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Frequency and Duration of Boarding for Pediatric Mental Health Conditions at Acute Care Hospitals in the US

JAMA : the journal of the American Medical Association, 2021-12, Vol.326 (22), p.2326

2021

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Prevalence of Children With Medical Complexity and Associations With Health Care Utilization and In-Hospital Mortality

JAMA pediatrics, 2022-06, Vol.176 (6), p.e220687

2022

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Epidemiology of pediatric hospitalizations at general hospitals and freestanding children's hospitals in the United States: 2019 update

Journal of hospital medicine, 2023-10, Vol.18 (10), p.908-917

2023

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Specialties Providing Ambulatory Care and Associated Health Care Utilization and Quality for Children With Medical Complexity

Academic pediatrics, 2023-11, Vol.23 (8), p.1542-1552

2023

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Pediatric Mental Health Hospitalizations at Acute Care Hospitals in the US, 2009-2019

JAMA : the journal of the American Medical Association, 2023-03, Vol.329 (12), p.1000

2023

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Rural–urban disparities in health care delivery for children with medical complexity and moderating effects of payer, disability, and community poverty

The Journal of rural health, 2024-03, Vol.40 (2), p.326-337

2024

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Pediatric Hospitalizations at Rural and Urban Teaching and Nonteaching Hospitals in the US, 2009-2019

JAMA network open, 2023-09, Vol.6 (9), p.e2331807-e2331807

2023

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"Idiopathic" pulmonary arterial hypertension in early infancy: Excluding NFU1 deficiency

Annals of pediatric cardiology, 2019-09, Vol.12 (3), p.325-328

2019

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Development of the Pediatric Hospitalization Admission Survey of Experience (PHASE) Measure

Pediatrics (Evanston), 2023-09, Vol.152 (3), p.1

2023

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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

Journal of inherited metabolic disease, 2015-11, Vol.38 (6), p.1147-1153

2015

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A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome

PloS one, 2014-11, Vol.9 (11), p.e112950-e112950

2014

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TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism

Journal of inherited metabolic disease, 2019-09, Vol.42 (5), p.898-908

2019

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Complex phenotype associated with mutation in the TANGO2 gene

European journal of paediatric neurology, 2017-06, Vol.21, p.e60-e60

2017

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Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

European journal of human genetics : EJHG, 2015-01, Vol.23 (1), p.41-48

2015

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Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy

European journal of paediatric neurology, 2017-06, Vol.21, p.e137-e137

2017

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De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation

Human genetics, 2014-11, Vol.133 (11), p.1359-1367

2014

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PP03.5 – 2756: Multiple symmetrical lipomatosis: An uncommon presentation of a mitochondrial disease

European journal of paediatric neurology, 2015-05, Vol.19, p.S37-S38

2015

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PP05.6 – 2896: Genotype-phenotype correlations and counseling in carriers of Filamin A gene mutations

European journal of paediatric neurology, 2015-05, Vol.19, p.S47-S48

2015

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Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase ( COQ2 )

European journal of paediatric neurology, 2013-11, Vol.17 (6), p.625-630

2013

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Characterization of CoQ10 biosynthesis in fibroblasts of patients with primary and secondary CoQ10 deficiency

Journal of inherited metabolic disease, 2014, Vol.37 (1), p.53-62

2014

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OP10 – 2707: Childhood-onset ataxic gait solved by muscle biopsy

European journal of paediatric neurology, 2015-05, Vol.19, p.S4-S4

2015

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PP03.14 – 2978: Massive early leukoencephalopathy caused by a pathogenic mutation in IBA57: A new clinical presentation for this recently described gene defect

European journal of paediatric neurology, 2015-05, Vol.19, p.S40-S40

2015

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Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisions

European journal of pediatrics, 2015-02, Vol.174 (2), p.267-270

2015

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Blue Native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects

Pediatric research, 2001-11, Vol.50 (5), p.658-665

2001

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Frequency and Duration of Boarding for Pediatric Mental Health Conditions at Acute Care Hospitals in the US

Prevalence of Children With Medical Complexity and Associations With Health Care Utilization and In-Hospital Mortality

Epidemiology of pediatric hospitalizations at general hospitals and freestanding children's hospitals in the United States: 2019 update

Specialties Providing Ambulatory Care and Associated Health Care Utilization and Quality for Children With Medical Complexity

Pediatric Mental Health Hospitalizations at Acute Care Hospitals in the US, 2009-2019

Rural–urban disparities in health care delivery for children with medical complexity and moderating effects of payer, disability, and community poverty

Pediatric Hospitalizations at Rural and Urban Teaching and Nonteaching Hospitals in the US, 2009-2019

"Idiopathic" pulmonary arterial hypertension in early infancy: Excluding NFU1 deficiency

Development of the Pediatric Hospitalization Admission Survey of Experience (PHASE) Measure

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients

A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome

TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism

Complex phenotype associated with mutation in the TANGO2 gene

Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy

De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation

PP03.5 – 2756: Multiple symmetrical lipomatosis: An uncommon presentation of a mitochondrial disease

PP05.6 – 2896: Genotype-phenotype correlations and counseling in carriers of Filamin A gene mutations

Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase ( COQ2 )

Characterization of CoQ10 biosynthesis in fibroblasts of patients with primary and secondary CoQ10 deficiency

OP10 – 2707: Childhood-onset ataxic gait solved by muscle biopsy

PP03.14 – 2978: Massive early leukoencephalopathy caused by a pathogenic mutation in IBA57: A new clinical presentation for this recently described gene defect

Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisions

Blue Native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects

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