Results 91 to 100 of about 5,300 (203)

A Case of Menorrhage Combined with Hypofibrinogenemia

The Tohoku Journal of Experimental Medicine, 1963
A rare case of hypofibrinogenemia combined with elevated fibrino(geno)-lysis at the time of expected menstruation was reported.
Maki, Masahiro, Takano, Atsushi
openaire   +3 more sources

IMR898033 Supplementary document - Supplemental material for Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report

, 2020
Supplemental material, IMR898033 Supplementary document for Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report by Leilei Gu, Bin Wang, Lu Liu, Qiaorong Gan, Xiaolong Liu, Lihong Chen and Li ...
Xiaolong Liu (265696), Li Chen (5749), Lihong Chen (12138), Lu Liu (171341), Qiaorong Gan (8712258), Leilei Gu (2066077), Bin Wang (30851)   +6 more
core   +1 more source

Usefulness of the APTT waveform for the diagnosis of DIC and prediction of the outcome or bleeding risk

Thrombosis Journal, 2019
Background The usefulness of the activated partial thromboplastin time (APTT) waveform has been reported in hemophilia, acquired hemophilia and monitoring for anticoagulants.
Kei Suzuki, Hideo Wada, Takeshi Matsumoto, Makoto Ikejiri, Kohshi Ohishi, Yoshiki Yamashita, Hiroshi Imai, Toshiaki Iba, Naoyuki Katayama   +8 more
doaj   +1 more source

Early Predictive Factors of Hypofibrinogenemia in Acute Trauma Patients

, 2018
Background: Uncontrolled hemorrhage still remains a major cause of trauma-associated mortality. The events resulting in acute traumatic coagulopathy, particularly hypofibrinogenemia, make control of bleeding difficult.
Shahram Paydar, Zahra Shayan, Behnam Dalfardi, Shahram Bolandparvaz, Leila Shayan, Jalal Saem   +5 more
core   +1 more source

Chiari I Malformation and Intramedullary Hemorrhage in a Female Patient with Klippel Trenaunay Syndrome: A Rare Case Report Study [PDF]

International Journal of Caring Sciences
Chiari I Malformation and Intramedullary Hemorrhage in a Female Patient with Klippel Trenaunay Syndrome: A Rare Case Report ...
Kalliopi Magounaki, Emmanouil Kalafatis, Dimitris Stergiou, Maria Tzaki, Dionysios Vekios, Aggelos Papakalos and Ioannis Kyriazis   +5 more
doaj  

Human Fibrinogen Concentrate and Fresh Frozen Plasma in the Management of Severe Acquired Hypofibrinogenemia in Children with Acute Lymphoblastic Leukemia: Results of a Retrospective Survey

, 2019
Objective of the Study:In this study we aimed to retrospectively evaluate how centers, belonging to the Associazione Italiana Ematologia e Oncologia Pediatrica (AIEOP), manage severe acquired hypofibrinogenemia in children with acute lymphoblastic ...
Putti M. C., Mura R. M., CORALLO, PAOLA CARMELA, Pollio B., Micalizzi C., Casale F., Giordano P., Luciani M., Colombini A., Grassi M., Testi A. M., Rizzari C., Tafuri S., Petruzziello F., Notarangelo L. D., De Leonardis F., Saracco P., Consarino C., Santoro N., Mastrodicasa E., Onofrillo D.   +20 more
core   +1 more source

Total knee arthroplasty in a patient with hypofibrinogenemia

, 2016
Patients with afibrinogenemia or hypofibrinogenemia present a unique challenge to the arthroplasty surgeon as fibrinogen is a key contributor to hemostasis.
Rubin, Lee E., Lee E. Rubin, MD, Truntzer, Jeremy N., Kalpit N. Shah, MD, Nacca, Christopher R., Christopher R. Nacca, MD, Shah, Kalpit N., Jeremy N. Truntzer, MD   +7 more
core   +1 more source

Diagnostic and management practices for inherited fibrinogen disorders: a nationwide survey of Italian Hemophilia Treatment Centers

Bleeding, Thrombosis and Vascular Biology
Background: inherited fibrinogen disorders are characterized by a spectrum of quantitative or qualitative fibrinogen deficiency associated with both a hemorrhagic and thrombotic risk.
Renato Marino, Silvia Linari, Marzia Leotta, Antonio Coppola, Chiara Biasoli, Maria Elisa Mancuso, Flora Peyvandi, Cristina Santoro, Ezio Zanon, Rita Carlotta Santoro   +9 more
doaj   +1 more source

Healed retinal vasculitis in a child with hypofibrinogenemia

Indian Journal of Ophthalmology. Case Reports
Dysfibrinogenemia is a hematological disorder resulting from a decreased or abnormal level of fibrinogen. We describe a child previously diagnosed with a case of hypofibrinogenemia, whose fundus evaluation revealed evidence of old retinal vasculitis.
Marushka Aguiar, Prachi Agashe, Ashish Doshi   +2 more
doaj   +1 more source

Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis

, 2006
Hypofibrinogenemia is a rare inherited disorder characterized by low levels of circulating fibrinogen, caused by mutations within 1 of the 3 fibrinogen genes.
Spahr, Laurent, Rougemont, A. L., Neerman Arbez, Marguerite, Male, P. J., Rubbia-Brandt, Laura   +4 more
core   +1 more source