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ELIZABETH FRIESEMA, M.D.
M.D.
Pediatrics Physician
NPI: 1992977763Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
MD60212397(WA)
Research & Publications (20)
Thyroid hormone transport by the human monocarboxylate transporter 8 and its rate-limiting role in intracellular metabolism.
PMID 16887882·Mol Endocrinol·2006
7-preclinical
Study of the transport of thyroid hormone by transporters of the SLC10 family.
PMID 19682536·Mol Cell Endocrinol·2010
7-preclinical
Transport of thyroxine and 3,3',5-triiodothyronine in human umbilical vein endothelial cells.
PMID 18948392·Endocrinology·2009
8-other
Genetic screening of a Dutch population with isolated GH deficiency (IGHD).
PMID 18785993·Clin Endocrinol (Oxf)·2009
7-preclinical
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations.
PMID 18636565·Hum Mutat·2009
8-other
Thyroid hormone transport and metabolism by organic anion transporter 1C1 and consequences of genetic variation.
PMID 18566113·Endocrinology·2008
4-observational
Organic anion transporter 1B1: an important factor in hepatic thyroid hormone and estrogen transport and metabolism.
PMID 18499754·Endocrinology·2008
7-preclinical
Effective cellular uptake and efflux of thyroid hormone by human monocarboxylate transporter 10.
PMID 18337592·Mol Endocrinol·2008
4-observational
Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8.
PMID 18187543·Endocrinology·2008
7-preclinical
Thyroid hormone transport by monocarboxylate transporters.
PMID 17574005·Best Pract Res Clin Endocrinol Metab·2007
6-review
Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine.
PMID 17356046·J Clin Endocrinol Metab·2007
8-other
Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter.
PMID 15980113·J Med Genet·2006
8-other
Novel neuroanatomical pathways for thyroid hormone action in the human anterior pituitary.
PMID 16498064·Eur J Endocrinol·2006
8-other
Mechanisms of disease: psychomotor retardation and high T3 levels caused by mutations in monocarboxylate transporter 8.
PMID 16957765·Nat Clin Pract Endocrinol Metab·2006
6-review
The monocarboxylate transporter 8 linked to human psychomotor retardation is highly expressed in thyroid hormone-sensitive neuron populations.
PMID 15661862·Endocrinology·2005
7-preclinical
Neuroanatomical pathways for thyroid hormone feedback in the human hypothalamus.
PMID 15840737·J Clin Endocrinol Metab·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
- 1708 E 44TH STREET
TACOMA, WA 98404 - Phone
- (253) 471-4553
Quick Facts
- NPI
- 1992977763
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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