117 related articles for article (PubMed ID: 22993897)
1. [X-linked thrombocytopenia with thalassemia in two families in Sweden. Consider hereditary causes of thrombocytopenia and bone marrow fibrosis].
Danielsson S; Merup M; Olsson L; Palmblad J; Aström M
Lakartidningen; 2012 Aug 22-Sep 4; 109(34-35):1474-7. PubMed ID: 22993897
[No Abstract] [Full Text] [Related]
2. X-linked thrombocytopenia with thalassemia displays bone marrow reticulin fibrosis and enhanced angiogenesis: comparisons with primary myelofibrosis.
Åström M; Hahn-Strömberg V; Zetterberg E; Vedin I; Merup M; Palmblad J
Am J Hematol; 2015 Mar; 90(3):E44-8. PubMed ID: 25421114
[TBL] [Abstract][Full Text] [Related]
3. Surgery of a cyanotic heart defect in an 11-year-old boy with thrombocytopenic thrombocytopathy and severe anemia due to a GATA-1 defect: hemostatic therapy.
Hoefer J; Streif W; Kilo J; Grimm M; Berger G; Velik-Salchner C
Klin Padiatr; 2012 Oct; 224(6):382-5. PubMed ID: 22915449
[TBL] [Abstract][Full Text] [Related]
4. Why the disorder induced by GATA1 Arg216Gln mutation should be called "X-linked thrombocytopenia with thalassemia" rather than "X-linked gray platelet syndrome".
Balduini CL; De Candia E; Savoia A
Blood; 2007 Oct; 110(7):2770-1; author reply 2771. PubMed ID: 17881640
[No Abstract] [Full Text] [Related]
5. Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemia.
Jamwal M; Aggarwal A; Sharma P; Bansal D; Maitra A; Das R
Blood Cells Mol Dis; 2020 Mar; 81():102391. PubMed ID: 31865264
[No Abstract] [Full Text] [Related]
6. [Hereditary thrombocytopenia-thrombocytopathy with myelofibrosis (author's transl)].
Delvallez N; Claisse JF; Faille N; Delobel J; Piussan C; Messerschmitt J
Sem Hop; 1980 Jun 18-25; 56(25-28):1154-8. PubMed ID: 6256862
[TBL] [Abstract][Full Text] [Related]
7. A novel GATA1 mutation (Stop414Arg) in a family with the rare X-linked blood group Lu(a-b-) phenotype and mild macrothrombocytic thrombocytopenia.
Singleton BK; Roxby DJ; Stirling JW; Spring FA; Wilson C; Poole J; Anstee DJ
Br J Haematol; 2013 Apr; 161(1):139-42. PubMed ID: 23278136
[No Abstract] [Full Text] [Related]
8. New germline GATA1 variant in females with anemia and thrombocytopenia.
Svidnicki MCCM; Filho MAF; Brandão MM; Dos Santos M; de Oliveira Dias R; Tavares RS; Assis-Mendonça GR; Traina F; Saad STO
Blood Cells Mol Dis; 2021 May; 88():102545. PubMed ID: 33611093
[TBL] [Abstract][Full Text] [Related]
9. First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β-thalassemia.
Singh N; Bhatia P; Jamwal M; Khadwal AR; Chhabra S; Hira JK; Das R; Sharma P
Int J Lab Hematol; 2023 Dec; 45(6):999-1002. PubMed ID: 37382348
[No Abstract] [Full Text] [Related]
10. [Agnogenic myelofibrosis].
Avilés A; Monroy L; Ambriz R; Butrón L; Pizzuto J
Gac Med Mex; 1981 Mar; 117(3):110-7. PubMed ID: 7327351
[No Abstract] [Full Text] [Related]
11. Captopril mitigates splenomegaly and myelofibrosis in the Gata1
Corey SJ; Jha J; McCart EA; Rittase WB; George J; Mattapallil JJ; Mehta H; Ognoon M; Bylicky MA; Summers TA; Day RM
J Cell Mol Med; 2018 Sep; 22(9):4274-4282. PubMed ID: 29971909
[TBL] [Abstract][Full Text] [Related]
12. [Polycythemia and splenomegaly in a 51-year-old woman].
Ribera JM; Abella E; Lloreta J
Med Clin (Barc); 1995 Jul; 105(5):191-6. PubMed ID: 7630233
[No Abstract] [Full Text] [Related]
13. Systemic lupus erythematosus presenting as myelofibrosis.
Konstantopoulos K; Terpos E; Prinolakis H; Kanta A; Variami E; Kanellopoulou G; Vaiopoulos G; Floros A; Androulaki A; Meletis J
Haematologia (Budap); 1998; 29(2):153-6. PubMed ID: 9728808
[TBL] [Abstract][Full Text] [Related]
14. X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation.
Tubman VN; Levine JE; Campagna DR; Monahan-Earley R; Dvorak AM; Neufeld EJ; Fleming MD
Blood; 2007 Apr; 109(8):3297-9. PubMed ID: 17209061
[TBL] [Abstract][Full Text] [Related]
15. Novel GATA1 mutation in residue D218 leads to macrothrombocytopenia and clinical bleeding problems.
Hermans C; De Waele L; Van Geet C; Freson K
Platelets; 2014; 25(4):305-7. PubMed ID: 23971719
[No Abstract] [Full Text] [Related]
16. Multiple myeloma with bone marrow biopsy features simulating concomitant chronic idiopathic myelofibrosis.
Schmidt U; Ruwe M; Leder LD
Nouv Rev Fr Hematol (1978); 1995; 37(2):159-63. PubMed ID: 7644355
[TBL] [Abstract][Full Text] [Related]
17. Autoimmune myelofibrosis. A steroid-responsive cause of bone marrow fibrosis associated with systemic lupus erythematosus.
Paquette RL; Meshkinpour A; Rosen PJ
Medicine (Baltimore); 1994 May; 73(3):145-52. PubMed ID: 8190037
[TBL] [Abstract][Full Text] [Related]
18. Hereditary thrombocytopenia. Report of three families.
Myllylä G; Pelkonen R; Ikkala E; Apajalahti J
Scand J Haematol; 1967 Dec; 4(6):441-52. PubMed ID: 6082223
[No Abstract] [Full Text] [Related]
19. [Early diagnosis of myelofibrosis].
Patakfalvi A; Zombai E; Gógl A
Z Gesamte Inn Med; 1969 Jul; 24(13):391-7. PubMed ID: 5384440
[No Abstract] [Full Text] [Related]
20. [Idiopathic myelofibrosis. Description of 6 cases and considerations on their clinical and diagnostic aspects].
Giardina MG; Matarazzo M; De Marco F; Varriale A; Cacciatore L
Recenti Prog Med; 1985 Nov; 76(11):571-5. PubMed ID: 4095373
[No Abstract] [Full Text] [Related]
[Next] [New Search]
