Search details
1.
Gillick competence: an inadequate guide to the ethics of involving adolescents in decision-making.
J Med Ethics
; 50(3): 157-162, 2024 Feb 20.
Article
in English
| MEDLINE | ID: mdl-37169548
2.
Emicizumab prophylaxis in haemophilia A with inhibitors: Three years follow-up from the UK Haemophilia Centre Doctors' Organisation (UKHCDO).
Haemophilia
; 29(3): 743-752, 2023 May.
Article
in English
| MEDLINE | ID: mdl-36811304
3.
A little bit pregnant: towards a pluralist account of non-sexual reproduction.
J Med Ethics
; 2023 Apr 13.
Article
in English
| MEDLINE | ID: mdl-37055160
4.
Management of children and adults with all stages of nodular lymphocyte predominant Hodgkin lymphoma - All StAGEs: A consensus-based position paper from the Hodgkin lymphoma subgroup of the UK National Cancer Research Institute.
Br J Haematol
; 197(6): 679-690, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35362554
5.
Reproduction misconceived: why there is no right to reproduce and the implications for ART access.
J Med Ethics
; 2022 Nov 08.
Article
in English
| MEDLINE | ID: mdl-36347604
6.
Immune tolerance induction in severe haemophilia A: A UKHCDO inhibitor and paediatric working party consensus update.
Haemophilia
; 27(6): 932-937, 2021 Nov.
Article
in English
| MEDLINE | ID: mdl-34403546
7.
Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Genet Med
; 22(4): 745-751, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31848469
8.
A single centre retrospective study of low dose prophylaxis with extended half-life factor IX for severe haemophilia B.
Haemophilia
; 26(2): 278-281, 2020 Mar.
Article
in English
| MEDLINE | ID: mdl-32083769
9.
CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing.
J Med Genet
; 55(2): 89-96, 2018 02.
Article
in English
| MEDLINE | ID: mdl-28918392
10.
Advanced stage nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents: clinical characteristics and treatment outcome - a report from the SFCE & CCLG groups.
Br J Haematol
; 177(1): 106-115, 2017 04.
Article
in English
| MEDLINE | ID: mdl-28220934
11.
Exploring the feasibility of delivering standardized genomic care using ophthalmology as an example.
Genet Med
; 19(9): 1032-1039, 2017 09.
Article
in English
| MEDLINE | ID: mdl-28301457
12.
Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal Disease.
Ophthalmology
; 124(7): 985-991, 2017 07.
Article
in English
| MEDLINE | ID: mdl-28341476
13.
Molecular findings from 537 individuals with inherited retinal disease.
J Med Genet
; 53(11): 761-767, 2016 Nov.
Article
in English
| MEDLINE | ID: mdl-27208204
14.
Relapsed or poorly responsive nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents - a report from the United Kingdom's Children's Cancer and Leukaemia Study Group.
Br J Haematol
; 173(3): 421-31, 2016 05.
Article
in English
| MEDLINE | ID: mdl-26996288
15.
A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias.
Br J Haematol
; 175(2): 318-330, 2016 Oct.
Article
in English
| MEDLINE | ID: mdl-27432187
16.
Correction: Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Genet Med
; 23(10): 2023, 2021 Oct.
Article
in English
| MEDLINE | ID: mdl-33353976
17.
Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease.
Ophthalmology
; 123(5): 1143-50, 2016 May.
Article
in English
| MEDLINE | ID: mdl-26872967
18.
Childhood and Adolescent nodular lymphocyte predominant Hodgkin lymphoma - A review of clinical outcome based on the histological variants.
Br J Haematol
; 171(2): 254-262, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26115355
19.
Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra.
Rheumatology (Oxford)
; 59(2): 448-451, 2020 02 01.
Article
in English
| MEDLINE | ID: mdl-31377798
20.
GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia.
Blood
; 122(24): 3908-17, 2013 Dec 05.
Article
in English
| MEDLINE | ID: mdl-24021668