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Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

Genetics in medicine, 2011-03, Vol.13 (3), p.255-262

2011

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Consensus treatment plans for periodic fever, aphthous stomatitis, pharyngitis and adenitis syndrome (PFAPA): a framework to evaluate treatment responses from the childhood arthritis and rheumatology research alliance (CARRA) PFAPA work group

Pediatric rheumatology online journal, 2020-04, Vol.18 (1), p.31-31, Article 31

2020

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Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia

Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.535-538.e2

2011

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Treatment escalation patterns to start biologics in refractory moderate juvenile dermatomyositis among members of the Childhood Arthritis and Rheumatology Research Alliance

Pediatric rheumatology online journal, 2023-01, Vol.21 (1), p.3-3, Article 3

2023

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Combination therapy with methotrexate and etanercept for refractory chronic recurrent multifocal osteomyelitis

Journal of rheumatology, 2011-04, Vol.38 (4), p.782

2011

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Correlation of Pediatric Residency Applicant Scoring With Mean Pediatric Milestone Assessment Scores for 2013-14 and 2014-15 Pediatric Interns at a Medium Sized Pediatric Residency Program

Academic pediatrics, 2016-08, Vol.16 (6), p.e5-e5

2016

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An evaluation of the utility of routine laboratory monitoring of juvenile idiopathic arthritis (JIA) patients using non-steroidal anti-inflammatory drugs (NSAIDs): a retrospective review

Pediatric rheumatology online journal, 2010-04, Vol.8 (1), p.11-11, Article 11

2010

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Childhood-Onset Systemic Lupus Erythematosus

Pediatrics in review, 2024-06, Vol.45 (6), p.316

2024

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Childhood Arthritis and Rheumatology Research Alliance Consensus Treatment Plans for New‐Onset Polyarticular Juvenile Idiopathic Arthritis

Arthritis care & research (2010), 2014-07, Vol.66 (7), p.1063-1072

2014

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Burnout in Pediatric Residents: Comparing Brief Screening Questions to the Maslach Burnout Inventory

Academic pediatrics, 2019-04, Vol.19 (3), p.251-255

2019

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Correlation Between Attending Physician and Resident Mean Milestones-Based Assessment Scores of Pediatric Residents (Research Abstract)

Academic pediatrics, 2017-07, Vol.17 (5), p.e55-e55

2017

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Intact Regulatory T‐Cell Function but Defective Generation of IL–17A‐Producing CD4+ T Cells in XIAP Deficiency

Journal of pediatric gastroenterology and nutrition, 2016-08, Vol.63 (2), p.218-225

2016

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American College of Rheumatology Provisional Criteria for Clinically Relevant Improvement in Children and Adolescents With Childhood‐Onset Systemic Lupus Erythematosus

Arthritis care & research (2010), 2019-05, Vol.71 (5), p.579-590

2019

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Consensus treatment plans for periodic fever, aphthous stomatitis, pharyngitis and adenitis syndrome PFAPA work group

Pediatric rheumatology online journal, 2020-04, Vol.18 (1)

2020

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Human phagocyte defect caused by aRac2mutation detected by means of neonatal screening for T-cell lymphopenia

Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.535

2011

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A Novel XIAP Mutation Detected by Genome Wide Sequencing Causes Early Onset Inflammatory Bowel Disease

Clinical immunology (Orlando, Fla.), 2010, Vol.135, p.S105-S105

2010

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An evaluation of the utility of routine laboratory monitoring of juvenile idiopathic arthritis

Pediatric rheumatology online journal, 2010-04, Vol.8, p.11

2010

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An evaluation of the utility of routine laboratory monitoring of juvenile idiopathic arthritis : a retrospective review

Pediatric rheumatology online journal, 2010-04, Vol.8, p.11

2010

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Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia

The Journal of allergy and clinical immunology, 2011, Vol.127 (2), p.535-538.e1-2

2011

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Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

Consensus treatment plans for periodic fever, aphthous stomatitis, pharyngitis and adenitis syndrome (PFAPA): a framework to evaluate treatment responses from the childhood arthritis and rheumatology research alliance (CARRA) PFAPA work group

Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia

Treatment escalation patterns to start biologics in refractory moderate juvenile dermatomyositis among members of the Childhood Arthritis and Rheumatology Research Alliance

Combination therapy with methotrexate and etanercept for refractory chronic recurrent multifocal osteomyelitis

Correlation of Pediatric Residency Applicant Scoring With Mean Pediatric Milestone Assessment Scores for 2013-14 and 2014-15 Pediatric Interns at a Medium Sized Pediatric Residency Program

An evaluation of the utility of routine laboratory monitoring of juvenile idiopathic arthritis (JIA) patients using non-steroidal anti-inflammatory drugs (NSAIDs): a retrospective review

Childhood-Onset Systemic Lupus Erythematosus

Childhood Arthritis and Rheumatology Research Alliance Biologic Disease‐Modifying Antirheumatic Drug Consensus Treatment Plans for Refractory Moderately Severe Juvenile Dermatomyositis

Childhood Arthritis and Rheumatology Research Alliance Consensus Treatment Plans for New‐Onset Polyarticular Juvenile Idiopathic Arthritis

Burnout in Pediatric Residents: Comparing Brief Screening Questions to the Maslach Burnout Inventory

Correlation Between Attending Physician and Resident Mean Milestones-Based Assessment Scores of Pediatric Residents (Research Abstract)

Intact Regulatory T‐Cell Function but Defective Generation of IL–17A‐Producing CD4+ T Cells in XIAP Deficiency

American College of Rheumatology Provisional Criteria for Clinically Relevant Improvement in Children and Adolescents With Childhood‐Onset Systemic Lupus Erythematosus

Consensus treatment plans for periodic fever, aphthous stomatitis, pharyngitis and adenitis syndrome PFAPA work group

Human phagocyte defect caused by aRac2mutation detected by means of neonatal screening for T-cell lymphopenia

A Novel XIAP Mutation Detected by Genome Wide Sequencing Causes Early Onset Inflammatory Bowel Disease

An evaluation of the utility of routine laboratory monitoring of juvenile idiopathic arthritis

An evaluation of the utility of routine laboratory monitoring of juvenile idiopathic arthritis : a retrospective review

Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia

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