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JESSICA ZEMAN, D.O.

D.O.

Critical Care Medicine (Internal Medicine) Physician

NPI: 1093869414IndividualAccepts Medicare

Specialties, Licenses & Credentials

Internal Medicine Physician

Internal Medicine

Code: 207R00000X

005239(AZ)
Pulmonary Disease Physician

Internal Medicine — Pulmonary Disease

Code: 207RP1001X

005239(AZ)
Critical Care Medicine (Internal Medicine) PhysicianPrimary

Internal Medicine — Critical Care Medicine

Code: 207RC0200X

005239(AZ)

CMS Specialties

PrimaryPULMONARY DISEASE

Additional

CRITICAL CARE (INTENSIVISTS)INTERNAL MEDICINE

Education

DES MOINES UNIVERSITY OF OSTEOPATHIC MEDICINE AND HEALTH SCIENCES

Class of 2006

Research & Publications (20)

Enzyme replacement therapy for Gaucher disease in twin pregnancy.
PMID 19349046·Int J Gynaecol Obstet·2009
5-case
Mucopolysaccharidosis type I in 21 Czech and Slovak patients: mutation analysis suggests a functional importance of C-terminus of the IDUA protein.
PMID 19396826·Am J Med Genet A·2009
8-other
TMEM70 protein - a novel ancillary factor of mammalian ATP synthase.
PMID 19103153·Biochim Biophys Acta·2009
7-preclinical
Common and specific emotion-related predictors of anxious and depressive symptoms in youth.
PMID 19039662·Child Psychiatry Hum Dev·2009
8-other
Loss of function of Sco1 and its interaction with cytochrome c oxidase.
PMID 19295170·Am J Physiol Cell Physiol·2009
8-other
Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.
PMID 18221507·BMC Genomics·2008
4-observational
Gene symbol: MECP2. Disease: Rett syndrome.
PMID 18846663·Hum Genet·2008
8-other
The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues.
PMID 18319067·Biochim Biophys Acta·2008
5-case
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates.
PMID 17698302·Early Hum Dev·2008
4-observational
Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
PMID 18846661·Hum Genet·2008
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

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Contact & Hours

Address
6677 W THUNDERBIRD RD, BLDG E
GLENDALE, AZ 85306

Quick Facts

NPI
1093869414
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
3
Locations
1
Years in Practice
20
Publications
20

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