Brenda Kohn, M.D.

Publications

Publications

1. Gold-von Simson G; Kohn B; Axelrod FB. "Cushing syndrome from topical foam steroid use in an adolescent male". Clinical pediatrics. 2006; 45: 97 (#J0115817)
2. Kamboj, Manmohan K; Zhou, Ping; Molofsky, Walter J; Franklin, Bonita; Shah, Bina; David, Raphael; Kohn, Brenda. "Hemorrhagic pituitary apoplexy in an 18 year-old male presenting as non-ketotic hyperglycemic coma (NKHC)". Journal of pediatric endocrinology & metabolism. 2005; 18: 611 (#J0125675)
3. Martin Rojas-Marcos, Patricia; David, Raphael; Kohn, Brenda. "Hormonal effects in infants conceived by assisted reproductive technology". Pediatrics. 2005; 116: 190 (#J0110222)
4. Kamboj MK; Axelrod FB; David R; Geffner ME; Novogroder M; Oberfield SE; Turco JH; Maayan C; Kohn B. "Growth hormone treatment in children with familial dysautonomia". Journal of pediatrics. 2004; 144: 63 (#J0067189)
5. Ping, Z; Kamboj, M; Pina, P; Marlon, A; Pelavin, P; Kohn, B. "Characterization of a severe 25-hydroxyvitamin D 1-alpha hydroxylase defect (Vitamin D Dependent Rickets type 1) in a novel family [abstract]". Pediatric research. 2003; 53: 151A (#J0052485)
6. Hiroi, N; Chrousos, GP; Kohn, B; Lafferty, A; Abu-Asab, M; Bonat, S; White, A; Bornstein, SR. "Adrenocortical-pituitary hybrid tumor causing Cushing's syndrome". Journal of clinical endocrinology & metabolism. 2001; 86: 2631 (#J0099683)
7. Chin D; Shackleton C; Prasad VK; Kohn B; David R; Imperato-McGinley J; Cohen H; McMahon DJ; Oberfield SE. "Increased 5alpha-reductase and normal 11beta-hydroxysteroid dehydrogenase metabolism of C19 and C21 steroids in a young population with polycystic ovarian syndrome". Journal of pediatric endocrinology & metabolism. 2000; 13: 253 (#J0009094)
8. Chin D; Sklar C; Donahue B; Uli N; Geneiser N; Allen J; Nirenberg A; David R; Kohn B; Oberfield SE. "Thyroid dysfunction as a late effect in survivors of pediatric medulloblastoma/primitive neuroectodermal tumors: a comparison of hyperfractionated versus conventional radiotherapy". Cancer. 1997; 80: 798 (#J0104478)
9. Kohn B; Day D; Alemzadeh R; Enerio D; Patel SV; Pelczar JV; Speiser PW. "Splicing mutation in CYP21 associated with delayed presentation of salt-wasting congenital adrenal hyperplasia". American journal of medical genetics. 1995; 57: 450 (#J0005475)

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