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GORDON ENNS, MD
MD
Emergency Medicine Physician
NPI: 1326000670Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
MD10734(OR)
Research & Publications (20)
Central nervous system therapy for lysosomal storage disorders.
PMID 18341388·Neurosurg Focus·2008
6-review
Neurologic damage and neurocognitive dysfunction in urea cycle disorders.
PMID 18708004·Semin Pediatr Neurol·2008
6-review
Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.
PMID 17538087·N Engl J Med·2007
3-trial
Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load.
PMID 16546428·Mol Genet Metab·2006
5-case
Postpartum "psychosis" in mild argininosuccinate synthetase deficiency.
PMID 15863597·Obstet Gynecol·2005
5-case
Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle.
PMID 16143021·Clin Genet·2005
5-case
Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency.
PMID 15303009·J Inherit Metab Dis·2004
5-case
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins.
PMID 12410200·J Pediatr·2002
5-case
The adolescent with an inborn error of metabolism: medical issues and transition to adulthood.
PMID 11986039·Adolesc Med·2002
6-review
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
PMID 10657835·J Pediatr·2000
5-case
Long-term outcome following pediatric liver transplantation for metabolic disorders.
PMID 19671092·Pediatr Transplant·2010
8-other
Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
PMID 19058814·J Pediatr·2009
5-case
Hypoplastic glomerulocystic kidney disease and hepatoblastoma: a potential association not caused by mutations in hepatocyte nuclear factor 1beta.
PMID 19564751·J Pediatr Hematol Oncol·2009
5-case
Novel deoxyguanosine kinase gene mutations and viral infection predispose apparently healthy children to fulminant liver failure.
PMID 19502998·J Pediatr Gastroenterol Nutr·2009
5-case
Mapping gene associations in human mitochondria using clinical disease phenotypes.
PMID 19390613·PLoS Comput Biol·2009
8-other
Pathological evidence of Wolman's disease following hematopoietic stem cell transplantation despite correction of lysosomal acid lipase activity.
PMID 19308038·Bone Marrow Transplant·2009
5-case
Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia.
PMID 19223582·Proc Natl Acad Sci U S A·2009
8-other
Successful pregnancy and cesarean delivery via noninvasive ventilation in mitochondrial myopathy.
PMID 19177045·J Perinatol·2009
5-case
Dopa-responsive dystonia presenting as delayed and awkward gait.
PMID 18358407·Pediatr Neurol·2008
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
- 280 MAPLE ST.
ASHLAND, OR 97520 - Phone
- (541) 201-4000
Quick Facts
- NPI
- 1326000670
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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