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Search Results to Sarah E. Soden

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

Item TypeName
Concept Child
Concept Child Abuse
Concept Child Development Disorders, Pervasive
Concept Child, Preschool
Concept Neurology
Academic Article Individualizing the use of medications in children: making Goldilocks happy.
Academic Article Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype.
Academic Article Clinical genome sequencing in an unbiased pediatric cohort.
Academic Article A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay.
Academic Article 24-hour provoked urine excretion test for heavy metals in children with autism and typically developing controls, a pilot study.
Academic Article Adopting orphans: comprehensive genetic testing of Mendelian diseases of childhood by next-generation sequencing.
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 Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome.
Academic Article Molecular diagnosis of infantile onset inflammatory bowel disease by exome sequencing.
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 The Future of Next-Generation Sequencing in Neurology.
Academic Article Clinical and Pharmacologic Considerations for Guanfacine Use in Very Young Children.
Academic Article PCDH19-related epileptic encephalopathy in a male mosaic for a truncating variant.
Academic Article GPR37L1 modulates seizure susceptibility: Evidence from mouse studies and analyses of a human GPR37L1 variant.
Academic Article Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease.
Academic Article Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings.
Academic Article Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing.
Academic Article Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Academic Article Parental understanding and attitudes following pharmacogenomic testing for pediatric neuropsychiatric patients.

Search Criteria
  • Child
  • Neurology