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GISELLE SCARANO, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1295420461Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Prenatal diagnosis of 46,XX testicular DSD. Molecular, cytogenetic, molecular-cytogenetic, and ultrasonographic evaluation.
PMID 19603386·Prenat Diagn·2009
5-case
Brain activity during the memorization of visual scenes from TV commercials: an application of high resolution EEG and steady state somatosensory evoked potentials technologies.
PMID 19619647·J Physiol Paris·2009
8-other
Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study.
PMID 19242930·Hum Mutat·2009
8-other
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
PMID 18566978·Birth Defects Res A Clin Mol Teratol·2008
8-other
Preferential associations between oral clefts and other major congenital anomalies.
PMID 18788868·Cleft Palate Craniofac J·2008
8-other
Assessing the memorization of TV commercials with the use of high resolution EEG: a pilot study.
PMID 19163528·Annu Int Conf IEEE Eng Med Biol Soc·2008
8-other
Al-Awadi/Raas-Rothschild syndrome: two new cases and review.
PMID 17431918·Am J Med Genet A·2007
5-case
Gastroschisis and associated defects: an international study.
PMID 17357116·Am J Med Genet A·2007
1-meta
Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation.
PMID 17661813·Clin Genet·2007
8-other
A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q.
PMID 17937430·Am J Med Genet A·2007
5-case
WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report.
PMID 16959810·Hum Reprod·2007
5-case
13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
PMID 17209130·J Med Genet·2007
8-other
Evidence for increased clinical severity of familial and sporadic Paget's disease of bone in Campania, southern Italy.
PMID 17002563·J Bone Miner Res·2006
4-observational
Reduced complexity rotation invariant texture classification using a blind deconvolution approach.
PMID 16402627·IEEE Trans Pattern Anal Mach Intell·2006
8-other
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene.
PMID 16600650·Mol Genet Metab·2006
8-other
Biosynthesis of Cd-bound phytochelatins by Phaeodactylum tricornutum and their speciation by size-exclusion chromatography and ion-pair chromatography coupled to ICP-MS.
PMID 16205894·Anal Bioanal Chem·2005
8-other
Biosynthesis of phytochelatins and arsenic accumulation in the marine microalga Phaeodactylum tricornutum in response to arsenate exposure.
PMID 16388398·Biometals·2005
8-other
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy.
PMID 16046620·Physiol Genomics·2005
8-other
Prenatal ultrasound diagnosis of cloacal exstrophy associated with myelocystocele complex by the 'elephant trunk-like' image and review of the literature.
PMID 15909284·Prenat Diagn·2005
5-case
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth.
PMID 15742365·Am J Med Genet A·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1600 SW ARCHER RD
GAINESVILLE, FL 32610 - Phone
- (352) 265-0076
Quick Facts
- NPI
- 1295420461
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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