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SIBYL RICKARD, M.D.
M.D.
Anatomic Pathology & Clinical Pathology Physician
NPI: 1932386372IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
MD436144(PA)
CMS Specialties
PrimaryPATHOLOGY
Education
JEFFERSON MEDICAL COLLEGE OF THOMAS JEFFERSON UNIVERSITY
Class of 2005
Research & Publications (13)
Plasma insulin-like growth factor I levels in rats are reduced by dietary supplementation of flaxseed or its lignan secoisolariciresinol diglycoside.
PMID 11078912·Cancer Lett·2000
7-preclinical
Urinary composition and postprandial blood changes in H-secoisolariciresinol diglycoside (SDG) metabolites in rats do not differ between acute and chronic SDG treatments.
PMID 10958827·J Nutr·2000
7-preclinical
Invariant chain+ N2a neuroblastoma cells stably expressing the class II MHC transactivator CIITA fail to stimulate anti-tumor immunity.
PMID 18952077·Exp Mol Pathol·2008
7-preclinical
Fractional delay estimation for blind source separation and localization of temporomandibular joint sounds.
PMID 18334386·IEEE Trans Biomed Eng·2008
8-other
The value of in-utero magnetic resonance imaging in ultrasound diagnosed foetal isolated cerebral ventriculomegaly.
PMID 17207696·Clin Radiol·2007
8-other
In utero magnetic resonance of non-isolated ventriculomegaly: Does ventricular size or morphology reflect pathology?
PMID 16978979·Clin Radiol·2006
8-other
Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS.
PMID 14981718·Am J Med Genet A·2004
8-other
The binding of human glial cell line-derived neurotrophic factor to heparin and heparan sulfate: importance of 2-O-sulfate groups and effect on its interaction with its receptor, GFRalpha1.
PMID 12626395·Glycobiology·2003
8-other
Analysis of GNAS1 and overlapping transcripts identifies the parental origin of mutations in patients with sporadic Albright hereditary osteodystrophy and reveals a model system in which to observe the effects of splicing mutations on translated and untranslated messenger RNA.
PMID 12624854·Am J Hum Genet·2003
4-observational
Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families.
PMID 11494963·J Med Genet·2001
8-other
Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cM.
PMID 11409867·Hum Genet·2001
5-case
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.
PMID 11134236·J Med Genet·2001
8-other
Importance of clinical evaluation and molecular testing in the branchio-oto-renal (BOR) syndrome and overlapping phenotypes.
PMID 10991693·J Med Genet·2000
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
- 601 PARK ST
HONESDALE, PA 18431 - Phone
- (570) 251-6655
Quick Facts
- NPI
- 1932386372
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 21
- Publications
- 13
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