Chalmers E, Cooper P, Forman K, Grimley C, Khair K, Minford A, et al. (November 2011). "Purpura fulminans: recognition, diagnosis and management". Archives of Disease in Childhood. 96 (11): 1066–1071. doi:10.1136/adc.2010.199919. PMID21233082. S2CID206846385.
Estellés A, Garcia-Plaza I, Dasí A, Aznar J, Duart M, Sanz G, et al. (August 1984). "Severe inherited "homozygous" protein C deficiency in a newborn infant". Thrombosis and Haemostasis. 52 (1): 53–56. doi:10.1055/s-0038-1661136. PMID6548587. S2CID1025282.
Gurgey A (1999). "Clinical manifestations in thrombotic children with factor V Leiden mutation". Pediatric Hematology and Oncology. 16 (3): 233–237. doi:10.1080/088800199277281. PMID10326221.
Levin M, Eley BS, Louis J, Cohen H, Young L, Heyderman RS (September 1995). "Postinfectious purpura fulminans caused by an autoantibody directed against protein S". The Journal of Pediatrics. 127 (3): 355–363. doi:10.1016/s0022-3476(95)70063-3. PMID7658262.
Adcock DM, Brozna J, Marlar RA (October 1990). "Proposed classification and pathologic mechanisms of purpura fulminans and skin necrosis". Seminars in Thrombosis and Hemostasis. 16 (4): 333–340. doi:10.1055/s-2007-1002686. PMID2281322.
Kondaveeti S, Hibberd ML, Booy R, Nadel S, Levin M (October 1999). "Effect of the Factor V Leiden mutation on the severity of meningococcal disease". The Pediatric Infectious Disease Journal. 18 (10): 893–896. doi:10.1097/00006454-199910000-00011. PMID10530586.
Adcock DM, Hicks MJ (October 1990). "Dermatopathology of skin necrosis associated with purpura fulminans". Seminars in Thrombosis and Hemostasis. 16 (4): 283–292. doi:10.1055/s-2007-1002681. PMID2281318.
Fourrier F, Lestavel P, Chopin C, Marey A, Goudemand J, Rime A, et al. (1990). "Meningococcemia and purpura fulminans in adults: acute deficiencies of proteins C and S and early treatment with antithrombin III concentrates". Intensive Care Medicine. 16 (2): 121–124. doi:10.1007/bf01699858. PMID2139671. S2CID10997888.
Páramo JA, Pérez JL, Serrano M, Rocha E (August 1990). "Types 1 and 2 plasminogen activator inhibitor and tumor necrosis factor alpha in patients with sepsis". Thrombosis and Haemostasis. 64 (1): 3–6. doi:10.1055/s-0038-1647143. PMID2274926. S2CID22756182.
Francis RB (October 1990). "Acquired purpura fulminans". Seminars in Thrombosis and Hemostasis. 16 (4): 310–325. doi:10.1055/s-2007-1002684. PMID2281320.
Marlar RA, Montgomery RR, Broekmans AW (April 1989). "Diagnosis and treatment of homozygous protein C deficiency. Report of the Working Party on Homozygous Protein C Deficiency of the Subcommittee on Protein C and Protein S, International Committee on Thrombosis and Haemostasis". The Journal of Pediatrics. 114 (4 Pt 1): 528–534. doi:10.1016/s0022-3476(89)80688-2. PMID2647943.
Dreyfus M, Masterson M, David M, Rivard GE, Müller FM, Kreuz W, et al. (1995). "Replacement therapy with a monoclonal antibody purified protein C concentrate in newborns with severe congenital protein C deficiency". Seminars in Thrombosis and Hemostasis. 21 (4): 371–381. doi:10.1055/s-2007-1000658. PMID8747700.
Monagle P, Andrew M, Halton J, Marlar R, Jardine L, Vegh P, et al. (April 1998). "Homozygous protein C deficiency: description of a new mutation and successful treatment with low molecular weight heparin". Thrombosis and Haemostasis. 79 (4): 756–761. doi:10.1055/s-0037-1615060. PMID9569188. S2CID3610434.
Gladson CL, Groncy P, Griffin JH (December 1987). "Coumarin necrosis, neonatal purpura fulminans, and protein C deficiency". Archives of Dermatology. 123 (12): 1701a–1706a. doi:10.1001/archderm.1987.01660360157029. PMID2961308.
Tuddenham EG, Takase T, Thomas AE, Awidi AS, Madanat FF, Abu Hajir MM, et al. (March 1989). "Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months". Thrombosis Research. 53 (5): 475–484. doi:10.1016/0049-3848(89)90202-8. PMID2660320.
Lerolle N, Carlotti A, Melican K, Aubey F, Pierrot M, Diehl JL, et al. (September 2013). "Assessment of the interplay between blood and skin vascular abnormalities in adult purpura fulminans". American Journal of Respiratory and Critical Care Medicine. 188 (6): 684–692. doi:10.1164/rccm.201302-0228oc. PMID23924269. S2CID31204154.
Manco-Johnson MJ, Abshire TC, Jacobson LJ, Marlar RA (November 1991). "Severe neonatal protein C deficiency: prevalence and thrombotic risk". The Journal of Pediatrics. 119 (5): 793–798. doi:10.1016/s0022-3476(05)80305-1. PMID1834822.
Chalmers E, Cooper P, Forman K, Grimley C, Khair K, Minford A, et al. (November 2011). "Purpura fulminans: recognition, diagnosis and management". Archives of Disease in Childhood. 96 (11): 1066–1071. doi:10.1136/adc.2010.199919. PMID21233082. S2CID206846385.
Estellés A, Garcia-Plaza I, Dasí A, Aznar J, Duart M, Sanz G, et al. (August 1984). "Severe inherited "homozygous" protein C deficiency in a newborn infant". Thrombosis and Haemostasis. 52 (1): 53–56. doi:10.1055/s-0038-1661136. PMID6548587. S2CID1025282.
Gurgey A (1999). "Clinical manifestations in thrombotic children with factor V Leiden mutation". Pediatric Hematology and Oncology. 16 (3): 233–237. doi:10.1080/088800199277281. PMID10326221.
Levin M, Eley BS, Louis J, Cohen H, Young L, Heyderman RS (September 1995). "Postinfectious purpura fulminans caused by an autoantibody directed against protein S". The Journal of Pediatrics. 127 (3): 355–363. doi:10.1016/s0022-3476(95)70063-3. PMID7658262.
Adcock DM, Brozna J, Marlar RA (October 1990). "Proposed classification and pathologic mechanisms of purpura fulminans and skin necrosis". Seminars in Thrombosis and Hemostasis. 16 (4): 333–340. doi:10.1055/s-2007-1002686. PMID2281322.
Kondaveeti S, Hibberd ML, Booy R, Nadel S, Levin M (October 1999). "Effect of the Factor V Leiden mutation on the severity of meningococcal disease". The Pediatric Infectious Disease Journal. 18 (10): 893–896. doi:10.1097/00006454-199910000-00011. PMID10530586.
Adcock DM, Hicks MJ (October 1990). "Dermatopathology of skin necrosis associated with purpura fulminans". Seminars in Thrombosis and Hemostasis. 16 (4): 283–292. doi:10.1055/s-2007-1002681. PMID2281318.
Fourrier F, Lestavel P, Chopin C, Marey A, Goudemand J, Rime A, et al. (1990). "Meningococcemia and purpura fulminans in adults: acute deficiencies of proteins C and S and early treatment with antithrombin III concentrates". Intensive Care Medicine. 16 (2): 121–124. doi:10.1007/bf01699858. PMID2139671. S2CID10997888.
Páramo JA, Pérez JL, Serrano M, Rocha E (August 1990). "Types 1 and 2 plasminogen activator inhibitor and tumor necrosis factor alpha in patients with sepsis". Thrombosis and Haemostasis. 64 (1): 3–6. doi:10.1055/s-0038-1647143. PMID2274926. S2CID22756182.
Francis RB (October 1990). "Acquired purpura fulminans". Seminars in Thrombosis and Hemostasis. 16 (4): 310–325. doi:10.1055/s-2007-1002684. PMID2281320.
Marlar RA, Montgomery RR, Broekmans AW (April 1989). "Diagnosis and treatment of homozygous protein C deficiency. Report of the Working Party on Homozygous Protein C Deficiency of the Subcommittee on Protein C and Protein S, International Committee on Thrombosis and Haemostasis". The Journal of Pediatrics. 114 (4 Pt 1): 528–534. doi:10.1016/s0022-3476(89)80688-2. PMID2647943.
Dreyfus M, Masterson M, David M, Rivard GE, Müller FM, Kreuz W, et al. (1995). "Replacement therapy with a monoclonal antibody purified protein C concentrate in newborns with severe congenital protein C deficiency". Seminars in Thrombosis and Hemostasis. 21 (4): 371–381. doi:10.1055/s-2007-1000658. PMID8747700.
"Human protein C: new preparations. Effective replacement therapy for some clotting disorders". Prescrire International. 12 (63): 11–13. February 2003. PMID12602374.
Hartman KR, Manco-Johnson M, Rawlings JS, Bower DJ, Marlar RA (1989). "Homozygous protein C deficiency: early treatment with warfarin". The American Journal of Pediatric Hematology/Oncology. 11 (4): 395–401. PMID2618972.
Monagle P, Andrew M, Halton J, Marlar R, Jardine L, Vegh P, et al. (April 1998). "Homozygous protein C deficiency: description of a new mutation and successful treatment with low molecular weight heparin". Thrombosis and Haemostasis. 79 (4): 756–761. doi:10.1055/s-0037-1615060. PMID9569188. S2CID3610434.
Gladson CL, Groncy P, Griffin JH (December 1987). "Coumarin necrosis, neonatal purpura fulminans, and protein C deficiency". Archives of Dermatology. 123 (12): 1701a–1706a. doi:10.1001/archderm.1987.01660360157029. PMID2961308.
Tuddenham EG, Takase T, Thomas AE, Awidi AS, Madanat FF, Abu Hajir MM, et al. (March 1989). "Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months". Thrombosis Research. 53 (5): 475–484. doi:10.1016/0049-3848(89)90202-8. PMID2660320.
Lerolle N, Carlotti A, Melican K, Aubey F, Pierrot M, Diehl JL, et al. (September 2013). "Assessment of the interplay between blood and skin vascular abnormalities in adult purpura fulminans". American Journal of Respiratory and Critical Care Medicine. 188 (6): 684–692. doi:10.1164/rccm.201302-0228oc. PMID23924269. S2CID31204154.
Wong VK, Hitchcock W, Mason WH (April 1989). "Meningococcal infections in children: a review of 100 cases". The Pediatric Infectious Disease Journal. 8 (4): 224–227. PMID2654860.
Manco-Johnson MJ, Abshire TC, Jacobson LJ, Marlar RA (November 1991). "Severe neonatal protein C deficiency: prevalence and thrombotic risk". The Journal of Pediatrics. 119 (5): 793–798. doi:10.1016/s0022-3476(05)80305-1. PMID1834822.
Chalmers E, Cooper P, Forman K, Grimley C, Khair K, Minford A, et al. (November 2011). "Purpura fulminans: recognition, diagnosis and management". Archives of Disease in Childhood. 96 (11): 1066–1071. doi:10.1136/adc.2010.199919. PMID21233082. S2CID206846385.
Estellés A, Garcia-Plaza I, Dasí A, Aznar J, Duart M, Sanz G, et al. (August 1984). "Severe inherited "homozygous" protein C deficiency in a newborn infant". Thrombosis and Haemostasis. 52 (1): 53–56. doi:10.1055/s-0038-1661136. PMID6548587. S2CID1025282.
Fourrier F, Lestavel P, Chopin C, Marey A, Goudemand J, Rime A, et al. (1990). "Meningococcemia and purpura fulminans in adults: acute deficiencies of proteins C and S and early treatment with antithrombin III concentrates". Intensive Care Medicine. 16 (2): 121–124. doi:10.1007/bf01699858. PMID2139671. S2CID10997888.
Páramo JA, Pérez JL, Serrano M, Rocha E (August 1990). "Types 1 and 2 plasminogen activator inhibitor and tumor necrosis factor alpha in patients with sepsis". Thrombosis and Haemostasis. 64 (1): 3–6. doi:10.1055/s-0038-1647143. PMID2274926. S2CID22756182.
Monagle P, Andrew M, Halton J, Marlar R, Jardine L, Vegh P, et al. (April 1998). "Homozygous protein C deficiency: description of a new mutation and successful treatment with low molecular weight heparin". Thrombosis and Haemostasis. 79 (4): 756–761. doi:10.1055/s-0037-1615060. PMID9569188. S2CID3610434.
Lerolle N, Carlotti A, Melican K, Aubey F, Pierrot M, Diehl JL, et al. (September 2013). "Assessment of the interplay between blood and skin vascular abnormalities in adult purpura fulminans". American Journal of Respiratory and Critical Care Medicine. 188 (6): 684–692. doi:10.1164/rccm.201302-0228oc. PMID23924269. S2CID31204154.
