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Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

Science translational medicine, 2014-12, Vol.6 (265), p.265ra168

2014

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Mercy TAPE for Calculation‐Free Height Estimation in Pediatric Rehabilitation Patients

PM & R, 2020-06, Vol.12 (6), p.538-545

2020

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Determining the impact of a clinic coordinator on patient access and clinic efficiency in a pediatric multidisciplinary spina bifida clinic using medical informatics

Journal of pediatric rehabilitation medicine, 2021-01, Vol.14 (4), p.661-666

2021

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Evaluation of the Mercy TAPE Height Estimation Method

PM & R, 2015-09, Vol.7 (9), p.S85-S85

2015

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Outcomes of a Structured Ambulatory Care Health Care Transition Approach in a Large Children's Hospital

Journal of adolescent health, 2023-11, Vol.73 (5), p.917-923

2023

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HSP and deafness: Neurocristopathy caused by a novel mosaic SOX10 mutation

Neurology. Genetics, 2017-06, Vol.3 (3), p.e151-e151

2017

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Poster 191: Further Workup of Phenotypic Bethlem Myopathy With Collagen Type VI Present on Muscle Biopsy: A Case Report

Archives of physical medicine and rehabilitation, 2008, Vol.89 (11), p.e82-e83

2008

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Poster 389 Internal Hemipelvectomy After Osteomyelitis in an Adolescent: A Case Report

PM & R, 2011, Vol.3 (10), p.S309-S309

2011

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Implementing a Nationally Recognized Pediatric-to-Adult Transitional Care Approach in a Major Children’s Hospital

Health & social work, 2018-02, Vol.43 (1), p.3-6

2018

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Improvement in survival and muscle function in an mdx/utrn −/− double mutant mouse using a human retinal dystrophin transgene

Neuromuscular disorders : NMD, 2006-03, Vol.16 (3), p.192-203

2006

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Transition to Adult Care in Youth with Epilepsy: One Center's Experience with a Transition Program and Its Integration within Telemedicine

Journal of pediatric epilepsy, 2020-12, Vol.9 (4), p.119-124

2020

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Learning Motivational Interviewing: A Pathway to Caring and Mindful Patient Encounters

Journal of pediatric nursing, 2016-09, Vol.31 (5), p.505-510

2016

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DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy

Neuromuscular disorders : NMD, 2009-11, Vol.19 (11), p.743-748

2009

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HSP and deafness: Neurocristopathy caused by a novel mosaic

Neurology. Genetics, 2017-05, Vol.3 (3)

2017

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PR_143

Archives of physical medicine and rehabilitation, 2006-11, Vol.87 (11), p.e28-e29

2006

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PR_143: Human Retinal Dystrophin Transgene Prevents Severe Myopathy and Lethality in Duchenne’s Muscular Dystrophy Model Mice

Archives of physical medicine and rehabilitation, 2006, Vol.87 (11), p.e28-e29

2006

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Improvement in survival and muscle function in an mdx, utrn −/− double mutant mouse using a human retinal dystrophin transgene

Neuromuscular disorders : NMD

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Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

Mercy TAPE for Calculation‐Free Height Estimation in Pediatric Rehabilitation Patients

Determining the impact of a clinic coordinator on patient access and clinic efficiency in a pediatric multidisciplinary spina bifida clinic using medical informatics

Evaluation of the Mercy TAPE Height Estimation Method

Outcomes of a Structured Ambulatory Care Health Care Transition Approach in a Large Children's Hospital

HSP and deafness: Neurocristopathy caused by a novel mosaic SOX10 mutation

Poster 191: Further Workup of Phenotypic Bethlem Myopathy With Collagen Type VI Present on Muscle Biopsy: A Case Report

Poster 389 Internal Hemipelvectomy After Osteomyelitis in an Adolescent: A Case Report

Implementing a Nationally Recognized Pediatric-to-Adult Transitional Care Approach in a Major Children’s Hospital

Improvement in survival and muscle function in an mdx/utrn −/− double mutant mouse using a human retinal dystrophin transgene

Transition to Adult Care in Youth with Epilepsy: One Center's Experience with a Transition Program and Its Integration within Telemedicine

Learning Motivational Interviewing: A Pathway to Caring and Mindful Patient Encounters

DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy

HSP and deafness: Neurocristopathy caused by a novel mosaic

PR_143

PR_143: Human Retinal Dystrophin Transgene Prevents Severe Myopathy and Lethality in Duchenne’s Muscular Dystrophy Model Mice

Improvement in survival and muscle function in an mdx, utrn −/− double mutant mouse using a human retinal dystrophin transgene

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