Back to Search
ANDREW GIANNOTTI, MD
MD
Addiction Medicine (Preventive Medicine) Physician
NPI: 1275509168Individual
Specialties, Licenses & Credentials
Addiction Medicine (Preventive Medicine) PhysicianPrimary
Preventive Medicine — Addiction Medicine
Code: 2083A0300X
MD61508969(WA)
Research & Publications (20)
Ellis-van Creveld Syndrome with hydrometrocolpos is not linked to chromosome arm 4p or 20p.
PMID 15054850·Am J Med Genet A·2004
5-case
Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome).
PMID 14616771·Clin Genet·2003
8-other
Malignant pancreatic endocrine tumor in a child with tuberous sclerosis.
PMID 14508401·Am J Surg Pathol·2003
5-case
Recurrence of HCV infection in liver transplant patients: evaluation of IgM anti-HCV and IgM anti-CMV.
PMID 12947847·Transplant Proc·2003
8-other
Impact of antiviral treatment on recurrence of hepatitis B virus infection and disease.
PMID 12947846·Transplant Proc·2003
8-other
Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome).
PMID 12923874·Am J Med Genet A·2003
8-other
Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
PMID 12815605·Hum Mutat·2003
8-other
Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxia.
PMID 12797454·Birth Defects Res A Clin Mol Teratol·2003
5-case
Deletion of the SHOX gene in patients with short stature of unknown cause.
PMID 12784295·Am J Med Genet A·2003
8-other
Glutathione metabolism and antioxidant enzymes in children with Down syndrome.
PMID 12756395·J Pediatr·2003
8-other
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies.
PMID 12702165·Clin Genet·2003
4-observational
SHOX mutations detected by FISH and direct sequencing in patients with short stature.
PMID 12566529·J Med Genet·2003
8-other
Two novel mutations of the human delta7-sterol reductase (DHCR7) gene in children with Smith-Lemli-Opitz syndrome.
PMID 12270273·Mol Cell Probes·2002
8-other
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies.
PMID 11954747·Eur J Pediatr·2002
4-observational
Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism.
PMID 11857750·Hum Mutat·2002
8-other
Intracranial effects of endotracheal suctioning in the acute phase of head injury.
PMID 11773824·J Neurosurg Anesthesiol·2002
8-other
Effect of removable orthodontic appliances on oral colonisation by mutans streptococci in children.
PMID 11767275·Eur J Oral Sci·2001
8-other
Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence.
PMID 11733399·Circulation·2001
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
- 9474 LATHROP INDUSTRIAL DR SW
TUMWATER, WA 98512 - Phone
- (360) 583-3340
Quick Facts
- NPI
- 1275509168
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile