Practical aspects of the two FIGO systems for management of abnormal uterine bleeding in the reproductive years

MG Munro - Best Practice & Research Clinical Obstetrics & …, 2017 - Elsevier
The FIGO systems defining the nomenclature and symptoms of abnormal uterine bleeding
(AUB) in the reproductive years (System 1) and the PALM-COEIN classification of causes of …

Gynaecological and obstetrical bleeding in women with factor XI deficiency–a systematic review

S Wiewel‐Verschueren, IJ Arendz, H M. Knol… - …, 2016 - Wiley Online Library
Introduction Menstrual bleeding, pregnancy and delivery present an intrinsic haemostatic
challenge to women with bleeding disorders such as factor XI (FXI) deficiency. Aim To …

Menstrual disorders and quality of life of women in an urban area of Puducherry: A community-based cross-sectional study

KB Laksham, R Selvaraj, SS Kar - Journal of family medicine and …, 2019 - journals.lww.com
Background: Menstrual disorders are common among women in reproductive age group
and affect their normal functioning and social life. Due to cultural reasons, menstrual …

Rare coagulation factor deficiencies: a countrywide screening data from India

S Shetty, T Shelar, D Mirgal, V Nawadkar, P Pinto… - …, 2014 - Wiley Online Library
As compared to haemophilia, although the clinical features and the management strategies
for rare coagulation factor deficiencies are discussed, little is known about them. This study …

Epidemiology of abnormal uterine bleeding

M Palep-Singh, A Prentice - Best Practice & Research Clinical Obstetrics & …, 2007 - Elsevier
Menstrual dysfunction is a common cause of referral to the gynaecology clinic, and the
problem has a considerable impact on the health status and the quality of life of women. The …

Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia

M Kannan, F Ahmad, BK Yadav… - … of Thrombosis and …, 2009 - Wiley Online Library
Background: Glanzmann thrombasthenia (GT) is an autosomal recessive inherited platelet
function defect that is characterized by reduction in, or absence of, platelet aggregation in …

Diagnosis of Glanzmann thrombasthenia by whole blood impedance analyzer (MEA) vs. light transmission aggregometry

A Albanyan, A Al‐Musa, R AlNounou… - … journal of laboratory …, 2015 - Wiley Online Library
Background Glanzmann thrombasthenia (GT) is a rare inherited platelet disorder that is
characterized by spontaneous or postprocedural bleeding. The diagnosis of GT depends on …

Etiology and diagnosis of heavy menstrual bleeding among adolescent and adult patients: a systematic review and meta-analysis of the literature

KJ Comishen, M Bhatt, K Yeung, J Irfan, A Zia… - Journal of Thrombosis …, 2024 - Elsevier
Background Heavy menstrual bleeding (HMB) is excessive menstrual blood loss that
interferes with an individual's quality of life. Many individuals with HMB are inadequately …

Comparison of platelet aggregation using light transmission and multiple electrode aggregometry in Glanzmann thrombasthenia

A Awidi, A Maqablah, M Dweik, N Bsoul, A Abu-Khader - Platelets, 2009 - Taylor & Francis
We examined platelet aggregation in platelet-rich plasma (PRP) and in whole blood in nine
patients with Thrombasthenia Glanzmann (TG). In PRP, aggregation was measured by …

Current understanding of von Willebrand's disease in women–some answers, more questions

PA Kouides - Haemophilia, 2006 - Wiley Online Library
Considerable progress has been made in the past decade in describing the obstetrical and
gynaecological aspects of von Willebrand's disease (VWD). In addition, epidemiological …