المؤلفون: Cirovic A; Center of Bone Biology, Institute of Anatomy, University of Belgrade - Faculty of Medicine, Dr Subotica 4/2, Belgrade, Serbia., Djuric M; Center of Bone Biology, Institute of Anatomy, University of Belgrade - Faculty of Medicine, Dr Subotica 4/2, Belgrade, Serbia., Milovanovic P; Center of Bone Biology, Institute of Anatomy, University of Belgrade - Faculty of Medicine, Dr Subotica 4/2, Belgrade, Serbia. drpmilovanovic@gmail.com.

المصدر: Endocrine [Endocrine] 2024 Aug; Vol. 85 (2), pp. 558-565. Date of Electronic Publication: 2024 Mar 14.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Humana Press Country of Publication: United States NLM ID: 9434444 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1559-0100 (Electronic) Linking ISSN: 1355008X NLM ISO Abbreviation: Endocrine Subsets: MEDLINE

مواضيع طبية MeSH: Osteoporosis*/etiology , Protein C Deficiency*/complications , Protein S Deficiency*/complications, Humans ; Protein C/metabolism ; Bone Density ; Animals ; Protein S/metabolism

المؤلفون: Chen X; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China., Yuan C; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China., Hu B; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China., Lu C; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China., Wang Y; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China., Han Z; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China., Zou M; Department of Neurology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325003, China. zouming625@163.com.

المصدر: Annals of hematology [Ann Hematol] 2024 Jun; Vol. 103 (6), pp. 2145-2155. Date of Electronic Publication: 2024 Mar 04.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0584 (Electronic) Linking ISSN: 09395555 NLM ISO Abbreviation: Ann Hematol Subsets: MEDLINE

مواضيع طبية MeSH: Protein C Deficiency*/genetics , Protein C Deficiency*/complications , Protein C*/genetics , Pedigree*, Humans ; Female ; Male ; Adult ; Middle Aged ; Retrospective Studies ; Venous Thrombosis/genetics ; Venous Thrombosis/blood ; Mutation, Missense ; Pulmonary Embolism/genetics ; Mutation

المؤلفون: Xie YH; 1 Department of Critical Care Medicine,The Second Affiliated Hospital of Chongqing Medical University,Chongqing 400010,China., Zhang A; 1 Department of Critical Care Medicine,The Second Affiliated Hospital of Chongqing Medical University,Chongqing 400010,China., Zeng HQ; 2 Department of Hematology,The Second Affiliated Hospital of Chongqing Medical University,Chongqing 400010,China., Cao YX; 1 Department of Critical Care Medicine,The Second Affiliated Hospital of Chongqing Medical University,Chongqing 400010,China.

المصدر: Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae [Zhongguo Yi Xue Ke Xue Yuan Xue Bao] 2024 Apr; Vol. 46 (2), pp. 293-296.

نوع المنشور: Case Reports; English Abstract

بيانات الدورية: Publisher: Zhongguo yi xue ke xue yuan Country of Publication: China NLM ID: 8006230 Publication Model: Print Cited Medium: Print ISSN: 1000-503X (Print) Linking ISSN: 1000503X NLM ISO Abbreviation: Zhongguo Yi Xue Ke Xue Yuan Xue Bao Subsets: MEDLINE

مواضيع طبية MeSH: Extracorporeal Membrane Oxygenation*/methods , Protein C Deficiency*/complications , Pulmonary Embolism*/therapy , Pulmonary Embolism*/etiology , Thrombectomy*/methods, Humans ; Male ; Frameshift Mutation ; Middle Aged

المؤلفون: Zhou S; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Wu X; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Song Y; Department of Clinical Hematology and osology, Shanghai Center of Clinical Laboratory, Shanghai, China., Li L; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Shi C; Department of Molecular Biology, Shanghai Center of Clinical Laboratory, Shanghai, China., Lai Z; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Ding Q; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Wu W; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Dai J; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Wang X; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China., Lu Y; Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

المصدر: Thrombosis and haemostasis [Thromb Haemost] 2024 May; Vol. 124 (5), pp. 459-470. Date of Electronic Publication: 2023 Nov 27.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: Thieme Country of Publication: Germany NLM ID: 7608063 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2567-689X (Electronic) Linking ISSN: 03406245 NLM ISO Abbreviation: Thromb Haemost Subsets: MEDLINE

مواضيع طبية MeSH: Protein C*/metabolism , Protein C*/genetics , Protein C*/chemistry , Protein C Deficiency*/genetics , Blood Coagulation*/genetics , Thrombin*/metabolism, Humans ; Glycosylation ; Female ; Mutation ; Thrombomodulin/genetics ; Thrombomodulin/metabolism ; Thrombomodulin/chemistry ; Thrombosis/genetics ; Thrombosis/blood ; HEK293 Cells ; Animals ; Protein Binding ; Serine ; Male ; Heterozygote

المؤلفون: Egami N; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan., Ishimura M; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan., Ochiai M; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.; Research Center for Environment and Developmental Medical Sciences, Kyushu University, Fukuoka, Japan., Ichiyama M; Department of Pediatrics, National Hospital Organization Kokura Medical Center, Kitakyushu, Japan., Inoue H; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan., Suenobu S; Division of General Pediatrics and Emergency Medicine, Department of Pediatrics, Oita University Faculty of Medicine, Yufu, Japan., Nishikubo T; Division of Neonatal Intensive Care, Center of Maternal-Fetal Medicine, Nara Medical University, Kashihara, Japan., Nogami K; Department of Pediatrics, Nara Medical University, Kashihara, Japan., Ishiguro A; Center for Postgraduate Education and Training, National Center for Child Health and Development, Setagaya-ku, Japan., Hotta T; Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospital, Fukuoka, Japan., Uchiumi T; Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospital, Fukuoka, Japan., Kang D; Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospital, Fukuoka, Japan., Ohga S; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

المصدر: Pediatric blood & cancer [Pediatr Blood Cancer] 2024 Mar; Vol. 71 (3), pp. e30824. Date of Electronic Publication: 2023 Dec 28.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: John Wiley Country of Publication: United States NLM ID: 101186624 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1545-5017 (Electronic) Linking ISSN: 15455009 NLM ISO Abbreviation: Pediatr Blood Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Protein S Deficiency*/complications , Protein S Deficiency*/diagnosis , Protein S Deficiency*/genetics , Thrombophilia*/complications , Thrombosis*/etiology , Thrombosis*/genetics , Protein C Deficiency*/genetics , Protein C Deficiency*/complications , Antithrombin III Deficiency*, Infant, Newborn ; Female ; Pregnancy ; Humans ; Retrospective Studies ; Prospective Studies ; Japan/epidemiology ; Protein C/genetics ; Anticoagulants ; Antithrombin III ; Antithrombins

المؤلفون: Mori F; Department of Research and Innovation, Kedrion Biopharma, Bolognana, Italy., Angelini C; Department of Research and Innovation, Kedrion Biopharma, Bolognana, Italy., Farina C; Department of Research and Innovation, Kedrion Biopharma, Bolognana, Italy.

المصدر: Vox sanguinis [Vox Sang] 2024 Mar; Vol. 119 (3), pp. 193-202. Date of Electronic Publication: 2023 Nov 28.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 0413606 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1423-0410 (Electronic) Linking ISSN: 00429007 NLM ISO Abbreviation: Vox Sang Subsets: MEDLINE

مواضيع طبية MeSH: Purpura Fulminans*/drug therapy , Purpura Fulminans*/genetics , Protein C Deficiency*/drug therapy, Infant, Newborn ; Humans ; Protein C/analysis ; Protein C/therapeutic use ; Protein S ; Plasma/chemistry

المؤلفون: Xu F; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Zhang K; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Xu Q; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Ye L; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Zeng M; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Jin Y; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Wang M; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China., Yang L; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015, China. YLH91@163.com.

المصدر: Annals of hematology [Ann Hematol] 2024 Feb; Vol. 103 (2), pp. 645-652. Date of Electronic Publication: 2023 Nov 10.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0584 (Electronic) Linking ISSN: 09395555 NLM ISO Abbreviation: Ann Hematol Subsets: MEDLINE

مواضيع طبية MeSH: Protein C Deficiency*/genetics , Protein C Deficiency*/diagnosis , Thrombophilia*, Humans ; Protein C/genetics ; Protein C/metabolism ; Mutation ; Mutation, Missense

SCR Disease Name: Thrombophilia, hereditary

المؤلفون: Tsuchihashi S; Department of Pediatrics, Graduate School of Medicine, Gunma University., Okuno H; Department of Pediatrics, Graduate School of Medicine, Gunma University., Kawashima J; Department of Pediatrics, Graduate School of Medicine, Gunma University., Yamato G; Department of Pediatrics, Graduate School of Medicine, Gunma University., Ogawa Y; Department of Hematology, Graduate School of Medicine, Gunma University., Uchiyama Y; Rare Disease Genomics, Yokohama City University Hospital.; Department of Human Genetics, Graduate School of Medicine, Yokohama City University., Matsumoto N; Department of Human Genetics, Graduate School of Medicine, Yokohama City University., Takizawa T; Department of Pediatrics, Graduate School of Medicine, Gunma University.

المصدر: [Rinsho ketsueki] The Japanese journal of clinical hematology [Rinsho Ketsueki] 2024; Vol. 65 (3), pp. 164-168.

نوع المنشور: Case Reports; English Abstract; Journal Article

بيانات الدورية: Publisher: Japan Society Of Clinical Hematology Country of Publication: Japan NLM ID: 2984782R Publication Model: Print Cited Medium: Print ISSN: 0485-1439 (Print) Linking ISSN: 04851439 NLM ISO Abbreviation: Rinsho Ketsueki Subsets: MEDLINE

مواضيع طبية MeSH: Fractures, Bone*/complications , Protein C Deficiency*/complications , Thrombosis*/complications, Child, Preschool ; Humans ; Infant, Newborn ; Male ; Anticoagulants ; Vitamin K ; Warfarin/therapeutic use

المؤلفون: Gibson D; Medicine, University of New South Wales, Sydney, New South Wales, Australia Damien.p.gibson@gmail.com.; Urology, Saint George Hospital, Kogarah, New South Wales, Australia., Zhong W; Urology, Saint George Hospital, Kogarah, New South Wales, Australia., Bajaj M; Urology, Saint George Hospital, Kogarah, New South Wales, Australia., Ranasinghe A; Urology, Saint George Hospital, Kogarah, New South Wales, Australia.

المصدر: BMJ case reports [BMJ Case Rep] 2023 Nov 01; Vol. 16 (11). Date of Electronic Publication: 2023 Nov 01.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 101526291 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-790X (Electronic) Linking ISSN: 1757790X NLM ISO Abbreviation: BMJ Case Rep Subsets: MEDLINE

مواضيع طبية MeSH: Protein C Deficiency*/complications , Protein C Deficiency*/diagnosis , Testicular Diseases*/etiology , Testicular Diseases*/complications , Stroke*/complications, Male ; Humans ; Testis/pathology ; Infarction/complications

المؤلفون: Cao Q; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China; Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA., Hao Z; College of Bioscience and Biotechnology, Yangzhou University, Yangzhou, Jiangsu, People's Republic of China., Li C; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China., Chen X; Department of Biology, the University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Gao M; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China., Jiang N; College of Bioscience and Biotechnology, Yangzhou University, Yangzhou, Jiangsu, People's Republic of China., Liu H; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China; Department of Cell Biology, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Shen Y; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China., Yang H; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China; First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China., Zhang S; Department of Cell Biology, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Yang A; Department of Cell Biology, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Li W; Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA. Electronic address: weikai@wustl.edu., Tie JK; Department of Biology, the University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA. Electronic address: jktie@email.unc.edu., Shen G; Henan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang, Henan, People's Republic of China; Department of Cell Biology, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China. Electronic address: shenba433@163.com.

المصدر: Journal of thrombosis and haemostasis : JTH [J Thromb Haemost] 2023 Nov; Vol. 21 (11), pp. 3124-3137. Date of Electronic Publication: 2023 Jun 29.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: England NLM ID: 101170508 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1538-7836 (Electronic) Linking ISSN: 15387836 NLM ISO Abbreviation: J Thromb Haemost Subsets: MEDLINE

مواضيع طبية MeSH: Protein C Deficiency*, Humans ; RNA Precursors/genetics ; RNA Precursors/metabolism ; Protein Sorting Signals/genetics ; RNA Splicing ; Mutation ; Mutation, Missense ; RNA, Messenger/genetics

SCR Disease Name: Thrombophilia, hereditary