Suchergebnisse - "Lentaigne, Claire"

PubPharm (28)

1

A single 1 g/kg dose of intravenous immunoglobulin is a safe and effective treatment for immune thrombocytopenia; results of the first HaemSTAR 'Flash-Mob' retrospective study incorporating 961 patients

enthalten in: British journal of haematology | 2022

von HaemSTAR Collaborators | Nicolson, P. | Perry, R. | +98

2

Clinical outcomes and the impact of prior oral anticoagulant use in patients with coronavirus disease 2019 admitted to hospitals in the UK - a multicentre observational study

enthalten in: British journal of haematology | 2022

von Arachchillage, D. | Rajakaruna, I. | Odho, Z. | +27

3

Clinical outcomes and the impact of prior oral anticoagulant use in patients with coronavirus disease 2019 admitted to hospitals in the UK — a multicentre observational study

enthalten in: British Journal of Haematology | 2022

von Arachchillage, D. | Rajakaruna, I. | Odho, Z. | +27

4

Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function

enthalten in: Haematologica | 2021

von Chan, M. | Hayman, M. | Sivapalaratnam, S. | +22

5

Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

enthalten in: Blood | 2019

von Lentaigne, C. | Greene, D. | Sivapalaratnam, S. | +28

CommentIn: Blood. 2019 Dec 5;134(23):2000-2002. - PMID 31805194

6

Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses

enthalten in: Haematologica | 2019

von van Oorschot, R. | Marneth, A. | Bergevoet, S. | +15

7

Germline selection shapes human mitochondrial DNA diversity

enthalten in: Science (New York, N.Y.) | 2019

von Wei, W. | Tuna, S. | Keogh, M. | +138

CommentIn: Nat Rev Genet. 2019 Aug;20(8):434-435. - PMID 31171864

8

Publisher Correction : Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

enthalten in: Scientific reports | 2018

von Farmery, J. | Smith, M. | NIHR BioResource - Rare Diseases | +101

ErratumFor: Sci Rep. 2018 Jan 22;8(1):1300. - PMID 29358629

9

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

enthalten in: American journal of human genetics | 2018

von Ito, Y. | Carss, K. | Duarte, S. | +118

10

Telomerecat : A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

enthalten in: Scientific reports | 2018

von Farmery, J. | Smith, M. | NIHR BioResource - Rare Diseases | +101

ErratumIn: Sci Rep. 2018 Sep 3;8(1):13376. - PMID 30177810