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DR. DORU BALI M.D.
M.D.
Emergency Medicine Physician
NPI: 1083651228IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
4301080205(MI)
Education
WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE
Class of 2002
Research & Publications (20)
Screening for Pompe disease using a rapid dried blood spot method: experience of a clinical diagnostic laboratory.
PMID 19533645·Muscle Nerve·2009
8-other
Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker.
PMID 19521244·Genet Med·2009
3-trial
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
Emerging therapies for glycogen storage disease type I.
PMID 19541498·Trends Endocrinol Metab·2009
6-review
Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: a case study.
PMID 18930676·Mol Genet Metab·2008
5-case
A case of congenital glycogen storage disease type IV with a novel GBE1 mutation.
PMID 18230843·J Child Neurol·2008
5-case
Methods for a prompt and reliable laboratory diagnosis of Pompe disease: report from an international consensus meeting.
PMID 18078773·Mol Genet Metab·2008
8-other
Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease.
PMID 17151339·Neurology·2007
4-observational
Glycogen storage disease type III-hepatocellular carcinoma a long-term complication?
PMID 17196294·J Hepatol·2007
5-case
Rapid diagnosis of late-onset Pompe disease by fluorometric assay of alpha-glucosidase activities in dried blood spots.
PMID 17270480·Mol Genet Metab·2007
8-other
Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.
PMID 16702880·Genet Med·2006
4-observational
The knowledge and perceptions of medical personnel relating to outcome after cardiac arrest.
PMID 16458410·Resuscitation·2006
8-other
Non-lethal congenital hypotonia due to glycogen storage disease type IV.
PMID 16528737·Am J Med Genet A·2006
5-case
The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease.
PMID 16702881·Genet Med·2006
8-other
Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy.
PMID 16275868·Circulation·2005
7-preclinical
Hepatocellular carcinoma in glycogen storage disease type Ia: a case series.
PMID 15877204·J Inherit Metab Dis·2005
5-case
Amylopectinosis disease isolated to the heart with normal glycogen branching enzyme activity and gene sequence.
PMID 15787805·Pediatr Transplant·2005
5-case
Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.
PMID 12736383·Pediatr Res·2003
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 4201 Saint Antoine St Ste 3R
Detroit, MI 48201 - Phone
- (313) 745-0003
Quick Facts
- NPI
- 1083651228
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 24
- Publications
- 20
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