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AMBRA FERRARIS, M.D.
M.D.
Internal Medicine Physician
NPI: 1255578399Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
25MA09295200(NJ)
Research & Publications (20)
Metastasis of malignant peritoneal epithelioid mesothelioma in endoscopic gastric biopsy: a diagnostic pitfall.
PMID 18794170·Int J Surg Pathol·2011
5-case
Neural tube defect in a 4000-year-old Egyptian infant mummy: a case of meningocele from the museum of anthropology and ethnography of Turin (Italy).
PMID 19136285·Eur J Paediatr Neurol·2009
5-case
GIGYF2 variants are not associated with Parkinson's disease in Italy.
PMID 19562763·Mov Disord·2009
8-other
Telomere length of donors influences granulocyte recovery in children after hematopoietic stem cell transplantation.
PMID 19229535·Ann Hematol·2009
8-other
Accelerated senescence in the kidneys of patients with type 2 diabetic nephropathy.
PMID 18768588·Am J Physiol Renal Physiol·2008
8-other
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts.
PMID 17693570·J Med Genet·2008
8-other
PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum.
PMID 18330912·Hum Mutat·2008
4-observational
Microarray analysis identifies a common set of cellular genes modulated by different HCV replicon clones.
PMID 18590516·BMC Genomics·2008
8-other
Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study.
PMID 18307263·Mov Disord·2008
5-case
Heterozygous mutations in genes causing parkinsonism: monogenic disorders go complex.
PMID 17582354·Lancet Neurol·2007
8-other
Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements.
PMID 17914726·Mov Disord·2007
8-other
Expansion of B cell precursors after unrelated cord blood transplantation for an adult patient.
PMID 17529999·Bone Marrow Transplant·2007
5-case
Combined test for UGT1A1 -3279T-->G and A(TA)nTAA polymorphisms best predicts Gilbert's syndrome in Italian pediatric patients.
PMID 16792515·Genet Test·2006
8-other
Contribution of IBD5 locus to clinical features of IBD patients.
PMID 16454837·Am J Gastroenterol·2006
4-observational
Absence of pathogenic mutations of the human telomerase RNA gene (hTERC) in patients with chronic myeloproliferative disorders.
PMID 16511512·Leukemia·2006
8-other
Relationship between CARD15, SLC22A4/5, and DLG5 polymorphisms and early-onset inflammatory bowel diseases: an Italian multicentric study.
PMID 16670523·Inflamm Bowel Dis·2006
4-observational
Clonal granulocytes in polycythaemia vera and essential thrombocythaemia have shortened telomeres.
PMID 16042688·Br J Haematol·2005
8-other
Analysis of CARD15 gene variants in Italian pediatric patients with inflammatory bowel diseases.
PMID 16126067·J Pediatr·2005
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
- 100 MADISON AVE, MORRISTOWN MEDICAL CENTER
MORRISTOWN, NJ 07960 - Phone
- (973) 656-6280
Quick Facts
- NPI
- 1255578399
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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