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GEORGIANNE ARNOLD, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1407885494Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
ME133480(FL)MD439538(PA)
Research & Publications (20)
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.
PMID 19157942·Mol Genet Metab·2009
6-review
A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency.
PMID 18155630·Mol Genet Metab·2008
6-review
Sensitivity and specificity of finger tapping test scores for the detection of suspect effort.
PMID 15814482·Clin Neuropsychol·2005
4-observational
Fe isotope variations in natural materials measured using high mass resolution multiple collector ICPMS.
PMID 14719878·Anal Chem·2004
8-other
Molybdenum isotope evidence for widespread anoxia in mid-Proterozoic oceans.
PMID 15066776·Science·2004
8-other
Prevalence of stimulant use for attentional dysfunction in children with phenylketonuria.
PMID 15159644·J Inherit Metab Dis·2004
8-other
Plasma amino acids profiles in children with autism: potential risk of nutritional deficiencies.
PMID 12959424·J Autism Dev Disord·2003
8-other
Barrett's esophagus-associated polypoid dysplasia: a case report and review of the literature.
PMID 12184548·Dig Dis Sci·2002
5-case
Steele-Richardson-Olszewski-syndrome: the relation of dopamine D2 receptor binding and subcortical lesions in MRI.
PMID 11956969·J Neural Transm (Vienna)·2002
4-observational
Steele-Richardson-Olszewski-syndrome: reduction of dopamine D2 receptor binding relates to the severity of midbrain atrophy in vivo: (123)IBZM SPECT and MRI study.
PMID 12112207·Mov Disord·2002
4-observational
Protein insufficiency and linear growth restriction in phenylketonuria.
PMID 12183721·J Pediatr·2002
4-observational
Iron and protein sufficiency and red cell indices in phenylketonuria.
PMID 11293470·J Am Coll Nutr·2001
8-other
Pyruvate carboxylase deficiency. Report of a case and additional evidence for the "mild" phenotype.
PMID 11583052·Clin Pediatr (Phila)·2001
5-case
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
Newborn screening for Krabbe disease: the New York State model.
PMID 19302934·Pediatr Neurol·2009
8-other
LC-MS/MS-based proteome profiling in Daphnia pulex and Daphnia longicephala: the Daphnia pulex genome database as a key for high throughput proteomics in Daphnia.
PMID 19383153·BMC Genomics·2009
7-preclinical
Evidence for estrogen-dependent uterine serpin (SERPINA14) expression during estrus in the bovine endometrial glandular epithelium and lumen.
PMID 19494250·Biol Reprod·2009
7-preclinical
A newcomer's guide to nano-liquid-chromatography of peptides.
PMID 19544020·Methods Mol Biol·2009
8-other
Broad neutralization of human immunodeficiency virus type 1 (HIV-1) elicited from human rhinoviruses that display the HIV-1 gp41 ELDKWA epitope.
PMID 19279101·J Virol·2009
7-preclinical
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
- 6535 NEMOURS PKWY
ORLANDO, FL 32827 - Phone
- (407) 567-4000
Quick Facts
- NPI
- 1407885494
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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