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RACHEL REISS CERONE MD
MD
Obstetrics & Gynecology Physician
NPI: 1083290654IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
ME173460(FL)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Education
UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL SCHOOL OF MEDICINE
Class of 2021
Research & Publications (20)
Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type.
PMID 18164228·Mol Genet Metab·2008
4-observational
Homocysteine, reactive oxygen species and nitric oxide in type 2 diabetes mellitus.
PMID 17188741·Thromb Res·2007
8-other
[Neonatal screening for congenital errors of metabolism by means of Tandem Mass: Italian experience].
PMID 17947884·Minerva Pediatr·2007
8-other
Effect of carnitine supplementation on lipid profile and anemia in children on chronic dialysis.
PMID 17277954·Pediatr Nephrol·2007
3-trial
von Willebrand factor multimer composition is modified following oral methionine load in women with thrombosis, but not in healthy women.
PMID 15870546·Blood Coagul Fibrinolysis·2005
8-other
Isolated sulphite oxidase deficiency: clinical and biochemical features in an Italian patient.
PMID 15065571·J Inherit Metab Dis·2004
5-case
Long-term follow-up of a patient with mild tetrahydrobiopterin-responsive phenylketonuria.
PMID 14741196·Mol Genet Metab·2004
5-case
Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure.
PMID 12644913·Pediatr Nephrol·2003
8-other
Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years.
PMID 14650352·Nutr Metab Cardiovasc Dis·2003
8-other
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features.
PMID 12060021·Epilepsia·2002
8-other
Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism.
PMID 11810299·Hum Genet·2002
8-other
Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings.
PMID 11237984·AJNR Am J Neuroradiol·2001
8-other
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia.
PMID 11596649·J Inherit Metab Dis·2001
5-case
Determination of lactic acid, pyruvic acid, and ketone bodies in serum and cerebrospinal fluid by HPLC.
PMID 11570270·Am Clin Lab·2001
8-other
Low total plasma homocysteine concentrations in patients with type 1 diabetes.
PMID 11347774·Diabetes Care·2001
4-observational
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases.
PMID 11315197·Neuropediatrics·2001
8-other
Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type III.
PMID 10942115·Hum Genet·2000
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
- 125 BAPTIST WAY STE 5A
PENSACOLA, FL 32503 - Phone
- (448) 227-6870
Quick Facts
- NPI
- 1083290654
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 5
- Publications
- 20
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