BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

33 related articles for article (PubMed ID: 38564005)

  • 1. 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]  

  • 2. Bernard-Soulier syndrome (hemorrhagiparous thrombocytic dystrophy).
    Lanza F
    Orphanet J Rare Dis; 2006 Nov; 1():46. PubMed ID: 17109744
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia.
    Sivapalaratnam S; Westbury SK; Stephens JC; Greene D; Downes K; Kelly AM; Lentaigne C; Astle WJ; Huizinga EG; Nurden P; Papadia S; Peerlinck K; Penkett CJ; Perry DJ; Roughley C; Simeoni I; Stirrups K; Hart DP; Tait RC; Mumford AD; ; Laffan MA; Freson K; Ouwehand WH; Kunishima S; Turro E
    Blood; 2017 Jan; 129(4):520-524. PubMed ID: 28064200
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene.
    Marzollo A; Zampieri S; Barozzi S; Yousaf MA; Quartararo J; De Rocco D; Faleschini M; Marconi C; Berti CC; Bozzi V; Russo G; Giordano P; Goffrini P; Bresolin S; Pastore A; Savoia A; Pecci A
    Br J Haematol; 2024 May; ():. PubMed ID: 38815995
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MPIG6B Gene-Related Myelofibrosis: A Rare Inherited Disease That Is Frequently Described in Arab Population.
    Attar LJ; Alelaimat A; Alshorman A; Aladily TN
    Avicenna J Med; 2024 Jan; 14(1):69-72. PubMed ID: 38694137
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genetic abnormalities of Bernard-Soulier syndrome.
    Kunishima S; Kamiya T; Saito H
    Int J Hematol; 2002 Nov; 76(4):319-27. PubMed ID: 12463594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A
    Skalníková M; Staňo Kozubík K; Trizuljak J; Vrzalová Z; Radová L; Réblová K; Holbová R; Kurucová T; Svozilová H; Štika J; Blaháková I; Dvořáčková B; Prudková M; Stehlíková O; Šmída M; Křen L; Smejkal P; Pospíšilová Š; Doubek M
    Int J Mol Sci; 2022 Jan; 23(2):. PubMed ID: 35055070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical phenotype in heterozygote and biallelic Bernard-Soulier syndrome--a case control study.
    Bragadottir G; Birgisdottir ER; Gudmundsdottir BR; Hilmarsdottir B; Vidarsson B; Magnusson MK; Larsen OH; Sorensen B; Ingerslev J; Onundarson PT
    Am J Hematol; 2015 Feb; 90(2):149-55. PubMed ID: 25370924
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations.
    Savoia A; Pastore A; De Rocco D; Civaschi E; Di Stazio M; Bottega R; Melazzini F; Bozzi V; Pecci A; Magrin S; Balduini CL; Noris P
    Haematologica; 2011 Mar; 96(3):417-23. PubMed ID: 21173099
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 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]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.