Dr. Charles E Schwartz MD
Psychiatrist | Psychiatry
415 Main St 15f New York NY, 10044About
Dr. Charles Schwartz is a psychiatrist practicing in Bronx, NY. Dr. Schwartz is a medical doctor specializing in the care of mental health patients. As a psychiatrist, Dr. Schwartz diagnoses and treats mental illnesses. Dr. Schwartz may treat patients through a variety of methods including medications, psychotherapy or talk therapy, psychosocial interventions and more, depending on each individual case. Different medications that a psychiatrist might prescribe include antidepressants, antipsychotic mediations, mood stabilizers, stimulants, sedatives and hypnotics. Dr. Schwartz treats conditions like depression, anxiety, OCD, eating disorders, bipolar disorders, personality disorders, insomnia, ADD and other mental illnesses.
Education and Training
Univ Of Ct Sch Of Med- Farmington Ct 1978
Univ Of Ct Sch Of Med 1978
University of Connecticut School of Medicine 1974
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN
Provider Details
Expert Publications
Data provided by the National Library of Medicine- X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.
- Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.
- Family MRX9 revisited: further evidence for locus heterogeneity in MRX.
- Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndrome.
- Detecting polymorphisms and mutations in candidate genes.
- Shashi XLMR syndrome: report of a second family.
- Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.
- Stocco dos Santos X-linked mental retardation syndrome: clinical elucidation and localization to Xp11.3-Xq21.3.
- A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
- X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome.
- Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly.
- Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequences.
- The FU gene and its possible protein isoforms.
- Mutation in the 5' alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome.
- A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor.
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