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GUSTAVO GRIECO, M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1073539755IndividualAccepts Medicare
Specialties, Licenses & Credentials
Interventional Cardiology Physician
Internal Medicine — Interventional Cardiology
Code: 207RI0011X
J2039(TX)
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
J2039(TX)
Education
OTHER
Class of 1984
Research & Publications (20)
Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism.
PMID 19517061·J Headache Pain·2009
8-other
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss.
PMID 19031088·Neurogenetics·2009
8-other
The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility.
PMID 19429006·Neurosci Lett·2009
8-other
Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs.
PMID 19414726·Neurology·2009
3-trial
Interferometer for ground-based observations of emitted spectral radiance from the troposphere: evaluation and retrieval performance.
PMID 18641761·Appl Opt·2008
8-other
Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
PMID 17292920·J Neurol Sci·2007
5-case
The wolframin His611Arg polymorphism influences medication overuse headache.
PMID 17719176·Neurosci Lett·2007
8-other
Dipyridamole plus aspirin: the best regimen for stroke prevention after noncardioembolic focal cerebral ischemia.
PMID 16567930·Cerebrovasc Dis·2006
8-other
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.
PMID 16636238·Neurology·2006
8-other
Skeletal muscle wasting in tumor-bearing rats is associated with MyoD down-regulation.
PMID 15870883·Int J Oncol·2005
7-preclinical
Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
PMID 16344534·Neurology·2005
8-other
Editorial comment--an approach to the estimation of the risk of TTP during clopidogrel therapy.
PMID 14757895·Stroke·2004
8-other
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.
PMID 14718707·Neurology·2004
5-case
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.
PMID 14745065·Neurology·2004
5-case
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.
PMID 12565915·Neuromuscul Disord·2003
5-case
Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
PMID 12815605·Hum Mutat·2003
8-other
Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders.
PMID 12782971·Psychiatr Genet·2003
8-other
Potential value of triple antiplatelet therapy for secondary stroke prevention.
PMID 14512584·Stroke·2003
1-meta
Increased muscle proteasome activity correlates with disease severity in gastric cancer patients.
PMID 12616123·Ann Surg·2003
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 6 locations total
- Address
- 1125 Cypress Station Dr Ste F4
Houston, TX 77090 - Phone
- (713) 897-7221
Locations (6)
Practice Location
1125 Cypress Station Dr Ste F4, Houston, TX
(713) 897-7221
Practice Location
17400 RED OAK DR, HOUSTON, TX
(281) 893-8640
Practice Location
920 Medical Plaza Dr Ste 500, Shenandoah, TX
(713) 897-7221
Practice Location
9180 PINECROFT DR STE 400, SHENANDOAH, TX
(713) 897-7221
Practice Location
21301 Kuykendahl Rd Ste F, Spring, TX
(713) 897-7221
Practice Location
9305 Pinecroft Dr Ste 300, The Woodlands, TX
(713) 897-7221
Quick Facts
- NPI
- 1073539755
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 6
- Years in Practice
- 42
- Publications
- 20
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