Наследственная афибриногенемия: обзор литературы и клинические наблюдения

ЕВ Яковлева, ВЛ Сурин, ДС Селиванова… - Терапевтический …, 2016 - cyberleninka.ru
Афибриногенемия относится к редким врожденным коагулопатиям, приводящим к
развитию угрожающих жизни кровотечений. При афибриногенемии уровень …

[HTML][HTML] Liver transplantation as a novel strategy for resolution of congenital afibrinogenemia in a pediatric patient

FF Corrales‐Medina, T Miloh, C O'Farrell… - Journal of Thrombosis …, 2020 - Elsevier
Fibrinogen replacement therapy is a treatment mainstay for patients with afibrinogenemia
and significant bleeding. A male infant with congenital afibrinogenemia and several …

Budd-Chiari syndrome associated with congenital afibrinogenaemia reversed after orthotopic liver transplant

VG Nikam, VW Dhakre, K Motwani… - … Case Reports CP, 2024 - casereports.bmj.com
A woman in her mid-20s, a known case of congenital afibrinogenaemia, presented with
abdominal pain and distension. She was diagnosed with decompensated liver cirrhosis due …

Hereditary afibrinogenemia: A literature review and clinical observations

EV Yakovleva, VL Surin, DS Selivanova… - Terapevticheskii …, 2016 - ter-arkhiv.ru
Afibrinogenemia is a rare congenital coagulopathy that leads to life-threatening bleeding. In
afibrinogenemia, plasma fibrinogen levels are less than 0.1 g/L. The clinical manifestations …

[HTML][HTML] Thrombosis in patients with hereditary fibrinogen deficiency

EV Yakovleva, VV Salomashkina, VL Surin… - Russian journal of …, 2022 - htjournal.ru
Introduction. In most cases, in patients with hereditary fibrinogen deficiency, clinical
manifestations are represented by bleeding of varying intensity and localization. However …

[HTML][HTML] Тромбозы у больных наследственной гипофибриногенемией

ЕВ Яковлева, ВВ Саломашкина… - Гематология и …, 2022 - cyberleninka.ru
Введение. В большинстве случаев у больных наследственным дефицитом
фибриногена клинические проявления представлены различными по интенсивности и …

Afibrinogénémie congénitale: un polymorphisme clinique et un défi thérapeutique.

F Badr, S Hajjaji, MA Hanafi, N Benajiba… - Revue Marocaine des …, 2024 - revues.imist.ma
Résumé Les déficits en fibrinogène sont un ensemble de maladies rares de la coagulation
subdivisées en fonction de la quantité et de la qualité du fibrinogène circulant …

Donor-to-recipient transmission of factor XII deficiency by orthotopic liver transplantation

H Elsiesy, M Shawakat, W Alhamoudi… - Baylor University …, 2019 - Taylor & Francis
Full article: Donor-to-recipient transmission of factor XII deficiency by orthotopic liver
transplantation Skip to Main Content Taylor and Francis Online homepage Taylor and Francis …

[PDF][PDF] Paul Calabresi Career Development Award for Clinical Oncology (K12) Total Costs: $130,000 PI: Robert Bradley, PhD 2022-2023 Sponsor: University of …

A Current - 2022 - bradleybiology.org
8. Kimble E, Cassaday R. Antibody and cellular immunotherapies for acute lymphoblastic
leukemia in adults. Leuk Lymphoma. 2021 Aug 17; 1-15. PMID: 34402732. 9. Wu B, Konnick …

[PDF][PDF] Afibrinogenemia acquired by liver transplant

S Milani, M Aliakbarian, S Amouian - Exp Clin Transplant, 2017 - researchgate.net
Liver transplant is a life-saving procedure in patients with end-stage liver disease. However,
this procedure may be associated with transmission of various deficiencies of proteins …