19 related articles for article (PubMed ID: 22915449)
1. Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 (G208R) mutation.
Dührsen U; Kratz CP; Flotho C; Lauenstein T; Bommer M; König E; Brittinger G; Heimpel H
Ann Hematol; 2011 Mar; 90(3):301-6. PubMed ID: 20922527
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. Outcome after repair of atrioventricular septal defect with tetralogy of Fallot.
Shuhaiber JH; Robinson B; Gauvreau K; Breitbart R; Mayer JE; Del Nido PJ; Pigula F
J Thorac Cardiovasc Surg; 2012 Feb; 143(2):338-43. PubMed ID: 21855095
[TBL] [Abstract][Full Text] [Related]
5. A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger.
Bastida JM; Malvestiti S; Boeckelmann D; Palma-Barqueros V; Wolter M; Lozano ML; Glonnegger H; Benito R; Zaninetti C; Sobotta F; Schilling FH; Morgan NV; Freson K; Rivera J; Zieger B
Cells; 2022 Oct; 11(20):. PubMed ID: 36291092
[TBL] [Abstract][Full Text] [Related]
6. Intracardiac repair of tetralogy of Fallot. Five-year review of 403 patients.
Chiariello L; Meyer J; Wukasch DC; Hallman GL; Cooley DA
J Thorac Cardiovasc Surg; 1975 Sep; 70(3):529-35. PubMed ID: 51950
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Tetralogy of Fallot and pulmonary atresia/ventricular septal defect.
Warnes CA
Cardiol Clin; 1993 Nov; 11(4):643-50. PubMed ID: 8252564
[TBL] [Abstract][Full Text] [Related]
9. GATA1 gene variants associated with thrombocytopenia and anemia.
Freson K; Wijgaerts A; Van Geet C
Platelets; 2017 Nov; 28(7):731-734. PubMed ID: 28895773
[No Abstract] [Full Text] [Related]
10.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
11.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
