Zobrazeno 1 - 10 of 20 pro vyhledávání: '"Heterozygous protein C deficiency"'
1
Late Onset of Clinical Symptoms and Recurrent Ecchymotic Skin Lesions in a 12-Year-Old Girl With a Severe Double Heterozygous Protein C Deficiency
Autor: Anne Demulder, Martine Alhenc-Gelas, Alina Ferster, Francis Corazza, Michèle Loop
Publikováno v: Journal of Pediatric Hematology/Oncology. 26:2-4
The authors describe a 12-year-old girl with late-onset clinical symptoms due to severe protein C deficiency. Protein C gene analysis showed double heterozygosity for two distinct mutations, associated with type I protein C deficiency. Her parents an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ebafcfdbf1619987e0f95c9772d3c80
https://doi.org/10.1097/00043426-200401000-00002
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2
Inherited Heterozygous Protein C Deficiency and Dysfunctional Protein S with Recurrent Venous Thrombotic Diseases. A Study of Three Generations of a Japanese Family
Autor: Akira Ito, Toshiyuki Sakata, Hiroshi Matsuo, Nobuko Tsushima, Toshikazu Hashizume, Keizaburo Oozono
Publikováno v: Internal Medicine. 31:1197-1200
We describe a rare occurence of a family affected with venous thrombosis, exhibiting a protein C (PC) deficiency and dysfunctional protein S (PS). The propositus and his father developed recurrent venous thrombosis. Their PC deficiency was characteri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7af873755bcfa796057b97e61e70d60
https://doi.org/10.2169/internalmedicine.31.1197
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3
Livedoid vasculopathy associated with heterozygous protein C deficiency
Autor: A. Boyvat, N. KundakC¸i, M.O.A. Babikir, E. Gürgey
Publikováno v: British Journal of Dermatology. 143:840-842
Livedoid vasculopathy is characterized by recurrent painful ulceration of the feet, ankles and legs that heals with residual white atrophic scars. For many years, livedoid vasculopathy has been considered to be a primary vasculitic process. Recently,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::771b1906a1261361de40065a7706b8e4
https://doi.org/10.1046/j.1365-2133.2000.03786.x
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5
Thrombophilic Risk Parameters in Juvenile »Idiopathic« Stroke Patients
Autor: M. Krause, E. Aygören-Pürsün, I. Scharrer, G. Ludwig, S. Ehrenforth
Publikováno v: 31st Hemophilia Symposium Hamburg 2000 ISBN: 9783540421313
Within the last decade, various genetic defects of proteins regulating blood coagulation, particularly those affecting the physiological anticoagulant systems, have been well established as risk factors of cerebrovascular disease in adults [8;22;23].
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c9616f59f9a53d73e1bc7bf571a71062
https://doi.org/10.1007/978-3-642-59383-3_36
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6
Central retinal vein thrombosis as an initial manifestation of heterozygous protein C deficiency: case report
Autor: Wilson Nadruz Junior, Carlos Eduardo Leite Arieta, Gustavo Araújo Covolo, Rodrigo Pessoa Cavalcanti Lira
Publikováno v: Arquivos Brasileiros de Oftalmologia, Vol 66, Iss 1, Pp 87-88 (2003)
The purpose of this paper is to report a case of central retinal vein thrombosis associated with isolated heterozygous protein C deficiency. Acute occlusion of the central retinal vein presents as one of the most dramatic pictures in ophthalmology. I
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25af5b1a50e4aa1d64ee64c64be7f4cd
https://doi.org/10.1590/s0004-27492003000100017
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8
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9
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Plný text Recenzováno Digitální knihovna AV ČR
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