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ERIC ROESSLER, MD
MD
Infectious Disease Physician
NPI: 1750904348IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
125.076160(IL)
Infectious Disease PhysicianPrimary
Internal Medicine — Infectious Disease
Code: 207RI0200X
036.163794(IL)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE IN NEW ORLEANS
Class of 2020
Research & Publications (20)
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.
PMID 19184110·Hum Genet·2009
7-preclinical
A novel SIX3 mutation segregates with holoprosencephaly in a large family.
PMID 19353631·Am J Med Genet A·2009
8-other
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
PMID 19603532·Hum Mutat·2009
8-other
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
PMID 19346217·J Med Genet·2009
8-other
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
PMID 19177455·Hum Mutat·2009
8-other
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
PMID 18538293·Am J Hum Genet·2008
7-preclinical
Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein.
PMID 18836447·Nat Genet·2008
7-preclinical
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
PMID 18791198·Hum Mol Genet·2008
4-observational
Inhibition of bFGF-receptor type 2 increases kidney damage and suppresses nephrogenic protein expression after ischemic acute renal failure.
PMID 18184769·Am J Physiol Regul Integr Comp Physiol·2008
7-preclinical
Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans.
PMID 17924340·Am J Hum Genet·2007
7-preclinical
Usefulness of a molecular strategy for the detection of bacterial DNA in patients with severe sepsis undergoing continuous renal replacement therapy.
PMID 17170546·Blood Purif·2007
4-observational
Functional analysis of mutations in TGIF associated with holoprosencephaly.
PMID 16962354·Mol Genet Metab·2007
5-case
Association of adrenal medullar and cortical nodular hyperplasia: a report of two cases with clinical and morpho-functional considerations.
PMID 17526953·Endocrine·2006
5-case
A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers.
PMID 16407397·Development·2006
7-preclinical
Impact of pregnancy on the function of transplanted kidneys.
PMID 15866678·Transplant Proc·2005
8-other
A previously unidentified amino-terminal domain regulates transcriptional activity of wild-type and disease-associated human GLI2.
PMID 15994174·Hum Mol Genet·2005
7-preclinical
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
PMID 14581620·Proc Natl Acad Sci U S A·2003
7-preclinical
SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activity.
PMID 12709790·Hum Genet·2003
8-other
Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia.
PMID 12503095·Am J Med Genet A·2003
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
- 5841 S MARYLAND AVE, M/C 5065
CHICAGO, IL 60637 - Phone
- (773) 834-9740
Quick Facts
- NPI
- 1750904348
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 6
- Publications
- 20
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