Aller au contenu principal
Profil bibliographique

Joanna Davies

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

34Publications signalées
572Citations signalées
0Affiliations récentes

Les domaines associés

Hemophilia Treatment and ResearchBlood Coagulation and Thrombosis MechanismsCoagulation, Bradykinin, Polyphosphates, and AngioedemaPlatelet Disorders and TreatmentsUterine Myomas and Treatments

Les publications récentes

Accès ouvert 2021 review OpenAlex

The Impact of Vitamin D Deficiency on the Severity of Symptoms and Mortality Rate among Adult Patients with Covid-19: A Systematic Review and Meta-Analysis

Maisa Hamed Al Kiyumi, Sanjay Kalra, Joanna Davies, Atul Kalhan

Introduction: We aimed to study the prevalence of vitamin D deficiency (VDD) in patients with COVID-19 infection and evaluate the impact of vitamin D levels on the severity of symptoms and the case fatality rate. Evidence Acquisition: A comprehensive literature search was …

om, in, gb (code pays fourni par la source)

17 citations Indian Journal of Endocrinology and Metabolism
2018 book-chapter OpenAlex

Gynecology

Joanna Davies, Rezan Abdul Kadir

The frequency and severity of gynecological bleeding have long been underestimated in women with inherited bleeding disorders (IBDs). Heavy menstrual bleeding (HMB) is the most common presenting symptom for women with IBD. Menstrual blood loss can be recorded with a high degree …

gb, us (code pays fourni par la source)

0 citations
Accès ouvert 2017 article OpenAlex

Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers

Irena Hudecova, Peiyong Jiang, Joanna Davies, Yuk Ming Dennis Lo et autres

Key Points Droplet digital PCR is an affordable and user-friendly method for the detection of F8 and F9 sequence variants in maternal plasma. Targeted MPS accurately determines fetal inheritance of F8 int22h-related inversions, using maternal plasma of pregnant hemophilia carriers.

hk, gb (code pays fourni par la source)

66 citations Blood
2016 article OpenAlex

The Management of Factor XI Deficiency in Pregnancy

Joanna Davies, Rezan Abdul Kadir

Management of factor XI (FXI) deficiency in pregnancy is complicated by lack of correlation between FXI level and bleeding risk. Clinicians should be vigilant about the potential for prolonged or excessive bleeding following miscarriage or termination of pregnancy, or postpartum hemorrhage (PPH). …

gb (code pays fourni par la source)

19 citations Seminars in Thrombosis and Hemostasis
2015 article OpenAlex

The role of rotational thromboelastometry in assessment of haemostasis during pregnancy in women with factor XI deficiency

Joanna Davies, Ann Harper, Rezan Abdul Kadir

Introduction Women with factor XI (FXI) deficiency are at an increased risk of bleeding complications at delivery. Obstetric management is complicated by a lack of correlation between FXI level and bleeding risk. Aim The aims of this study were to assess the …

gb (code pays fourni par la source)

13 citations Haemophilia
2015 review OpenAlex

Mode of delivery and cranial bleeding in newborns with haemophilia: a systematic review and meta‐analysis of the literature

Joanna Davies, Rezan Abdul Kadir

OBJECTIVES: Cranial bleeding at birth can result in significant neurological morbidity in newborns with haemophilia. The optimum mode of delivery (MOD) of a potentially affected foetus remains controversial. AIM: The aim of this review is to ascertain overall incidence of cranial bleeding …

gb (code pays fourni par la source)

59 citations Haemophilia
2014 article OpenAlex

PFM.18 UK variation in prenatal management of Congenital Adrenal Hyperplasia

CL Mercer, Michelle M. Coleman, Joanna Davies, DG Wellesley

Introduction Congenital adrenal hyperplasia (CAH) is a relatively common condition with a population carrier frequency of 1:50. Antenatal administration of dexamethasone treatment has been used to reduce virilisation in affected female offspring. There is however, considerable national/international variability regarding this treatment, including …

gb (code pays fourni par la source)

0 citations Archives of Disease in Childhood Fetal & Neonatal
2013 article OpenAlex

The Effect Of Thrombotic Markers On The Severity Of Bleeding Symptoms In Women With Inherited Bleeding Disorders

Susan Halimeh, Joanna Davies, Rezan Abdul Kadir

Background Women with inherited bleeding disorders demonstrate heterogenicity in bleeding symptoms that do not always correlate to underlying clotting factor levels. This is problematic when predicting the bleeding risk, especially when haemostatic challenge is anticipated. The effect of thrombotic variables in reducing …

gb (code pays fourni par la source)

0 citations Blood
Accès ouvert 2013 article OpenAlex

Pregnancy complications and obstetric care in women with inherited bleeding disorders

Rezan Abdul Kadir, Joanna Davies, Rochelle Winikoff, Debra Pollard et autres

Women with inherited bleeding disorders (IBD) require the input of a multidisciplinary team to improve outcomes of pregnancy. The role of the haemophilia nurse within the multidisciplinary team is to provide educational and emotional support to the women and to facilitate and …

gb, ca, it (code pays fourni par la source)

119 citations Haemophilia

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.