135 related articles for article (PubMed ID: 15461630)
21. A Rare Cause of Isolated Prolonged Activated Partial Thromboplastin Time: An Overview of Prekallikrein Deficiency and the Contact System.
Riano I; Prasongdee K
J Investig Med High Impact Case Rep; 2021; 9():23247096211012187. PubMed ID: 33940978
[TBL] [Abstract][Full Text] [Related]
22. Laboratory diagnosis and molecular classification of von Willebrand disease.
Gadisseur A; Hermans C; Berneman Z; Schroyens W; Deckmyn H; Michiels JJ
Acta Haematol; 2009; 121(2-3):71-84. PubMed ID: 19506352
[TBL] [Abstract][Full Text] [Related]
23. [Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-gene].
Maak B; Kochhan L; Heuchel P; Jenderny J
Hamostaseologie; 2009 May; 29(2):187-9. PubMed ID: 19404525
[TBL] [Abstract][Full Text] [Related]
24. Prekallikrein deficiency in a dog.
Okawa T; Yanase T; Shimokawa Miyama T; Hiraoka H; Baba K; Tani K; Okuda M; Mizuno T
J Vet Med Sci; 2011 Jan; 73(1):107-11. PubMed ID: 20736516
[TBL] [Abstract][Full Text] [Related]
25. [Factor XI deficiency caused by a mutation of Gly400Val].
Sato T; Iyama S; Araki N; Murase K; Sato Y; Kobune M; Takimoto R; Matsunaga T; Kato J; Kuroda H; Niitsu Y
Rinsho Ketsueki; 2007 Feb; 48(2):148-50. PubMed ID: 17370644
[TBL] [Abstract][Full Text] [Related]
26. Severe prekallikrein deficiencies due to homozygous C529Y mutations.
François D; Trigui N; Leterreux G; Flaujac C; Horellou MH; Mazaux L; Vignon D; Conard J; de Mazancourt P
Blood Coagul Fibrinolysis; 2007 Apr; 18(3):283-6. PubMed ID: 17413767
[TBL] [Abstract][Full Text] [Related]
27. Severe high-molecular-weight kininogen deficiency due to a homozygous c.1456C > T nonsense variant in a large Chinese family.
Yang J; Fan L; Qiao Y; Zhao Y; Zhu T
J Thromb Thrombolysis; 2020 Nov; 50(4):989-994. PubMed ID: 32185598
[TBL] [Abstract][Full Text] [Related]
28. c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans.
Adenaeuer A; Ezigbo ED; Fawzy Nazir H; Barco S; Trinchero A; Laubert-Reh D; Strauch K; Wild PS; Lackner KJ; Lämmle B; Rossmann H
J Thromb Haemost; 2021 Jan; 19(1):147-152. PubMed ID: 33073460
[TBL] [Abstract][Full Text] [Related]
29. Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene.
Rubio-Cabezas O; Díaz González F; Aragonés A; Argente J; Campos-Barros A
Pediatr Diabetes; 2008 Jun; 9(3 Pt 1):245-9. PubMed ID: 18298419
[TBL] [Abstract][Full Text] [Related]
30. A novel mutation in the biliverdin reductase-A gene combined with liver cirrhosis results in hyperbiliverdinaemia (green jaundice).
Gåfvels M; Holmström P; Somell A; Sjövall F; Svensson JO; Ståhle L; Broomé U; Stål P
Liver Int; 2009 Aug; 29(7):1116-24. PubMed ID: 19580635
[TBL] [Abstract][Full Text] [Related]
31. [Prolonged activated partial thromboplastin time (aPTT): not always indicative of increased risk of bleeding].
van der Pas AJ; Leebeek FW; Perry DJ; Castel A; van Esser JW
Ned Tijdschr Geneeskd; 2009; 153():B42. PubMed ID: 19785809
[TBL] [Abstract][Full Text] [Related]
32. Replacement therapy in a patient with congenital prekallikrein deficiency undergoing surgery.
Shigekiyo T; Fujino O
Int J Hematol; 1992 Aug; 56(1):89-93. PubMed ID: 1391808
[TBL] [Abstract][Full Text] [Related]
33. Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.
Ivaskevicius V; Windyga J; Baran B; Schroeder V; Junen J; Bykowska K; Seifried E; Kohler HP; Oldenburg J
Haemophilia; 2007 Sep; 13(5):649-57. PubMed ID: 17880458
[TBL] [Abstract][Full Text] [Related]
34. A case of prekallikrein deficiency resulting in severe recurrent mucosal hemorrhage.
Dasanu CA; Alexandrescu DT
Am J Med Sci; 2009 Nov; 338(5):429-30. PubMed ID: 19773642
[TBL] [Abstract][Full Text] [Related]
35. [Prekallikrein (Fletcher Factor) Deficiency and Prolongation of APTT Reaction].
Dietzel H; Lutze G; Kätzel R; Liebscher K
Med Klin (Munich); 2003 Oct; 98(10):587-90. PubMed ID: 14586514
[TBL] [Abstract][Full Text] [Related]
36. Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: definite evidence for the non-penetrance of the C2362F mutation.
Castaman G; Bertoncello K; Bernardi M; Eikenboom JC; Budde U; Rodeghiero F
Am J Hematol; 2007 May; 82(5):376-80. PubMed ID: 17109387
[TBL] [Abstract][Full Text] [Related]
37. [MYH associated polyposis: severe phenotype in the homozygosity for the 1103delC mutation].
De Ferro SM; Lage P; Suspiro A; Fidalgo P; Fragoso S; Baltazar C; Vitoriano I; Rodrigues P; Albuquerque C; Leitão CN
Acta Med Port; 2007; 20(3):243-7. PubMed ID: 17868535
[TBL] [Abstract][Full Text] [Related]
38. Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion.
Hewitt J; Ballard JN; Nelson TN; Smith VC; Griffiths TA; Pritchard S; Wu JK; Wadsworth LD; Casey B; MacGillivray RT
Br J Haematol; 2005 Feb; 128(3):380-5. PubMed ID: 15667541
[TBL] [Abstract][Full Text] [Related]
39. [Prekallikrein deficiency: a rare cause of a significant prolongation of the activated partial thromboplastin time. Apropos of a case].
Abecassis L; Poupin F; Forceville X; Tapie-Meurgue M; Amiot JF
Cah Anesthesiol; 1991; 39(6):421-3. PubMed ID: 1773371
[No Abstract] [Full Text] [Related]
40. Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation.
Aquaron R; Bergé-Lefranc JL; Pellissier JF; Montfort MF; Mayan M; Figarella-Branger D; Coquet M; Serratrice G; Pouget J
Neuromuscul Disord; 2007 Mar; 17(3):235-41. PubMed ID: 17324573
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
