150 related articles for article (PubMed ID: 29218739)
21. [Analysis of a hereditary protein C deficient consanguineous pedigree caused by Phe139Val homozygous mutation].
Yang LH; Zhu LQ; Wang YY; Xie HX; Xie YS; Jin YH; Wang MS; Chen BC; Yang XL
Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):767-70. PubMed ID: 24103874
[TBL] [Abstract][Full Text] [Related]
22. Severe clinical presentation of protein C deficiency in a type I/II compound heterozygote newborn.
Fernandez-Burriel M
Thromb Haemost; 2005 Jul; 94(1):216-8. PubMed ID: 16113807
[No Abstract] [Full Text] [Related]
23. A novel mutation c.1048A>T at codon 350(Lys>Stop) in PROC gene causing neonatal purpura fulminans.
Jain R; T L; Chandran J; Jayandharan GR; Palle A; Moses PD
Blood Coagul Fibrinolysis; 2013 Dec; 24(8):890-2. PubMed ID: 24158118
[TBL] [Abstract][Full Text] [Related]
24. Protein C deficiency.
Goldenberg NA; Manco-Johnson MJ
Haemophilia; 2008 Nov; 14(6):1214-21. PubMed ID: 19141162
[TBL] [Abstract][Full Text] [Related]
25. A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy.
Millar DS; Allgrove J; Rodeck C; Kakkar VV; Cooper DN
Blood Coagul Fibrinolysis; 1994 Aug; 5(4):647-9. PubMed ID: 7841323
[TBL] [Abstract][Full Text] [Related]
26. A novel frameshift mutation Gly239Serfs*8 in the PROC gene results in protein C deficiency in a Korean patient.
Park SH; Jang S; Yang HK; Shim H; Park CJ; Chi HS; Oh YM
Ann Hematol; 2012 Nov; 91(11):1829-30. PubMed ID: 22588326
[No Abstract] [Full Text] [Related]
27. Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months.
Tuddenham EG; Takase T; Thomas AE; Awidi AS; Madanat FF; Abu Hajir MM; Kernoff PB; Hoffbrand AV
Thromb Res; 1989 Mar; 53(5):475-84. PubMed ID: 2660320
[TBL] [Abstract][Full Text] [Related]
28. A Novel Protein C Mutation Causing Neonatal Purpura Fulminans.
Devi R U; Bharathi S M; Kawankar N
Indian Pediatr; 2016 Nov; 53(11):1019-1021. PubMed ID: 27889735
[TBL] [Abstract][Full Text] [Related]
29. Severe homozygous protein C deficiency: identification of a splice site missense mutation (184, Q-->H) in exon 7 of the protein C gene.
Soria JM; Brito D; Barceló J; Fontcuberta J; Botero L; Maldonado J; Estivill X; Sala N
Thromb Haemost; 1994 Jul; 72(1):65-9. PubMed ID: 7974377
[TBL] [Abstract][Full Text] [Related]
30. The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
Yang LH; Zheng FX; Chen Y; Jin YH; Zhang Z; Xie HX; Yang XL; Wang MS; Chen BC
Blood Coagul Fibrinolysis; 2014 Dec; 25(8):824-30. PubMed ID: 24911457
[TBL] [Abstract][Full Text] [Related]
31. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
Tjeldhorn L; Sandset PM; Haugbro K; Skretting G
Thromb Res; 2010 Mar; 125(3):230-4. PubMed ID: 19535131
[TBL] [Abstract][Full Text] [Related]
32. Successful treatment of homozygous protein C deficiency by hepatic transplantation.
Casella JF; Lewis JH; Bontempo FA; Zitelli BJ; Markel H; Starzl TE
Lancet; 1988 Feb; 1(8583):435-8. PubMed ID: 2893866
[TBL] [Abstract][Full Text] [Related]
33. Neonatal Purpura Fulminans, a rare genetic disorder due to protein C deficiency: A case report.
Irfan Kazi SG; Siddiqui E; Habib I; Tabassum S; Afzal B; Khan IQ
J Pak Med Assoc; 2018 Mar; 68(3):463-465. PubMed ID: 29540887
[TBL] [Abstract][Full Text] [Related]
34. A case of purpura fulminans is caused by homozygous delta8857 mutation (protein C-nagoya) and successfully treated with activated protein C concentrate.
Nakayama T; Matsushita T; Hidano H; Suzuki C; Hamaguchi M; Kojima T; Saito H
Br J Haematol; 2000 Sep; 110(3):727-30. PubMed ID: 10997987
[TBL] [Abstract][Full Text] [Related]
35. En bloc heterotopic auxiliary liver and bilateral renal transplant in a patient with homozygous protein C deficiency.
Angelis M; Pegelow CH; Khan FA; Verzaro R; Tzakis AG
J Pediatr; 2001 Jan; 138(1):120-2. PubMed ID: 11148525
[TBL] [Abstract][Full Text] [Related]
36. A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction.
Wypasek E; Pankiw-Bembenek O; Potaczek DP; Alhenc-Gelas M; Trebacz J; Undas A
Int J Cardiol; 2013 Sep; 167(5):e146-8. PubMed ID: 23643436
[No Abstract] [Full Text] [Related]
37. Paediatric presentation and outcome of congenital protein C deficiency in Japan.
Ohga S; Kang D; Kinjo T; Ochiai M; Doi T; Ishimura M; Kayamori Y; Urata M; Yamamoto J; Suenobu SI; Kanegane H; Ikenoue T; Shirahata A; Hara T
Haemophilia; 2013 May; 19(3):378-84. PubMed ID: 23379934
[TBL] [Abstract][Full Text] [Related]
38. Molecular characterization of novel splice site mutation causing protein C deficiency.
Al-Hamed MH; AlBatniji F; AlDakheel GA; El-Faraidi H; Al-Zahrani A; Al-Abbass F; Imtiaz F
Blood Coagul Fibrinolysis; 2016 Jul; 27(5):585-8. PubMed ID: 26656900
[TBL] [Abstract][Full Text] [Related]
39. Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.
Fidalgo T; Martinho P; Salvado R; Manco L; Oliveira AC; Pinto CS; Gonçalves E; Marques D; Sevivas T; Martins N; Ribeiro ML
Eur J Haematol; 2015 Oct; 95(4):294-307. PubMed ID: 25533856
[TBL] [Abstract][Full Text] [Related]
40. Protein C Deficiency.
Dinarvand P; Moser KA
Arch Pathol Lab Med; 2019 Oct; 143(10):1281-1285. PubMed ID: 30702334
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
