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Journal of Child Neurology
|
July 5, 2012
Confounding diagnoses in the neurodevelopmental disabilities population: a child with hearing loss, absence epilepsy, and attention-deficit hyperactivity disorder (ADHD)
Eboni I Lance, Bruce K Shapiro
Journal of Child Neurology
|
September 25, 2007
Expansion of the deletion 13q syndrome phenotype: a case report
Eboni I Lance, Barbara R DuPont, Kenton R Holden
Proteomics. Clinical Applications
|
October 8, 2014
Proteomic and biomarker studies and neurological complications of pediatric sickle cell disease
Eboni I Lance, James F Casella, Allen D Everett, et al.
Research in Developmental Disabilities
|
December 18, 2013
Association between regression and self injury among children with autism
Eboni I Lance, Janet M York, Li-Ching Lee, et al.
Pediatric Blood & Cancer
|
November 19, 2019
Brain-derived neurotrophic factor levels in pediatric sickle cell disease
Eboni I Lance, Emily Barron-Casella, Allen D Everett, et al.
Pediatric Neurology
|
December 3, 2014
Stimulant use in patients with sturge-weber syndrome: safety and efficacy
Eboni I Lance, Kira E Lanier, T Andrew Zabel, et al.
Clinical Pediatrics
|
October 12, 2014
Disparities in identification of comorbid diagnoses in children with ADHD
Tanjala T Gipson, Eboni I Lance, Rebecca A Albury, et al.
SAGE Open Medical Case Reports
|
November 1, 2018
Successful treatment of choreo-athetotic movements in a patient with an EEF1A2 gene variant
Eboni I Lance, Martin Kronenbuerger, Julie S Cohen, et al.
Clinical Pediatrics
|
July 8, 2015
Risk Factors for Attention and Behavioral Issues in Pediatric Sickle Cell Disease
Eboni I Lance, Anne M Comi, Michael V Johnston, et al.
British Journal of Haematology
|
December 1, 2022
Current developmental screening practices in young children with sickle cell disease
Chibuzo J Aguwa, Alicia D Cannon, James F Casella, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Journal of Child Neurology
|
July 5, 2012
Confounding diagnoses in the neurodevelopmental disabilities population: a child with hearing loss, absence epilepsy, and attention-deficit hyperactivity disorder (ADHD)
Eboni I Lance, Bruce K Shapiro
Journal of Child Neurology
|
September 25, 2007
Expansion of the deletion 13q syndrome phenotype: a case report
Eboni I Lance, Barbara R DuPont, Kenton R Holden
Proteomics. Clinical Applications
|
October 8, 2014
Proteomic and biomarker studies and neurological complications of pediatric sickle cell disease
Eboni I Lance, James F Casella, Allen D Everett, et al.
Research in Developmental Disabilities
|
December 18, 2013
Association between regression and self injury among children with autism
Eboni I Lance, Janet M York, Li-Ching Lee, et al.
Pediatric Blood & Cancer
|
November 19, 2019
Brain-derived neurotrophic factor levels in pediatric sickle cell disease
Eboni I Lance, Emily Barron-Casella, Allen D Everett, et al.
Pediatric Neurology
|
December 3, 2014
Stimulant use in patients with sturge-weber syndrome: safety and efficacy
Eboni I Lance, Kira E Lanier, T Andrew Zabel, et al.
Clinical Pediatrics
|
October 12, 2014
Disparities in identification of comorbid diagnoses in children with ADHD
Tanjala T Gipson, Eboni I Lance, Rebecca A Albury, et al.
SAGE Open Medical Case Reports
|
November 1, 2018
Successful treatment of choreo-athetotic movements in a patient with an EEF1A2 gene variant
Eboni I Lance, Martin Kronenbuerger, Julie S Cohen, et al.
Clinical Pediatrics
|
July 8, 2015
Risk Factors for Attention and Behavioral Issues in Pediatric Sickle Cell Disease
Eboni I Lance, Anne M Comi, Michael V Johnston, et al.
British Journal of Haematology
|
December 1, 2022
Current developmental screening practices in young children with sickle cell disease
Chibuzo J Aguwa, Alicia D Cannon, James F Casella, et al.
Page
of 2