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Artificial intelligence in paediatric radiology: Future opportunities

British journal of radiology, 2021-01, Vol.94 (1117), p.20200975-20200975

2021

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Early clinical applications for imaging at microscopic detail: microfocus computed tomography (micro-CT)

British journal of radiology, 2017-07, Vol.90 (1075), p.20170113-20170113

2017

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Phenotypic and Genotypic Characterisation of Inflammatory Bowel Disease Presenting Before the Age of 2 years

Journal of Crohn's and colitis, 2017-01, Vol.11 (1), p.60-69

2017

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The impact of the COVID-19 pandemic on antimicrobial prescribing at a specialist paediatric hospital: an observational study

Journal of antimicrobial chemotherapy, 2022-03, Vol.77 (4), p.1185-1188

2022

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3D printing from microfocus computed tomography (micro-CT) in human specimens: education and future implications

British journal of radiology, 2018-07, Vol.91 (1088), p.20180306-20180306

2018

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Placenta as a reservoir of stem cells: an underutilized resource?

British medical bulletin, 2013-03, Vol.105 (1), p.43-68

2013

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A mouse model of Proteus syndrome

Human molecular genetics, 2019-09, Vol.28 (17), p.2920-2936

2019

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Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function

The journal of clinical endocrinology and metabolism, 2007-03, Vol.92 (3), p.991-999

2007

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Clusterin, a Haploinsufficient Tumor Suppressor Gene in Neuroblastomas

JNCI : Journal of the National Cancer Institute, 2009-05, Vol.101 (9), p.663-677

2009

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X-ray phase contrast tomography; proof of principle for post-mortem imaging

British journal of radiology, 2016-01, Vol.89 (1058), p.20150565-20150565

2016

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Cushing syndrome in a child due to pro-opiomelanocortin (POMC) secretion from a yolk sac tumor

European journal of endocrinology, 2017-02, Vol.176 (2), p.K1-K7

2017

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Tubulointerstitial nephritis, uveitis, hearing loss and vestibular failure: TINU-atypical Cogan's overlap syndrome

Rheumatology (Oxford, England), 2012-05, Vol.51 (5), p.950-952

2012

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PAX5 Expression in Nonhematopoietic Tissues: Reappraisal of Previous Studies

American journal of clinical pathology, 2010-03, Vol.133 (3), p.407-415

2010

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Impaired expression of endometrial differentiation markers and complement regulatory proteins in patients with recurrent pregnancy loss associated with antiphospholipid syndrome

Molecular human reproduction, 2006-07, Vol.12 (7), p.435-442

2006

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The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

Human molecular genetics, 2002-12, Vol.11 (26), p.3267-3272

2002

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017 Pulmonary renal syndrome in Henoch-Schönlein purpura: a life-threatening complication

Rheumatology (Oxford, England), 2018-04, Vol.57 (suppl_3)

2018

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Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred

Nephrology, dialysis, transplantation, 2007-01, Vol.22 (1), p.259-263

2007

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P43 Immunoglobulin G4-related disease in a 10 year-old girl with multisystem involvement

Rheumatology (Oxford, England), 2019-10, Vol.58 (Supplement_4)

2019

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Takayasu arteritis in infancy

Rheumatology (Oxford, England), 2013-11, Vol.52 (11), p.2093-2095

2013

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The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

Human molecular genetics, 2002-12, Vol.11 (26), p.3267-3272

2002

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Maternal serum concentrations of pregnancy associated placental protein A and pregnancy specific β-1-glycoprotein in multifetal pregnancies before and after fetal reduction

Human reproduction (Oxford), 1996-04, Vol.11 (4), p.900-902

1996

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Takayasu arteritis in infancy

Rheumatology (Oxford, England), 2013, Vol.52 (11), p.2093-2095

2013

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Tubulointerstitial nephritis, uveitis, hearing loss and vestibular failure: TINU-atypical Cogan's overlap syndrome

Rheumatology (Oxford, England), 2012, Vol.51 (5), p.950-952

2012

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Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred

Nephrology Dialysis Transplantation, 2007, Vol.22 (1), p.259-263

2007

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Artificial intelligence in paediatric radiology: Future opportunities

Early clinical applications for imaging at microscopic detail: microfocus computed tomography (micro-CT)

Phenotypic and Genotypic Characterisation of Inflammatory Bowel Disease Presenting Before the Age of 2 years

The impact of the COVID-19 pandemic on antimicrobial prescribing at a specialist paediatric hospital: an observational study

3D printing from microfocus computed tomography (micro-CT) in human specimens: education and future implications

Placenta as a reservoir of stem cells: an underutilized resource?

A mouse model of Proteus syndrome

Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function

Clusterin, a Haploinsufficient Tumor Suppressor Gene in Neuroblastomas

X-ray phase contrast tomography; proof of principle for post-mortem imaging

Cushing syndrome in a child due to pro-opiomelanocortin (POMC) secretion from a yolk sac tumor

Tubulointerstitial nephritis, uveitis, hearing loss and vestibular failure: TINU-atypical Cogan's overlap syndrome

PAX5 Expression in Nonhematopoietic Tissues: Reappraisal of Previous Studies

Impaired expression of endometrial differentiation markers and complement regulatory proteins in patients with recurrent pregnancy loss associated with antiphospholipid syndrome

The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

017 Pulmonary renal syndrome in Henoch-Schönlein purpura: a life-threatening complication

Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred

P43 Immunoglobulin G4-related disease in a 10 year-old girl with multisystem involvement

Takayasu arteritis in infancy

The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

Maternal serum concentrations of pregnancy associated placental protein A and pregnancy specific β-1-glycoprotein in multifetal pregnancies before and after fetal reduction

Takayasu arteritis in infancy

Tubulointerstitial nephritis, uveitis, hearing loss and vestibular failure: TINU-atypical Cogan's overlap syndrome

Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred

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