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Results of search for 'su:"Protein C Deficiency"', page 39 of 78
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Authors
Aiach, M
Alhenc-Gelas, M
Bertina, R M
Bovill, E G
Conard, J
Cooper, D N
De Stefano, V
Emmerich, J
Gandrille, S
Girolami, A
Kakkar, V V
Long, G L
Mannucci, P M
Marlar, R A
Miyata, T
Reitsma, P H
Rosendaal, F R
Sakata, T
Simioni, P
Tripodi, A
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Adolescent
Adult
Aged
Antithrombin III Deficiency
Female
Humans
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Middle Aged
Protein C
Protein C Deficiency
Protein S Deficiency
Risk Factors
Thrombosis
analysis
blood
complications
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etiology
genetics
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761.
Molecular genetics of venous thromboembolism.
[electronic resource]
by
Dahlbäck, B
Producer:
19950912
In:
Annals of medicine
vol. 27
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762.
Management strategy in purpura fulminans with multiple organ failure in children.
[electronic resource]
by
Sheridan, R L
Briggs, S E
Remensnyder, J P
Tompkins, R G
Producer:
19961121
In:
Burns : journal of the International Society for Burn Injuries
vol. 22
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763.
Thrombotic complications of BMT: association with protein C deficiency.
[electronic resource]
by
Gordon, B G
Haire, W D
Patton, D F
Manno, P J
Reed, E C
Producer:
19930317
In:
Bone marrow transplantation
vol. 11
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764.
Cutaneous heparin necrosis in a patient with heterozygous protein S deficiency.
[electronic resource]
by
Libow, L F
DiPreta, E A
Dyksterhouse, D L
Producer:
19970827
In:
Cutis
vol. 59
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765.
[Protein C deficiency manifested as pulmonary aretery thromboembolism induced by oral contraceptive].
[electronic resource]
by
Takami, Hirokazu
Fukushima, Kazuyuki
Takizawa, Masataka
Kodama, Takahide
Uozumi, Hiroki
Kobayakawa, Naoshi
Takeuchi, Hiroaki
Aoyagi, Teruhiko
Producer:
20070501
In:
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine
vol. 96
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766.
Late onset warfarin-induced skin necrosis.
[electronic resource]
by
Xin, Chongmei
Hu, Dongyan
Li, Ming
Producer:
20190619
In:
Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia
vol. 154
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767.
Protein C deficiency: identification of a novel two-base pair insertion and two point mutations in exon 7 of the protein C gene in Spanish families.
[electronic resource]
by
Soria, J M
Fontcuberta, J
Borrell, M
Estivill, X
Sala, N
Producer:
19930610
In:
Human mutation
vol. 1
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768.
The clinical expression of hereditary protein C and protein S deficiency: a relation to clinical thrombotic risk factors and to levels of protein C and protein S?
[electronic resource]
by
Henkens, C M
van der Meer, J
Hillege, J L
van der Schaaf, W
Bom, V J
Halie, M R
Producer:
19931201
In:
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
vol. 4
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769.
Severe homozygous protein C deficiency: identification of a splice site missense mutation (184, Q-->H) in exon 7 of the protein C gene.
[electronic resource]
by
Soria, J M
Brito, D
Barceló, J
Fontcuberta, J
Botero, L
Maldonado, J
Estivill, X
Sala, N
Producer:
19941227
In:
Thrombosis and haemostasis
vol. 72
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770.
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis.
[electronic resource]
by
Millar, D S
Grundy, C B
Bignell, P
Moffat, E H
Martin, R
Kakkar, V V
Cooper, D N
Producer:
19930629
In:
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
vol. 4
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771.
Congenital thrombophilia.
[electronic resource]
by
Walker, I D
Producer:
19980316
In:
Bailliere's clinical obstetrics and gynaecology
vol. 11
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772.
Warfarin-induced skin necrosis associated with acquired protein C deficiency.
[electronic resource]
by
Parsi, Kurosh
Younger, Ian
Gallo, John
Producer:
20030328
In:
The Australasian journal of dermatology
vol. 44
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773.
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
[electronic resource]
by
Kemahli, S
Alhenc-Gelas, M
Gandrille, S
Aiach, M
Akar, N
Cin, S
Producer:
19981021
In:
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
vol. 9
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774.
A case of purpura fulminans secondary to transient protein C deficiency as a complication of chickenpox infection.
[electronic resource]
by
Canpolat, Cengiz
Bakir, Mustafa
Producer:
20020611
In:
The Turkish journal of pediatrics
vol. 44
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775.
Thromboepidemiology: identifying patients with heritable risk for thrombin-mediated thromboembolic events.
[electronic resource]
by
Tran, Maichi
Spencer, Frederick A
Producer:
20050502
In:
American heart journal
vol. 149
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776.
Severe protein C deficiency is associated with organ dysfunction in patients with severe sepsis.
[electronic resource]
by
Shaw, Andrew D
Vail, George M
Haney, Douglas J
Xie, Jin
Williams, Mark D
Producer:
20120410
In:
Journal of critical care
vol. 26
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777.
[A case of superior mesenteric venous thrombosis due to protein C deficiency in a patient with duodenal ulcer bleeding].
[electronic resource]
by
Woo, Jae Gon
Lee, Ji Eun
Kwon, Oh Un
Jung, Kyoung Won
Jung, Chang Wook
Cho, Dae Hyeon
Yu, Kil Jong
Shim, Sang Goon
Producer:
20110520
In:
The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi
vol. 57
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778.
[Hereditary thrombophilia testing and its therapeutic impact on venous thromboembolism disease: Results from a retrospective single-center study of 162 patients].
[electronic resource]
by
Allain, J-S
Gueret, P
Le Gallou, T
Cazalets, C
Lescoat, A
Jego, P
Producer:
20170421
In:
La Revue de medecine interne
vol. 37
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779.
Protein C and protein S deficiencies may be related to survival among hemodialysis patients.
[electronic resource]
by
Ichinose, Mayuri
Sasagawa, Naru
Chiba, Tetsuo
Toyama, Katsuhide
Kayamori, Yuzo
Kang, Dongchon
Producer:
20200831
In:
BMC nephrology
vol. 20
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780.
[Paget-Schroetter syndrome and combined deficiency of blood coagulation inhibitors--antithrombin III and protein C].
[electronic resource]
by
Prosviriakova, I G
Makatsariia, A D
Producer:
19900829
In:
Akusherstvo i ginekologiia
no. 3
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