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Search Results to Sarah E. Soden

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following properties of Soden, Sarah

PropertyValue
keywords Developmental & Behavioral Medicine
keywords Developmental delay

One or more keywords matched the following items that are connected to Soden, Sarah

Item TypeName
Concept Arsenic
Concept Base Sequence
Concept Chelating Agents
Concept Developmental Disabilities
Concept Child Development Disorders, Pervasive
Concept Dextromethorphan
Concept Dextrorphan
Concept Succimer
Concept DNA
Concept Dose-Response Relationship, Drug
Concept Pharmaceutical Preparations
Concept Glutarates
Concept Microfilament Proteins
Concept Oxidoreductases
Concept Phosphotransferases
Concept Potassium
Concept Recombinant Proteins
Concept RNA, Messenger
Concept Transcription Factors
Concept Ubiquinone
Concept Glucuronosyltransferase
Concept Cadherins
Concept Guanfacine
Concept Connexins
Concept Metals, Heavy
Concept Cytochrome P-450 CYP2D6
Concept Electron Transport Complex I
Concept Receptors, G-Protein-Coupled
Concept Oxidoreductases Acting on CH-CH Group Donors
Concept Glutaryl-CoA Dehydrogenase
Concept Shab Potassium Channels
Concept Interleukin-10 Receptor alpha Subunit
Concept Drug Dosage Calculations
Concept Adrenergic alpha-2 Receptor Agonists
Concept Cytochrome P-450 CYP2C19
Academic Article Individualizing the use of medications in children: making Goldilocks happy.
Academic Article In vivo characterization of CYP2D6*12, *29 and *84 using dextromethorphan as a probe drug: a case report.
Academic Article A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay.
Academic Article 15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features.
Academic Article Nutrition, physical activity, and bone mineral density in youth with autistic spectrum disorders.
Academic Article De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies.
Academic Article Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Academic Article Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease.

Search Criteria
  • Drug
  • Development