-
1
-
-
0024603102
-
Diagnosis and treatment of homozygous protein C deficiency
-
Marlar RA, Montgomery RR, Broekmans AW. Diagnosis and treatment of homozygous protein C deficiency. J Pediatr. 1989;114(4 pt 1):528-534
-
(1989)
J Pediatr
, vol.114
, Issue.4 PART 1
, pp. 528-534
-
-
Marlar, R.A.1
Montgomery, R.R.2
Broekmans, A.W.3
-
2
-
-
0025475202
-
Hereditary protein C deficiency: A review of the genetics, clinical presentation, diagnosis and treatment
-
Marlar RA, Mastovich S. Hereditary protein C deficiency: a review of the genetics, clinical presentation, diagnosis and treatment. Blood Coagul Fibrinolysis. 1990;1(3): 319-330
-
(1990)
Blood Coagul Fibrinolysis
, vol.1
, Issue.3
, pp. 319-330
-
-
Marlar, R.A.1
Mastovich, S.2
-
3
-
-
41949101630
-
Severe congenital protein C deficiency: Description of a new mutation and prophylactic protein C therapy and in vivo pharmacokinetics
-
Tcheng WY, Dovat S, Gurel Z, Donkin J, Wong W. Severe congenital protein C deficiency: description of a new mutation and prophylactic protein C therapy and in vivo pharmacokinetics. J Pediatr Hematol Oncol. 2008; 30(2):166-171
-
(2008)
J Pediatr Hematol Oncol
, vol.30
, Issue.2
, pp. 166-171
-
-
Tcheng, W.Y.1
Dovat, S.2
Gurel, Z.3
Donkin, J.4
Wong, W.5
-
4
-
-
0029617466
-
Replacement therapy with a monoclonal antibody purified protein C concentrate in newborns with severe congenital protein C deficiency
-
Dreyfus M, Masterson M, David M, et al. Replacement therapy with monoclonal antibody purified protein C concentrate in newborns with severe congenital protein C deficiency. Semin Thromb Hemost. 1995; 21(4):371-381 (Pubitemid 26013109)
-
(1995)
Seminars in Thrombosis and Hemostasis
, vol.21
, Issue.4
, pp. 371-381
-
-
Dreyfus, M.1
Masterson, M.2
David, M.3
Rivard, G.E.4
Muller, F.-M.5
Kreuz, W.6
Beeg, T.7
Minford, A.8
Allgrove, J.9
Cohen, J.D.10
Christoph, J.11
Bergmann, F.12
Mitchell, V.E.13
Haworth, C.14
Nelson, K.15
Schwarz, H.P.16
-
5
-
-
0030044808
-
Purpura fulminans in severe congenital protein C deficiency: Monitoring of treatment with protein C concentrate
-
DOI 10.1007/BF02115621
-
Müller FM, Ehrenthal W, Hafner G, Schranz D. Purpura fulminans in severe congenital protein C deficiency: monitoring of treatment with protein C concentrate. Eur J Pediatr. 1996;155(1):20-25 (Pubitemid 26004667)
-
(1996)
European Journal of Pediatrics
, vol.155
, Issue.1
, pp. 20-25
-
-
Muller, F.-M.1
Ehrenthal, W.2
Hafner, G.3
Schranz, D.4
-
6
-
-
0029077128
-
Homozygous protein C deficiency: Management with protein C concentrate
-
Baliga V, Thwaites R, Tillyer ML, Minford A, Parapia L, Allgrove J. Homozygous protein C deficiency: management with protein C concentrate. Eur J Pediatr. 1995;154(7): 534-538
-
(1995)
Eur J Pediatr
, vol.154
, Issue.7
, pp. 534-538
-
-
Baliga, V.1
Thwaites, R.2
Tillyer, M.L.3
Minford, A.4
Parapia, L.5
Allgrove, J.6
-
7
-
-
1642496931
-
Diagnosis and treatment of a newborn with homozygous protein C deficiency
-
DOI 10.1080/08035250310007411
-
Salonvaara M, Kuismanen K, Mononen T, Riikonen P. Diagnosis and treatment of a newborn with homozygous protein C deficiency. Acta Paediatr. 2004;93(1): 137-139 (Pubitemid 38134735)
-
(2004)
Acta Paediatrica, International Journal of Paediatrics
, vol.93
, Issue.1
, pp. 137-139
-
-
Salonvaara, M.1
Kuismanen, K.2
Mononen, T.3
Riikonen, P.4
-
8
-
-
0033142912
-
Ophthalmic manifestation of congenital protein C deficiency
-
Hattenbach LO, Beeg T, Kreuz W, Zubcov A. Ophthalmic manifestation of congenital protein C deficiency. J AAPOS. 1999;3(3): 188-190
-
(1999)
J AAPOS
, vol.3
, Issue.3
, pp. 188-190
-
-
Hattenbach, L.O.1
Beeg, T.2
Kreuz, W.3
Zubcov, A.4
-
9
-
-
0028342423
-
Ophthalmic manifestations of neonatal protein C deficiency
-
Cassels-Brown A, Minford AM, Chatfield SL, Bradbury JA. Ophthalmic manifestations of neonatal protein C deficiency. Br J Ophthalmol. 1994;78(6):486-487 (Pubitemid 24186291)
-
(1994)
British Journal of Ophthalmology
, vol.78
, Issue.6
, pp. 486-487
-
-
Cassels-Brown, A.1
Minford, A.M.B.2
Chatfield, S.L.3
Bradbury, J.A.4
-
10
-
-
0021911725
-
Coumarin prophylaxis for fulminant purpura syndrome due to homozygous protein C deficiency
-
Garcia-Plaza I, Jiminez-Astroga C, Borrego D, Marty ML. Coumarin prophylaxis for fulminant purpura syndrome due to homozygous protein C deficiency. Lancet. 1985; 1(8429):634-635 (Pubitemid 15133903)
-
(1985)
Lancet
, vol.1
, Issue.8429
, pp. 634-635
-
-
Garcia-Plaza, I.1
Jimenez-Astorga, C.2
Borrego, D.3
Marty, M.L.4
-
11
-
-
0021086761
-
Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant
-
Branson HE, Marble R, Katz J, Griffin JH. Inherited protein C deficiency and coumarinresponsive chronic relapsing purpura fulminans in a newborn infant. Lancet. 1983; 2(8360):1165-1168 (Pubitemid 14243933)
-
(1983)
Lancet
, vol.2
, Issue.8360
, pp. 1165-1168
-
-
Branson, H.E.1
Katz, J.2
Marble, R.3
Griffin, J.H.4
-
12
-
-
0021233839
-
Severe homozygous protein C deficiency
-
Sills RH, Marlar RA, Montgomery RR, Deshpande GN, Humbert JR. Severe homozygous protein C deficiency. J Pediatr. 1984;105(3): 409-413 (Pubitemid 14072123)
-
(1984)
Journal of Pediatrics
, vol.105
, Issue.3
, pp. 409-413
-
-
Sills, R.H.1
Marlar, R.A.2
Montgomery, R.R.3
-
13
-
-
0021930913
-
Neonatal purpura fulminans: A genetic disorder related to the absence of protein C in blood
-
Marciniak E, Wilson D, Marlar RA. Neonatal purpura fulminans: a genetic disorder related to the absence of protein C in blood. Blood. 1985;65(1):15-20 (Pubitemid 15191032)
-
(1985)
Blood
, vol.65
, Issue.1
, pp. 15-20
-
-
Marciniak, E.1
Wilson, H.D.2
Marlar, R.A.3
-
14
-
-
34548491155
-
Treatment of inherited protein C deficiency by replacement therapy with the French purified plasma-derived protein C concentrate (PROTEXEL)
-
DOI 10.1111/j.1423-0410.2007.00953.x
-
Dreyfus M, Ladouzi A, Chambost H, et al; PROTEXEL Study Group. Treatment of inherited protein C deficiency by replacement therapy with the French purified plasmaderived protein C concentrate (PROTEXEL). Vox Sanguinis. 2007;93(3):233-240 (Pubitemid 47373987)
-
(2007)
Vox Sanguinis
, vol.93
, Issue.3
, pp. 233-240
-
-
Dreyfus, M.1
Ladouzi, A.2
Chambost, H.3
Gruel, Y.4
Tardy, B.5
Ffrench, P.6
Bridey, F.7
Tellier, Z.8
Dreyfus, M.9
Tardy, B.10
Conard, J.11
Chambost, H.12
Ffrench, P.13
Kiffer, B.14
Viard, P.15
Gruel, Y.16
Borel-Derlon, A.17
Lequerrec, A.18
-
15
-
-
0347634503
-
Activated Protein C Concentrate Reverses Purpura Fulminans in Severe Genetic Protein C Deficiency
-
DOI 10.1097/00043426-200401000-00008
-
Manco-Johnson MJ, Knapp-Clevenger R. Activated protein C concentrate reverses purpura fulminans in severe genetic protein C deficiency. J Pediatr Hematol Oncol. 2004; 26(1):25-27 (Pubitemid 38095629)
-
(2004)
Journal of Pediatric Hematology/Oncology
, vol.26
, Issue.1
, pp. 25-27
-
-
Manco-Johnson, M.J.1
Knapp-Clevenger, R.2
-
16
-
-
0028919868
-
Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His
-
Alhenc-Gelas M, Emmerich J, Gandrille S, et al. Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His. Blood Coagul Fibrinolysis. 1995;6(1): 35-41
-
(1995)
Blood Coagul Fibrinolysis
, vol.6
, Issue.1
, pp. 35-41
-
-
Alhenc-Gelas, M.1
Emmerich, J.2
Gandrille, S.3
-
17
-
-
0035143083
-
En bloc heterotopic auxiliary liver and bilateral renal transplant in a patient with homozygous protein C deficiency
-
DOI 10.1067/mpd.2001.109199
-
Angelis M, Pegelow CH, Khan FA, Verzaro R, Tzakis AG. En bloc heterotopic auxiliary liver and bilateral renal transplant in a patient with homozygous protein C deficiency. J Pediatr. 2001;138(1):120-122 (Pubitemid 32097154)
-
(2001)
Journal of Pediatrics
, vol.138
, Issue.1
, pp. 120-122
-
-
Angelis, M.1
Pegelow, C.H.2
Khan, F.A.3
Verzaro, R.4
Tzakis, A.G.5
-
18
-
-
0026409651
-
Treatment of homozygous protein C deficiency and neonatal purpura fulminans with a purified protein C concentrate
-
Dreyfus M, Mangy JF, Bridey F, et al. Treatment of homozygous protein C deficiency and neonatal purpura fulminans with a purified protein C concentrate. N Engl J Med. 1991;325(22):1565-1568
-
(1991)
N Engl J Med
, vol.325
, Issue.22
, pp. 1565-1568
-
-
Dreyfus, M.1
Mangy, J.F.2
Bridey, F.3
-
19
-
-
0033781467
-
A case of purpura fulminans is caused by homozygous Δ8857 mutation (protein C-Nagoya) and successfully treated with activated protein C concentrate
-
Nakayama T, Matsushita T, Hidano H, et al. A case of purpura fulminans is caused by homozygous Δ8857 mutation (protein C-Nagoya) and successfully treated with activated protein C concentrate. Br J Haematol. 2000;110(3):727-730
-
(2000)
Br J Haematol
, vol.110
, Issue.3
, pp. 727-730
-
-
Nakayama, T.1
Matsushita, T.2
Hidano, H.3
-
20
-
-
0033058659
-
Long-term management of homozygous protein C deficiency: Replacement therapy with subcutaneous purified protein C concentrate
-
Sanz-Rodriguez C, Gil-Fernández JJ, Zapater P, et al. Long-term management of homozygous protein C deficiency: replacement therapy with subcutaneous purified protein C concentrate. Thromb Haemost. 1999; 81(6):887-890 (Pubitemid 29312702)
-
(1999)
Thrombosis and Haemostasis
, vol.81
, Issue.6
, pp. 887-890
-
-
Sanz-Rodriguez, C.1
Gil-Fernandez, J.J.2
Zapater, P.3
Pinilla, I.4
Granados, E.5
De Soria, V.G.-G.6
Cano, J.7
Sala, N.8
Fernandez-Ranada, J.M.9
Gomez, N.G.10
-
21
-
-
33745924383
-
Management of neonatal purpura fulminans with severe protein C deficiency
-
Sen K, Roy A. Management of neonatal purpura fulminans with severe protein C defi- ciency. Indian Pediatr. 2006;43(6):542-545 (Pubitemid 44049658)
-
(2006)
Indian Pediatrics
, vol.43
, Issue.6
, pp. 542-545
-
-
Sen, K.1
Roy, A.2
-
22
-
-
0027186461
-
Replacement therapy with a purified protein C concentrate during initiation of oral anticoagulation in severe protein C congenital deficiency
-
De Stefano V, Mastrangelo S, Schwarz HP, et al. Replacement therapy with a purified protein C concentrate during initiation of oral anticoagulation in severe protein C congenital deficiency. Thromb Haemost. 1993; 70(2):247-249 (Pubitemid 23222477)
-
(1993)
Thrombosis and Haemostasis
, vol.70
, Issue.2
, pp. 247-249
-
-
De Stefano, V.1
Mastrangelo, S.2
Schwarz, H.P.3
Pola, P.4
Flore, R.5
Bizzi, B.6
Leone, G.7
-
23
-
-
0031981018
-
Homozygous protein C deficiency: Description of a new mutation and successful treatment with low molecular weight heparin
-
Monagle P, Andrew M, Halton J, et al. Homozygous protein C deficiency: description of a new mutation and successful treatment with low molecular weight heparin. Thromb Haemost. 1998;79(4):756-761 (Pubitemid 28163850)
-
(1998)
Thrombosis and Haemostasis
, vol.79
, Issue.4
, pp. 756-761
-
-
Monagle, P.1
Andrew, M.2
Halton, J.3
Marlar, R.4
Jardine, L.5
Vegh, P.6
Johnston, M.7
Webber, C.8
Massicotte, M.P.9
-
24
-
-
4444285402
-
Subcutaneous administration of protein C concentrate
-
DOI 10.1080/08880010490477365
-
Mathias M, Khair K, Burgess C, Liesner R. Subcutaneous administration of protein C concentrate. Pediatr Hematol Oncol. 2004; 21(6):551-556 (Pubitemid 39166878)
-
(2004)
Pediatric Hematology and Oncology
, vol.21
, Issue.6
, pp. 551-556
-
-
Mathias, M.1
Khair, K.2
Burgess, C.3
Liesner, R.4
-
25
-
-
0029968541
-
Treatment of homozygous protein C deficiency with subcutaneous protein C concentrate
-
DOI 10.1046/j.1365-2141.1996.4691021.x
-
Minford AMB, Parapia LA, Stainforth C, Lee D. Treatment of homozygous protein C defi- ciency with subcutaneous protein C concentrate. Br J Haematol. 1996;93(1):215-216 (Pubitemid 26132398)
-
(1996)
British Journal of Haematology
, vol.93
, Issue.1
, pp. 215-216
-
-
Minford, A.M.B.1
Parapia, L.A.2
Stainforth, C.3
Lee, D.4
-
26
-
-
0023911084
-
Homozygous protein C deficiency: Observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy
-
Peters C, Casella JF, Marlar RA, Montgomery RR, Zinkham WH. Homozygous protein C deficiency: observations on the nature of the molecular abnormality and effectiveness of warfarin therapy. Pediatrics. 1988; 81(2):272-276 (Pubitemid 18060608)
-
(1988)
Pediatrics
, vol.81
, Issue.2
, pp. 272-276
-
-
Peters, C.1
Casella, J.F.2
Marlar, R.A.3
Montgomery, R.R.4
Zinkham, W.H.5
-
27
-
-
0023858403
-
Successful treatment of homozygous protein C deficiency by hepatic transplantation
-
Casella JF, Bontempo FA, Markel H, Lewis JH, Zitelli BJ, Starzl TE. Successful treatment of homozygous protein C deficiency by hepatic transplantation. Lancet. 1988;1(8583): 435-438
-
(1988)
Lancet
, vol.1
, Issue.8583
, pp. 435-438
-
-
Casella, J.F.1
Bontempo, F.A.2
Markel, H.3
Lewis, J.H.4
Zitelli, B.J.5
Starzl, T.E.6
-
28
-
-
59449110175
-
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. Long-term survival of a child with homozygous protein C deficiency successfully treated with living donor liver transplantation. Pediatr Transplant. 2009;13(2): 251-254
-
(2009)
Pediatr Transplant
, vol.13
, Issue.2
, pp. 251-254
-
-
Lee, M.J.1
Kim, K.M.2
Kim, J.S.3
Kim, Y.J.4
Lee, Y.J.5
Ghim, T.T.6
|