Prof. Randi Jenssen Hagerman M.D.
Pediatrician | Developmental ? Behavioral Pediatrics
4307 Redbud Pl Davis CA, 95616About
Dr. Randi Hagerman is a pediatrician practicing in Davis, CA. Dr. Hagerman is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Hagerman diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Hagerman can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
Stanford Univ Sch Of Med- Stanford Ca 1975
Board Certification
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report.
- Fragile X syndrome and selective mutism.
- Compound heterozygous female with fragile X syndrome.
- Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome.
- Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutation.
- FMRP expression as a potential prognostic indicator in fragile X syndrome.
- Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development.
- Epilepsy and EEG findings in males with fragile X syndrome.
- Sensory-modulation disruption, electrodermal responses, and functional behaviors.
- Clinical involvement and protein expression in individuals with the FMR1 premutation.
- Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.
- Profile of cognitive functioning in women with the fragile X mutation.
- Sensory modulation dysfunction in children with attention-deficit-hyperactivity disorder.
- A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.
- Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.
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SUTTER MEDICAL CENTER, SACRAMENTOl
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2000 SUTTER PLACE DAVIS CA 95616