BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 32516168)

  • 1. Familial macro thrombocytopenia: role of genetics where morphology fails.
    Chaudhary H; Jindal A; Guleria S; Sharma S; Sachdeva MUS; Ahluwalia J
    Blood Coagul Fibrinolysis; 2020 Jul; 31(5):333-334. PubMed ID: 32516168
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diagnosis and treatment of
    Rabbolini DJ; Chun Y; Latimer M; Kunishima S; Fixter K; Valecha B; Tan P; Chew LP; Kile BT; Burt R; Radhakrishnan K; Bird R; Ockelford P; Gabrielli S; Chen Q; Stevenson WS; Ward CM; Morel-Kopp MC
    Platelets; 2018 Dec; 29(8):793-800. PubMed ID: 29090586
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial cases with MYH9 disorders caused by MYH9 S96L mutation.
    Murayama S; Akiyama M; Namba H; Wada Y; Ida H; Kunishima S
    Pediatr Int; 2013 Feb; 55(1):102-4. PubMed ID: 23409987
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MYH9 Associated nephropathy.
    Furlano M; Arlandis R; Venegas MDP; Novelli S; Crespi J; Bullich G; Ayasreh N; Remacha Á; Ruiz P; Lorente L; Ballarín J; Matamala A; Ars E; Torra R
    Nefrologia (Engl Ed); 2019; 39(2):133-140. PubMed ID: 30471777
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan.
    Huang YC; Shih YH; Lin CY; Chiu PF; Kuo SF; Lin JS; Shen MC
    Int J Hematol; 2020 Dec; 112(6):878-882. PubMed ID: 32712863
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Management of patients with severe Epstein syndrome: Review of four patients who received living-donor renal transplantation.
    Hashimoto J; Hamasaki Y; Takahashi Y; Kubota M; Yanagisawa T; Itabashi Y; Muramatsu M; Kawamura T; Kumagai N; Ohwada Y; Sakai K; Shishido S
    Nephrology (Carlton); 2019 Apr; 24(4):450-455. PubMed ID: 29532554
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sporadic Epstein syndrome with macrothrombocytopenia, sensorineural hearing loss and renal failure.
    Makino S; Kunishima S; Ikumi A; Awaguni H; Shinozuka J; Tanaka S; Maruyama R; Imashuku S
    Pediatr Int; 2015 Oct; 57(5):977-81. PubMed ID: 26387855
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital thrombocytopenia with nephritis - The first case of MYH9 related disorder in Serbia.
    Kuzmanović M; Kunishima S; Putnik J; Stajić N; Paripović A; Bogdanović R
    Vojnosanit Pregl; 2014 Apr; 71(4):395-8. PubMed ID: 24783421
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Malta (MYH9 Associated Elastin Aggregation) Syndrome: Germline Variants in MYH9 Cause Rare Sweat Duct Proliferations and Irregular Elastin Aggregations.
    Fewings E; Ziemer M; Hörtnagel K; Reicherter K; Larionov A; Redman J; Goldgraben MA; Pepler A; Hearn T; Firth H; Ha T; Schaller J; Adams DJ; Rytina E; van Steensel M; Tischkowitz M
    J Invest Dermatol; 2019 Oct; 139(10):2238-2241.e6. PubMed ID: 31125547
    [No Abstract]   [Full Text] [Related]  

  • 10. Renal Biopsy-induced Hematoma and Infection in a Patient with Asymptomatic May-Hegglin Anomaly.
    Matsumoto T; Yanagihara T; Yoshizaki K; Tsuchiya M; Terasaki M; Nagahama K; Shimizu A; Kunishima S; Maeda M
    J Nippon Med Sch; 2021 Dec; 88(6):579-584. PubMed ID: 33692298
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.
    Verver EJ; Topsakal V; Kunst HP; Huygen PL; Heller PG; Pujol-Moix N; Savoia A; Benazzo M; Fierro T; Grolman W; Gresele P; Pecci A
    Ear Hear; 2016; 37(1):112-20. PubMed ID: 26226608
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Hereditary sensorineural hearing impairment and macrothrombocytopenia: a rare MYH9 gene mutation].
    Böttcher A; Knecht R; Busch CJ; Lörincz BB; Dalchow CV
    HNO; 2013 Feb; 61(2):159-60, 162-5. PubMed ID: 23223919
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An interesting case of thrombocytopenia in pregnancy.
    Garcia-Horton A; Chin-Yee I; Lam S
    Int J Hematol; 2020 Aug; 112(2):139-140. PubMed ID: 32557127
    [No Abstract]   [Full Text] [Related]  

  • 14. Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report.
    Ciftciler R; Balasar Ö; Keyik H; Ciftciler AE
    Transfus Apher Sci; 2023 Aug; 62(4):103710. PubMed ID: 37076359
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
    Pecci A; Klersy C; Gresele P; Lee KJ; De Rocco D; Bozzi V; Russo G; Heller PG; Loffredo G; Ballmaier M; Fabris F; Beggiato E; Kahr WH; Pujol-Moix N; Platokouki H; Van Geet C; Noris P; Yerram P; Hermans C; Gerber B; Economou M; De Groot M; Zieger B; De Candia E; Fraticelli V; Kersseboom R; Piccoli GB; Zimmermann S; Fierro T; Glembotsky AC; Vianello F; Zaninetti C; Nicchia E; Güthner C; Baronci C; Seri M; Knight PJ; Balduini CL; Savoia A
    Hum Mutat; 2014 Feb; 35(2):236-47. PubMed ID: 24186861
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents.
    Kunishima S; Kitamura K; Matsumoto T; Sekine T; Saito H
    Br J Haematol; 2014 Jun; 165(6):885-7. PubMed ID: 24611568
    [No Abstract]   [Full Text] [Related]  

  • 17. [Renal diseases related to MYH9 disorders].
    Galeano D; Zanoli L; L'Imperio V; Fatuzzo P; Granata A
    G Ital Nefrol; 2017 Apr; 34(2):40-57. PubMed ID: 28682562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Report of a young girl with MYH9 mutation and review of the literature.
    Landi D; Lockhart E; Miller SE; Datto M; Rehder C; Kanaly A; Thornburg CD
    J Pediatr Hematol Oncol; 2012 Oct; 34(7):538-40. PubMed ID: 23007341
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A De Novo Mutation in MYH9 in a Child With Severe and Prolonged Macrothrombocytopenia.
    Li K; Jin R; Xu W; Shen Y; Lu K; Wu X
    J Pediatr Hematol Oncol; 2021 Jan; 43(1):e7-e10. PubMed ID: 32520844
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Avatrombopag improves thrombocytopenia in MYH9-related disorder following eltrombopag treatment failure.
    Arif AR; Zhao M; Chen W; Xue M; Luo S; Wang Y
    Platelets; 2022 Nov; 33(8):1307-1311. PubMed ID: 35791514
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.