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Academic Journal

Efficacy of factor VIII/von Willebrand factor concentrate Alphanate in preventing excessive bleeding during surgery in subjects with von Willebrand disease.

Subjects: Hemostasis, Surgical*; Factor VIII/Factor VIII/Factor VIII/*therapeutic use ; Hemostatics/Hemostatics/Hemostatics/*therapeutic use

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2008 Mar; Vol. 14 (2), pp. 271-5. Date of Electronic Publication: 2008 Jan 08.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Desmopressin (DDAVP) use in patients with von Willebrand disease: A single-centre retrospective review of test response and clinical outcomes.

Subjects: Tranexamic Acid*/Tranexamic Acid*/Tranexamic Acid*/therapeutic use ; von Willebrand Diseases*/von Willebrand Diseases*/von Willebrand Diseases*/drug therapy; Adolescent

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2023 Jul; Vol. 29 (4), pp. 1095-1103. Date of Electronic Publication: 2023 May 31.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Women and girls with haemophilia: A retrospective cohort study in China.

  • Authors : Zhang W; State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin Key Laboratory of Gene Therapy for Blood Diseases, CAMS Key Laboratory of Gene Therapy for Blood Diseases, Tianjin, China.; Li K

Subjects: Hemophilia A*/Hemophilia A*/Hemophilia A*/complications ; Hemophilia A*/Hemophilia A*/Hemophilia A*/epidemiology ; Hemophilia A*/Hemophilia A*/Hemophilia A*/genetics

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2023 Mar; Vol. 29 (2), pp. 578-590. Date of Electronic Publication: 2023 Jan 03.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Global epidemiology of factor XI deficiency: A targeted review of the literature and foundation reports.

  • Authors : Zhang X; CERobs Consulting, LLC., Wrightsville Beach, North Carolina, USA.; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Subjects: Factor XI Deficiency*/Factor XI Deficiency*/Factor XI Deficiency*/epidemiology ; Factor XI Deficiency*/Factor XI Deficiency*/Factor XI Deficiency*/genetics; Humans

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2023 Mar; Vol. 29 (2), pp. 423-434. Date of Electronic Publication: 2022 Nov 11.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Pharmacokinetics of perioperative FVIII in adult patients with haemophilia A: An external validation and development of an alternative population pharmacokinetic model.

  • Authors : Zhu J; Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina Eshelman School of Pharmacy, Chapel Hill, North Carolina, USA.; Wu YS

Subjects: Hemophilia A*/Hemophilia A*/Hemophilia A*/drug therapy ; Hemostatics*; Adult

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2021 Nov; Vol. 27 (6), pp. 974-983. Date of Electronic Publication: 2021 Aug 17.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Genetic causes of haemophilia in women and girls.

  • Authors : Miller CH; Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.; Bean CJ

Subjects: Hemophilia A*/Hemophilia A*/Hemophilia A*/genetics ; Hemophilia B*/Hemophilia B*/Hemophilia B*/genetics; Factor IX/Factor IX/Factor IX/genetics

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2021 Mar; Vol. 27 (2), pp. e164-e179. Date of Electronic Publication: 2020 Dec 13.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Diagnosis of von Willebrand disease in Western Mexico.

  • Authors : Zavelia Padilla-Romo MG; División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.; Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.

Subjects: von Willebrand Diseases*/von Willebrand Diseases*/von Willebrand Diseases*/diagnosis ; von Willebrand Diseases*/von Willebrand Diseases*/von Willebrand Diseases*/epidemiology; Hemorrhage

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2021 Jan; Vol. 27 (1), pp. e78-e87. Date of Electronic Publication: 2020 Nov 20.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Menstrual and obstetrical bleeding in women with inherited platelet receptor defects-A systematic review.

  • Authors : Punt MC; Van Creveldkliniek, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.; Schuitema PCE

Subjects: Blood Platelets/Blood Platelets/Blood Platelets/*pathology ; Menorrhagia/Menorrhagia/Menorrhagia/*etiology ; Postpartum Hemorrhage/Postpartum Hemorrhage/Postpartum Hemorrhage/*etiology

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2020 Mar; Vol. 26 (2), pp. 216-227. Date of Electronic Publication: 2020 Jan 31.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Efficacy and safety of a VWF/FVIII concentrate (wilate ® ) in inherited von Willebrand disease patients undergoing surgical procedures.

Subjects: Factor VIII/Factor VIII/Factor VIII/*therapeutic use ; von Willebrand Diseases/von Willebrand Diseases/von Willebrand Diseases/*surgery; Adolescent

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2017 Mar; Vol. 23 (2), pp. 264-272. Date of Electronic Publication: 2016 Dec 27.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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Academic Journal

Low-factor consumption for major surgery in haemophilia B with long-acting recombinant glycoPEGylated factor IX.

  • Authors : Escobar MA; University of Texas Health Science Center and the Gulf States Hemophilia and Thrombophilia Center, Houston, TX, USA.; Tehranchi R

Subjects: Factor IX/Factor IX/Factor IX/*therapeutic use ; Hemophilia B/Hemophilia B/Hemophilia B/*drug therapy ; Hemophilia B/Hemophilia B/Hemophilia B/*surgery

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2017 Jan; Vol. 23 (1), pp. 67-76. Date of Electronic Publication: 2016 Aug 01.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited

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