Results 21 to 30 of about 278,057 (291)

Inhibitors in Patients with Congenital Bleeding Disorders Other Than Hemophilia [PDF]

open access: yes, 2017
The most worrying complication of replacement therapy for severe hemophilia A and B is currently the occurrence of inhibitory alloantibodies against infused factor VIII and factor IX, respectively.
Franchini, Massimo   +6 more
core   +1 more source

Inhibitors to factor VII in congenital factor VII deficiency [PDF]

open access: yesHaemophilia, 2014
We performed a prospective study of FVII inhibitor occurrence in a large number of patients with FVII deficiency who had received replacement therapy for spontaneous or traumatic bleeding episodes, major or minor surgical interventions or prophylaxis.Inhibitor development was detected in 2.6% (3/115) of patients, but the incidence of de novo inhibitors
Batorova A   +11 more
openaire   +3 more sources

Congenital factor VII deficiency presenting first time as isolated recurrent hematuria at late age

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2019
Hematological conditions rarely present as isolated hematuria. Factor VII deficiency is a rare congenital coagulopathy inherited as autosomal recessive pattern. It usually presents a severe life-threatening bleeding at an early age.
Suman Sethi   +5 more
doaj   +1 more source

Generation of a human induced pluripotent stem cell line, YCMi002-A, from a Factor VII deficiency patient carrying F7 mutations

open access: yesStem Cell Research, 2020
Factor VII (FVII) deficiency is the most common among the rare bleeding disorders, which is caused by mutations in coagulation factor VII. Clinical features caused by FVII deficiency vary from mild or asymptomatic to fatal cerebral hemorrhage.
Do-Hun Kim   +3 more
doaj   +1 more source

Replacement therapy for bleeding episodes in factor VII deficiency: A prospective evaluation [PDF]

open access: yes, 2013
Patients with inherited factor VII (FVII) deficiency display different clinical phenotypes requiring ad hoc management. This study evaluated treatments for spontaneous and traumatic bleeding using data from the Seven Treatment Evaluation Registry (STER).
Auerswald,G   +14 more
core   +1 more source

Successful Treatment of Intracranial Hemorrhage with Recombinant Activated Factor VII in a Patient with Newly Diagnosed Acute Myeloid Leukemia: A Case Report and Review of the Literature [PDF]

open access: yes, 2015
Intracranial hemorrhage (ICH) is a common complication in acute myeloid leukemia (AML) patients with an incidence rate of 6.3% [1]. Bleeding disorders related to disseminated intravascular coagulation (DIC) are common complications in AML cases [2 ...
Daniel Johnson   +10 more
core   +3 more sources

Vitamin K as a diet supplement with impact in human health: current evidence in age-related idseases [PDF]

open access: yes, 2020
Vitamin K health benefits have been recently widely shown to extend beyond blood homeostasis and implicated in chronic low-grade inflammatory diseases such as cardiovascular disease, osteoarthritis, dementia, cognitive impairment, mobility disability ...
Araujo, Nuna C. P.   +3 more
core   +1 more source

Asymptomatic intracranial hemorrhage in a newborn with congenital factor VII deficiency and successful treatment with recombinant activated factor VII

open access: yesThe Turkish Journal of Pediatrics, 2018
Intracranial hemorrhage is considered the most common cause of death in newborns with congenital factor VII (FVII) deficiency. Recombinant activated FVII (rFVIIa) provides specific replacement therapy, however there is limited experience with its ...
Zeynep İnce   +5 more
doaj   +1 more source

Dental extraction in congenital factor Vll deficiency with inhibitor – a case report

open access: yesThe Journal of Haemophilia Practice, 2021
Hereditary factor VII (FVII) deficiency is a rare bleeding disorder with autosomal recessive inheritance, and FVII deficiency with an inhibitor is extremely rare.
Nayar Geeta   +3 more
doaj   +1 more source

The Arecibo Galaxy Environment Survey VII : A Dense Filament With Extremely Long HI Streams [PDF]

open access: yes, 2014
We present completed observations of the NGC 7448 galaxy group and background volume as part of the blind neutral hydrogen Arecibo Galaxy Environment Survey (AGES).
Davies, J. I.   +5 more
core   +1 more source

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