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WILLIAM CROWLEY, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1417709189Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome.
PMID 19021638·Clin Genet·2009
8-other
Safety of frequent venous blood sampling in a pediatric research population.
PMID 19026428·J Pediatr·2009
4-observational
GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism.
PMID 19567835·Proc Natl Acad Sci U S A·2009
8-other
Inhibition of luteinizing hormone secretion by testosterone in men requires aromatization for its pituitary but not its hypothalamic effects: evidence from the tandem study of normal and gonadotropin-releasing hormone-deficient men.
PMID 18073301·J Clin Endocrinol Metab·2008
8-other
Kisspeptin and GPR54: discovery of a novel pathway in reproduction.
PMID 18601695·J Neuroendocrinol·2008
6-review
Central blockade of oxytocin receptors during mid-late gestation reduces amplitude of slow afterhyperpolarization in supraoptic oxytocin neurons.
PMID 18812459·Am J Physiol Endocrinol Metab·2008
7-preclinical
The relative role of gonadal sex steroids and gonadotropin-releasing hormone pulse frequency in the regulation of follicle-stimulating hormone secretion in men.
PMID 18445673·J Clin Endocrinol Metab·2008
8-other
Use of informatics and information technologies in the clinical research enterprise within US academic medical centers: progress and challenges from 2005 to 2007.
PMID 18525452·J Investig Med·2008
8-other
Relative roles of inhibin B and sex steroids in the negative feedback regulation of follicle-stimulating hormone in men across the full spectrum of seminiferous epithelium function.
PMID 18270253·J Clin Endocrinol Metab·2008
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
Interplay between dose and frequency of GnRH administration in determining pituitary gonadotropin responsiveness.
PMID 18063854·Neuroendocrinology·2008
4-observational
Mass spectrometric and physiological validation of a sensitive, automated, direct immunoassay for serum estradiol using the Architect.
PMID 18023274·Clin Chim Acta·2008
8-other
New genes controlling human reproduction and how you find them.
PMID 18596868·Trans Am Clin Climatol Assoc·2008
6-review
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
PMID 17235395·J Clin Invest·2007
5-case
Neuroendocrine actions and regulation of hypothalamic neuropeptide Y during lactation.
PMID 17241697·Peptides·2007
6-review
Effect of continuous intravenous administration of human metastin 45-54 on the neuroendocrine activity of the hypothalamic-pituitary-testicular axis in the adult male rhesus monkey (Macaca mulatta).
PMID 17412800·Endocrinology·2007
7-preclinical
Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
PMID 17959774·Proc Natl Acad Sci U S A·2007
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
- 259 1ST ST
MINEOLA, NY 11501 - Phone
- (203) 448-7044
Quick Facts
- NPI
- 1417709189
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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