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Priapism in sickle‐cell disease; incidence, risk factors and complications – an international multicentre study

BJU international, 2002-12, Vol.90 (9), p.898-902

2002

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High prevalence of low bone mass in thalassaemia major

British journal of haematology, 1998-12, Vol.103 (4), p.911-915

1998

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Wheezing Symptoms and Parental Asthma Are Associated with a Physician Diagnosis of Asthma in Children with Sickle Cell Anemia

The Journal of pediatrics, 2014-04, Vol.164 (4), p.821-826.e1

2014

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Compound heterozygosity for haemoglobin S and haemoglobin E

British journal of haematology, 2000-03, Vol.108 (3), p.463-463

2000

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Combination therapy with interferon alpha and ribavirin for chronic hepatitis C virus infection in thalassaemic patients

British journal of haematology, 1997-09, Vol.98 (4), p.850-855

1997

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The burden of poverty in children with haemoglobinopathies presenting to a London tertiary referral centre

Archives of disease in childhood, 2012-05, Vol.97 (Suppl 1), p.A91-A91

2012

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Sickle cell disease

Clinical medicine (London, England), 2001-11, Vol.1 (6), p.441-446

2001

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Incidence of endocrine complications and clinical disease severity related to genotype analysis and iron overload in patients with β-thalassaemia

European journal of haematology, 1997-08, Vol.59 (2), p.76-81

1997

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Psychosocial and clinical burden of thalassaemia intermedia and its implications for prenatal diagnosis

Archives of disease in childhood, 1995-05, Vol.72 (5), p.408-412

1995

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Register cannot replace prospective studies in sickle cell disease [letter]

BMJ. British medical journal (International ed.), 1999-03, Vol.318 (7184), p.671

International edition, 1999

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The effects of neonatal screening for sickle cell disorders on lifetime treatment costs and early deaths avoided: a modelling approach

Journal of public health (Oxford, England), 2000-12, Vol.22 (4), p.500-511

2000

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High incidence of osteoporosis in thalassaemia major

Journal of pediatric endocrinology & metabolism : JPEM, 1998, Vol.11 Suppl 3, p.975

1998

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Red cell deformability in oral contraceptive pill users with sickle cell anaemia

British journal of haematology, 1999-03, Vol.104 (4), p.868-870

1999

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Hydroxyurea therapy for sickle cell disease in Britain

BMJ. British medical journal (International ed.), 1998-06, Vol.316 (7146), p.1689

International edition, 1998

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A Prospective Diary Study of Stuttering Priapism in Adolescents and Young Men With Sickle Cell Anemia: Report of an International Randomized Control Trial—The Priapism in Sickle Cell Study

Journal of andrology, 2011-07, Vol.32 (4), p.375-382

2011

Volltextzugriff (PDF)

Mingrelian SNP Genotype Data

Schurr, Theodore

2023

Volltextzugriff (PDF)

Laboratory investigation of platelet function: a review of methodology

Journal of clinical pathology, 1986-07, Vol.39 (7), p.701-712

1986

Volltextzugriff (PDF)

Low incidence of non-A, non-B post-transfusion hepatitis in London confirmed by hepatitis C virus serology

The Lancet (British edition), 1991-03, Vol.337 (8744), p.753-757

1991

Volltextzugriff (PDF)

Salmonella bacteraemia in children with sickle cell disease

Archives of disease in childhood, 2012-05, Vol.97 (Suppl 1), p.A89-A89

2012

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The effect of ovarian steroids on sickle cell deformability

Clinical and laboratory haematology, 1998-06, Vol.20 (3), p.151-154

1998

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Clonal Rearrangement and Expression of the T Cell Receptor β Gene and Involvement of the Breakpoint Cluster Region in Blast Crisis of CGL

Blood, 1986-02, Vol.67 (2), p.533-536

1986

Volltextzugriff (PDF)

Register cannot replace prospective studies in sickle cell disease

BMJ (Online), 1999-03, Vol.318 (7184), p.671

1999

Volltextzugriff (PDF)

Hydroxyurea therapy for sickle cell disease in Britain. Disappointing recruitment despite promising results

BMJ (Online), 1998-06, Vol.316 (7146), p.1689

1998

Volltextzugriff (PDF)

Successful bone marrow transplant for Fanconi anaemia in transformation

Bone marrow transplantation (Basingstoke), 1994-07, Vol.14 (1), p.151-153

1994

Volltextzugriff (PDF)

G409(P) An evaluation of the transition to adult care for young patients with sickle cell disease

Archives of disease in childhood, 2015-04, Vol.100 (Suppl 3), p.A168-A169

2015

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Priapism in sickle‐cell disease; incidence, risk factors and complications – an international multicentre study

High prevalence of low bone mass in thalassaemia major

Wheezing Symptoms and Parental Asthma Are Associated with a Physician Diagnosis of Asthma in Children with Sickle Cell Anemia

Compound heterozygosity for haemoglobin S and haemoglobin E

Combination therapy with interferon alpha and ribavirin for chronic hepatitis C virus infection in thalassaemic patients

The burden of poverty in children with haemoglobinopathies presenting to a London tertiary referral centre

Sickle cell disease

Incidence of endocrine complications and clinical disease severity related to genotype analysis and iron overload in patients with β-thalassaemia

Psychosocial and clinical burden of thalassaemia intermedia and its implications for prenatal diagnosis

Register cannot replace prospective studies in sickle cell disease [letter]

The effects of neonatal screening for sickle cell disorders on lifetime treatment costs and early deaths avoided: a modelling approach

High incidence of osteoporosis in thalassaemia major

Red cell deformability in oral contraceptive pill users with sickle cell anaemia

Hydroxyurea therapy for sickle cell disease in Britain

A Prospective Diary Study of Stuttering Priapism in Adolescents and Young Men With Sickle Cell Anemia: Report of an International Randomized Control Trial—The Priapism in Sickle Cell Study

Mingrelian SNP Genotype Data

Laboratory investigation of platelet function: a review of methodology

Low incidence of non-A, non-B post-transfusion hepatitis in London confirmed by hepatitis C virus serology

Salmonella bacteraemia in children with sickle cell disease

The effect of ovarian steroids on sickle cell deformability

Clonal Rearrangement and Expression of the T Cell Receptor β Gene and Involvement of the Breakpoint Cluster Region in Blast Crisis of CGL

Register cannot replace prospective studies in sickle cell disease

Hydroxyurea therapy for sickle cell disease in Britain. Disappointing recruitment despite promising results

Successful bone marrow transplant for Fanconi anaemia in transformation

G409(P) An evaluation of the transition to adult care for young patients with sickle cell disease

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