L. Quittell

发表

Staphylococcus aureus Nasal Colonization Among Pediatric Cystic Fibrosis Patients and Their Household Contacts

F. Lowy, L. Saiman, A. Dozor, 2009, The Pediatric infectious disease journal.

Adherence with tobramycin inhaled solution and health care utilization

L. Saiman, A. Quittner, B. Briesacher, 2011, BMC pulmonary medicine.

Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health.

Karen A Robinson, C. Goss, K. Robinson, 2007, American journal of respiratory and critical care medicine.

Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism.

M. Knowles, R. Boucher, Z. Zhou, 1999, The New England journal of medicine.

Understanding of safety monitoring in clinical trials by individuals with CF or their parents: A qualitative analysis.

L. Saiman, A. Kern‐Goldberger, L. Quittell, 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Management of non-tuberculous mycobacteria in patients with cystic fibrosis.

L. Quittell, 2004, Paediatric respiratory reviews.

Respiratory microbiology of patients with cystic fibrosis in the United States, 1995 to 2005.

L. Saiman, H. Quinton, B. Marshall, 2009, Chest.

Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator.

A. Prince, L. Saiman, H. Zar, 1995, The Journal of pediatrics.

Clinical spectrum in homozygotes and compound heterozygotes inheriting cystic fibrosis mutation 3849 + 10kbC > T: significance for geneticists.

M. Bialer, C. Denning, L. Quittell, 1995, American journal of medical genetics.

Severe respiratory viral infections in children with history of asymptomatic or mild COVID‐19

P. Zachariah, S. Lovinsky-Desir, L. Quittell, 2021, Pediatric pulmonology.

The Scientific and Social Implications of Unblinding a Study Subject

L. Quittell, 2018, The American journal of bioethics : AJOB.

Impact of colonizing organism in the respiratory tract on the incidence, duration, and time between subsequent hospitalizations among patients with cystic fibrosis.

E. Larson, Jianfang Liu, B. Cohen, 2019, American journal of infection control.

Cystic fibrosis carrier screening in Hispanics.

K. Valverde, H. Zar, C. Denning, 1995, American journal of human genetics.

Pneumocystis carinii pneumonia in infants given adrenocorticotropic hormone for infantile spasms.

C. Foley, M. Fisher, L. Quittell, 1987, The Journal of pediatrics.

Pseudomonas aeruginosa endophthalmitis after lung transplantation for cystic fibrosis.

A. Prince, N. Neu, M. Bye, 1997, The Pediatric infectious disease journal.

Defective CFTR increases synthesis and mass of sphingolipids that modulate membrane composition and lipid signaling Published, JLR Papers in Press, January 14, 2009.

T. Worgall, L. Quittell, F. Keyserman, 2009, Journal of Lipid Research.

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT).

M. White, G. Dolganov, V. Baranov, 1991, Genomics.

Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelines.

J. Yankaskas, B. Marshall, P. Mogayzel, 2007, The Journal of pediatrics.

Facial palsy and idiopathic intracranial hypertension in twins with cystic fibrosis and hypovitaminosis A.

C. Chiriboga, Morris H. Scantlebury, L. Quittell, 2011, Pediatric neurology.

Cystic fibrosis

M. Bye, L. Quittell, J. Ewig, 2004, Lung.

Cell phone intervention to improve adherence: Cystic fibrosis care team, patient, and parent perspectives

Lisa Saiman, L. Saiman, A. Quittner, 2010, Pediatric pulmonology.

Long-term treatment with oral N-acetylcysteine: affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial.

C. Goss, J. Clancy, L. Herzenberg, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Identification of cystic fibrosis mutations.

M. Leppert, V. Baranov, M. Dean, 1991, Advances in experimental medicine and biology.

Infection control knowledge, attitudes, and practices among cystic fibrosis patients and their families

M. Cabana, L. Saiman, Haomiao Jia, 2012, Pediatric pulmonology.

Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothorax.

K. Robinson, P. Flume, B. Marshall, 2010, American journal of respiratory and critical care medicine.

Quantitative analysis of longitudinal response to aerosolized granulocyte-macrophage colony-stimulating factor in two adolescents with autoimmune pulmonary alveolar proteinosis.

D. Cornfield, M. Goris, B. Trapnell, 2009, Chest.

Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health.

C. Goss, K. Robinson, P. Flume, 2007, American journal of respiratory and critical care medicine.

Perceptions of safety monitoring in CF clinical studies and potential impact on future study participation.

L. Saiman, A. Dozor, L. Quittell, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.