G. Hall

发表

A. Qureshi, G. Hall, 2013 .

Guideline for investigation and management of adults and children presenting with a thrombocytosis

P. Campbell, A. Green, W. Erber, 2010, British journal of haematology.

Anaplastic lymphoma kinase‐positive anaplastic large cell lymphoma: current and future perspectives in adult and paediatric disease

G. Hall, G. Collins, T. Eyre, 2014, European journal of haematology.

Kasabach–merritt syndrome: pathogenesis and management

G. Hall, 2001 .

Kasabach–Merritt syndrome: caveats of diagnosis and management

G. Hall, I. Hann, P. Maggs, 2000 .

Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations

I. Roberts, I. Dokal, G. Hall, 1996, British journal of haematology.

G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction.

C. Klein, A. Dell, H. Morris, 2011, Glycobiology.

Resection alone in 58 children with limited stage, lymphocyte‐predominant Hodgkin lymphoma–experience from the European network group on pediatric Hodgkin lymphoma

D. Hasenclever, W. Wallace, D. Körholz, 2007, Cancer.

Cytogenetic and Molecular Genetic Aspects of Childhood Myeloproliferative/Myelodysplastic Disorders

G. Hall, 2002, Acta Haematologica.

Acute leukaemia in children: diagnosis and management

C. Mitchell, G. Hall, Rachel T. Clarke, 2009, BMJ : British Medical Journal.

Treatment of Children & Adolescents with Early Stage Nodular Lymphocyte Predominant Hodgkin Lymphoma with a Low Intensity Short Duration Chemotherapy Regimen [CVP] - on Behalf of the EuroNet-PHL Group.

D. Hasenclever, W. Wallace, D. Körholz, 2006 .

Advanced stage nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents: clinical characteristics and treatment outcome – a report from the SFCE & CCLG groups

T. Leblanc, A. Shankar, J. Landman-Parker, 2017, British journal of haematology.

Natural history of GATA1 mutations in Down syndrome.

P. Vyas, I. Roberts, A. O'marcaigh, 2004, Blood.

Childhood myeloid leukaemias.

G. Hall, Georgina W. Hall, 2001, Best practice & research. Clinical haematology.

A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

D. Ferguson, D. Higgs, A. Schuh, 2016, British journal of haematology.

A NOVEL MUTATION (NONSENSE β 127) IN EXON 3 OF THE β GLOBIN GENE PRODUCES A VARIABLE THALASSAEMIC PHENOTYPE

S. Thein, T. Sura, G. Hall, 1991 .

Beta thalassaemia in the indigenous British population

R. Barnetson, S. Thein, G. Hall, 1992, British journal of haematology.

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

P. McKay, A. Shankar, P. Fielding, 2022, British journal of haematology.

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

A. Shankar, G. Hall, J. Hayward, 2016, British journal of haematology.

Childhood and Adolescent nodular lymphocyte predominant Hodgkin lymphoma ‐ A review of clinical outcome based on the histological variants

A. Shankar, G. Hall, J. Hayward, 2015, British journal of haematology.

Shwachman–Diamond syndrome: UK perspective

G. Hall, J. Dodge, P. Dale, 2006, Archives of Disease in Childhood.

Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee

M. Makris, D. Hart, P. Collins, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Major bleeding disorders: diagnosis, classification, management and recent developments in haemophilia

G. Hall, N. Bhatnagar, 2017, Archives of Disease in Childhood.

A single centre retrospective study of low dose prophylaxis with extended half‐life factor IX for severe haemophilia B

N. Curry, G. Hall, M. Desborough, 2020, Haemophilia : the official journal of the World Federation of Hemophilia.

SOX3 deletion in mouse and human is associated with persistence of the craniopharyngeal canal.

M. Dattani, P. Thomas, H. Stewart, 2014, The Journal of clinical endocrinology and metabolism.

A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia

D. Higgs, J. Traeger-Synodinos, E. Kanavakis, 1993 .

Meiotic recombination in an Irish family with beta-thalassaemia

R. Barnetson, S. Thein, G. Hall, 1993, Human Genetics.

Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra

S. McGowan, V. Buckle, C. Babbs, 2019, Rheumatology.

GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia.

A. Curley, P. Campbell, P. Vyas, 2013, Blood.

Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia

I. Macaulay, N. Potter, P. Van Loo, 2021, Nature Cancer.

Guideline for the diagnosis and management of myelofibrosis

A. Mead, A. Green, R. Mesa, 2012, British journal of haematology.

Is this immune thrombocytopenic purpura?

J. Thachil, G. Hall, 2007, Archives of Disease in Childhood.

Nonsense codon mutations in the terminal exon of the beta-globin gene are not associated with a reduction in beta-mRNA accumulation: a mechanism for the phenotype of dominant beta-thalassemia.

S. Thein, G. Hall, Georgina W. Hall, 1994, Blood.

G371 Defining transient abnormal myelopoiesis (TAM) and silent tam in neonates with down syndrome

A. Curley, P. Vyas, A. Roy, 2016 .

CHAPTER 15 – Congenital dyserythropoietic anemias

W. Wood, G. Hall, R. Renella, 2011 .

Trilineage Perturbation of Hematopoiesis In Neonates with Down Syndrome

P. Vyas, A. Roy, I. Roberts, 2010 .

Guidelines for the investigation and management of nodular lymphocyte predominant Hodgkin lymphoma

T. Marafioti, P. McKay, P. Fielding, 2016, British journal of haematology.

Incidence, management, and outcome of high‐grade transformation of nodular lymphocyte predominant hodgkin lymphoma: Long‐term outcomes from a 30‐year experience

K. Gatter, G. Hall, G. Collins, 2015, American journal of hematology.

Treatment outcome after low intensity chemotherapy [CVP] in children and adolescents with early stage nodular lymphocyte predominant Hodgkin's lymphoma - an Anglo-French collaborative report.

D. Hasenclever, T. Leblanc, W. Wallace, 2012, European journal of cancer.

Outcome of children with nodular lymphocyte predominant Hodgkin lymphoma – a Children's Cancer and Leukaemia Group report

C. R. Pinkerton, W. Wallace, K. McCarthy, 2007, British journal of haematology.

Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia

A. Shakoori, A. Segal, D. Linch, 2012, British journal of haematology.

A MUTATION IN THE POLYADENYLATION SIGNAL OF THE α2 GLOBIN GENE (AATAA→AATA–) AS A CAUSE OF α THALASSAEMIA IN ASIAN INDIANS

D. Higgs, G. Hall, P. Murphy, 1994, British journal of haematology.

Abnormalities of the spleen: a systematic approach to a child with enlarged spleen and splenic dysfunction

E. Louka, G. Hall, 2022, Paediatrics and Child Health.

Emicizumab prophylaxis in haemophilia A with inhibitors: Three years follow‐up from the UK Haemophilia Centre Doctors’ Organisation (UKHCDO)

H. Xiang, D. Hart, B. Palmer, 2023, Haemophilia : the official journal of the World Federation of Hemophilia.

A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemia.

D. Higgs, E. Kanavakis, S. Thein, 1993, British journal of haematology.

Pediatric Hodgkin Lymphoma

L. Constine, S. Daw, C. Schwartz, 2020, Hodgkin Lymphoma.

A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

D. Ferguson, D. Higgs, A. Schuh, 2016, British journal of haematology.

Unusually severe heterozygous beta-thalassemia: evidence for an interacting gene affecting globin translation.

S. Thein, W. Wood, S. Watt, 1998, Blood.

Pediatric Hodgkin Lymphoma

L. Constine, S. Daw, C. Schwartz, 2020, Hodgkin Lymphoma.

Guideline for investigation and management of adults and children presenting with a thrombocytosis

P. Campbell, A. Green, W. Erber, 2010, British journal of haematology.

Digital pathology in pediatric nodular lymphocyte-predominant Hodgkin lymphoma: correlation with treatment response

D. Hasenclever, W. Wallace, D. Körholz, 2023, Blood Advances.