Dr. Michael Paul Wajnrajch M.D.
Endocronologist (Pediatric) | Pediatric Endocrinology
462 1st Ave Suite 3c New York NY, 10016About
Dr. Michael Wajnrajch is a pediatric endocrinologist practicing in New York, NY. Dr. Wajnrajch specializes in growth, puberty, diabetes or other disorders related to hormones that produce certain conditions in children and growing young adults. Pediatric endocrinologists possess copious knowledge on hormone chemicals and how they can affect other parts of the body and their functions.
Education and Training
Technion-Israel Inst Of Tech- Fac Of Med- Haifa- Israel 1989
Ruth and Bruce Rappaport Faculty of Medicine 1989
Board Certification
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Heritable disorders of pituitary development.
- Effect of different growth hormone (GH) mutants on the regulation of GH-receptor gene transcription in a human hepatoma cell line.
- Genetic disorders of human growth.
- Growth Hormone Releasing Hormone (GHRH) and the GHRH Receptor.
- Congenital hypopituitarism as a cause of undetectable estriol levels in the maternal triple-marker screen.
- Physiological and pathological growth hormone secretion.
- Limited efficacy of growth hormone (GH) during transition of GH-deficient patients from adolescence to adulthood: a phase III multicenter, double-blind, randomized two-year trial.
- Safety of growth hormone treatment in children born small for gestational age: the US trial and KIGS analysis.
- Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene.
- Gender of pediatric recombinant human growth hormone recipients in the United States and globally.
- Predictors of first-year growth response to a fixed-dose growth hormone treatment in children born small for gestational age: results of an open-label, multicenter trial in the United States.
- Impaired reproduction in adult male, but not female, rats following juvenile treatment with the aromatase inhibitor, exemestane.
- Growth hormone deficiency and central precocious puberty in Klinefelter syndrome: report of a case and review of KIGS database.
- A four-year, open-label, multi-center, randomized, two-arm study of Genotropin® in patients with idiopathic short stature: comparison of an individualized, target-driven treatment regimen to standard dosing of Genotropin® - analysis of two-year data.
- A 4-Year, Open-Label, Multicenter, Randomized Trial of Genotropin® Growth Hormone in Patients with Idiopathic Short Stature: Analysis of 4-Year Data Comparing Efficacy, Efficiency, and Safety between an Individualized, Target-Driven Regimen and Stand
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