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3. Quantitative Characterization of Respiratory Patterns on Dynamic Higher Temporal Resolution MRI to Stratify Postacute Covid‐19 Patients by Cardiopulmonary Symptom Burden

Author

Azour, Lea, primary, Rusinek, Henry, additional, Mikheev, Artem, additional, Landini, Nicholas, additional, Keerthivasan, Mahesh Bharath, additional, Maier, Christoph, additional, Bagga, Barun, additional, Bruno, Mary, additional, Condos, Rany, additional, Moore, William H., additional, and Chandarana, Hersh, additional

Published
2024
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4. Disease Severity and Quality of Life in Patients With Idiopathic Pulmonary Fibrosis: A Cross-Sectional Analysis of the IPF-PRO Registry

Author

Asi, Wael, Baker, Albert, Beegle, Scott, Belperio, John A., Condos, Rany, Cordova, Francis, Culver, Daniel A., de Andrade, Joao A.M., Dilling, Daniel, Flaherty, Kevin R., Glassberg, Marilyn, Gulati, Mridu, Guntupalli, Kalpalatha, Gupta, Nishant, Hajari Case, Amy, Hotchkin, David, Huie, Tristan, Kaner, Robert, Kim, Hyun, Kreider, Maryl, Lancaster, Lisa, Lasky, Joseph, Lederer, David, Lee, Doug, Liesching, Timothy, Lipchik, Randolph, Lobo, Jason, Mageto, Yolanda, Menon, Prema, Morrison, Lake, Namen, Andrew, Oldham, Justin, Raj, Rishi, Ramaswamy, Murali, Russell, Tonya, Sachs, Paul, Safdar, Zeenat, Sigal, Barry, Silhan, Leann, Strek, Mary, Suliman, Sally, Tabak, Jeremy, Walia, Rajat, Whelan, Timothy P., O’Brien, Emily C., Hellkamp, Anne S., Neely, Megan L., Swaminathan, Aparna, Bender, Shaun, Snyder, Laurie D., Conoscenti, Craig S., Todd, Jamie L., Palmer, Scott M., and Leonard, Thomas B.

Published
2020
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6. Comparison of Clinical Measures Among Interstitial Lung Disease (ILD) Patients with Usual Interstitial Pneumonia (UIP) Patterns on High-Resolution Computed Tomography

Author

Gibson, Charlisa D., Bhatt, Alok, Deshwal, Himanshu, Li, Xiaochun, Goldberg, Judith D., Ko, Jane, and Condos, Rany

Subjects
Medical research -- Comparative analysis, Bacterial pneumonia -- Comparative analysis, Societies -- Comparative analysis, Pulmonary fibrosis -- Comparative analysis, Comorbidity -- Comparative analysis, Medical colleges -- Comparative analysis, CT imaging -- Comparative analysis, Associations, institutions, etc. -- Comparative analysis, Diagnostic imaging -- Comparative analysis, Medicine, Experimental -- Comparative analysis, Lung diseases, Obstructive -- Comparative analysis, Smoking -- Comparative analysis, Pneumonia -- Comparative analysis, Health
Abstract

Purpose Idiopathic Pulmonary Fibrosis is a progressive and fatal interstitial lung disease (ILD) characterized by a typical radiographic or histologic usual interstitial pneumonia (UIP) pattern. In 2018, diagnostic categories of UIP based on computed tomography patterns were revised by the Fleischner Society. The study aimed to describe differences in comorbidities and spirometry in ILD patients that were characterized by high-resolution computed tomography (HRCT) images as having a typical, probable, indeterminate, and alternative diagnosis of UIP. Methods We retrospectively studied 80 ILD patients from 2017 to 2019. Typical UIP was defined using the Fleischner Society diagnostic criteria for IPF. Atypical UIP was reached by consensus after a multidisciplinary clinical-radiological-pathological review of patient data. Baseline characteristics, comorbidities, and spirometry were compared among the four subgroups. Results Among 80 patients, 59% were male, 61% had a history of smoking, and the mean age was 67.7 ± 10 years (SD). A typical UIP pattern was more frequently observed among patients with chronic obstructive pulmonary disease (COPD) (p < 0.001) and pulmonary hypertension (p = 0.03). Of 30 patients with COPD, 14 had emphysema, while 10 had IPF. After adjusting for forced expiratory volume in one second (FEV.sub.1) in liters, change of FEV.sub.1% from baseline to 6-12 months, age, and sex, only COPD remained significantly associated with typical UIP (p = 0.018). Tobacco use was not significantly associated with any radiographic type (p = 0.199). Conclusion Typical UIP was prevalent among COPD/emphysema patients. Although smoking has a strong association with IPF, we did not find a significant association with smoking and typical UIP in our cohort., Author(s): Charlisa D. Gibson [sup.1], Alok Bhatt [sup.1], Himanshu Deshwal [sup.1], Xiaochun Li [sup.2], Judith D. Goldberg [sup.2], Jane Ko [sup.3], Rany Condos [sup.1] Author Affiliations: (1) grid.137628.9, 0000 0004 [...]

Published
2020
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7. Advances in Targeted Therapy for Progressive Fibrosing Interstitial Lung Disease

Author

Gibson, Charlisa D., Kugler, Matthias C., Deshwal, Himanshu, Munger, John S., and Condos, Rany

Subjects
Lung diseases -- Care and treatment -- Development and progression, Mortality, Immune response -- Health aspects, Medical colleges -- Health aspects, Drug approval -- Health aspects, Evidence-based medicine -- Health aspects, Health
Abstract

Progressive fibrosing interstitial lung disease (PF-ILD) has been redefined as a new clinical syndrome that shares similar genetics, pathophysiology, and natural history to idiopathic pulmonary fibrosis (IPF). IPF is the most common form of idiopathic interstitial pneumonias, which is progressive in nature and is associated with significant mortality. Therapies targeting an inflammatory and/or immune response have not been consistently effective or well tolerated in patients with IPF. The two antifibrotic drugs approved for IPF treatment, nintedanib and pirfenidone, have been shown to reduce lung function decline in PF-ILD. Novel uses of antifibrotic therapy are emerging due to a paucity of evidence-based treatments for multiple ILD subtypes. In this review, we describe the current body of knowledge on antifibrotic therapy and immunomodulators in PF-ILD, drawing from experience in IPF where appropriate., Author(s): Charlisa D. Gibson [sup.1], Matthias C. Kugler [sup.1], Himanshu Deshwal [sup.1], John S. Munger [sup.1], Rany Condos [sup.1] Author Affiliations: (1) grid.137628.9, 0000 0004 1936 8753, Division of Pulmonary [...]

Published
2020
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10. Respiratory care in familial dysautonomia: Systematic review and expert consensus recommendations

Author

Kazachkov, Mikhail, Palma, Jose-Alberto, Norcliffe-Kaufmann, Lucy, Bar-Aluma, Bat-El, Spalink, Christy L., Barnes, Erin P., Amoroso, Nancy E., Balou, Stamatela M., Bess, Shay, Chopra, Arun, Condos, Rany, Efrati, Ori, Fitzgerald, Kathryn, Fridman, David, Goldenberg, Ronald M., Goldhaber, Ayelet, Kaufman, David A., Kothare, Sanjeev V., Levine, Jeremiah, Levy, Joseph, Lubinsky, Anthony S., Maayan, Channa, Moy, Libia C., Rivera, Pedro J., Rodriguez, Alcibiades J., Sokol, Gil, Sloane, Mark F., Tan, Tina, and Kaufmann, Horacio

Published
2018
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11. Emerging Therapeutic Options for Refractory Pulmonary Sarcoidosis: The Evidence and Proposed Mechanisms of Action.

Author

Nelson, Nathaniel C., Kogan, Rebecca, Condos, Rany, and Hena, Kerry M.

Subjects
SARCOIDOSIS, PATIENT experience, REFRACTORY materials, DISEASE progression, PATIENTS' attitudes
Abstract

Sarcoidosis is a systemic disease with heterogenous clinical phenotypes characterized by non-necrotizing granuloma formation in affected organs. Most disease either remits spontaneously or responds to corticosteroids and second-line disease-modifying therapies. These medications are associated with numerous toxicities that can significantly impact patient quality-of-life and often limit their long-term use. Additionally, a minority of patients experience chronic, progressive disease that proves refractory to standard treatments. To date, there are limited data to guide the selection of alternative third-line medications for these patients. This review will outline the pathobiological rationale behind current and emerging therapeutic agents for refractory or drug-intolerant sarcoidosis and summarize the existing clinical evidence in support of their use. [ABSTRACT FROM AUTHOR]

Published
2024
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13. Disparities in Lung Transplant among Patients with Idiopathic Pulmonary Fibrosis: An Analysis of the IPF-PRO Registry

Author

Swaminathan, Aparna C., primary, Hellkamp, Anne S., additional, Neely, Megan L., additional, Bender, Shaun, additional, Paoletti, Luca, additional, White, Eric S., additional, Palmer, Scott M., additional, Whelan, Timothy P. M., additional, Dilling, Daniel F., additional, Baker, Albert, additional, Beegle, Scott, additional, Belperio, John A., additional, Condos, Rany, additional, Cordova, Francis, additional, Culver, Daniel A., additional, Fitzgerald, John, additional, Flaherty, Kevin R., additional, Gibson, Kevin, additional, Gulati, Mridu, additional, Guntupalli, Kalpalatha, additional, Gupta, Nishant, additional, Case, Amy Hajari, additional, Hotchkin, David, additional, Huie, Tristan J., additional, Kaner, Robert J., additional, Kim, Hyun J., additional, Lancaster, Lisa H., additional, Lasky, Joseph A., additional, Lee, Doug, additional, Liesching, Timothy, additional, Lipchik, Randolph, additional, Lobo, Jason, additional, Luckhardt, Tracy R., additional, Mageto, Yolanda, additional, Menon, Prema, additional, Morrison, Lake, additional, Namen, Andrew, additional, Oldham, Justin M., additional, Paul, Tessy, additional, Zhang, David, additional, Porteous, Mary, additional, Raj, Rishi, additional, Ramaswamy, Murali, additional, Russell, Tonya, additional, Sachs, Paul, additional, Safdar, Zeenat, additional, Shafazand, Shirin, additional, Siddiqi, Ather, additional, Sigal, Barry, additional, Strek, Mary E., additional, Suliman, Sally, additional, Tabak, Jeremy, additional, and Walia, Rajat, additional

Published
2022
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14. The clinical impact of the Covid-19 pandemic first wave on patients with cystic fibrosis in New York

Author

Simonson, Joseph L., primary, Esposito, Christine, additional, Frantzen, Theresa, additional, Henthorne, Katherine, additional, Espinal, Aileen, additional, Romano, Serena, additional, Ramdeo, Ramona, additional, Trentacoste, Jessica, additional, Tsang, Donna, additional, LaVecchia, Geralyn, additional, Abdullah, Robert, additional, Berdella, Maria, additional, Bonitz, Lynn, additional, Condos, Rany, additional, Constantinescu, Andrei, additional, DeCelie-Germana, Joan K., additional, DiMango, Emily, additional, Draine, Myah, additional, Gimeli, Tara, additional, Giusti, Robert, additional, Guzman, Jessenia, additional, Hammouda, Soumia, additional, Keating, Claire, additional, Kier, Catherine, additional, Lennox, Alison T., additional, Liriano, Carmen, additional, Messer, Zachary, additional, Plachta, Amy, additional, Sadeghi, Hossein, additional, Schwind, Elinor, additional, Stables-Carney, Teresa, additional, Walker, Patricia, additional, and Wang, Janice, additional

Published
2022
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16. THE CLINICAL IMPACT OF COVID-19 ON CYSTIC FIBROSIS PATIENTS IN NEW YORK

Author

Simonson, Joseph, primary, ESPOSITO, Christine, additional, Frantzen, Theresa, additional, Henthorne, Katherine, additional, Ramdeo, Ramona, additional, Trentacoste, Jessica, additional, Tsang, Donna, additional, La Vecchia, Geralyn, additional, Abdullah, Robert, additional, Berdella, Maria, additional, Bonitz, Lynn, additional, Condos, Rany, additional, Constantinescu, Andrei, additional, DeCelie- Germana, Joan, additional, Di Mango, Emily, additional, Giusti, Robert, additional, Keating, Claire, additional, Kier, Catherine, additional, Lennox, Alison, additional, Sadeghi, Hossein, additional, Walker, Patricia, additional, and Wang, Janice, additional

Published
2021
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18. Antifibrotic Drug Use in Patients with Idiopathic Pulmonary Fibrosis. Data from the IPF-PRO Registry

Author

Salisbury, Margaret L., primary, Conoscenti, Craig S., additional, Culver, Daniel A., additional, Yow, Eric, additional, Neely, Megan L., additional, Bender, Shaun, additional, Hartmann, Nadine, additional, Palmer, Scott M., additional, Leonard, Thomas B., additional, Baker, Albert, additional, Beegle, Scott, additional, Belperio, John, additional, Condos, Rany, additional, Cordova, Francis, additional, Dilling, Daniel, additional, Fitzgerald, John, additional, Flaherty, Kevin R., additional, Gibson, Kevin, additional, Gulati, Mridu, additional, Guntupalli, Kalpalatha, additional, Gupta, Nishant, additional, Case, Amy Hajari, additional, Hotchkin, David, additional, Huie, Tristan, additional, Kaner, Robert, additional, Kim, Hyun, additional, Lancaster, Lisa, additional, Lasky, Joseph A., additional, Lee, Doug, additional, Liesching, Timothy, additional, Lipchik, Randolph, additional, Lobo, Jason, additional, Luckhardt (formerly Joao de Andrade), Tracy, additional, Mageto, Yolanda, additional, Malik, Numaan, additional, Menon, Prema, additional, Morrison, Lake, additional, Namen, Andrew, additional, Oldham, Justin, additional, Paul, Tessy, additional, Podolanczuk, Anna, additional, Porteous, Mary, additional, Raj, Rishi, additional, Ramaswamy, Murali, additional, Russell, Tonya, additional, Sachs, Paul, additional, Safdar, Zeenat, additional, Shafazand, Shirin, additional, Siddiqi, Ather, additional, Sigal, Barry, additional, Strek, Mary, additional, Suliman, Sally, additional, Tabak, Jeremy, additional, Walia, Rajat, additional, and Whelan, Timothy, additional

Published
2020
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22. Disease Severity and Quality of Life in Patients With Idiopathic Pulmonary Fibrosis

Author

O’Brien, Emily C., primary, Hellkamp, Anne S., additional, Neely, Megan L., additional, Swaminathan, Aparna, additional, Bender, Shaun, additional, Snyder, Laurie D., additional, Culver, Daniel A., additional, Conoscenti, Craig S., additional, Todd, Jamie L., additional, Palmer, Scott M., additional, Leonard, Thomas B., additional, Asi, Wael, additional, Baker, Albert, additional, Beegle, Scott, additional, Belperio, John A., additional, Condos, Rany, additional, Cordova, Francis, additional, de Andrade, Joao A.M., additional, Dilling, Daniel, additional, Flaherty, Kevin R., additional, Glassberg, Marilyn, additional, Gulati, Mridu, additional, Guntupalli, Kalpalatha, additional, Gupta, Nishant, additional, Hajari Case, Amy, additional, Hotchkin, David, additional, Huie, Tristan, additional, Kaner, Robert, additional, Kim, Hyun, additional, Kreider, Maryl, additional, Lancaster, Lisa, additional, Lasky, Joseph, additional, Lederer, David, additional, Lee, Doug, additional, Liesching, Timothy, additional, Lipchik, Randolph, additional, Lobo, Jason, additional, Mageto, Yolanda, additional, Menon, Prema, additional, Morrison, Lake, additional, Namen, Andrew, additional, Oldham, Justin, additional, Raj, Rishi, additional, Ramaswamy, Murali, additional, Russell, Tonya, additional, Sachs, Paul, additional, Safdar, Zeenat, additional, Sigal, Barry, additional, Silhan, Leann, additional, Strek, Mary, additional, Suliman, Sally, additional, Tabak, Jeremy, additional, Walia, Rajat, additional, and Whelan, Timothy P., additional

Published
2020
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23. Associations between resources and practices of ILD centers and outcomes in patients with idiopathic pulmonary fibrosis: data from the IPF-PRO Registry.

Author

de Andrade, Joao A., Kulkarni, Tejaswini, Neely, Megan L., Hellkamp, Anne S., Case, Amy Hajari, Culver, Daniel A., Guntupalli, Kalpalatha, Bender, Shaun, Conoscenti, Craig S., Snyder, Laurie D., the IPF-PRO Registry Investigators, Baker, Albert, Beegle, Scott, Belperio, John A., Condos, Rany, Cordova, Francis, Dilling, Daniel, Fitzgerald, John, Silhan, Leann, and Flaherty, Kevin R.

Subjects
IDIOPATHIC pulmonary fibrosis, TREATMENT effectiveness, LUNG transplantation, BENCHMARKING (Management), INTERSTITIAL lung diseases, PERFORMANCE management
Abstract

Background: Performance benchmarks for the management of idiopathic pulmonary fibrosis (IPF) have not been established. We used data from the IPF-PRO Registry, an observational registry of patients with IPF managed at sites across the US, to examine associations between the characteristics of the enrolling sites and patient outcomes.Methods: An online survey was used to collect information on the resources, operations, and self-assessment practices of IPF-PRO Registry sites that enrolled ≥ 10 patients. Site variability in 1-year event rates of clinically relevant outcomes, including death, death or lung transplant, and hospitalization, was assessed. Models were adjusted for differences in patient case mix by adjusting for known predictors of each outcome. We assessed whether site-level heterogeneity existed for each patient-level outcome, and if so, we investigated potential drivers of the heterogeneity.Results: All 27 sites that enrolled ≥ 10 patients returned the questionnaire. Most sites were actively following > 100 patients with IPF (70.4%), had a lung transplant program (66.7%), and had a dedicated ILD nurse leader (77.8%). Substantial heterogeneity was observed in the event rates of clinically relevant outcomes across the sites. After controlling for patient case mix, there were no outcomes for which the site variance component was significantly different from 0, but the p-value for hospitalization was 0.052. Starting/completing an ILD-related quality improvement project in the previous 2 years was associated with a lower risk of hospitalization (HR 0.60 [95% CI 0.44, 0.82]; p = 0.001).Conclusions: Analyses of data from patients with IPF managed at sites across the US found no site-specific characteristics or practices that were significantly associated with clinically relevant outcomes after adjusting for patient case mix. Trial registration ClinicalTrials.gov, NCT01915511. Registered 5 August 2013, https://clinicaltrials.gov/ct2/show/NCT01915511. [ABSTRACT FROM AUTHOR]

Published
2022
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29. Hospitalizations in patients with idiopathic pulmonary fibrosis.

Author

Kim, Hyun J., Snyder, Laurie D., Adegunsoye, Ayodeji, Neely, Megan L., Bender, Shaun, White, Eric S., Conoscenti, Craig S., Strek, Mary E., The IPF-PRO Registry Investigators, Baker, Albert, Beegle, Scott, Belperio, John A., Condos, Rany, Cordova, Francis, Culver, Daniel A., Dilling, Daniel, Fitzgerald, John, Silhan, Leann, Flaherty, Kevin R., and Gibson, Kevin

Subjects
IDIOPATHIC pulmonary fibrosis, HOSPITAL care, TREATMENT effectiveness, PULMONARY hypertension, PULMONARY function tests
Abstract

Background: Hospitalizations are common among patients with idiopathic pulmonary fibrosis (IPF). We investigated the impact of hospitalizations on outcomes in patients with IPF.Methods: The IPF-PRO Registry is an observational US registry that enrolled patients with IPF that was diagnosed or confirmed at the enrolling center in the previous 6 months. Associations between patient characteristics and hospitalization, and between hospitalization and mortality, were analyzed using Cox regression models.Results: A total of 1002 patients with IPF were enrolled into the IPF-PRO Registry. Over a median follow-up time of 23.7 months (maximum: 67.0 months), 568 patients (56.7%) had at least one hospitalization. Of these patients, 319 (56.2%) had at least one respiratory-related hospitalization and 120 (21.1%) had at least one hospitalization with ventilatory support. Younger age (HR 0.68 [95% CI 0.55, 0.84] per 5-year increase for patients < 62 years), lower BMI (0.96 [0.93, 0.98] per 1-point increase), lower FVC % predicted (0.90 [0.83, 0.97] per 10% increase), oxygen use at rest (2.85 [2.18, 3.72]) and history of pulmonary hypertension (2.02 [1.37, 2.96]) at enrollment were associated with an increased risk of respiratory-related hospitalization during follow-up. In a multivariable model, there was an eightfold increase in the risk of mortality during hospitalization or within 90 days of discharge compared with outside of this period. The risk of mortality associated with a respiratory hospitalization or a hospitalization with ventilatory support was even greater.Conclusions: Data from the IPF-PRO Registry demonstrate that hospitalizations are common among patients with IPF. The risk of mortality during hospitalization or within 90 days of discharge was high, particularly among patients who were hospitalized for a respiratory cause or received ventilatory support. Trial registration ClinicalTrials.gov, NCT01915511. Registered 5 August 2013, https://clinicaltrials.gov/ct2/show/NCT01915511. [ABSTRACT FROM AUTHOR]

Published
2021
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34. Non-tuberculosis mycobacterium related bronchiectasis is associated with oral commensals in the lower airway

Author

Sulaiman, Imran, primary, Wu, Benjamin, additional, Tsay, Jun-Chieh, additional, Li, Yonghua, additional, Scott, Adrienne, additional, Basavaraj, Ashwin, additional, Bessich, Jamie, additional, Michaud, Gaetane, additional, Rafeq, Samaan, additional, Donington, Jessica, additional, Condos, Rany, additional, Kamelhar, David, additional, Addrizzo-Harris, Doreen, additional, and Segal, Leopoldo, additional

Published
2019
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38. Circulating matrix metalloproteinases and tissue metalloproteinase inhibitors in patients with idiopathic pulmonary fibrosis in the multicenter IPF-PRO Registry cohort.

Author

Todd, Jamie L., Vinisko, Richard, Liu, Yi, Neely, Megan L., Overton, Robert, Flaherty, Kevin R., Noth, Imre, Newby, L. Kristin, Lasky, Joseph A., Olman, Mitchell A., Hesslinger, Christian, Leonard, Thomas B., Palmer, Scott M., Belperio, John A., on behalf of the IPF-PRO Registry investigators, Asi, Wael, Baker, Albert, Beegle, Scott, Condos, Rany, and Cordova, Francis

Subjects
IDIOPATHIC pulmonary fibrosis, TISSUE inhibitors of metalloproteinases, MATRIX metalloproteinases, CARBOXYHEMOGLOBIN, CARBON monoxide, EXTRACELLULAR matrix
Abstract

Background: Matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMPs) play important roles in the turnover of extracellular matrix and in the pathogenesis of idiopathic pulmonary fibrosis (IPF). This study aimed to determine the utility of circulating MMPs and TIMPs in distinguishing patients with IPF from controls and to explore associations between MMPs/TIMPs and measures of disease severity in patients with IPF.Methods: The IPF cohort (n = 300) came from the IPF-PRO Registry, an observational multicenter registry of patients with IPF that was diagnosed or confirmed at the enrolling center in the past 6 months. Controls (n = 100) without known lung disease came from a population-based registry. Generalized linear models were used to compare circulating concentrations of MMPs 1, 2, 3, 7, 8, 9, 12, and 13 and TIMPs 1, 2, and 4 between patients with IPF and controls, and to investigate associations between circulating levels of these proteins and measures of IPF severity. Multivariable models were fit to identify the MMP/TIMPs that best distinguished patients with IPF from controls.Results: All the MMP/TIMPs analyzed were present at significantly higher levels in patients with IPF compared with controls except for TIMP2. Multivariable analyses selected MMP8, MMP9 and TIMP1 as top candidates for distinguishing patients with IPF from controls. Higher concentrations of MMP7, MMP12, MMP13 and TIMP4 were significantly associated with lower diffusion capacity of the lung for carbon monoxide (DLCO) % predicted and higher composite physiologic index (worse disease). MMP9 was associated with the composite physiologic index. No MMP/TIMPs were associated with forced vital capacity % predicted.Conclusions: Circulating MMPs and TIMPs were broadly elevated among patients with IPF. Select MMP/TIMPs strongly associated with measures of disease severity. Our results identify potential MMP/TIMP targets for further development as disease-related biomarkers. [ABSTRACT FROM AUTHOR]

Published
2020
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39. Evaluation of the airway microbiome in nontuberculous mycobacteria disease

Author

Sulaiman, Imran, primary, Wu, Benjamin G., additional, Li, Yonghua, additional, Scott, Adrienne S., additional, Malecha, Patrick, additional, Scaglione, Benjamin, additional, Wang, Jing, additional, Basavaraj, Ashwin, additional, Chung, Samuel, additional, Bantis, Katrina, additional, Carpenito, Joseph, additional, Clemente, Jose C., additional, Shen, Nan, additional, Bessich, Jamie, additional, Rafeq, Samaan, additional, Michaud, Gaetene, additional, Donington, Jessica, additional, Naidoo, Charissa, additional, Theron, Grant, additional, Schattner, Gail, additional, Garofano, Suzette, additional, Condos, Rany, additional, Kamelhar, David, additional, Addrizzo-Harris, Doreen, additional, and Segal, Leopoldo N., additional

Published
2018
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48. Evaluation of subjective effects of aripiprazole and methamphetamine in methamphetamine-dependent volunteers

Author

Newton, Thomas F., primary, Reid, Malcolm S., additional, De La Garza, Richard, additional, Mahoney, James J., additional, Abad, Antonio, additional, Condos, Rany, additional, Palamar, Joseph, additional, Halkitis, Perry N., additional, Mojisak, Jurji, additional, Anderson, Ann, additional, Li, Shou-Hua, additional, and Elkashef, Ahmed, additional

Published
2008
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49. Gene expression profiles of bronchoalveolar cells in pulmonary TB

Author

Raju, Bindu, primary, Hoshino, Yoshihiko, additional, Belitskaya-Lévy, Ilana, additional, Dawson, Rod, additional, Ress, Stanley, additional, Gold, Jeffrey A., additional, Condos, Rany, additional, Pine, Richard, additional, Brown, Stuart, additional, Nolan, Anna, additional, Rom, William N., additional, and Weiden, Michael D., additional

Published
2008
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