(3):132-7.

PMID:
12164595
18.

Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome.

Wang H, Chuhjo T, Yasue S, Omine M, Nakao S.

Blood. 2002 Dec 1;100(12):3897-902. Epub 2002 Aug 8.

19.

A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins.

Schrezenmeier H, Hertenstein B, Wagner B, Raghavachar A, Heimpel H.

Exp Hematol. 1995 Jan;23(1):81-7. Erratum in: Exp Hematol 1995 Feb;23(2):181.

PMID:
7995374
20.

Acquired aplastic anemia.

Young NS.

Ann Intern Med. 2002 Apr 2;136(7):534-46. Review.

PMID:
11926789

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