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Injury patterns associated with hypotension in pediatric trauma patients: A national trauma database review

The journal of trauma and acute care surgery, 2015-06, Vol.78 (6), p.1143-1148

2015

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The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene

Journal of human genetics, 2004-06, Vol.49 (6), p.308-311

2004

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

American journal of human genetics, 2012-01, Vol.90 (1), p.152-160

2012

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Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

European journal of human genetics : EJHG, 2012-07, Vol.20 (7), p.806-809

2012

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Imaging of the elbow in children with wrist fracture: an unnecessary source of radiation and use of resources?

Pediatric radiology, 2015-07, Vol.45 (8), p.1169-1173

2015

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Isolated Head Injury Is a Cause of Shock in Pediatric Trauma Patients

Pediatric emergency care, 2013-08, Vol.29 (8), p.879-883

2013

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Contribution of early weight gain to childhood overweight and metabolic health: a longitudinal study (EarlyBird 36)

Pediatrics (Evanston), 2009-01, Vol.123 (1), p.e67-e73

2009

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Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy

Human gene therapy, 2013-12, Vol.24 (12), p.993-1006

2013

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Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness

PloS one, 2014-08, Vol.9 (8), p.e104163-e104163

2014

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Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype-Phenotype Correlation and Functional Investigation of Cone Opsin Variants

Human mutation, 2014-11, Vol.35 (11), p.1354-1362

2014

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Muscle Biopsy Findings in Combination With Myositis‐Specific Autoantibodies Aid Prediction of Outcomes in Juvenile Dermatomyositis

Arthritis & rheumatology (Hoboken, N.J.), 2016-11, Vol.68 (11), p.2806-2816

2016

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Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease

Annals of the rheumatic diseases, 2015-01, Vol.74 (1), p.204-210

2015

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Efficacy and Safety of Cyclophosphamide Treatment in Severe Juvenile Dermatomyositis Shown by Marginal Structural Modeling

Arthritis & rheumatology (Hoboken, N.J.), 2018-05, Vol.70 (5), p.785-793

2018

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Histological heterogeneity in a large clinical cohort of juvenile idiopathic inflammatory myopathy: analysis by myositis autoantibody and pathological features

Neuropathology and applied neurobiology, 2019-08, Vol.45 (5), p.495-512

2019

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Retrospective analysis of infliximab and adalimumab treatment in a large cohort of juvenile dermatomyositis patients

Arthritis research & therapy, 2020-04, Vol.22 (1), p.79-79, Article 79

2020

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Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients

Journal of rheumatology, 2017-04, Vol.44 (4), p.488-492

2017

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Blue cone monochromacy: causative mutations and associated phenotypes

Molecular vision, 2009-05, Vol.15, p.876-884

2009

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A national registry for juvenile dermatomyositis and other paediatric idiopathic inflammatory myopathies: 10 years' experience; the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory Myopathies

Rheumatology (Oxford, England), 2011-01, Vol.50 (1), p.137-145

2011

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Treatment-related adverse events associated with a modified UK ALLR3 induction chemotherapy backbone for childhood relapsed/refractory acute lymphoblastic leukemia

Pediatric blood & cancer, 2016-11, Vol.63 (11), p.1943-1948

2016

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Identification of attentional and hyperactivity problems in primary care: a report from pediatric research in office settings and the ambulatory sentinel practice network

Pediatrics (Evanston), 1999-03, Vol.103 (3), p.E38-e38

1999

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Comparison of children with onset of juvenile dermatomyositis symptoms before or after their fifth birthday in a UK and Ireland juvenile dermatomyositis cohort study

Arthritis care & research (2010), 2012-11, Vol.64 (11), p.1665-1672

2012

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Behavior of Insulin Resistance and Its Metabolic Correlates in Prepubertal Children: A Longitudinal Study (EarlyBird 32)

Diabetes care, 2007-11, Vol.30 (11), p.2962-2964

2007

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Trends, associations and predictions of insulin resistance in prepubertal children (EarlyBird 29)

Pediatric diabetes, 2008-06, Vol.9 (3pt1), p.214-220

2008

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Autoantibodies to a 140‐kd protein in juvenile dermatomyositis are associated with calcinosis

Arthritis and rheumatism, 2009-06, Vol.60 (6), p.1807-1814

2009

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Injury patterns associated with hypotension in pediatric trauma patients: A national trauma database review

The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

Imaging of the elbow in children with wrist fracture: an unnecessary source of radiation and use of resources?

Isolated Head Injury Is a Cause of Shock in Pediatric Trauma Patients

Contribution of early weight gain to childhood overweight and metabolic health: a longitudinal study (EarlyBird 36)

Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy

Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness

Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype-Phenotype Correlation and Functional Investigation of Cone Opsin Variants

Muscle Biopsy Findings in Combination With Myositis‐Specific Autoantibodies Aid Prediction of Outcomes in Juvenile Dermatomyositis

Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease

Efficacy and Safety of Cyclophosphamide Treatment in Severe Juvenile Dermatomyositis Shown by Marginal Structural Modeling

Histological heterogeneity in a large clinical cohort of juvenile idiopathic inflammatory myopathy: analysis by myositis autoantibody and pathological features

Retrospective analysis of infliximab and adalimumab treatment in a large cohort of juvenile dermatomyositis patients

Anti-HMGCR Autoantibodies in Juvenile Idiopathic Inflammatory Myopathies Identify a Rare but Clinically Important Subset of Patients

Blue cone monochromacy: causative mutations and associated phenotypes

A national registry for juvenile dermatomyositis and other paediatric idiopathic inflammatory myopathies: 10 years' experience; the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory Myopathies

Treatment-related adverse events associated with a modified UK ALLR3 induction chemotherapy backbone for childhood relapsed/refractory acute lymphoblastic leukemia

Identification of attentional and hyperactivity problems in primary care: a report from pediatric research in office settings and the ambulatory sentinel practice network

Comparison of children with onset of juvenile dermatomyositis symptoms before or after their fifth birthday in a UK and Ireland juvenile dermatomyositis cohort study

Behavior of Insulin Resistance and Its Metabolic Correlates in Prepubertal Children: A Longitudinal Study (EarlyBird 32)

Trends, associations and predictions of insulin resistance in prepubertal children (EarlyBird 29)

Autoantibodies to a 140‐kd protein in juvenile dermatomyositis are associated with calcinosis

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