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MICHAEL GEFFNER, MD
MD
Pediatric Neurodevelopmental Disabilities Physician
NPI: 1619199551Individual
Specialties, Licenses & Credentials
Pediatric Neurodevelopmental Disabilities PhysicianPrimary
Pediatrics — Neurodevelopmental Disabilities
Code: 2080P0008X
MA68792(NJ)
Research & Publications (20)
Optic nerve hypoplasia in North America: a re-appraisal of perinatal risk factors.
PMID 19141149·Acta Ophthalmol·2010
8-other
Use of recombinant human growth hormone in children with thalassemia.
PMID 19153505·Horm Res·2009
8-other
Efficacy of recombinant human interleukin-10 in prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis in subjects with increased risk.
PMID 19214137·Pancreas·2009
4-observational
Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy.
PMID 19523546·Bone·2009
5-case
For debate: Aromatase inhibitors to augment height: have we lost our inhibitions?
PMID 18367995·Pediatr Endocrinol Rev·2008
6-review
Neuroradiographic, endocrinologic, and ophthalmic correlates of adverse developmental outcomes in children with optic nerve hypoplasia: a prospective study.
PMID 18250116·Pediatrics·2008
8-other
The 88th Annual Meeting of the Endocrine Society, June 24-27, 2006, Boston MA, USA: selected pediatric presentations.
PMID 18368001·Pediatr Endocrinol Rev·2008
8-other
Impact of the primary aetiology upon the clinical outcome of adults with childhood-onset GH deficiency.
PMID 17984238·Eur J Endocrinol·2007
4-observational
Increased aggression and activity level in 3- to 11-year-old girls with congenital adrenal hyperplasia (CAH).
PMID 17673215·Horm Behav·2007
4-observational
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
Compound heterozygosity of a frameshift mutation in the coding region and a single base substitution in the promoter of the ACTH receptor gene in a family with isolated glucocorticoid deficiency.
PMID 17128564·J Pediatr Endocrinol Metab·2006
5-case
Improvement in risk factors for metabolic syndrome and insulin resistance in overweight youth who are treated with lifestyle intervention.
PMID 16682491·Pediatrics·2006
8-other
A hypocalcemic child with a novel activating mutation of the calcium-sensing receptor gene: successful treatment with recombinant human parathyroid hormone.
PMID 16608894·J Clin Endocrinol Metab·2006
5-case
Endocrinological and auxological abnormalities in young children with optic nerve hypoplasia: a prospective study.
PMID 16423602·J Pediatr·2006
8-other
Interferon alfa-2b in combination with ribavirin for the treatment of chronic hepatitis C in children: efficacy, safety, and pharmacokinetics.
PMID 16250032·Hepatology·2005
2-rct
Baseline characteristics and response to 2 years of growth hormone (GH) replacement of hypopituitary patients with GH deficiency due to adult-onset craniopharyngioma in comparison with patients with nonfunctioning pituitary adenoma: data from KIMS (Pfizer International Metabolic Database).
PMID 15928246·J Clin Endocrinol Metab·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1 MERCK DR, WS3D-90
WHITEHOUSE STATION, NJ 08889 - Phone
- (908) 423-3426
Quick Facts
- NPI
- 1619199551
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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