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MARIAH HILDEBRAND, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1063216729Individual
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)
3D imaging of diatoms with ion-abrasion scanning electron microscopy.
PMID 19269330·J Struct Biol·2009
8-other
Clinical value of FDG-PET/CT for the diagnosis of human immunodeficiency virus-associated fever of unknown origin: a retrospective study.
PMID 19306513·Nucl Med Commun·2009
8-other
A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family.
PMID 19215054·Am J Med Genet A·2009
8-other
Recruiting older adults into a physical activity promotion program: Active Living Every Day offered in a naturally occurring retirement community.
PMID 19574541·Gerontologist·2009
8-other
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.
PMID 19274735·Laryngoscope·2009
8-other
Phenomic determinants of genomic variation in autism spectrum disorders.
PMID 19625284·J Med Genet·2009
8-other
Diverse and conserved nano- and mesoscale structures of diatom silica revealed by atomic force microscopy.
PMID 19659911·J Microsc·2009
8-other
Human male infertility caused by mutations in the CATSPER1 channel protein.
PMID 19344877·Am J Hum Genet·2009
7-preclinical
Functional coupling between mGluR1 and Cav3.1 T-type calcium channels contributes to parallel fiber-induced fast calcium signaling within Purkinje cell dendritic spines.
PMID 19657020·J Neurosci·2009
7-preclinical
Mutation in the COCH gene is associated with superior semicircular canal dehiscence.
PMID 19161137·Am J Med Genet A·2009
8-other
A self-propagating system for Ge incorporation into nanostructured silica.
PMID 18802602·Chem Commun (Camb)·2008
8-other
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.
PMID 18941426·Genet Med·2008
7-preclinical
A catechol-O-methyltransferase that is essential for auditory function in mice and humans.
PMID 18794526·Proc Natl Acad Sci U S A·2008
7-preclinical
Activation of corticotropin-releasing factor receptor 1 selectively inhibits CaV3.2 T-type calcium channels.
PMID 18292205·Mol Pharmacol·2008
4-observational
Direct inhibition of the DNA-binding activity of POU transcription factors Pit-1 and Brn-3 by selective binding of a phenyl-furan-benzimidazole dication.
PMID 18440973·Nucleic Acids Res·2008
8-other
Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1.
PMID 18688868·Am J Med Genet A·2008
5-case
Rebeccamycin derivatives as dual DNA-damaging agents and potent checkpoint kinase 1 inhibitors.
PMID 18768386·Mol Pharmacol·2008
7-preclinical
Biomineralization at the nanoscale learning from diatoms.
PMID 19195546·Methods Cell Biol·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
- CLEVELAND CLINIC AKRON GENERAL, 1 AKRON GENERAL AVE.
AKRON, OH 44307 - Phone
- (330) 334-6000
Quick Facts
- NPI
- 1063216729
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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