150 related articles for article (PubMed ID: 29218739)
1. Successful liver transplantation for homozygous protein C deficiency with a type II mutation using a heterozygous living related donor.
Boucher AA; Luchtman-Jones L; Nathan JD; Palumbo JS
Am J Hematol; 2018 Mar; 93(3):462-466. PubMed ID: 29218739
[No Abstract] [Full Text] [Related]
2. Long-term follow-up of homozygote protein C deficiency after multimodal therapy.
Monagle K; Ignjatovic V; Hardikar W; Newall F; Monagle P
J Pediatr Hematol Oncol; 2014 Oct; 36(7):e452-5. PubMed ID: 24136027
[TBL] [Abstract][Full Text] [Related]
3. Successful living domino liver transplantation in a child with protein C deficiency.
Matsunami M; Ishiguro A; Fukuda A; Sasaki K; Uchida H; Shigeta T; Kanazawa H; Sakamoto S; Ohta M; Nakadate H; Horikawa R; Nakazawa A; Ishige M; Mizuta K; Kasahara M
Pediatr Transplant; 2015 May; 19(3):E70-4. PubMed ID: 25712501
[TBL] [Abstract][Full Text] [Related]
4. Purpura fulminans in congenital protein C deficiency successfully treated with fresh frozen plasma and thrombomodulin.
Hayami T; Yamaguchi A; Kato T; Tanaka T; Nishizawa Y; Yanagi T; Taga T; Matsumoto S; Uchiumi T; Fujimoto N
J Dermatol; 2018 Jun; 45(6):e165-e166. PubMed ID: 29265490
[No Abstract] [Full Text] [Related]
5. Prenatal diagnosis in a family with purfura fulminans.
Shanbhag S; Pai N; Ghosh K; Shetty S
Blood Coagul Fibrinolysis; 2015 Apr; 26(3):350. PubMed ID: 25803516
[No Abstract] [Full Text] [Related]
6. A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period.
Unal S; Gumruk F; Yigit S; Tuncer M; Tavil B; Cil O; Takci S; Urata M; Hotta T; Kang D; Cetin M
Pediatr Blood Cancer; 2014 Apr; 61(4):763-4. PubMed ID: 24115609
[TBL] [Abstract][Full Text] [Related]
7. Long-term survival of a child with homozygous protein C deficiency successfully treated with living donor liver transplantation.
Lee MJ; Kim KM; Kim JS; Kim YJ; Lee YJ; Ghim TT
Pediatr Transplant; 2009 Mar; 13(2):251-4. PubMed ID: 18482214
[TBL] [Abstract][Full Text] [Related]
8. Severe purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation.
Demirel N; Bas AY; Okumus N; Zenciroglu A; Yarali N
Pediatr Hematol Oncol; 2009 Nov; 26(8):597-600. PubMed ID: 19954370
[No Abstract] [Full Text] [Related]
9. Protein C (PROC) gene mutations in two Indian families with purpura fulminans.
Pai N; Shetty S; Ghosh K
Ann Hematol; 2010 Aug; 89(8):835-6. PubMed ID: 20077116
[No Abstract] [Full Text] [Related]
10. Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C Deficiency.
Martin G; Thomas MA; Wei XC; Le D
J Pediatr Hematol Oncol; 2021 Aug; 43(6):e763-e765. PubMed ID: 33165188
[TBL] [Abstract][Full Text] [Related]
11. A novel homozygous missense mutation (Val 325-->Ala) in the protein C gene causing neonatal purpura fulminans.
Witt I; Beck S; Seydewitz HH; Tasangil C; Schenck W
Blood Coagul Fibrinolysis; 1994 Aug; 5(4):651-3. PubMed ID: 7841324
[TBL] [Abstract][Full Text] [Related]
12. Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.
Abu-Amero KK; Owaidah TM; Al-Mahed M
J Thromb Haemost; 2006 May; 4(5):1152-3. PubMed ID: 16689776
[No Abstract] [Full Text] [Related]
13. Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
Barg AA; Dardik R; Levin C; Koren A; Levy-Mendelovich S; Pode-Shakked B; Kenet G
Acta Haematol; 2021; 144(3):327-331. PubMed ID: 32980846
[TBL] [Abstract][Full Text] [Related]
14. A novel compound heterozygous form of severe protein C deficiency causing bleeding without purpura fulminans.
Herrick NL; Geddis AE; Lovejoy AE; Kim J; Schiff D; Thornburg CD
Pediatr Blood Cancer; 2017 Nov; 64(11):. PubMed ID: 28485122
[No Abstract] [Full Text] [Related]
15. Chronic disseminated intravascular coagulation and childhood-onset skin necrosis resulting from homozygosity for a protein C Gla domain mutation, Arg15Trp.
Steinkamp M; Geva A; Joffe S; Lapp CN; Neufeld EJ
J Pediatr Hematol Oncol; 2002 Nov; 24(8):685-8. PubMed ID: 12439046
[TBL] [Abstract][Full Text] [Related]
16. Homozygous type I Protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene.
Park HJ; Song KS; Nah BM; Choi JR; Kim MJ
J Thromb Haemost; 2005 Mar; 3(3):593-5. PubMed ID: 15748260
[No Abstract] [Full Text] [Related]
17. Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort study.
Limperger V; Klostermeier UC; Kenet G; Holzhauer S; Alhenc Gelas M; Finckh U; Junker R; Heller C; Zieger B; Kurnik K; Knöfler R; Mesters R; Halimeh S; Nowak-Göttl U
Br J Haematol; 2014 Nov; 167(3):385-93. PubMed ID: 25039884
[TBL] [Abstract][Full Text] [Related]
18. Hereditary protein C deficiency caused by novel compound heterozygous mutants in a Chinese pedigree: A case report.
Li Y; Cai R; Wang W; Feng Q; Gao X; Liu P; Liu M; Qi C
Transfus Apher Sci; 2019 Oct; 58(5):685-687. PubMed ID: 31521534
[TBL] [Abstract][Full Text] [Related]
19. Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
Kemahli S; Alhenc-Gelas M; Gandrille S; Aiach M; Akar N; Cin S
Blood Coagul Fibrinolysis; 1998 Jun; 9(4):351-4. PubMed ID: 9690806
[TBL] [Abstract][Full Text] [Related]
20. [Gene diagnosis of four patients with protein C deficiency].
Gao B; Zhou RF; Ouyang J; Chen B; Xu Y; Li P
Zhonghua Xue Ye Xue Za Zhi; 2016 Nov; 37(11):966-970. PubMed ID: 27995882
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
