Results 21 to 30 of about 448,079 (362)

Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature [PDF]

BMC Medical Genetics, 2006
Background Unbalanced chromosomal translocations may present with a variety of clinical and laboratory findings and provide insight into the functions of genes on the involved chromosomal segments.
Meck Jeanne M, Brooks Brian P, Haddad Bassem R, Bendavid Claude, Blain Delphine, Toretsky Jeffrey A   +5 more
doaj   +2 more sources

A Comparison between Recombinant Activated Factor VII (Aryoseven) and Novoseven in Patients with Congenital Factor VII Deficiency [PDF]

Clinical and applied thrombosis/hemostasis, 2015
In order to establish the efficacy and biosimilar nature of AryoSeven to NovoSeven in the treatment of congenital factor VII (FVII) deficiency, patients received either agent at 30 1/4g/kg, intravenously per week for 4 weeks, in a randomized fashion. The
Abolghasemi, H., Ahmadinejad, M., Baghaeipour, M.R., Dehdezi, B.K., Eshghi, P., Faranoush, M., Fayazfar, R., Heshmat, R., Hoorfar, H., Kamyar, K., Karimi, M., Khoeiny, B., Managhchi, M., Mehrvar, A., Mirbehbahani, N.B., Naderi, M., Toogeh, G.   +16 more
core   +2 more sources

Acute myeloid leukemia: A rare cause of acquired isolated factor VII deficiency [PDF]

Leukemia Research Reports
Background: Acquired factor VII deficiency remains a rare pathology. Only 5 prior reported cases of aFVIID associated with acute myeloid leukemia (AML) have been described in the literature.
Zaineb Mlayah, Haifa Hafsa, Alaa Ghorbel, Nader Slama, Sara Boukhris, Mohamed-Adnene Laatiri   +5 more
doaj   +2 more sources

Isolated congenital factor VII deficiency [PDF]

, 2019
Congenital factor VII (FVII) (proconvertin) is a rare autosomal recessive bleeding disorder. Bleeding manifestations and clinical findings vary widely, ranging from being asymptomatic to life-threatening bleeding. Intracranial bleeding is relatively less
Mahalinge, Manisha, Merchant, Saira, Meshram, Rajkumar, Somkuwar, Anand Suresh, Somkuwar, Tushar, Waghmare, Mukesh   +5 more
core   +4 more sources

Factor VII Deficiency in Systemic Mastocytosis with an Associated Myeloid Neoplasm [PDF]

Hematology Reports
Factor VII (FVII) deficiency is a rare bleeding disorder that can be classified as congenital or acquired, and the majority of acquired cases are due to vitamin K deficiency or liver disease. Isolated acquired FVII deficiency is a rare occurrence and has
Giorgio Rosati, Sofia Camerlo, Alessandro Fornari, Valerio Marci, Barbara Montaruli, Alessandro Morotti   +5 more
doaj   +2 more sources

Anticoagulation Therapy Considerations in Factor VII Deficiency [PDF]

Drug Safety - Case Reports, 2016
Factor VII (FVII) deficiency is the most prevalent rare bleeding disorder in the USA and affects approximately 1 out of every 500,000 people. Warfarin inhibits the synthesis of FVII, in addition to other clotting factors. Warfarin is contraindicated in patients with bleeding tendencies or blood dyscrasias; therefore, the literature regarding the use of
Kathy E. Komperda, Julie A. Fusco, Eric J. Paulus, Gabriel Park   +3 more
openaire   +4 more sources

Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children

The Application of Clinical Genetics, 2017
Chanchai Traivaree,1 Chalinee Monsereenusorn,1 Arunotai Meekaewkunchorn,2 Premsak Laoyookhong,3 Saranya Suwansingh,4 Boonchai Boonyawat5 1Division of Hematology/Oncology, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine ...
Traivaree C, Monsereenusorn C, Meekaewkunchorn A, Laoyookhong P, Suwansingh S, Boonyawat B   +5 more
doaj   +2 more sources

Congenital factor VII deficiency [PDF]

British Journal of Anaesthesia, 2010
R Mandhyan, Alankar Tiwari, G Cherian
openalex   +3 more sources

Continuous infusion of recombinant activated factor VII: a review of data in congenital hemophilia with inhibitors and congenital factor VII deficiency

Journal of Blood Medicine, 2018
Madhvi Rajpurkar,1 David L Cooper2 1Division of Hematology/Oncology, Carman and Ann Adams Department of Pediatrics, Wayne State University School of Medicine, Children’s Hospital of Michigan, Detroit, MI, USA; 2Clinical, Medical and Regulatory ...
Rajpurkar M, Cooper DL
doaj   +2 more sources

Molecular characterization of iranian patients with inherited coagulation factor VII deficiency

Balkan Journal of Medical Genetics, 2017
Coagulation factor VII (FVII) is a key enzyme of the extrinsic coagulation cascade that is predominantly produced by hepatocytes. The F7 gene mutations cause FVII deficiency with considerable molecular and phenotypic heterogeneity.
Shahbazi S, Mahdian R, Karimi K, Mashayekhi A   +3 more
doaj   +2 more sources