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MICHAEL HILDEBRANDT, MD
MD
Family Medicine Physician
NPI: 1881655926Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
25437(MN)
Research & Publications (20)
Genetic diversity and function in the human cytosolic sulfotransferases.
PMID 16801938·Pharmacogenomics J·2007
7-preclinical
Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studies.
PMID 15358107·Biochem Biophys Res Commun·2004
8-other
Pharmacogenomics of platinum-based chemotherapy in NSCLC.
PMID 19442035·Expert Opin Drug Metab Toxicol·2009
6-review
Towards a clinico-pathological classification of granule cell dispersion in human mesial temporal lobe epilepsies.
PMID 19277686·Acta Neuropathol·2009
4-observational
Increased reelin promoter methylation is associated with granule cell dispersion in human temporal lobe epilepsy.
PMID 19287316·J Neuropathol Exp Neurol·2009
8-other
Calculation of NNTs in RCTs with time-to-event outcomes: a literature review.
PMID 19302699·BMC Med Res Methodol·2009
6-review
[Conflicts of interest and clinical drug trials -- impact of the pharmaceutical industry and the impingement on the integrity of medical science].
PMID 19554889·Z Evid Fortbild Qual Gesundhwes·2009
8-other
Genetic variations in the PI3K/PTEN/AKT/mTOR pathway are associated with clinical outcomes in esophageal cancer patients treated with chemoradiotherapy.
PMID 19164214·J Clin Oncol·2009
8-other
Very important pharmacogene summary: sulfotransferase 1A1.
PMID 19451861·Pharmacogenet Genomics·2009
6-review
Clinical prediction of postoperative seizure control: structural, functional findings and disease histories.
PMID 18838399·J Neurol Neurosurg Psychiatry·2009
8-other
Different presurgical characteristics and seizure outcomes in children with focal cortical dysplasia type I or II.
PMID 18513354·Epilepsia·2009
8-other
Breast cancer risk reduction and membrane-bound catechol O-methyltransferase genetic polymorphisms.
PMID 18632656·Cancer Res·2008
8-other
Gemcitabine and cytosine arabinoside cytotoxicity: association with lymphoblastoid cell expression.
PMID 18757419·Cancer Res·2008
8-other
Glutathione s-transferase p1: gene sequence variation and functional genomic studies.
PMID 18559526·Cancer Res·2008
7-preclinical
Brillouin scattering spectra in high-power single-frequency ytterbium doped fiber amplifiers.
PMID 18825235·Opt Express·2008
8-other
In vivo detection of hepatitis C virus (HCV) RNA in the brain in a case of encephalitis: evidence for HCV neuroinvasion.
PMID 18215154·Eur J Neurol·2008
5-case
White matter angiopathy is common in pediatric patients with intractable focal epilepsies.
PMID 18266747·Epilepsia·2008
4-observational
Testing whether genetic variation explains correlation of quantitative measures of gene expression, and application to genetic network analysis.
PMID 18444230·Stat Med·2008
8-other
Proteasome beta subunit pharmacogenomics: gene resequencing and functional genomics.
PMID 18519783·Clin Cancer Res·2008
8-other
Non-invasive detection of hippocampal sclerosis: correlation between metabolite alterations detected by (1)H-MRS and neuropathology.
PMID 18035849·NMR Biomed·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 100 STATE AVE
FARIBAULT, MN 55021 - Phone
- (507) 334-3921
Quick Facts
- NPI
- 1881655926
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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