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RYAN SCHULTZ, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1245083146Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Memory with emotional content, brain amygdala and Alzheimer's disease.
PMID 19154540·Acta Neurol Scand·2009
8-other
The structure of intelligence in children and adults with high functioning autism.
PMID 18444708·Neuropsychology·2008
4-observational
Preclinical development of Alimta (Pemetrexed, LY231514), a multitargeted antifolate.
PMID 16265884·Prog Drug Res·2005
6-review
The role of the fusiform face area in social cognition: implications for the pathobiology of autism.
PMID 12639338·Philos Trans R Soc Lond B Biol Sci·2003
8-other
Potential of p38 MAP kinase inhibitors in the treatment of cancer.
PMID 12790339·Prog Drug Res·2003
6-review
Genetics of childhood disorders: XLIII. Autism, part 2: neural foundations.
PMID 12364850·J Am Acad Child Adolesc Psychiatry·2002
8-other
Genetics of childhood disorders: XXVI. Williams syndrome and brain-behavior relationships.
PMID 11349707·J Am Acad Child Adolesc Psychiatry·2001
8-other
The cognitive subscale of the "Alzheimer's Disease Assessment Scale" in a Brazilian sample.
PMID 11593304·Braz J Med Biol Res·2001
8-other
Abnormal ventral temporal cortical activity during face discrimination among individuals with autism and Asperger syndrome.
PMID 10768694·Arch Gen Psychiatry·2000
4-observational
Cytotoxicity and ultrastructural changes in H9c2(2-1) cells treated with pavetamine, a novel polyamine.
PMID 19095003·Toxicon·2010
7-preclinical
Radiography, computed tomography and virtual bronchoscopy in four dogs and two cats with lung lobe torsion.
PMID 19508491·J Small Anim Pract·2009
4-observational
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
PMID 19404256·Nature·2009
8-other
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
PMID 19404257·Nature·2009
8-other
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
PMID 19500772·Am J Hum Genet·2009
8-other
Comment on "Patel JR, Heldens JGM. Review of companion animal viral diseases and immunoprophylaxis" (Vaccine 2009;27:491-504).
PMID 19428859·Vaccine·2009
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2650 RIDGE AVE STE 1304
EVANSTON, IL 60201 - Phone
- (847) 570-2700
Quick Facts
- NPI
- 1245083146
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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