BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

85 related articles for article (PubMed ID: 23422342)

  • 1. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias.
    Acharya SS; Coughlin A; Dimichele DM;
    J Thromb Haemost; 2004 Feb; 2(2):248-56. PubMed ID: 14995986
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology.
    Mumford AD; Ackroyd S; Alikhan R; Bowles L; Chowdary P; Grainger J; Mainwaring J; Mathias M; O'Connell N;
    Br J Haematol; 2014 Nov; 167(3):304-26. PubMed ID: 25100430
    [No Abstract]   [Full Text] [Related]  

  • 3. National strategic advocacy to manage patients with inherited bleeding disorders in low and lower-middle income countries.
    Chuansumrit A; Ruchutrakul T; Sirachainan N; Kitpoka P; Panuwannakorn M; Panburana P; Suwannuraks M; Sri-Udomporn N; Kijkunasathian C; Jaovisidha S; Utamakul C; Natesirinilkul R; Pongtanakul B; Traivaree C; Komvilaisak P; Suwantaroj E; Sosothikul D; Angchaisuksiri P; Rojnuckarin P
    Expert Rev Hematol; 2023; 16(12):1063-1076. PubMed ID: 38100503
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Not Available].
    Casini A; Al-Samkari H; Hayward C; Peyvandi F
    Haemophilia; 2024 Apr; 30 Suppl 3():60-69. PubMed ID: 38494995
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mining of mortality-related findings in rare bleeding disorders: a retrospective study from two centers.
    Rafieemehr H; Dorgalaleh A; Mansouritorghabeh H
    Blood Res; 2020 Nov; 55(4):213-6. PubMed ID: 33232939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Contributions to the evolution of knowledge about hereditary hemorrhagic disorders.
    Roberts HR
    Cell Mol Life Sci; 2007 Mar; 64(5):517-21. PubMed ID: 17256091
    [No Abstract]   [Full Text] [Related]  

  • 7. A British Society for Haematology guideline on the assessment and management of bleeding risk prior to invasive procedures.
    Lester W; Bent C; Alikhan R; Roberts L; Gordon-Walker T; Trenfield S; White R; Forde C; Arachchillage DJ;
    Br J Haematol; 2024 May; 204(5):1697-1713. PubMed ID: 38517351
    [No Abstract]   [Full Text] [Related]  

  • 8. Rare Inherited Bleeding Disorders in The Middle East.
    Mazhari A; Khajavi M; Mansouritorghabeh H
    Transfus Med Rev; 2024 Apr; 38(2):150825. PubMed ID: 38579548
    [No Abstract]   [Full Text] [Related]  

  • 9. Case report: Superficial siderosis after brachial plexus avulsion.
    Decramer T; Theys T; Smetcoren C; van Loon J; Thijs V
    Clin Neurol Neurosurg; 2016 Apr; 143():104-6. PubMed ID: 26914142
    [No Abstract]   [Full Text] [Related]  

  • 10. Rapid and Specific Diagnosis of Extrapulmonary Tuberculosis by Immunostaining of Tissues and Aspirates With Anti-MPT64.
    Purohit MR; Sviland L; Wiker H; Mustafa T
    Appl Immunohistochem Mol Morphol; 2017 Apr; 25(4):282-288. PubMed ID: 26766121
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Burning mouth syndrome.
    Thoppay JR; De Rossi SS; Ciarrocca KN
    Dent Clin North Am; 2013 Jul; 57(3):497-512. PubMed ID: 23809306
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comparison and critical evaluation of six published extraction and clean-up procedures for aflatoxin M1 in liquid milk.
    Shepherd MJ; Holmes M; Gilbert J
    J Chromatogr; 1986 Feb; 354():305-15. PubMed ID: 3084526
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hereditary heterozygous factor VII deficiency in patients undergoing surgery : Clinical relevance].
    Woehrle D; Martinez M; Bolliger D
    Anaesthesist; 2016 Oct; 65(10):746-754. PubMed ID: 27586406
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Rare bleeding disorders and invasive procedures].
    Bonhomme F; Schved JF; Giansily-Blaizot M; Samama CM; de Moerloose P
    Ann Fr Anesth Reanim; 2013 Mar; 32(3):198-205. PubMed ID: 23422342
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern Iran.
    Mahmoodi M; Peyvandi F; Afrasiabi A; Ghaffarpasand F; Karimi M
    Blood Coagul Fibrinolysis; 2011 Jul; 22(5):396-401. PubMed ID: 21451397
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal recessive deficiencies of coagulation factors.
    Peyvandi F; Asselta R; Mannucci PM
    Rev Clin Exp Hematol; 2001 Dec; 5(4):369-88. PubMed ID: 11844134
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pregnancy and rare bleeding disorders.
    Kadir R; Chi C; Bolton-Maggs P
    Haemophilia; 2009 Sep; 15(5):990-1005. PubMed ID: 19298378
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The rare inherited coagulation disorders.
    Bolton-Maggs PH
    Pediatr Blood Cancer; 2013; 60 Suppl 1():S37-40. PubMed ID: 23109366
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare bleeding disorders in children: identification and primary care management.
    Acharya SS
    Pediatrics; 2013 Nov; 132(5):882-92. PubMed ID: 24127475
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 5.