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DR. ABIGAIL ELIZABETH BEGGS M.D.
M.D.
Critical Care Medicine (Internal Medicine) Physician
NPI: 1518200393IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
140285(CA)
Pulmonary Disease Physician
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
140285(CA)
Sleep Medicine (Internal Medicine) Physician
Internal Medicine — Sleep Medicine
Code: 207RS0012X
140285(CA)
Critical Care Medicine (Internal Medicine) PhysicianPrimary
Internal Medicine — Critical Care Medicine
Code: 207RC0200X
140285(CA)
Education
OTHER
Class of 2011
Research & Publications (20)
Localization of parathyroid adenomas using 11C-methionine positron emission tomography.
PMID 15657506·Nucl Med Commun·2005
4-observational
Use of co-registered 11C-methionine PET and computed tomography for the localisation of parathyroid adenomas.
PMID 14579103·Eur J Nucl Med Mol Imaging·2003
5-case
F-18 FDG-positron emission tomographic scanning and Wegener's granulomatosis.
PMID 12352111·Clin Nucl Med·2002
5-case
FDG-PET as a "metabolic biopsy" tool in non-lung lesions with indeterminate biopsy.
PMID 11914894·Eur J Nucl Med Mol Imaging·2002
4-observational
A pilot study of ultrasound guided Durasphere injection in the treatment of faecal incontinence.
PMID 19438887·Colorectal Dis·2010
8-other
Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency.
PMID 19346529·Hum Mol Genet·2009
7-preclinical
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
PMID 19562689·Hum Mutat·2009
8-other
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.
PMID 19291799·Muscle Nerve·2009
8-other
The exon 55 deletion in the nebulin gene--one single founder mutation with world-wide occurrence.
PMID 19232495·Neuromuscul Disord·2009
8-other
Genomics and breast cancer: the different levels of inherited susceptibility.
PMID 19092772·Eur J Hum Genet·2009
8-other
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
PMID 19061985·Am J Hum Genet·2008
8-other
Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia.
PMID 18535205·Blood·2008
5-case
The DCC gene and colorectal cancer: the story is more complex.
PMID 18266884·Colorectal Dis·2008
8-other
Acute appendicitis is characterized by a uniform and highly selective pattern of inflammatory gene expression.
PMID 19079191·Mucosal Immunol·2008
8-other
Dynamic regulation of endothelial NOS mediated by competitive interaction with alpha-actinin-4 and calmodulin.
PMID 18180332·FASEB J·2008
7-preclinical
AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis.
PMID 18434328·Hum Mol Genet·2008
7-preclinical
Type I interferon-inducible gene expression in blood is present and reflects disease activity in dermatomyositis and polymyositis.
PMID 17968926·Arthritis Rheum·2007
8-other
Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy.
PMID 17537630·Neuromuscul Disord·2007
8-other
Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2.
PMID 17160903·Am J Hum Genet·2007
8-other
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
- 2020 ZONAL AVE # IRD720
LOS ANGELES, CA 90089 - Phone
- (323) 409-7184
Locations (3)
Quick Facts
- NPI
- 1518200393
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 3
- Years in Practice
- 15
- Publications
- 20
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