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Description of posterior fossa syndrome in children after posterior fossa brain tumor surgery

Journal of pediatric oncology nursing, 1995-10, Vol.12 (4), p.181-187

1995

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Rhinovirus illnesses during infancy predict subsequent childhood wheezing

Journal of Allergy and Clinical Immunology, 2005-09, Vol.116 (3), p.571-577

2005

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Height-for-age z scores increase despite increasing height deficits among children in 5 developing countries

The American journal of clinical nutrition, 2014-09, Vol.100 (3), p.821-825

2014

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Reduced-intensity conditioning for hematopoietic cell transplant for HLH and primary immune deficiencies

Blood, 2018-09, Vol.132 (13), p.1438-1451

2018

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Children with access to improved sanitation but not improved water are at lower risk of stunting compared to children without access: a cohort study in Ethiopia, India, Peru, and Vietnam

BMC public health, 2017-01, Vol.17 (1), p.110-19, Article 110

2017

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Rapid identification of pathogens from positive blood cultures by multiplex polymerase chain reaction using the FilmArray system

Diagnostic microbiology and infectious disease, 2012-12, Vol.74 (4), p.349-355

2012

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A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures

Cell, 2018-02, Vol.172 (5), p.924-936.e11

2018

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Growth faltering and recovery in children aged 1–8 years in four low- and middle-income countries: Young Lives

Public health nutrition, 2014-09, Vol.17 (9), p.2131-2137

2014

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An adenovirus 4 outbreak amongst staff in a pediatric ward manifesting as keratoconjunctivitis—a possible failure of contact and aerosol infection control

American journal of infection control, 2016-05, Vol.44 (5), p.602-604

2016

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Longitudinal speech perception and language performance in pediatric cochlear implant users: the effect of age at implantation

Ear and hearing, 2014-03, Vol.35 (2), p.148-160

2014

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Coagulopathy is Prevalent and Associated with Adverse Outcomes in Transfused Pediatric Trauma Patients

The Journal of pediatrics, 2012-02, Vol.160 (2), p.204-209.e3

2012

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Controlled Trial of Two Incremental Milk-Feeding Rates in Preterm Infants

The New England journal of medicine, 2019-10, Vol.381 (15), p.1434-1443

2019

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A longitudinal investigation of the relationship between maternal mind-mindedness and theory of mind

British journal of developmental psychology, 2015-11, Vol.33 (4), p.434-445

2015

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The addition of sirolimus to tacrolimus/methotrexate GVHD prophylaxis in children with ALL: a phase 3 Children's Oncology Group/Pediatric Blood and Marrow Transplant Consortium trial

Blood, 2014-03, Vol.123 (13), p.2017-2025

2014

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RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features

American journal of human genetics, 2020-12, Vol.107 (6), p.1157-1169

2020

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De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome

American journal of human genetics, 2019-03, Vol.104 (3), p.542-552

2019

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Implementation of a pediatric trauma massive transfusion protocol: one institution's experience

Transfusion (Philadelphia, Pa.), 2012-06, Vol.52 (6), p.1228-1236

2012

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Periods of child growth up to age 8 years in Ethiopia, India, Peru and Vietnam: Key distal household and community factors

Social science & medicine (1982), 2013-11, Vol.97, p.278-287

2013

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Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness

Molecular genetics & genomic medicine, 2018-03, Vol.6 (2), p.186-199

2018

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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American journal of human genetics, 2019-05, Vol.104 (5), p.948-956

2019

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Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing

American journal of medical genetics. Part A, 2015-05, Vol.167A (5), p.1026-1032

2015

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Description of posterior fossa syndrome in children after posterior fossa brain tumor surgery

Rhinovirus illnesses during infancy predict subsequent childhood wheezing

Height-for-age z scores increase despite increasing height deficits among children in 5 developing countries

Reduced-intensity conditioning for hematopoietic cell transplant for HLH and primary immune deficiencies

Risk- and response-based classification of childhood B-precursor acute lymphoblastic leukemia: a combined analysis of prognostic markers from the Pediatric Oncology Group (POG) and Children's Cancer Group (CCG)

Children with access to improved sanitation but not improved water are at lower risk of stunting compared to children without access: a cohort study in Ethiopia, India, Peru, and Vietnam

Rapid identification of pathogens from positive blood cultures by multiplex polymerase chain reaction using the FilmArray system

A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures

Growth faltering and recovery in children aged 1–8 years in four low- and middle-income countries: Young Lives

An adenovirus 4 outbreak amongst staff in a pediatric ward manifesting as keratoconjunctivitis—a possible failure of contact and aerosol infection control

Longitudinal speech perception and language performance in pediatric cochlear implant users: the effect of age at implantation

Coagulopathy is Prevalent and Associated with Adverse Outcomes in Transfused Pediatric Trauma Patients

Controlled Trial of Two Incremental Milk-Feeding Rates in Preterm Infants

A longitudinal investigation of the relationship between maternal mind-mindedness and theory of mind

Amino acid substitution at peptide-binding pockets of HLA class I molecules increases risk of severe acute GVHD and mortality

Improving statistical power in severe malaria genetic association studies by augmenting phenotypic precision

The addition of sirolimus to tacrolimus/methotrexate GVHD prophylaxis in children with ALL: a phase 3 Children's Oncology Group/Pediatric Blood and Marrow Transplant Consortium trial

RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features

De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome

Implementation of a pediatric trauma massive transfusion protocol: one institution's experience

Periods of child growth up to age 8 years in Ethiopia, India, Peru and Vietnam: Key distal household and community factors

Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness

Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing

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