42 related articles for article (PubMed ID: 23414566)
1. Correction of murine Bernard-Soulier syndrome by lentivirus-mediated gene therapy.
Kanaji S; Kuether EL; Fahs SA; Schroeder JA; Ware J; Montgomery RR; Shi Q
Mol Ther; 2012 Mar; 20(3):625-32. PubMed ID: 22044935
[TBL] [Abstract][Full Text] [Related]
2. Bernard-Soulier syndrome caused by two novel heterozygous
Zhang S; Ling J; Cui K; Zhan S; Zheng J; Wang W; Fan J; Hu S
Hematology; 2024 Dec; 29(1):2334642. PubMed ID: 38564005
[TBL] [Abstract][Full Text] [Related]
3. Bernard-Soulier syndrome (hemorrhagiparous thrombocytic dystrophy).
Lanza F
Orphanet J Rare Dis; 2006 Nov; 1():46. PubMed ID: 17109744
[TBL] [Abstract][Full Text] [Related]
4. Bernard-Soulier syndrome caused by a novel GP1BB variant and 22q11.2 deletion.
Nagoshi R; Sakamoto A; Imai T; Uchiyama T; Kaname T; Kunishima S; Ishiguro A
Int J Hematol; 2024 Apr; ():. PubMed ID: 38625506
[TBL] [Abstract][Full Text] [Related]
5. WY-14643, a novel antiplatelet and antithrombotic agent targeting the GPIbα receptor.
Cao C; Yang Q; Xia X; Chen Z; Liu P; Wu X; Hu H; Ding Z; Li X
Thromb Res; 2024 Apr; 238():41-51. PubMed ID: 38669962
[TBL] [Abstract][Full Text] [Related]
6. Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion.
Kunishima S; Imai T; Kobayashi R; Kato M; Ogawa S; Saito H
Pediatr Int; 2013 Aug; 55(4):434-7. PubMed ID: 23566026
[TBL] [Abstract][Full Text] [Related]
7. Novel Compound Heterozygous Mutations in Two Families With Bernard-Soulier Syndrome.
Minkov M; Zeitlhofer P; Zoubek A; Kager L; Panzer S; Haas OA
Front Pediatr; 2020; 8():589812. PubMed ID: 33553065
[No Abstract] [Full Text] [Related]
8. A Novel Mutation in
Barozzi S; Bozzi V; De Rocco D; Giangregorio T; Noris P; Savoia A; Pecci A
Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638529
[TBL] [Abstract][Full Text] [Related]
9. Structure-function of platelet glycoprotein Ib-IX.
Quach ME; Li R
J Thromb Haemost; 2020 Dec; 18(12):3131-3141. PubMed ID: 32735697
[TBL] [Abstract][Full Text] [Related]
10. Novel nonsense mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome.
Kunishima S; Matsushita T; Ito T; Kamiya T; Saito H
Am J Hematol; 2002 Dec; 71(4):279-84. PubMed ID: 12447957
[TBL] [Abstract][Full Text] [Related]
11. Bernard-Soulier syndrome: novel nonsense mutation in GPIbbeta gene affecting GPIb-IX complex expression.
Hadjkacem B; Elleuch H; Gargouri J; Gargouri A
Ann Hematol; 2009 May; 88(5):465-72. PubMed ID: 18825380
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of the mutations in Bernard-Soulier syndrome.
Savoia A; Kunishima S; De Rocco D; Zieger B; Rand ML; Pujol-Moix N; Caliskan U; Tokgoz H; Pecci A; Noris P; Srivastava A; Ward C; Morel-Kopp MC; Alessi MC; Bellucci S; Beurrier P; de Maistre E; Favier R; Hézard N; Hurtaud-Roux MF; Latger-Cannard V; Lavenu-Bombled C; Proulle V; Meunier S; Négrier C; Nurden A; Randrianaivo H; Fabris F; Platokouki H; Rosenberg N; HadjKacem B; Heller PG; Karimi M; Balduini CL; Pastore A; Lanza F
Hum Mutat; 2014 Sep; 35(9):1033-45. PubMed ID: 24934643
[TBL] [Abstract][Full Text] [Related]
13. Novel Bernard-Soulier syndrome variants caused by compound heterozygous mutations (case I) or a cytoplasmic tail truncation (case II) of GPIbα.
Yamamoto N; Akamatsu N; Sakuraba H; Matsuno K; Hosoya R; Nogami H; Kasahara K; Mitsuyama S; Arai M
Thromb Res; 2013 Apr; 131(4):e160-7. PubMed ID: 23414566
[TBL] [Abstract][Full Text] [Related]
14. Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations.
Kunishima S; Sako M; Yamazaki T; Hamaguchi M; Saito H
Eur J Haematol; 2006 Dec; 77(6):501-12. PubMed ID: 16978236
[TBL] [Abstract][Full Text] [Related]
15. Bernard-Soulier syndrome: an update.
Andrews RK; Berndt MC
Semin Thromb Hemost; 2013 Sep; 39(6):656-62. PubMed ID: 23929303
[TBL] [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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]