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TARA MAXWELL, MD
MD
Pediatric Endocrinology Physician
NPI: 1467795450Individual
Specialties, Licenses & Credentials
Pediatric Endocrinology PhysicianPrimary
Pediatrics — Pediatric Endocrinology
Code: 2080P0205X
280123(MA)
Research & Publications (20)
Predicting abundance-body size relationships in functional and taxonomic subsets of food webs.
PMID 16927102·Oecologia·2006
7-preclinical
Experience with hospice: reflections from third-year medical students.
PMID 12572971·J Palliat Med·2002
8-other
Exploring the management of bone metastasis according to the Roy Adaptation Model.
PMID 11517850·Oncol Nurs Forum·2001
6-review
Replication of long-bone length QTL in the F9-F10 LG,SM advanced intercross.
PMID 19306044·Mamm Genome·2009
7-preclinical
Cholinesterase inhibitor and N-methyl-D-aspartic acid receptor antagonist use in older adults with end-stage dementia: a survey of hospice medical directors.
PMID 19622011·J Palliat Med·2009
4-observational
Inferring population mutation rate and sequencing error rate using the SNP frequency spectrum in a sample of DNA sequences.
PMID 19318520·Mol Biol Evol·2009
8-other
Irinotecan pharmacogenetics: influence of pharmacodynamic genes.
PMID 18347181·Clin Cancer Res·2008
8-other
Sampling strategies to evaluate the status of offshore soft sediment assemblages.
PMID 18353403·Mar Pollut Bull·2008
7-preclinical
Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studies.
PMID 18413369·J Med Genet·2008
5-case
Quantitative trait loci associated with susceptibility to therapy-related acute murine promyelocytic leukemia in hCG-PML/RARA transgenic mice.
PMID 18552208·Blood·2008
7-preclinical
Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
PMID 18798325·Am J Med Genet A·2008
5-case
Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform.
PMID 18178633·J Med Genet·2008
4-observational
Acetylcholinesterase inhibitor and N-methyl-D-aspartic acid receptor antagonist use among hospice enrollees with a primary diagnosis of dementia.
PMID 18588406·J Palliat Med·2008
8-other
Palliative care benchmarks from academic medical centers.
PMID 17298257·J Palliat Med·2007
4-observational
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster.
PMID 17431905·Am J Med Genet A·2007
5-case
Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.
PMID 17506097·Am J Med Genet A·2007
5-case
Response to Carlson/Morrison guest editorial: "evaluating palliative care programs: let's do it right".
PMID 17592970·J Palliat Med·2007
8-other
Numerical and functional defects of blood dendritic cells in early- and late-stage breast cancer.
PMID 17923873·Br J Cancer·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 1 JOSLIN PL
BOSTON, MA 02215 - Phone
- (617) 309-2400
Quick Facts
- NPI
- 1467795450
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 3
- Publications
- 20
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