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ANH INNES, M.D.
M.D.
Pulmonary Disease Physician
NPI: 1982803573Individual
Specialties, Licenses & Credentials
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
A79839(CA)
Research & Publications (20)
Ex vivo sputum analysis reveals impairment of protease-dependent mucus degradation by plasma proteins in acute asthma.
PMID 19423716·Am J Respir Crit Care Med·2009
4-observational
Epithelial mucin stores are increased in the large airways of smokers with airflow obstruction.
PMID 17035444·Chest·2006
8-other
Dark chocolate inhibits platelet aggregation in healthy volunteers.
PMID 12944249·Platelets·2003
3-trial
Genetic landmarks through philately: Woodrow Wilson 'Woody' Guthrie and Huntington disease.
PMID 12030890·Clin Genet·2002
8-other
Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature.
PMID 11471171·Am J Med Genet·2001
5-case
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy.
PMID 10625081·Pediatr Res·2000
5-case
Influenza vaccination in asthma: a primary care experience.
PMID 10695063·Br J Gen Pract·2000
4-observational
Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.
PMID 19481194·Am J Hum Genet·2009
7-preclinical
Fluctuating hearing loss associated with Halo vest application.
PMID 18976511·J Laryngol Otol·2009
5-case
Cystic schwannoma of the cervical plexus masquerading as a type II second branchial cleft cyst.
PMID 18418621·Eur Arch Otorhinolaryngol·2009
5-case
Efficacy and safety of certolizumab pegol monotherapy every 4 weeks in patients with rheumatoid arthritis failing previous disease-modifying antirheumatic therapy: the FAST4WARD study.
PMID 19015206·Ann Rheum Dis·2009
4-observational
Chitotriosidase is the primary active chitinase in the human lung and is modulated by genotype and smoking habit.
PMID 18845328·J Allergy Clin Immunol·2008
4-observational
An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier.
PMID 18348271·Am J Med Genet A·2008
5-case
The detection of advanced chronic kidney disease by surveillance of elevated plasma creatinines--a five-year experience.
PMID 18390892·Nephrol Dial Transplant·2008
8-other
Costello syndrome associated with novel germline HRAS mutations: an attenuated phenotype?
PMID 18247425·Am J Med Genet A·2008
5-case
Unique disease heritage of the Dutch-German Mennonite population.
PMID 18348259·Am J Med Genet A·2008
6-review
Clinical genetics and the Hutterite population: a review of Mendelian disorders.
PMID 18348266·Am J Med Genet A·2008
6-review
Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome.
PMID 17603801·Am J Med Genet A·2007
8-other
Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy.
PMID 17712733·Neuropediatrics·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- BOX 0130, 505 PARNASSUS AVENUE
SAN FRANCISCO, CA 94143 - Phone
- (415) 476-9456
Quick Facts
- NPI
- 1982803573
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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