Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00034925.xml
Download PDF
Hamostaseologie 1990; 10(03): 125-129
DOI: 10.1055/s-0038-1655195
DOI: 10.1055/s-0038-1655195
Originalarbeiten
Das Protein-C-System bei Kindern
Further Information
Publication History
Publication Date:
02 July 2018 (online)
-
LITERATUR
- 1 Bertina RM, Broekmans AW, van der Linden IK, Mertens K. Protein C deficiency in a Dutch family with thrombotic disease. Thromb Haemost 1982; 48: 1-5.
- 2 Bertina RM, Broekmans AW, Krommenhoeke-van Es C, van Wijngaarden A. The use of a functional and immunologic assay for plasma protein C in the study of the heterogeneity of congenital protein C deficiency. Thromb Haemost 1984; 51: 1-5.
- 3 Bertina RM. Persönliche Mitteilung. 1988
- 4 Broekmans AW, Bertina RM, Loeliger EA, Hofmann V, Klingemann HG. Protein C and the development of skin necrosis during anticoagulant therapy. Thromb Haemost 1983; 49: 251 (Letter)
- 5 Broekmans AW, van der Linden IK, Veltkamp JJ, Bertina RM. Prevalence of isolated protein C deficiency in patients with venous thromboembolic disease and in the population. Thromb Haemost 1983; 50: 350 (Abstr 1096)
- 6 Broekmans AW, Conard J. Hereditary protein C deficiency. In: Bertina RM. (ed). Protein C and Related Protein S. Edinburgh, London, Melbourne. New York: Churchill Livingstone; 1988: 160-81.
- 7 Branson HE, Katz J, Marble R, Griffin JH. Inherited protein C deficiency and coumarin responsive chronic relapsing purpura fulminans in a newborn infant. Lancet 1983; II: 1165-68.
- 8 Casella JF, Bontempo FA, Markel H, Lewis JH, Zitelli BJ, Stark TE. Successful treatment of homozygous protein C deficiency by hepatic transplantation. Lancet 1988; I: 435-38.
- 9 Clouse LH, Comp PC. The regulation of hemostasis: the protein C system. N Engl J Med 1986; 314: 1298-304.
- 10 Dusser A, Boyer-Neumann C, Wolf M. Temporary protein C deficiency associated with cerebral arterial thombosis in childhood. J Pediatr 1988; 113: 849-51.
- 11 Estelles A, Garcia-Plaza I, Dasi A, Aznar J, Duart M, Sanz G, Perez-Requejo JL, Espana F, Jimenez C, Abeledo G. Severe inherited »homozygous« protein C deficiency in a newborn infant. Thromb Haemost 1984; 52: 53-56.
- 12 Fernandez JA, Estelles A, Gilabert J, Espana F, Aznar J. Functional and immunological protein S in normal pregnant women and in full-term newborns. Thromb Haemost 1989; 61: 474-78.
- 13 Foster DC, Yoshitake S, Davie EW. The nucleotide sequence of the gene for human protein C. Proc Natl Acad Sci 1985; 82: 4673-77.
- 14 Garcia-Plaza I, Jimenez-Astorga C, Borrego D, Marty ML. Coumarin prophylaxis for fulminant purpura syndrome due to homozygous protein C deficiency. Lancet 1985; I: 634-35.
- 15 Gladson CL, Scharrer I, Hach V, Beck KH, Griffin JH. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis. Thromb Haemost 1988; 59: 18-22.
- 16 Griffin JH, Evatt B, Zimmermann TS, Kleiss AJ, Wideman C. Deficiency of protein C in congenital thrombotic disease. J Clin Invest 1981; 68: 1370-73.
- 17 Gruppo RA, Leimer B, Francis RB, Marlar RA, Gilberstein E. Protein C deficiency resulting from possible double heterozygosity and its response to Danazol. Blood 1988; 71: 370-74.
- 18 Heeb MJ, Griffin JH. Biochemistry of protein S. In: Bertina RM. (ed). Protein C and Related Proteins. Edinburgh, London, Melbourne, New York: Churchill Livingstone; 1988: 55-70.
- 19 Hintz G, Weil J, Buchmann S, Azzam A, Auberger K, Beck C. Homozygoter Säugling in einer Sippe mit erheblichem Protein-C-Mangel. Klin Wschr 1987; 62: 183-93.
- 20 International Committee for Standardization in Haematology and International Committee on Thrombosis and Haemostasis (ICSH-ICTH) Recommendations for reporting prothrombin time in oral anticoagulant control. Acta Haematol (Basel) 1985; 72: 405-07.
- 21 Israels SJ, Seshia SS. Childhood stroke associated with protein C or S deficiency. J Pediatr 1987; 111: 562-64.
- 22 Karpatkin M, Mannucci P, Bhogal M, Vigano S, Nardi M. Low protein C in the neonatal period. Br J Haemat 1986; 62: 137-42.
- 23 Kemkes-Matthes B. Heterozygous protein C deficiency type I. Blut 1989; 58: 201-06.
- 24 Klingemann HG, Broekmans AW, Bertina RM, Egbring R, Loeliger EA. Protein-CMangel Risikofaktor für venöse Thrombosen. Klin Wschr 1984; 62: 975-78.
- 25 Malm J, Bennhagen R, Holmberg L, Dahlbäck B. Plasma concentrations of C 4 bbinding protein and vitamin K-dependent protein S in term and preterm infants: low levels of protein S-C4b-binding protein complexes. Br J Haematol 1988; 68: 445-49.
- 26 Marciniak E, Wilson HD, Marlar RA. Neonatal purpura fulminans : A genetic disorder related to absence of protein C in blood. Blood 1985; 65: 15-20.
- 27 Manabe SI, Matsuda M. Homozygous protein C deficiency combined with heterozygous dysplasminogenaemia in a 21-year-old thrombophilic. Thromb Res 1985; 39: 333-41.
- 28 Manco-Johnson M, Hays T, Warady BA, Marlar RA. Severe protein C deficiency in newborn infants. J Pediatr 1988; 113: 359-63.
- 29 Marlar RA, Endres-Brooks J, Müller Ch. Serial studies of protein C and its plasma inhibitor in patients with disseminated intravascular coagulation. Blood 1985; 66: 59-63.
- 30 Marlar RA, Montgomery RR, Madden RM. Homozygous protein C deficiency. In: Bertina RM. (ed). Protein C and Related Proteins. Edinburgh, London, Melbourne, New York: Churchill Livingstone; 1988: 182-95.
- 31 Marlar RA, Montgomery RR, Broekmans AW. the Working Party. Diagnosis and treatment of homozygous protein C deficiency. J Pediatr 1989; 114: 528-34.
- 32 Matsuda M, Sugo T, Sakata Y, Murayama H, Mimuro J, Tanabe S, Yoshitake S. A thrombotic state due to an abnormal protein C. N Engl J Med 1988; 319: 1265-68.
- 33 Miletich J, Sherman L, Broze G. Absence of thrombosis in subjects with heterozygous protein C deficiency. N Engl J Med 1987; 317: 991-96.
- 34 Moalic P, Gruel Y, Body G, Foloppe P, Delahousse B, Leroy J. Levels and plasma distributions of free and C4b-BP-bound protein S in human fetuses and full-term newborns. Thromb Res 1988; 49: 471-80.
- 35 Özsoylu S, Cengiz B, Karament A. Purpura fulminans in a case of protein C deficiency. Eur J Pediatr 1988; 147: 209-12.
- 36 Peters C, Casella JF, Marlar RA, Montgomery RR, Zinkham WH. Homozygous protein C deficiency: observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy. Pediatrics 1988; 81: 272-76.
- 37 Polack B, Pauzol P, Amiral J. Protein C level at birth. Thromb Haemost 1984; 52: 188-91.
- 38 Powars DR, Rogers ZR, Patch MJ, McGehee WG, Francis Jr RB. Purpura fulminans in meningococcemia: association with acquired deficiencies of protein C and S. N Engl J Med 1987; 317: 571-72.
- 39 Pulido JS, Lingua RW, Cristol S, Byrne S. Protein C deficiency associated with vitreous hemorrhage in a neonate. Am J Ophthalmol 1987; 104: 546-47.
- 40 Rappaport ES, Speights VO, Helbert B, Trowbridge A, Koops B, Montgomery RR, Marlar RA. Protein C deficiency. South Med J 1987; 80: 240-42.
- 41 Rogers PCJ, Silva MP, Carter JEJ, Wadsworth LD. Renal vein thrombosis and response to therapy in a newborn due to protein C deficiency. Eur J Pediatr 1989; 149: 124-25.
- 42 Schenck W. Persönliche Mitteilung..
- 43 Schwarz HP, Muntean W, Watzke H, Richter B, Griffin JH. Low total protein S antigen but high protein S activity due to decreased C4b-binding protein in neonates. Blood 1988; 71: 562-65.
- 44 Sills RH, Marlar RA, Montgomery RR, Deshphande GN, Humbert JR. Severe homozygous protein C deficiency. J Pediatr 1984; 105: 409-13.
- 45 Seligsohn U, Berger A, Abend M. Homozygous protein C deficiency manifested by massive thrombosis in the newborn. N Engl J Med 1984; 310: 559-62.
- 46 Stenflo J. The biochemistry of protein C. In: Bertina RM. (ed). Protein C and Related Proteins. Edinburgh, London, Melbourne, New York: Churchill Livingstone; 1988: 21-54.
- 47 Suzuki K. Protein C inhibitor. In: Bertina RM. (ed). Protein C and Related Proteins. Edinburgh, London, Melbourne, New York: Churchill Livingstone: 1988: 106-16.
- 48 Thaiss H. Protein C im Neugeborenen-, Säuglingsund Kindesalter. In: Sutor AH, Kiinzer W. (Hrsg). Physiologie und Pathophysiologie des Vitamin K. Grenzach/Wyhlen: Editiones Roche; 1986: 75-78.
- 49 Thomas AE, Edward GD, Tuddenham D, Takase T, Awidi A, Hoffbrand V. Homozygous severe protein C deficiency. Br J Haematol 1986; 64: 828-29 (Abstr)
- 50 Tuddenham EGD, Takase T, Thomas AE, Awidi AS, Madanat FF, Hajir MMA, Kernoff PBA, Hoffbrand AV. Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months. Thromb Res 1989; 53: 475-84.
- 51 Uysal S, Anlar B, Altay C, Kirazli S. Role of protein C in childhood cerebrovascular occlusive accidents. Eur J Pediatr 1988; 149: 216-18.
- 52 Vicente V, Maia R, Alberca I, Tamagnini GPT, Borrasca AL. Congenital deficiency of vitamin K-dependent coagulation factors and protein C. Thromb Haemost 1984; 51: 343-46.
- 53 Von Mühlendahl KE, Witt I. In Vorbereitung..
- 54 Wehinger H, Geiger E, Freudenberg V, Schurmann J, Alexandrakis E, Witt I. Schwerer hereditärer Protein-C-Mangel bei einem Neugeborenen mit Purpura fulminans erfolgreiche Behandlung mit Phenprocoumon. Klin Pädiat 1985; 197: 116-20.
- 55 Wehinger H, Witt I. Protein C deficiency in a newborn infant with purpura fulminans. In: Witt I. (ed). Protein C, Biochemical and Medical Aspects. Berlin, New York: de Gruyter; 1985: 117-24.
- 56 Yuen P, Cheung A, Lin HJ, Ho F, Mimuro J, Yoshida N, Aoki N. Purpura fulminans in a Chinese boy with congenital protein C deficiency. Pediatrics 1986; 77: 670-76.