305 related articles for article (PubMed ID: 20514618)
1. Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I.
Vannier C; Behnisch W; Bartsch I; Sandrock K; Ertle F; Schmidt K; Busse A; Superti-Furga A; Kulozik A; Santoso S; Zieger B
Klin Padiatr; 2010 May; 222(3):150-3. PubMed ID: 20514618
[TBL] [Abstract][Full Text] [Related]
2. Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.
Sandrock K; Halimeh S; Wiegering V; Kappert G; Sauer K; Deeg N; Busse E; Zieger B
Klin Padiatr; 2012 Apr; 224(3):174-8. PubMed ID: 22513797
[TBL] [Abstract][Full Text] [Related]
3. Abnormal processing of the glycoprotein IIb transcript due to a nonsense mutation in exon 17 associated with Glanzmann's thrombasthenia.
Tomiyama Y; Kashiwagi H; Kosugi S; Shiraga M; Kanayama Y; Kurata Y; Matsuzawa Y
Thromb Haemost; 1995 May; 73(5):756-62. PubMed ID: 7482399
[TBL] [Abstract][Full Text] [Related]
4. Classification of Iranian patients with Glanzmann's Thrombasthenia using a flow cytometric method.
Farsinejad A; Abolghasemi H; Kazemi A; Aghaiipour M; Hadjati E; Faranoush M; Jazebi M; Ala F
Platelets; 2011; 22(5):321-7. PubMed ID: 21526886
[TBL] [Abstract][Full Text] [Related]
5. Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin.
Ruan C; Gu J; Wang X; Chu X; Pan J
Thromb Haemost; 1993 Jan; 69(1):64-9. PubMed ID: 8095357
[TBL] [Abstract][Full Text] [Related]
6. Homozygous Cys542-->Arg substitution in GPIIIa in a Swiss patient with type I Glanzmann's thrombasthenia.
Ruan J; Schmugge M; Clemetson KJ; Cazes E; Combrie R; Bourre F; Nurden AT
Br J Haematol; 1999 May; 105(2):523-31. PubMed ID: 10233432
[TBL] [Abstract][Full Text] [Related]
7. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
Tokgoz H; Torun Ozkan D; Caliskan U; Akar N
Platelets; 2015; 26(8):779-82. PubMed ID: 25734216
[TBL] [Abstract][Full Text] [Related]
8. [Mutation screening and prenatal diagnosis of a pedigree with Glanzmann's thrombasthenia].
Li W; Liu JL; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):251-5. PubMed ID: 21644217
[TBL] [Abstract][Full Text] [Related]
9. Role of RFLP using TspRI for carrier detection in Glanzmann's thrombasthenia: a report on two families.
Kannan M; Yadav BK; Ahmad F; Saxena R
Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e158-62. PubMed ID: 19170775
[TBL] [Abstract][Full Text] [Related]
10. Glanzmann's thrombasthenia: updated.
Nair S; Ghosh K; Kulkarni B; Shetty S; Mohanty D
Platelets; 2002 Nov; 13(7):387-93. PubMed ID: 12487785
[TBL] [Abstract][Full Text] [Related]
11. A new variant of Glanzmann's thrombasthenia (Strasbourg I). Platelets with functionally defective glycoprotein IIb-IIIa complexes and a glycoprotein IIIa 214Arg----214Trp mutation.
Lanza F; Stierlé A; Fournier D; Morales M; André G; Nurden AT; Cazenave JP
J Clin Invest; 1992 Jun; 89(6):1995-2004. PubMed ID: 1602006
[TBL] [Abstract][Full Text] [Related]
12. A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombasthenia.
Grimaldi CM; Chen F; Scudder LE; Coller BS; French DL
Blood; 1996 Sep; 88(5):1666-75. PubMed ID: 8781422
[TBL] [Abstract][Full Text] [Related]
13. Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India.
Vijapurkar M; Ghosh K; Shetty S
Platelets; 2009 Feb; 20(1):35-40. PubMed ID: 19172520
[TBL] [Abstract][Full Text] [Related]
14. A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.
Losonczy G; Rosenberg N; Kiss C; Kappelmayer J; Vereb G; Kerényi A; Balogh I; Muszbek L
Thromb Haemost; 2005 May; 93(5):904-9. PubMed ID: 15886807
[TBL] [Abstract][Full Text] [Related]
15. Biochemical and molecular basis of Glanzmann's thrombasthenia.
Perutelli P; Mori PG
Haematologica; 1992; 77(5):421-6. PubMed ID: 1483593
[TBL] [Abstract][Full Text] [Related]
16. Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations.
Sandrock-Lang K; Oldenburg J; Wiegering V; Halimeh S; Santoso S; Kurnik K; Fischer L; Tsakiris DA; Sigl-Kraetzig M; Brand B; Bührlen M; Kraetzer K; Deeg N; Hund M; Busse E; Kahle A; Zieger B
Thromb Haemost; 2015 Apr; 113(4):782-91. PubMed ID: 25373348
[TBL] [Abstract][Full Text] [Related]
17. Molecular genetic analysis of a compound heterozygote for the glycoprotein (GP) IIb gene associated with Glanzmann's thrombasthenia: disruption of the 674-687 disulfide bridge in GPIIb prevents surface exposure of GPIIb-IIIa complexes.
González-Manchón C; Fernández-Pinel M; Arias-Salgado EG; Ferrer M; Alvarez MV; García-Muñoz S; Ayuso MS; Parrilla R
Blood; 1999 Feb; 93(3):866-75. PubMed ID: 9920835
[TBL] [Abstract][Full Text] [Related]
18. A novel (288delC) mutation in exon 2 of GPIIb associated with type I Glanzmann's thrombasthenia.
Tao J; Arias-Salgado EG; González-Manchón C; Díaz-Cremades J; Ayuso MS; Parrilla R
Br J Haematol; 2000 Oct; 111(1):96-103. PubMed ID: 11091187
[TBL] [Abstract][Full Text] [Related]
19. Description of 10 new mutations in platelet glycoprotein IIb (alphaIIb) and glycoprotein IIIa (beta3) genes.
Vinciguerra C; Bordet JC; Beaune G; Grenier C; Dechavanne M; Négrier C
Platelets; 2001 Dec; 12(8):486-95. PubMed ID: 11798398
[TBL] [Abstract][Full Text] [Related]
20. [Analysis of the GPIIb and GPIIIa genes in patients with Glanzmann's thrombasthenia].
Yasunaga M; Ryo R; Adachi M; Sugano W; Yoshida A; Nakayama K; Saigo K; Yasunaga K; Yamaguchi N
Rinsho Ketsueki; 1992 Feb; 33(2):133-8. PubMed ID: 1635160
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
