Sherwin A. Gillman
University of California, Irvine
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Featured researches published by Sherwin A. Gillman.
The Journal of Allergy and Clinical Immunology | 1996
William C. Howland; Robert J. Dockhorn; Sherwin A. Gillman; Gary Gross; Darcy Hille; Brandon Simpsonf; John A. Furstf; Gary Feiss; Joseph A. Smith
BACKGROUND One of the risks associated with the use of oral corticosteroids is suppression of adrenocortical function. Triamcinolone acetonide (TAA) aqueous nasal spray administered once daily (110 micrograms and 220 micrograms) has been shown to reduce allergic rhinitis symptoms. OBJECTIVE This multicenter, placebo-controlled, double-blind study determined the effects of TAA aqueous nasal spray, placebo, and oral prednisone on adrenocortical function in patients with allergic rhinitis. METHODS Sixty-four patients received TAA aqueous nasal spray (220 micrograms or 440 micrograms), oral prednisone (10 mg), or placebo once daily for 6 weeks. Adrenocortical function was assessed after cosyntropin stimulation for 6 hours before treatment and after 6 weeks of treatment. RESULTS There was no statistically significant effect on adrenocortical function in patients who received either dose of TAA aqueous nasal spray compared with placebo. In contrast, prednisone produced statistically significant (p < 0.001) reductions in adrenocortical function compared with placebo; reductions occurred in both the mean 6-hour plasma cortisol levels and mean change in 6-hour plasma cortisol levels from pretreatment. CONCLUSION This study demonstrated that, unlike oral prednisone, TAA aqueous nasal spray, in therapeutic doses, did not alter adrenocortical function and was comparable to treatment with placebo in its absence of measurable effects on adrenocortical function.
Pediatric Research | 2014
Bryan M. Harvey; Jane E. Langford; Lucien F. Harthoorn; Sherwin A. Gillman; Todd D. Green; Richard H. Schwartz; A. Wesley Burks
Background:To evaluate the effects of an amino acid–based formula (AAF) with synbiotics on growth and tolerance in healthy infants. The hypoallergenicity of this AAF with synbiotics was evaluated in subjects with cow’s milk allergy (CMA).Methods:Study 1: 115 full-term, healthy infants randomly received an AAF with synbiotics or a commercially available AAF for 16 wk. Subjects’ weight, length, and head circumference were primary outcome measures. Stool characteristics and gastrointestinal (GI) symptoms were secondary outcome measures. Clinical examinations, dietary intake, clinical laboratory results, and adverse events were recorded. Study 2: hypoallergenicity of the AAF with synbiotics was evaluated in 30 infants and children with immunoglobulin E (IgE)–mediated CMA using a double-blind, placebo-controlled food challenge, and a 7-d feeding period.Results:Study 1: comparable results in growth parameters and tolerance were observed for both groups. Minimal differences were observed in stool characteristics and GI symptoms throughout the study. Study 2: all 30 subjects with IgE-mediated CMA completed the study with no allergic reactions detected to challenges.Conclusion:These studies demonstrate that an AAF with synbiotics is safe and well tolerated and promotes normal growth when fed to healthy full-term infants as the sole source of nutrition and is hypoallergenic in subjects with CMA.
The Journal of Pediatrics | 1989
Mark Ellis; Irene Haydik; Sherwin A. Gillman; Leo H. Cummins; Mitchell S. Cairo
and a !ys!ne analogue (MK-521): disposition in man. Br J Clin Pharmacol 1982;14:357-62. 10. Hitchens M, Hand EL, Mulcahy WS. Radioimmunoassay for angiotensin converting enzyme inhibitors. Ligand Q 1981; 4:43. 11. Ferguson RK, Vlasses PH, Swanson BN, et al. Effects of enalapril, a new converting enzyme inhibitor, in hypertension. Clin Pharmacol Ther 1982;32:48-53. 12. Dickstein K, Till AE, Aarsland T, et al. The pharmacokinetics of enalapril in hospitalized patients with congestive heart failure. Br J Clin pharmacol 1987;23:403-10. 13. Biol!az J, Schelling JL, Des Combes J, et al. Enalapril maleate and a lysine analogue (MK-521) in normal volunteers: relationship between plasma drug levels and the renin angiotensin system. Br J Clin Pharmacol 1982;14:363-8. 14. Till AE, Gomez H J, Hichens M, et al. Pharmacokinetics of repeated single oral doses of enalapril maleate (MK-421) in normal volunteers. Biopharm Drug Dispos 1984;5:372-80. 15. Schwartz JB, Addison AT, Abernethy DR, et al. Altered pharmacokinetics and pharmacodynamics of enalapril in patients with congestive heart failure versus patients with hypertension [Abstract]. J Am Coil Cardiol 1985;5:544. 16. Shaddy RE, Teitel DF, Brett C. Short-term hemodynamic effects of eaptopril in infants with congestive heart failure. Am J Dis Child 1988;142:100-5. 17. Bengur AR, Beekman RH, Rocchini AP, et al. Hemodynamic effects of eaptopril in children with congestive or restrictive cardiomyopathy [Abstract]. J Am Coil Cardiol 1988; 11 (suppl A):28A. 18. Artman M, Graham TP. Guidelines for vasodilator therapy of congestive heart failure in infants and children. Am Heart J 1987;113:994-1005.
The Journal of Allergy and Clinical Immunology | 1978
Peter P. Kozak; Jan Gallup; Leo H. Cummins; Sherwin A. Gillman
The concentration of molds isolated in 68 homes of allergic patients in southern California using the Andersen volumetric sampler varied from a minimum of 36 to a maximum of 5,984 isolate/M3 air sampled. The most frequently isolated included Cladosporium, Penicillium species. Alternaria, Sterile (Non-sporulating) Mycelium, Epicoccum, Aspergillus species, Aureobasidium and Dreschlera. Statistically significant higher mold isolates were associated with high shade and high levels of organic debris near the home and poor landscaping and landscape maintenance. Low concentrations of mold isolates were associated with the presence of a central electrostatic filtration system and good compliance with dust controls. The viable mold spore levels were lower in homes where the electrostatic filtration unit was operated continuously rather than intermittently. No statistically significant correlations could be made between indoor mold isolates and any of the following: number and age of the occupants, age and size of home, month of survey or the presence of indoor plants.
The Journal of Allergy and Clinical Immunology | 1977
Peter P. Kozak; Leo H. Cummins; Sherwin A. Gillman
Pediatrics | 1977
Leo H. Cummins; Peter P. Kozak; Sherwin A. Gillman
JAMA Pediatrics | 1977
Stanley P. Galant; Sherwin A. Gillman; Leo H. Cummins; Peter P. Kozak; John J. Orcutt
The Journal of Allergy and Clinical Immunology | 1988
R.Michael Sly; James P. Kemp; John A. Anderson; C. Warren Bierman; Milan L. Brandon; Herbert A. Bronstein; Earl B. Brown; Paul Chervinsky; Frederick C. Cogen; Robert J. Dockhorn; James G. Easton; Constantine J. Falliers; Ira Finegold; Sidney Friedlaender; Clifton T. Furukawa; Sherwin A. Gillman; Leonard S. Girsh; Israel Glazer; Nathan I. Handelman; Paul J. Hannaway; Leslie Hendeles; William E. Hermance; Gregory J. Kadlec; Roger M. Katz; Herbert S. Kaufman; Allan Knight; Daniel Kordansky; Richard A. Krumholz; James M. Labraico; Gilbert Lanoff
The Journal of Allergy and Clinical Immunology | 1988
Mark Ellis; Irene Haydik; Sherwin A. Gillman; Leo H. Cummins; Mitchell S. Cairo
Pediatrics | 1978
Peter P. Kozak; Leo H. Cummins; Sherwin A. Gillman