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LARRY LAZARO, M.D.
M.D.
Internal Medicine Physician
NPI: 1568449007IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
4301069069(MI)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 1991
Research & Publications (16)
Influence of cyclic strain and decorin deficiency on 3D cellularized collagen matrices.
PMID 18394699·Biomaterials·2008
7-preclinical
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.
PMID 18253926·Hum Mutat·2008
8-other
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy.
PMID 17993579·J Med Genet·2008
5-case
Predictors of weight maintenance after hospital discharge in adolescent anorexia nervosa.
PMID 17080450·Int J Eat Disord·2007
8-other
In vitro characterization of the human biotransformation pathways of aplidine, a novel marine anti-cancer drug.
PMID 16633717·Invest New Drugs·2007
8-other
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assays.
PMID 16428367·Arch Dis Child·2006
4-observational
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations.
PMID 15635066·J Med Genet·2005
8-other
Phenotypic and molecular variability of the holoprosencephalic spectrum.
PMID 15266610·Am J Med Genet A·2004
8-other
Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
PMID 15221788·Hum Mutat·2004
8-other
Enteroviral meningoencephalitis after anti-CD20 (rituximab) treatment.
PMID 12539090·Clin Infect Dis·2003
5-case
Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.
PMID 12522553·Hum Genet·2003
8-other
Bone mineral density in male adolescents with anorexia nervosa.
PMID 12014794·J Am Acad Child Adolesc Psychiatry·2002
8-other
Adolescent anorexia nervosa: the catch-up effect in bone mineral density after recovery.
PMID 11589535·J Am Acad Child Adolesc Psychiatry·2001
8-other
Compatibility and stability of the investigational polypeptide marine anticancer agent kahalalide F in infusion devices.
PMID 11561686·Invest New Drugs·2001
7-preclinical
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.
PMID 11039582·Eur J Hum Genet·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1721 S STEPHENSON AVE
IRON MOUNTAIN, MI 49801 - Phone
- (810) 692-4030
Quick Facts
- NPI
- 1568449007
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 35
- Publications
- 16
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