339 related articles for article (PubMed ID: 20514633)
1. Inherited disorders of platelet function in pediatric clinical practice: a diagnostic challenge.
Streif W; Knöfler R; Eberl W
Klin Padiatr; 2010 May; 222(3):203-8. PubMed ID: 20514633
[TBL] [Abstract][Full Text] [Related]
2. The level of laboratory testing required for diagnosis or exclusion of a platelet function disorder using platelet aggregation and secretion assays.
Mezzano D; Quiroga T; Pereira J
Semin Thromb Hemost; 2009 Mar; 35(2):242-54. PubMed ID: 19408197
[TBL] [Abstract][Full Text] [Related]
3. [Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)].
Knöfler R; Eberl W; Schulze H; Bakchoul T; Bergmann F; Gehrisch S; Geisen C; Gottstein S; Halimeh S; Harbrecht U; Kappert G; Kirchmaier C; Kehrel B; Lösche W; Krause M; Mahnel R; Meyer O; Pilgrimm AK; Pillitteri D; Rott H; Santoso S; Siegemund A; Schambeck C; Scheer M; Schmugge M; Scholl T; Strauss G; Zieger B; Zotz R; Hermann M; Streif W
Hamostaseologie; 2014; 34(3):201-12. PubMed ID: 24903476
[TBL] [Abstract][Full Text] [Related]
4. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders.
Gupta PK; Charan VD; Saxena R
Ann Hematol; 2007 Jun; 86(6):403-7. PubMed ID: 17375300
[TBL] [Abstract][Full Text] [Related]
5. [Clinical and laboratory aspects of the Aspirin-like defect as hereditary thrombocytopathy].
Rolf N; Bugert P; Gehrisch S; Siegert G; Suttorp M; Knöfler R
Hamostaseologie; 2009 May; 29(2):177-83. PubMed ID: 19404514
[TBL] [Abstract][Full Text] [Related]
6. Testing for inherited platelet defects in clinical laboratories in Germany, Austria and Switzerland. Results of a survey carried out by the Permanent Paediatric Group of the German Thrombosis and Haemostasis Research Society (GTH).
Streif W; Oliveri M; Weickardt S; Eberl W; Knoefler R;
Platelets; 2010; 21(6):470-8. PubMed ID: 20635849
[TBL] [Abstract][Full Text] [Related]
7. The spectrum of inherited bleeding disorders in pediatrics.
El-Bostany EA; Omer N; Salama EE; El-Ghoroury EA; Al-Jaouni SK
Blood Coagul Fibrinolysis; 2008 Dec; 19(8):771-5. PubMed ID: 19002043
[TBL] [Abstract][Full Text] [Related]
8. Genetic testing in the diagnostic evaluation of inherited platelet disorders.
Nurden AT; Fiore M; Pillois X; Nurden P
Semin Thromb Hemost; 2009 Mar; 35(2):204-12. PubMed ID: 19408193
[TBL] [Abstract][Full Text] [Related]
9. A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience.
Mokhtar GM; Tantawy AA; Adly AA; Telbany MA; El Arab SE; Ismail M
Blood Coagul Fibrinolysis; 2012 Jul; 23(5):411-8. PubMed ID: 22610136
[TBL] [Abstract][Full Text] [Related]
10. Diagnostic tool for Glanzmann's thrombasthenia clinicopathologic spectrum.
Ali N; Moiz B; Shaikh U; Adil S; Rizvi B; Rahman Y
J Coll Physicians Surg Pak; 2008 Feb; 18(2):91-4. PubMed ID: 18454893
[TBL] [Abstract][Full Text] [Related]
11. Inherited traits affecting platelet function.
Salles II; Feys HB; Iserbyt BF; De Meyer SF; Vanhoorelbeke K; Deckmyn H
Blood Rev; 2008 May; 22(3):155-72. PubMed ID: 18180086
[TBL] [Abstract][Full Text] [Related]
12. An update on pediatric bleeding disorders: bleeding scores, benign joint hypermobility, and platelet function testing in the evaluation of the child with bleeding symptoms.
O'Brien SH
Am J Hematol; 2012 May; 87 Suppl 1():S40-4. PubMed ID: 22460356
[TBL] [Abstract][Full Text] [Related]
13. [Membrane glycoproteins of human platelets: structures, functions, and abnormalities in Glanzmann's thrombasthenia and Bernard-Soulier syndrome].
Ando Y; Fusegawa H; Kawada T; Tanaka Y; Watanabe K; Kobayashi N
Rinsho Byori; 1989 Dec; 37(12):1344-52. PubMed ID: 2614964
[TBL] [Abstract][Full Text] [Related]
14. [Children with hemorrhagic diathesis: correct diagnostic and therapeutic approach].
Carnelli V; Dozzi M; Gibelli M; Giovanniello A; Riva F; Seidita C; Stucchi C
Pediatr Med Chir; 1990; 12(1):1-13. PubMed ID: 2198546
[TBL] [Abstract][Full Text] [Related]
15. Inherited disorders of platelet function.
Matthews DC
Pediatr Clin North Am; 2013 Dec; 60(6):1475-88. PubMed ID: 24237983
[TBL] [Abstract][Full Text] [Related]
16. Platelet disorders in adolescents.
Philipp CS
J Pediatr Adolesc Gynecol; 2010 Dec; 23(6 Suppl):S11-4. PubMed ID: 20869280
[TBL] [Abstract][Full Text] [Related]
17. Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory.
Karimi M; Haghpanah S; Amirhakimi A; Afrasiabi A; Dehbozorgian J; Nasirabady S
Blood Coagul Fibrinolysis; 2009 Dec; 20(8):642-5. PubMed ID: 19710607
[TBL] [Abstract][Full Text] [Related]
18. [Skin and mucous membrane hemorrhages: clinical assessment, study sequence and relative frequency of hereditary diseases of the hemostasis in a Chilean population].
Quiroga T; Pérez M; Rodríguez S; Muñoz B; Aranda E; Morales M; Verdugo P; Pereira J; Mezzano D
Rev Med Chil; 1997 Apr; 125(4):409-18. PubMed ID: 9460281
[TBL] [Abstract][Full Text] [Related]
19. Functional platelet defects and their laboratory evaluation.
Bowie EJ; Owen CA
Southeast Asian J Trop Med Public Health; 1979 Jun; 10(2):234-40. PubMed ID: 524147
[TBL] [Abstract][Full Text] [Related]
20. PFA-100 system: a new method for assessment of platelet dysfunction.
Mammen EF; Comp PC; Gosselin R; Greenberg C; Hoots WK; Kessler CM; Larkin EC; Liles D; Nugent DJ
Semin Thromb Hemost; 1998; 24(2):195-202. PubMed ID: 9579642
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
