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ROBERT HALLER, M.D.
M.D.
Diagnostic Radiology Physician
NPI: 1639113293IndividualAccepts Medicare
Education
CLVLND CLINIC LERNER COLLEGE OF MED OF CASE WSTN RSV UNIVERSITY
Class of 1988
Research & Publications (20)
Fat metabolism during exercise in patients with mitochondrial disease.
PMID 19273755·Arch Neurol·2009
3-trial
Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease.
PMID 19433441·Brain·2009
4-observational
Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle.
PMID 19483197·Hum Mol Genet·2009
7-preclinical
Effect of changes in fat availability on exercise capacity in McArdle disease.
PMID 19506137·Arch Neurol·2009
2-rct
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions.
PMID 19664747·Am J Hum Genet·2009
8-other
Resistance training in patients with single, large-scale deletions of mitochondrial DNA.
PMID 18984605·Brain·2008
8-other
Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance.
PMID 18304497·Am J Hum Genet·2008
8-other
Isolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS protein.
PMID 18334481·J Biol Chem·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4853 GALAXY PKWY, SUITE I
CLEVELAND, OH 44128 - Phone
- (216) 831-9786
Quick Facts
- NPI
- 1639113293
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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