B J Rosenstein
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Explore the profile of B J Rosenstein including associated specialties, affiliations and a list of published articles.
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91
Citations
1690
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Recent Articles
1.
Schulze K, Cutchins C, Rosenstein B, Germain-Lee E, OBrien K
Osteoporos Int
. 2006 Mar;
17(5):731-40.
PMID: 16505982
Few longitudinal data are available characterizing bone development in adolescents with cystic fibrosis (CF) although this is a critical time for bone mineralization. Dual energy X-ray absorptiometry (DXA) scans were...
2.
Evaluation of the culture of safety: survey of clinicians and managers in an academic medical center
Pronovost P, Weast B, Holzmueller C, Rosenstein B, Kidwell R, Haller K, et al.
Qual Saf Health Care
. 2003 Dec;
12(6):405-10.
PMID: 14645754
Background: Despite the emphasis on patient safety in health care, few organizations have evaluated the extent to which safety is a strategic priority or their culture supports patient safety. In...
3.
Lai H, FitzSimmons S, Allen D, Kosorok M, Rosenstein B, Campbell P, et al.
N Engl J Med
. 2000 Mar;
342(12):851-9.
PMID: 10727589
Background: It is uncertain whether the growth impairment that occurs in children during long-term treatment with glucocorticoids persists after the medication is discontinued and ultimately affects adult height. Methods: We...
4.
Rosenstein B
Clin Chest Med
. 1998 Oct;
19(3):423-41, v.
PMID: 9759547
Cystic fibrosis (CF) should be considered in patients with a wide variety of clinical presentations and of diverse racial and ethnic backgrounds. In most cases the diagnosis is suggested by...
5.
Rosenstein B, Cutting G
J Pediatr
. 1998 May;
132(4):589-95.
PMID: 9580754
The diagnostic criteria proposed here are not likely to cover every possible clinical scenario, and there will be clinical dilemmas. For the vast majority of patients with CF, the diagnosis...
6.
Hamosh A, FitzSimmons S, Macek Jr M, Knowles M, Rosenstein B, Cutting G
J Pediatr
. 1998 Mar;
132(2):255-9.
PMID: 9506637
No large-scale studies of the incidence or disease severity of cystic fibrosis (CF) in black patients have been reported to date. In this study, the CF Foundation National Patient Registry...
7.
8.
Macek Jr M, Mackova A, Hamosh A, HILMAN B, Selden R, Lucotte G, et al.
Am J Hum Genet
. 1997 May;
60(5):1122-7.
PMID: 9150159
Cystic fibrosis (CF)--an autosomal recessive disorder caused by mutations in CF transmembrane conductance regulator (CFTR) and characterized by abnormal chloride conduction across epithelial membranes, leading to chronic lung and exocrine...
9.
Warren W, Hamosh A, Egan M, Rosenstein B
J Pediatr
. 1997 Apr;
130(4):658-60.
PMID: 9108869
We describe a patient in whom newborn immunoreactive trypsin screening and mutation analysis suggested a diagnosis of cystic fibrosis; however, the clinical course and sweat test results were not consistent...
10.
Laube B, Auci R, Shields D, Christiansen D, Lucas M, Fuchs H, et al.
Am J Respir Crit Care Med
. 1996 Feb;
153(2):752-60.
PMID: 8564129
We tested the hypothesis that recombinant human deoxyribonuclease 1 (rhDNase) reduces airflow obstruction and improves mucociliary clearance in patients with cystic fibrosis (CF), and that improvements seen in FEV1 and...