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DAVID GUNTHER, M.D.
M.D.
Addiction Medicine (Family Medicine) Physician
NPI: 1467426536IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine Physician
Family Medicine
Code: 207Q00000X
82112(MA)
Addiction Medicine (Family Medicine) PhysicianPrimary
Family Medicine — Addiction Medicine
Code: 207QA0401X
82112(MA)
Education
OTHER
Class of 1994
Research & Publications (17)
Cyclical Cushing syndrome presenting in infancy: an early form of primary pigmented nodular adrenocortical disease, or a new entity?
PMID 15240590·J Clin Endocrinol Metab·2004
8-other
Meticillin-resistant Staphylococcus aureus contamination of healthcare workers' uniforms in long-term care facilities.
PMID 19100661·J Hosp Infect·2009
4-observational
[Immunoassay rapid test for influenza diagnosis in institutions for elderly people: a four-year surveillance with the GROG Géronto-Alsace].
PMID 18835108·Pathol Biol (Paris)·2009
3-trial
Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle.
PMID 18713863·Proc Natl Acad Sci U S A·2008
7-preclinical
[Respiratory tract infections in institutions for elderly people: the GROG Géronto-Alsace, strategy of surveillance and alert].
PMID 17997251·Med Mal Infect·2007
8-other
Growth hormone treatment of early growth failure in toddlers with Turner syndrome: a randomized, controlled, multicenter trial.
PMID 17595258·J Clin Endocrinol Metab·2007
4-observational
A Gender Assessment Team: experience with 250 patients over a period of 25 years.
PMID 17575501·Genet Med·2007
4-observational
A case of true hermaphroditism reveals an unusual mechanism of twinning.
PMID 17165045·Hum Genet·2007
5-case
Hypocalciuric hypercalcemia presenting as neonatal rib fractures: a newly described mutation of the calcium-sensing receptor gene.
PMID 17110864·Pediatr Emerg Care·2006
5-case
Attenuating growth in children with profound developmental disability: a new approach to an old dilemma.
PMID 17018459·Arch Pediatr Adolesc Med·2006
5-case
Differences in follicle-stimulating hormone secretion between 45,X monosomy Turner syndrome and 45,X/46,XX mosaicism are evident at an early age.
PMID 16968797·J Clin Endocrinol Metab·2006
4-observational
Onset of acquired autoimmune hypothyroidism in infancy: a presentation of delayed gross-motor development and rhabdomyolysis.
PMID 16429278·Eur J Pediatr·2006
5-case
Oxide nanoparticle uptake in human lung fibroblasts: effects of particle size, agglomeration, and diffusion at low concentrations.
PMID 16382966·Environ Sci Technol·2005
8-other
Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life.
PMID 15342833·Pediatrics·2004
8-other
Growth failure in early life: an important manifestation of Turner syndrome.
PMID 12053087·Horm Res·2002
8-other
Androgen-accelerated bone maturation in mice is not attenuated by Faslodex, an estrogen receptor blocker.
PMID 11336922·Bone·2001
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1601 WASHINGTON ST
BOSTON, MA 02118 - Phone
- (617) 425-2000
Quick Facts
- NPI
- 1467426536
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 32
- Publications
- 17
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