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50 Years of ERIC
50 Years of ERIC
The Education Resources Information Center (ERIC) is celebrating its 50th Birthday! First opened on May 15th, 1964 ERIC continues the long tradition of ongoing innovation and enhancement.

Learn more about the history of ERIC here. PDF icon

Showing 1 to 15 of 69 results
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Braverman, Nancy E.; D'Agostino, Maria Daniela; MacLean, Gillian E. – Developmental Disabilities Research Reviews, 2013
The peroxisome biogenesis disorders (PBD) are a heterogeneous group of autosomal recessive disorders in which peroxisome assembly is impaired, leading to multiple peroxisome enzyme deficiencies, complex developmental sequelae and progressive disabilities. Mammalian peroxisome assembly involves the protein products of 16 "PEX" genes;…
Descriptors: Genetic Disorders, Congenital Impairments, Biochemistry, Symptoms (Individual Disorders)
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Wolfe, Lynne A.; Krasnewich, Donna – Developmental Disabilities Research Reviews, 2013
The congenital disorders of glycosylation (CDG) are a rapidly growing group of inborn errors of metabolism that result from defects in the synthesis of glycans. Glycosylation is a major post-translational protein modification and an estimated 2% of the human genome encodes proteins for glycosylation. The molecular bases for the current 60…
Descriptors: Mental Retardation, Congenital Impairments, Metabolism, Comorbidity
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Prada, Carlos E.; Grabowski, Gregory A. – Developmental Disabilities Research Reviews, 2013
Background: The lysosomal--autophagocytic system diseases (LASDs) affect multiple body systems including the central nervous system (CNS). The progressive CNS pathology has its onset at different ages, leading to neurodegeneration and early death. Methods: Literature review provided insight into the current clinical neurological findings,…
Descriptors: Genetic Disorders, Neurological Impairments, Symptoms (Individual Disorders), Pathology
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Matern, Dietrich; Oglesbee, Devin; Tortorelli, Silvia – Developmental Disabilities Research Reviews, 2013
Newborn screening (NBS) is a public health program aimed at identifying treatable conditions in presymptomatic newborns to avoid premature mortality, morbidity, and disabilities. Currently, every newborn in the Unites States is screened for at least 29 conditions where evidence suggests that early detection is possible and beneficial. With new or…
Descriptors: Genetic Disorders, Neurological Impairments, Neonates, Health Programs
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Feudtner, Chris; Brosco, Jeffrey P. – Developmental Disabilities Research Reviews, 2011
People with intellectual disability (ID) have a long history of discrimination and stigmatization, and a more recent history of pride and self-advocacy. The early history suggests that people with ID are a vulnerable population and deserve special research protections as do some other groups; the disability rights movement of the late 20th century…
Descriptors: Mental Retardation, Self Advocacy, Ethics, Sampling
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Lantos, John D. – Developmental Disabilities Research Reviews, 2011
Public policy surrounding newborn screening is in flux. New technology allows more screening for more diseases at lower cost. Traditional criteria for target diseases have been criticized by leading health policymakers. The example of newborn screening for Krabbe disease highlights many of the dilemmas associated with population-based screening…
Descriptors: Pilot Projects, Diseases, Neonates, Public Policy
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Waggoner, Darrel J.; Tan, Christopher A. – Developmental Disabilities Research Reviews, 2011
Newborn screening (NBS), since its implementation in the 1960s, has traditionally been successful in reducing mortality and disability in children with a range of different conditions. Lysosomal storage disorders (LSD) are a heterogeneous group of inherited metabolic diseases that result from lysosomal dysfunction. Based on available treatment and…
Descriptors: Disability Identification, Reading Achievement, Screening Tests, Neonates
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Bauer, Sarah C.; Msall, Michael E. – Developmental Disabilities Research Reviews, 2011
Children with autism spectrum disorders (ASD) have unique developmental and behavioral phenotypes, and they have specific challenges with communication, social skills, and repetitive behaviors. At this time, no single etiology for ASD has been identified. However, evidence from family studies and linkage analyses suggests that genetic factors play…
Descriptors: Trend Analysis, Genetic Disorders, Autism, Genetics
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Booth, Karin Vander Ploeg – Developmental Disabilities Research Reviews, 2011
Individuals with intellectual disabilities experience health disparities and disparities in accessing health care services compared to individuals within the general population. In order to eliminate these disparities the contributors to them must be understood. In this article, we aim to describe a recent reconceptualization of health and…
Descriptors: Down Syndrome, Access to Health Care, Mental Retardation, Racial Differences
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Acharya, Kruti – Developmental Disabilities Research Reviews, 2011
Down syndrome is the most common cause of intellectual disability. In the United States, it is recommended that prenatal testing for Down syndrome be offered to all women. Because of this policy and consequent public perception, having Down syndrome has become a disadvantage in the prenatal period. However, in the postnatal period, there may be…
Descriptors: Screening Tests, Pregnancy, Down Syndrome, Parents
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Bell, Emily; Wallace, Tessa; Chouinard, Isabelle; Shevell, Michael; Racine, Eric – Developmental Disabilities Research Reviews, 2011
Faced with the limitations of currently available mainstream medical treatments and interventions, parents of children with neurodevelopmental disorders often seek information about unproven interventions. These interventions frequently have undetermined efficacy and uncertain safety profiles. In this article, we present a general background and…
Descriptors: Physical Disabilities, Developmental Disabilities, Cerebral Palsy, Parents
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Depositario-Cabacar, Dewi Frances T.; Zelleke, Tesfaye-Getaneh – Developmental Disabilities Research Reviews, 2010
Children with developmental disabilities are at increased risk for epilepsy with a prevalence rate higher than the general population. Some of the more common developmental disorders in childhood and the features of epilepsy in these conditions are discussed. Specifically, autism, cerebral palsy, mental retardation, and attention deficit and…
Descriptors: Epilepsy, Mental Retardation, Quality of Life, Developmental Disabilities
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Robb, Adelaide S. – Developmental Disabilities Research Reviews, 2010
Children with autism and autism spectrum disorders have a high rate of irritability and aggressive symptoms. In one study up to 20% of children with autism have symptoms of irritability and aggression including aggression, severe tantrums, and deliberate self injurious behavior (Lecavalier [2006] "J. Autism Dev. Disord." 36:1101-1114.). These…
Descriptors: Self Destructive Behavior, Autism, Aggression, Antisocial Behavior
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Donahue, Pamela K.; Robinson, Karen A. – Developmental Disabilities Research Reviews, 2010
Few interventions and treatments for premature infants have undergone the rigors of a randomized controlled trial (RCT), the cornerstone of evidence-based healthcare. Multiple barriers in establishing a quality evidence base for the care of preterm infants are examined including the systematic exclusion of children from drug trials, vulnerability…
Descriptors: Evidence, Premature Infants, At Risk Persons, Barriers
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Bauer, Sarah C.; Msall, Michael E. – Developmental Disabilities Research Reviews, 2010
In the past 20 years, many advances (e.g., maternal steroids and surfactant) have changed the course of neonatal medicine. As a result, extremely preterm infants survive medical complications that were previously fatal. Once they are discharged from the neonatal intensive care unit, preterm infants may continue to experience a spectrum of medical…
Descriptors: School Readiness, Early Intervention, Premature Infants, Child Development
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