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The impact of early identification of permanent childhood hearing impairment on speech and language outcomes

Archives of disease in childhood, 2012-07, Vol.97 (7), p.648-653

2012

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The effect of lead time to treatment and of age of onset on developmental outcome at 4 years in infantile spasms: Evidence from the United Kingdom Infantile Spasms Study

Epilepsia (Copenhagen), 2011-07, Vol.52 (7), p.1359-1364

2011

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Language Ability after Early Detection of Permanent Childhood Hearing Impairment

The New England journal of medicine, 2006-05, Vol.354 (20), p.2131-2141

2006

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The underlying etiology of infantile spasms (West syndrome): Information from the United Kingdom Infantile Spasms Study (UKISS) on contemporary causes and their classification

Epilepsia (Copenhagen), 2010-10, Vol.51 (10), p.2168-2174

2010

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Developmental and epilepsy outcomes at age 4 years in the UKISS trial comparing hormonal treatments to vigabatrin for infantile spasms: a multi-centre randomised trial

Archives of disease in childhood, 2010-05, Vol.95 (5), p.382-386

2010

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Reduction of Health Status 7 Years After Addition of Chemotherapy to Craniospinal Irradiation for Medulloblastoma: A Follow-Up Study in PNET 3 Trial Survivors—on Behalf of the CCLG (formerly UKCCSG)

Journal of clinical oncology, 2007-09, Vol.25 (27), p.4239-4245

2007

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The United Kingdom Infantile Spasms Study comparing vigabatrin with prednisolone or tetracosactide at 14 days: a multicentre, randomised controlled trial

The Lancet (British edition), 2004-11, Vol.364 (9447), p.1773-1778

2004

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CD43 in the nucleus and cytoplasm of lung cancer is a potential therapeutic target

International journal of cancer, 2013-04, Vol.132 (8), p.1761-1770

2013

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Randomized, controlled trial of acetazolamide and furosemide in posthemorrhagic ventricular dilation in infancy: follow-up at 1 year

Pediatrics (Evanston), 2001-09, Vol.108 (3), p.597

2001

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R-Ras is required for murine dendritic cell maturation and CD4+ T-cell priming

Blood, 2012-02, Vol.119 (7), p.1693-1701

2012

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The economic costs of congenital bilateral permanent childhood hearing impairment

Pediatrics (Evanston), 2006-04, Vol.117 (4), p.1101

2006

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Health status and health-related quality of life preference-based outcomes of children who are aged 7 to 9 years and have bilateral permanent childhood hearing impairment

Pediatrics (Evanston), 2007-11, Vol.120 (5), p.1044

2007

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Effects of Maturation on Parameters Used for Pass/Fail Criteria in Neonatal Hearing Screening Programmes Using Evoked Otoacoustic Emissions

Audiology & neurotology, 2007-01, Vol.12 (4), p.226-233

2007

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Methodological factors involved in neonatal screening using transient-evoked otoacoustic emissions and automated auditory brainstem response testing

Hearing research, 2003-08, Vol.182 (1), p.65-76

2003

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The diagnosis of brain tumours in children: a guideline to assist healthcare professionals in the assessment of children who may have a brain tumour

Archives of disease in childhood, 2010-07, Vol.95 (7), p.534-539

2010

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Progression from first symptom to diagnosis in childhood brain tumours

European journal of pediatrics, 2012, Vol.171 (1), p.87-93

2012

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An audit of paediatric epilepsy care

Archives of disease in childhood, 1998-08, Vol.79 (2), p.145-148

1998

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Neonatal screening for hearing impairment

Archives of disease in childhood, 2000-11, Vol.83 (5), p.377-383

Kennedy, Colin R

2000

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Universal newborn screening for permanent childhood hearing impairment : an 8-year follow-up of a controlled trial. Commentary

The Lancet (British edition), 2005, Vol.366 (9486), p.660-662

2005

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Standardized quantitative assessment of brain tumor survivors treated within clinical trials in childhood

International journal of cancer, 1999, Vol.83 (S12), p.77-82

1999

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Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q

Epilepsy research, 2002-02, Vol.48 (3), p.169-179

2002

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Mutations in the human LARGE gene cause MCD1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan

Human molecular genetics, 2003, Vol.12 (21), p.2853-2861

2003

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Advances in neurology

Archives of Disease in Childhood, 1996-09, Vol.75 (3), p.251-255

Kennedy, C R

1996

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Small terminal deletions of the long arm of chromosome 2: Two new cases

American journal of medical genetics, 1994-12, Vol.53 (4), p.366-369

1994

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Effect of treatment delay, age, and stroke severity on the effects of intravenous thrombolysis with alteplase for acute ischaemic stroke: a meta-analysis of individual patient data from randomised trials

The Lancet (British edition), 2014-11, Vol.384 (9958), p.1929-1935

2014

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The impact of early identification of permanent childhood hearing impairment on speech and language outcomes

The effect of lead time to treatment and of age of onset on developmental outcome at 4 years in infantile spasms: Evidence from the United Kingdom Infantile Spasms Study

Language Ability after Early Detection of Permanent Childhood Hearing Impairment

The underlying etiology of infantile spasms (West syndrome): Information from the United Kingdom Infantile Spasms Study (UKISS) on contemporary causes and their classification

Developmental and epilepsy outcomes at age 4 years in the UKISS trial comparing hormonal treatments to vigabatrin for infantile spasms: a multi-centre randomised trial

Reduction of Health Status 7 Years After Addition of Chemotherapy to Craniospinal Irradiation for Medulloblastoma: A Follow-Up Study in PNET 3 Trial Survivors—on Behalf of the CCLG (formerly UKCCSG)

The United Kingdom Infantile Spasms Study comparing vigabatrin with prednisolone or tetracosactide at 14 days: a multicentre, randomised controlled trial

CD43 in the nucleus and cytoplasm of lung cancer is a potential therapeutic target

Randomized, controlled trial of acetazolamide and furosemide in posthemorrhagic ventricular dilation in infancy: follow-up at 1 year

R-Ras is required for murine dendritic cell maturation and CD4+ T-cell priming

The economic costs of congenital bilateral permanent childhood hearing impairment

Health status and health-related quality of life preference-based outcomes of children who are aged 7 to 9 years and have bilateral permanent childhood hearing impairment

Effects of Maturation on Parameters Used for Pass/Fail Criteria in Neonatal Hearing Screening Programmes Using Evoked Otoacoustic Emissions

Methodological factors involved in neonatal screening using transient-evoked otoacoustic emissions and automated auditory brainstem response testing

The diagnosis of brain tumours in children: a guideline to assist healthcare professionals in the assessment of children who may have a brain tumour

Progression from first symptom to diagnosis in childhood brain tumours

An audit of paediatric epilepsy care

Neonatal screening for hearing impairment

Universal newborn screening for permanent childhood hearing impairment : an 8-year follow-up of a controlled trial. Commentary

Standardized quantitative assessment of brain tumor survivors treated within clinical trials in childhood

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q

Mutations in the human LARGE gene cause MCD1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan

Advances in neurology

Small terminal deletions of the long arm of chromosome 2: Two new cases

Effect of treatment delay, age, and stroke severity on the effects of intravenous thrombolysis with alteplase for acute ischaemic stroke: a meta-analysis of individual patient data from randomised trials

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