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THERESA GREBE, M.D.
M.D.
NPI: 1346202991Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
18774(AZ)
Research & Publications (15)
The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle.
PMID 18495510·Mol Genet Metab·2008
4-observational
Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype.
PMID 11078563·Am J Med Genet·2000
5-case
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
8-other
Celecoxib dilates guinea-pig coronaries and rat aortic rings and amplifies NO/cGMP signaling by PDE5 inhibition.
PMID 17383621·Cardiovasc Res·2007
7-preclinical
Montelukast exerts no acute direct effect on NO synthases.
PMID 16815057·Pulm Pharmacol Ther·2007
7-preclinical
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
PMID 17172942·Genet Med·2006
5-case
Further delineation of Kabuki syndrome in 48 well-defined new individuals.
PMID 15690370·Am J Med Genet A·2005
8-other
(4R)-3-Allenyl-4-(diphenylmethyl)oxazolidin-2-one, an unsubstituted allenamide.
PMID 15528834·Acta Crystallogr C·2004
8-other
Organization of the receptor-kinase signaling array that regulates Escherichia coli chemotaxis.
PMID 12119289·J Biol Chem·2002
8-other
The first successful base-promoted isomerization of propargyl amides to chiral ynamides. Applications in ring-closing metathesis of ene-ynamides and tandem RCM of diene-ynamides.
PMID 12098261·Org Lett·2002
8-other
Affinity profile at alpha(1)- and alpha(2)-adrenoceptor subtypes and in vitro cardiovascular actions of (+)-boldine.
PMID 12044805·Eur J Pharmacol·2002
4-observational
Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.
PMID 11829489·Genomics·2002
7-preclinical
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.
PMID 11685205·Nat Genet·2001
8-other
Failure of AH11110A to functionally discriminate between alpha(1)-adrenoceptor subtypes A, B and D or between alpha(1)- and alpha(2)-adrenoceptors.
PMID 11275009·Eur J Pharmacol·2001
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
- 1919 E THOMAS RD
PHOENIX, AZ 85016 - Phone
- (602) 546-1000
Quick Facts
- NPI
- 1346202991
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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