A glossary of terms and concepts found in the Nemours HSP policies and procedures. References and resources are located in the policy noted by HSP### after each definition.
- Centers and Labs
- Center for Clinical and Applied Genomics
- Center for Cardiac Research
- Center for Clinical Diagnostics
- Center for Pediatric Auditory and Speech Sciences (CPASS)
- Center for Endocrinology, Diabetes and Metabolic Disorders
- 2009 Progress Report
- Hypoglycemia in Children with T1DM: Mechanisms and Prevention
- Placebo-controlled Trial to Assess Anastrozole (ARIMIDEX)
- Therapeutic Intervention on Cardiovascular Risk Markers
- Nutrients & Hormones: Effects in Boys with Disordered Growth
- Patients with T1DM: Relation to Glycemic Variability
- Glutathione Homeostasis in Adolescent Type I Diabetes
- Study of the Effect of Continuous Subcutaneous Insulin Infusion
- C-Type Natriuretic Peptide levels in healthy children
- Amino-Terminal Propeptide of C-Type Natriuretic Peptide
- Multi-Center Studies
- Center for Pediatric Psychology Research
- Center for Pediatric Lung Research
- Center for Childhood Cancer Research
- Center for Pediatric Research
- Center for Pediatric Clinical Research and Development
- Center for Orthopedics Research and Development (CORD)
- Center for Pharmacogenomics and Translational Research
- Center for Integrative Pediatric Obesity Care
- Core Laboratories
- Clinical Trials
- Algorithms for Processing of Self-Monitoring Blood Glucose Data
- Amblyopia Treatment Studies
- Behavior Therapy for Families of Diabetic Adolescents
- Continuous Glucose Sensors in Youth: Biobehavioral Study
- Family Management of Childhood Diabetes (Type 1)
- Family Management of Childhood Diabetes: Clinical Site
- Home-Based Versus Office-Based Family Therapy for Diabetes
- Effect of a high-frequency, low-magnitude vibration on bone
- Cystic Fibrosis Foundation Patient Registry
- Vesicoureteral Reflux Study
- Clinical Lab Services
- Clinical Immunology
- Gastroenterology Clinical Laboratory
- Molecular Diagnostics
- Allan-Herndon-Dudley Syndrome
- Autosomal Dominant Leukodystrophy
- Barth Syndrome
- Cardio-Facio-Cutaneous Syndrome
- Costello Syndrome
- Duchenne Muscular Dystrophy
- Emery-Dreifuss Muscular Dystrophy
- Escobar Syndrome
- Familial Isolated Hypoparathyroidism
- Fatal Infantile Cardioencephalomyopathy
- Feingold Syndrome
- GJB2 & GJB6 Related Disorders
- Hypomyelination and Congenital Cataract
- Microcephalic Osteodysplastic Primordial Dwarfism, Type II
- NKX2-1 Related Disorders
- Noonan/LEOPARD Syndrome
- Pelizaeus-Merzbacher-Like Disease
- Pendred Syndrome and DFNB4
- Pelizaeus Merzbacher Disease
- Rett Syndrome
- Spinal Muscular Atrophy
- TARP Syndrome
- Timothy Syndrome
- TRPV4-Related Neuropathies
- TRPV4-Related Skeletal Dysplasias
- Transplant Molecular Diagnostics
- Muscle Enzyme Histochemistry Lab
- Faculty and Staff
- Committees
- Human Subject Protections: NOHSP
- Education
- Publications
- Technology Transfer
- IDeA Networks of Biomedical Research Excellence
- Delaware Health Sciences Alliance
- Contact Us