Dr. Sarah M. Edwards DO
Adolescent Psychiatrist | Child & Adolescent Psychiatry
701 W PRATT ST BALTIMORE MD, 21201About
Dr. Sarah Edwards practices Child & Adolescent Psychiatry in BALTIMORE, MD. Dr. Edwards evaluates patients throughout childhood and adolescence using many different procedures, in order to determine what treatments must be carried out in order to properly assess their symptoms. Child & Adolescent Psychiatrists are trained and certified to administer psychotherapy, medication, and many other means of treatment. Dr. Edwards seeks to improve each patients quality of life.
Education and Training
Chicago College of Osteopathic Medicine of Midwestern University 2005
Board Certification
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN- Child and Adolescent Psychiatry
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53.
- God must love galectins; he made so many of them.
- Evolution of the proximal promoter region of the mammalian growth hormone gene.
- Human gene mutation database-a biomedical information and research resource.
- Molecular analysis of the genotype-phenotype relationship in factor X deficiency.
- Molecular analysis of the 5'-flanking region of the neurofibromatosis type 1 (NF1) gene: identification of five sequence variants.
- Molecular genetic analysis of severe protein C deficiency.
- Promoter shuffling has occurred during the evolution of the vertebrate growth hormone gene.
- Hypermethylation of the neurofibromatosis type 1 (NF1) gene promoter is not a common event in the inactivation of the NF1 gene in NF1-specific tumours.
- Protein S deficiency: a database of mutations--summary of the first update.
- Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
- Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions.
- Identification of an intronic regulatory element in the human protein C (PROC) gene.
- Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease.
- Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence.
Treatments
- Attention Deficit Hyperactivity Disorder (adhd)
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