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Results of search for 'su:"Factor XII Deficiency"', page 17 of 23
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Authors
Aznar, J
Colman, R W
Fischer, M
Gailani, David
Gallimore, M J
Girolami, A
Girolami, Antonio
Girolami, B
Griffin, J H
Halbmayer, W M
Haushofer, A
Hayashi, H
Jin, Yanhui
Lombardi, A M
Lämmle, B
Mannhalter, C
Renné, Thomas
Saito, H
Wang, Mingshan
Yang, Lihong
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Adult
Aged
Animals
Blood Coagulation
Blood Coagulation Disorders
Factor XII
Factor XII Deficiency
Female
Humans
Kallikreins
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Partial Thromboplastin Time
Prekallikrein
analysis
blood
complications
etiology
genetics
metabolism
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Results
321.
[Analysis of an hereditary coagulation factor XII deficiency in a consanguineous pedigree].
[electronic resource]
by
Zhang, Yang
Xie, Hai-xiao
Wang, Ming-shan
Jin, Yan-hui
Xie, Yao-sheng
Zheng, Fang-xiu
Producer:
20120412
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 28
Online resources:
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322.
Influence of factor XII deficiency on activated partial thromboplastin time (aPTT) in critically ill patients.
[electronic resource]
by
Bachler, Mirjam
Niederwanger, Christian
Hell, Tobias
Höfer, Judith
Gerstmeyr, Dominic
Schenk, Bettina
Treml, Benedikt
Fries, Dietmar
Producer:
20200219
In:
Journal of thrombosis and thrombolysis
vol. 48
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323.
Reduction of salivary tissue factor (thromboplastin) activity by warfarin therapy.
[electronic resource]
by
Zacharski, L R
Rosenstein, R
Producer:
19790426
In:
Blood
vol. 53
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324.
[Acute lung injury as a consequence of fresh frozen plasma administration in a patient with factor XII deficiency].
[electronic resource]
by
San Juan-Álvarez, M
Sánchez-Zamora, P
de la Flor-Robledo, M
Producer:
20161013
In:
Revista espanola de anestesiologia y reanimacion
vol. 61
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325.
Gene dosage effects for coagulation factors XII (F12) and XIII subunit A (F13A) in a case of partial monosomy 6p resulting from a maternal pericentric inversion of chromosome 6.
[electronic resource]
by
Narahara, K
Seno, Y
Nishibayashi, Y
Hiramoto, K
Nanba, H
Kikkawa, K
Kimoto, H
Producer:
19880919
In:
Jinrui idengaku zasshi. The Japanese journal of human genetics
vol. 32
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326.
Orthognathic surgery in a patient with Noonan's syndrome.
[electronic resource]
by
Sugar, A W
Ezsias, A
Bloom, A L
Morcos, W E
Producer:
19940418
In:
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
vol. 52
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327.
Orbital subperiosteal hemorrhage in a patient with factor VIII and factor XII Deficiency.
[electronic resource]
by
Oh, Joo Youn
Khwarg, Sang In
Producer:
20050210
In:
Journal of pediatric ophthalmology and strabismus
vol. 41
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328.
Kallikrein and prekallikrein levels in a large number of congenital clotting deficiencies and abnormalities.
[electronic resource]
by
Patrassi, G M
Martinelli, S
Vianello, C
Girolami, A
Producer:
19830225
In:
Folia haematologica (Leipzig, Germany : 1928)
vol. 109
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329.
Role of Factor XII in hemostasis and thrombosis: clinical implications.
[electronic resource]
by
Renné, Thomas
Gailani, David
Producer:
20070904
In:
Expert review of cardiovascular therapy
vol. 5
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330.
Current update on cellular and molecular mechanisms of hereditary angioedema.
[electronic resource]
by
Walford, Hannah H
Zuraw, Bruce L
Producer:
20140702
In:
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
vol. 112
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331.
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage.
[electronic resource]
by
Zou, Anqing
Wang, Mingshan
Jin, Yanhui
Cheng, Xiaoli
Su, Kankan
Yang, Lihong
Producer:
20180803
In:
International journal of hematology
vol. 107
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332.
Contact system dependent fibrinolytic activity in vivo: observations in healthy subjects and factor XII deficient patients.
[electronic resource]
by
Levi, M
Hack, C E
de Boer, J P
Brandjes, D P
Büller, H R
ten Cate, J W
Producer:
19930113
In:
Agents and actions. Supplements
vol. 38 ( Pt 2)
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333.
Contact factor deficiencies and cardiopulmonary bypass surgery: detection of the defect and monitoring of heparin.
[electronic resource]
by
van Veen, Joost Jair
Laidlaw, Stuart
Swanevelder, Justin
Harvey, Nicholas
Watson, Chris
Kitchen, Steve
Makris, Mike
Producer:
20090309
In:
European journal of haematology
vol. 82
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334.
Coagulation on endothelial cells: the underexposed part of Virchow's Triad.
[electronic resource]
by
Geenen, Irma L A
Post, Mark J
Molin, Daniel G M
Schurink, Geert W H
Maessen, Jos G
van Oerle, Rene
ten Cate, Hugo
Spronk, Henri M H
Producer:
20130418
In:
Thrombosis and haemostasis
vol. 108
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335.
The novel acceptor splice site mutation 11396(G-->A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients.
[electronic resource]
by
Schloesser, M
Hofferbert, S
Bartz, U
Lutze, G
Lämmle, B
Engel, W
Producer:
19960126
In:
Human molecular genetics
vol. 4
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336.
A comparison of the effects of factor XII deficiency and prekallikrein deficiency on thrombus formation.
[electronic resource]
by
Kokoye, Yasin
Ivanov, Ivan
Cheng, Qiufang
Matafonov, Anton
Dickeson, S Kent
Mason, Shauna
Sexton, Daniel J
Renné, Thomas
McCrae, Keith
Feener, Edward P
Gailani, David
Producer:
20161220
In:
Thrombosis research
vol. 140
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337.
Lemierre's syndrome complicating bacterial pharyngitis in a patient with undiagnosed factor XII deficiency.
[electronic resource]
by
Hlibczuk, Veronica
Producer:
20070717
In:
The Journal of emergency medicine
vol. 32
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338.
[Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation].
[electronic resource]
by
Yang, Lihong
Jin, Saiyan
Ji, Weidan
Cheng, Xiaoli
Li, Xiaolong
Jin, Yanhui
Wang, Mingshan
Producer:
20180605
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 35
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339.
Formation of an association between factor XII and kallikrein in human plasma--significance of storage of plasma and the functional state of plasma kallikrein.
[electronic resource]
by
Hoem, N O
Johannesen, S
Briseid, K
Producer:
19921119
In:
Thrombosis research
vol. 66
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340.
Abnormal proteolytic degradation of von Willebrand factor after desmopressin infusion in a new subtype of von Willebrand disease (ID).
[electronic resource]
by
Lopez-Fernandez, M F
Gonzalez-Boullosa, R
Blanco-Lopez, M J
Perez, M
Batlle, J
Producer:
19910325
In:
American journal of hematology
vol. 36
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