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READE QUINTON, MD
MD
Anatomic Pathology Physician
NPI: 1689141335Individual
Specialties, Licenses & Credentials
Anatomic Pathology PhysicianPrimary
Pathology — Anatomic Pathology
Code: 207ZP0101X
64436(MN)
Research & Publications (20)
Enclomiphene, an estrogen receptor antagonist for the treatment of testosterone deficiency in men.
PMID 19204885·IDrugs·2009
6-review
Estrogen biosynthesis in human H295 adrenocortical carcinoma cells.
PMID 19026713·Mol Cell Endocrinol·2009
8-other
Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations.
PMID 18710468·Clin Endocrinol (Oxf)·2009
8-other
Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.
PMID 18559922·J Clin Endocrinol Metab·2008
7-preclinical
Selecting forensic pathology as a career: a survey of the past with an eye on the future.
PMID 18520476·Am J Forensic Med Pathol·2008
8-other
Impact of standardised reporting in adrenocortical carcinoma: a single centre clinicopathological review.
PMID 18515402·J Clin Pathol·2008
8-other
The role of the aryl hydrocarbon receptor-interacting protein gene in familial and sporadic pituitary adenomas.
PMID 18381572·J Clin Endocrinol Metab·2008
8-other
Therapeutic response to metformin in an underweight patient with polycystic ovarian syndrome.
PMID 18222436·Fertil Steril·2008
5-case
The investigation and management of severe hyperandrogenism pre- and postmenopause: non-tumor disease is strongly associated with metabolic syndrome and typically responds to insulin-sensitization with metformin.
PMID 18210332·Gynecol Endocrinol·2008
8-other
Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.
PMID 18177653·Fertil Steril·2008
5-case
Health-related quality of life instruments in studies of adult men with testosterone deficiency syndrome: a critical assessment.
PMID 19090941·J Sex Med·2008
1-meta
Insulin resistance causing severe postmenopausal hyperandrogenism.
PMID 18005967·Int J Gynaecol Obstet·2008
5-case
Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
PMID 18596921·J Clin Invest·2008
5-case
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
PMID 17235395·J Clin Invest·2007
5-case
The burden of testosterone deficiency syndrome in adult men: economic and quality-of-life impact.
PMID 17627750·J Sex Med·2007
1-meta
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.
PMID 17535987·J Clin Endocrinol Metab·2007
8-other
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
PMID 16764984·Mol Cell Endocrinol·2006
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
- 200 1ST ST SW
ROCHESTER, MN 55905 - Phone
- (507) 284-2511
Quick Facts
- NPI
- 1689141335
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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