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SURA LYONNET, M.D.
M.D.
Emergency Medicine Physician
NPI: 1881122257IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
4301112533(MI)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
UNIVERSITY OF TOLEDO COLLEGE OF MEDICINE
Class of 2017
Research & Publications (20)
Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families.
PMID 19643772·J Med Genet·2010
8-other
Evaluation of methods for amplification of picogram amounts of total RNA for whole genome expression profiling.
PMID 19470167·BMC Genomics·2009
4-observational
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.
PMID 19234473·Nat Genet·2009
5-case
In Vitro studies of non poly alanine PHOX2B mutations argue against a loss-of-function mechanism for congenital central hypoventilation.
PMID 19058226·Hum Mutat·2009
8-other
Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease.
PMID 19666486·Proc Natl Acad Sci U S A·2009
8-other
Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance.
PMID 18854860·Eur J Hum Genet·2009
5-case
Conotruncal heart defects in three patients with congenital disorder of glycosylation type Ia (CDG Ia).
PMID 19357119·J Med Genet·2009
5-case
Sporadic case of unusual facies, cerebral vascular anomalies and developmental delay.
PMID 19057380·Clin Dysmorphol·2009
5-case
Long-range regulation at the SOX9 locus in development and disease.
PMID 19473998·J Med Genet·2009
6-review
Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.
PMID 19002211·Eur J Hum Genet·2009
5-case
Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.
PMID 19306335·Hum Mutat·2009
8-other
Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome.
PMID 19235238·Hum Mutat·2009
8-other
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.
PMID 19126570·J Med Genet·2009
8-other
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
PMID 18449898·Hum Mutat·2008
8-other
Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutions.
PMID 18945804·RNA·2008
8-other
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders.
PMID 18781618·Hum Mutat·2008
8-other
Human neural crest cells display molecular and phenotypic hallmarks of stem cells.
PMID 18689800·Hum Mol Genet·2008
7-preclinical
Delineation of late onset hypoventilation associated with hypothalamic dysfunction syndrome.
PMID 18670370·Pediatr Res·2008
7-preclinical
Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells.
PMID 18591412·J Exp Med·2008
8-other
Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma.
PMID 18923523·Nature·2008
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
- 200 N MADISON ST
MARSHALL, MI 49068 - Phone
- (269) 781-4271
Quick Facts
- NPI
- 1881122257
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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