Research Topics
| Lewis RubinSummaryAffiliation: University of California Country: USA Publications
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Publications
Iloprost inhalation solution for the treatment of pulmonary arterial hypertensionHenry H Hsu
CoTherix, Inc, 5000 Shoreline Court, San Francisco, CA 94080, USA
Expert Opin Pharmacother 6:1921-30. 2005..This article reviews iloprost inhalation solution, the most recently approved form of prostacyclin therapy that is delivered directly to the lungs by inhalation...
Function of Kv1.5 channels and genetic variations of KCNA5 in patients with idiopathic pulmonary arterial hypertensionCarmelle V Remillard
Department of Medicine, University of California San Diego, 9500 Gilman Dr, MC 0725, La Jolla, CA 92093 0725, USA
Am J Physiol Cell Physiol 292:C1837-53. 2007..g., nicotine and ET-1); 2) novel SNPs in KCNA5 are present in IPAH patients; and 3) SNPs in the promoter and translated regions of KCNA5 may underlie the altered expression and/or function of Kv1.5 channels in PASMC from IPAH patients...
Systemic sclerosis-associated pulmonary hypertension: why disease-specific composite endpoints are neededChristopher P Denton
Centre for Rheumatology, Royal Free Campus, University College Medical School, London, NW3 2PF, UK
Arthritis Res Ther 13:114. 2011..Failure to take this into account may compromise progress in managing PAH in SSc...
Clinical trials and basic research: defining mechanisms and improving treatment in connective tissue diseaseLewis J Rubin
Division of Pulmonary and Critical Care Medicine, University of California San Diego, Campus Point Drive, La Jolla, California 92037 7381, USA
Arthritis Res Ther 9:S10. 2007....
Diagnosis and management of pulmonary arterial hypertension: ACCP evidence-based clinical practice guidelinesLewis J Rubin
Division of Pulmonary and Critical Care Medicine, University of California, San Diego School of Medicine, La Jolla, USA
Chest 126:4S-6S. 2004
Diagnosis and management of pulmonary arterial hypertension: ACCP evidence-based clinical practice guidelinesLewis J Rubin
Division of Pulmonary and Critical Care Medicine, University of California, San Diego School of Medicine, La Jolla, USA
Chest 126:7S-10S. 2004
Treatment of pulmonary arterial hypertension due to scleroderma: challenges for the futureLewis J Rubin
University of California, San Diego School of Medicine, 9300 Campus Point Drive, La Jolla, CA 92032, USA
Rheum Dis Clin North Am 34:191-7; viii. 2008..It also provides a glimpse into the future, based on recent developments in the field that hold promise for enhancing the treatment of this disease...
Pulmonary arterial hypertension: a look to the futureLewis J Rubin
Pulmonary Vascular Center, University of California San Diego School of Medicine, La Jolla, California, USA
J Am Coll Cardiol 43:89S-90S. 2004..This summary provides a brief overview of future directions in the field...
Current and future management of chronic thromboembolic pulmonary hypertension: from diagnosis to treatment responsesLewis J Rubin
University of California, San Diego, CA, USA
Proc Am Thorac Soc 3:601-7. 2006..Continued research and clinical trials investigating possible applications of new medical treatments are required...
Perspective on the optimal endpoints for pulmonary arterial hypertension trialsLewis Rubin
University of California, San Diego School of Medicine, La Jolla, California 92037, USA
Curr Opin Pulm Med 16:S43-6. 2010..Time to clinical worsening (TTCW) may represent an alternative, and although it is being considered as a primary endpoint in future trials, it will ultimately require refinement before it can be broadly applied...
Bosentan: a dual endothelin receptor antagonistLewis J Rubin
Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of California at San Diego, School of Medicine, 9300 Campus Point Drive, 7372, La Jolla, CA 92037, USA
Expert Opin Investig Drugs 11:991-1002. 2002....
Long-term treatment with sildenafil citrate in pulmonary arterial hypertension: the SUPER-2 studyLewis J Rubin
Department of Medicine, University of California at San Diego, UCSD Medical Center Thornton, 9300 Campus Point Dr MC 7372, La Jolla, CA 92037, USA
Chest 140:1274-83. 2011..The long-term safety and tolerability of sildenafil treatment of pulmonary arterial hypertension (PAH) were assessed...
Metabolic dysfunction in the pathogenesis of pulmonary hypertensionLewis J Rubin
University of California, San Diego, La Jolla, CA 92093, USA
Cell Metab 12:313-4. 2010..2010) found that increased fatty acid oxidation and a shift in the glycolysis/glucose oxidation ratio may be central to the pathogenesis of this process, suggesting that these abnormalities comprise novel treatment targets...
Bosentan therapy for pulmonary arterial hypertensionLewis J Rubin
Division of Pulmonary and Critical Care Medicine, University of California at San Diego, La Jolla 92037 1330, USA
N Engl J Med 346:896-903. 2002..The present trial investigated the effect of bosentan on exercise capacity in a larger number of patients and compared two doses...
Pulmonary arterial hypertensionLewis J Rubin
University of California, San Diego, School of Medicine, 9300 Campus Point Drive, La Jolla, CA 92037, USA
Proc Am Thorac Soc 3:111-5. 2006..The article reviews the classification of diseases associated with PAH, the current understanding of its pathogenesis, and the contemporary approach to therapy...
Endothelin in health and disease: endothelin receptor antagonists in the management of pulmonary artery hypertensionNick H S Kim
Division of Pulmonary and Critical Care Medicine, University of California, San Diego, La Jolla, CA 92037-1300, USA
J Cardiovasc Pharmacol Ther 7:9-19. 2002..Current classification and management of PAH are reviewed, along with the promise of greatly improved treatment generated by recent and ongoing clinical trials using ERAs...
Preoperative partitioning of pulmonary vascular resistance correlates with early outcome after thromboendarterectomy for chronic thromboembolic pulmonary hypertensionNick H S Kim
University of California, San Diego, 9300 Campus Point Dr, M/C 7381, La Jolla, CA 92037-1300, USA
Circulation 109:18-22. 2004..Patients with CTEPH and Rup value <60% appear to be at highest risk...
The right ventricle in pulmonary hypertensionKelly M Chin
Division of Pulmonary and Critical Care Medicine, University of California, San Diego School of Medicine, La Jolla, California, USA
Coron Artery Dis 16:13-8. 2005..The article will review the normal structure and function of the right ventricle and summarize the impact of PAH and its treatments on right ventricular function...
Cellular and molecular mechanisms of pulmonary vascular remodeling: role in the development of pulmonary hypertensionMehran Mandegar
Department of Medicine, School of Medicine, University of California, San Diego, La Jolla 92093, USA
Microvasc Res 68:75-103. 2004....
Bosentan inhibits transient receptor potential channel expression in pulmonary vascular myocytesNaomi Kunichika
Department of Medicine, University of California, San Diego, La Jolla, California, USA
Am J Respir Crit Care Med 170:1101-7. 2004..The greater effect of bosentan on IPAH-PASMCs than on normal PASMCs suggests that increased TRPC6 expression and function may be involved in the overgrowth of PASMCs in patients with IPAH...
Safety and efficacy of inhaled treprostinil as add-on therapy to bosentan in pulmonary arterial hypertensionRichard N Channick
UCSD Medical Center, La Jolla, California 92037, USA
J Am Coll Cardiol 48:1433-7. 2006..This study evaluated the safety and efficacy of inhaled treprostinil as add-on therapy to oral bosentan in patients with pulmonary arterial hypertension (PAH)...
Enhanced expression of transient receptor potential channels in idiopathic pulmonary arterial hypertensionYing Yu
Department of Medicine, School of Medicine, University of California at San Diego, La Jolla, CA 92093, USA
Proc Natl Acad Sci U S A 101:13861-6. 2004..TRPC channel overexpression may be partially responsible for the increased PASMC proliferation and pulmonary vascular medial hypertrophy in IPAH patients...
Long-term ambrisentan therapy for the treatment of pulmonary arterial hypertensionRonald J Oudiz
LA Biomedical Research Institute at Harbor UCLA Medical Center, Torrance, California, USA
J Am Coll Cardiol 54:1971-81. 2009..This study evaluated the safety and efficacy of ambrisentan for a period of 2 years in patients with pulmonary arterial hypertension (PAH)...
Endothelin receptor antagonists in pulmonary arterial hypertensionRichard N Channick
Pulmonary and Critical Care Division, University of California, San Diego, California, USA
J Am Coll Cardiol 43:62S-67S. 2004..The selective endothelin receptor-A antagonists sitaxsentan and ambrisentan are currently undergoing investigation...
Longterm survival among patients with scleroderma-associated pulmonary arterial hypertension treated with intravenous epoprostenolDavid B Badesch
Department of Medicine, University of Colorado Denver, Denver, Colorado, USA
J Rheumatol 36:2244-9. 2009..v.) infusion in an uncontrolled open-label 3-year extension study following an initial randomized, controlled 12-week study...
Identification of putative endothelial progenitor cells (CD34+CD133+Flk-1+) in endarterectomized tissue of patients with chronic thromboembolic pulmonary hypertensionWeijuan Yao
Division of Pulmonary and Critical Care Medicine, Dept of Medicine, MTF 252, Univ of California, San Diego, 9200 Gilman Dr, MC 0725, La Jolla, CA 92093 0725, USA
Am J Physiol Lung Cell Mol Physiol 296:L870-8. 2009..It is possible that the microenvironment provided by thromboemboli may promote these putative progenitor cells to differentiate and enhance intimal remodeling...
Successful withdrawal of long-term epoprostenol therapy for pulmonary arterial hypertensionNick H Kim
Pulmonary Vascular Center, University of California, San Diego, CA, La Jolla 92037, USA
Chest 124:1612-5. 2003..7 years (range, 2.4 to 13.5 years) CONCLUSION: Epoprostenol may sufficiently reverse the pathogenic process in select patients with PAH to allow a transition to less complex and less invasive treatment modalities...
Is methamphetamine use associated with idiopathic pulmonary arterial hypertension?Kelly M Chin
Department of Internal Medicine, Division of Pulmonary and Critical Care Medicine, St. Paul University Hospital, Dallas, TX, USA
Chest 130:1657-63. 2006..5; p < 0.0001) more likely to have used stimulants than patients with CTEPH. CONCLUSIONS: Patients with idiopathic PAH are significantly more likely to have used stimulants than patients with other forms of pulmonary hypertension...
Chronic thromboembolic pulmonary hypertensionTimothy L Williamson
Division of Pulmonary and Critical Care Medicine, University of California, San Diego, La Jolla 92037, USA
Prog Cardiovasc Dis 45:203-12. 2002..Definitive treatment requires surgical resection of thromboembolic material. The role of medical therapy remains to be defined...
Successful liver transplantation in a child with severe portopulmonary hypertension treated with epoprostenolAhmed Laving
Division of Pediatric Gastroenterology and Nutrition, University of California, San Diego, California 92103, USA
J Pediatr Gastroenterol Nutr 41:466-8. 2005
Measures of response in clinical trials of systemic sclerosis: the Combined Response Index for Systemic Sclerosis (CRISS) and Outcome Measures in Pulmonary Arterial Hypertension related to Systemic Sclerosis (EPOSS)Dinesh Khanna
David Geffen School at University of California, Los Angeles, CA, USA
J Rheumatol 36:2356-61. 2009..CRISS and EPOSS are being developed through the OMERACT process. Through Delphi process and literature review significant progress has been made for both indices, and prospective data are being collected...
A functional single-nucleotide polymorphism in the TRPC6 gene promoter associated with idiopathic pulmonary arterial hypertensionYing Yu
Department of Medicine, University of California, San Diego, La Jolla, CA 92093 0725, USA
Circulation 119:2313-22. 2009..This study sought to identify single-nucleotide polymorphisms (SNPs) in the TRPC6 gene promoter that are associated with IPAH and have functional significance in regulating TRPC6 activity in PASMCs...
Validation of the 6 min walk test according to the OMERACT filter: a systematic literature review by the EPOSS-OMERACT groupJerome Avouac
Division of Rheumatology, Department of Medicine, David Geffen School at UCLA, 1000 Veteran Avenue, Room 32 59, Los Angeles, CA 90095 1670, USA
Ann Rheum Dis 69:1360-3. 2010..To assess the validity of the 6 min walk test (6MWT) in pulmonary arterial hypertension secondary to systemic sclerosis (PAH-SSc) according to the OMERACT filter...
Upregulation of Na+/Ca2+ exchanger contributes to the enhanced Ca2+ entry in pulmonary artery smooth muscle cells from patients with idiopathic pulmonary arterial hypertensionShen Zhang
Dept of Medicine, University of California, San Diego, La Jolla, CA 92093 0725, USA
Am J Physiol Cell Physiol 292:C2297-305. 2007..These observations indicate that the upregulated NCX1 and enhanced Ca(2+) entry via the reverse mode of Na(+)/Ca(2+) exchange are an additional mechanism responsible for the elevated [Ca(2+)](cyt) in PASMC from IPAH patients...
Evaluation and management of the patient with pulmonary arterial hypertensionLewis J Rubin
University of California, San Diego, Medical Center, La Jolla, California 92037-7381, USA
Ann Intern Med 143:282-92. 2005..In this review, the authors present approaches to the diagnosis and management of pulmonary arterial hypertension, using a hypothetical case to highlight the key management points...
Bone morphogenetic proteins induce apoptosis in human pulmonary vascular smooth muscle cellsShen Zhang
Dept of Medicine, UCSD Medical Center, 200 West Arbor Dr, San Diego, CA 92103 8382, USA
Am J Physiol Lung Cell Mol Physiol 285:L740-54. 2003..Inhibition of BMP-induced PASMC apoptosis in PPH patients may play an important role in the development of pulmonary vascular medial hypertrophy in these patients...
Nitric oxide induces apoptosis by activating K+ channels in pulmonary vascular smooth muscle cellsStefanie Krick
Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of California School of Medicine, 200 W. Arbor Dr, San Diego, CA 92103-8382, USA
Am J Physiol Heart Circ Physiol 282:H184-93. 2002..The resulting increase in K+ efflux leads to cytosolic K+ loss and eventual apoptosis volume decrease and apoptosis. NO-induced apoptosis may also be related to mitochondrial membrane depolarization in PASMC...
Worldwide physician education and training in pulmonary hypertension: pulmonary vascular disease: the global perspectiveC Gregory Elliott
Department of Medicine, Division of Pulmonary and Critical Care Medicine, Intermountain Medical Center, Murray, UT 84157 7000, USA
Chest 137:85S-94S. 2010..Political, economic, and cultural barriers must be identified and overcome as part of any strategic plan. Global education should include training objectives for generalist, non-PH specialist, and PH specialist physicians...
Prednisolone inhibits PDGF-induced nuclear translocation of NF-kappaB in human pulmonary artery smooth muscle cellsAiko Ogawa
Department of Medicine, University of California, San Diego, La Jolla, CA 92093 0725, USA
Am J Physiol Lung Cell Mol Physiol 295:L648-57. 2008....
Hemodynamic and functional assessment of patients with sickle cell disease and pulmonary hypertensionAnastasia Anthi
Vascular Medicine Branch, Clinical Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 2089, USA
Am J Respir Crit Care Med 175:1272-9. 2007..Although pulmonary hypertension (PH) is a common complication of sickle cell disease (SCD) associated with high mortality, there exist few data characterizing hemodynamics and cardiopulmonary function in this population...
Medical therapy for pulmonary arterial hypertension: updated ACCP evidence-based clinical practice guidelinesDavid B Badesch
University of Colorado Health Sciences Center, Box C 272, 4200 E Ninth Ave, Denver, CO 80262, USA
Chest 131:1917-28. 2007..Due to the complexity of the diagnostic evaluation required and the treatment options available, referral of patients with PAH to a specialized center continues to be strongly recommended...
Central venous blood oxygen saturation monitoring in patients with chronic pulmonary arterial hypertension treated with continuous IV epoprostenol: correlation with measurements of hemodynamics and plasma brain natriuretic peptide levelsKelly M Chin
Department of Internal Medicine, University of Texas Southwestern Pulmonary Hypertension Program, 5909 Harry Hines Blvd, Dallas, TX 75235 9254, USA
Chest 132:786-92. 2007....
High prevalence of elevated clotting factor VIII in chronic thromboembolic pulmonary hypertensionDiana Bonderman
Department of Internal Medicine II, Division of Cardiology, University of Vienna, Wahringer Gurtel 18 20, 1090 Vienna, Austria
Thromb Haemost 90:372-6. 2003..0001) and PAH patients (22%, p = 0.022). We can conclude that elevated plasma FVIII is the first prothrombotic factor identified in a large proportion of CTEPH patients...
Effects of the dual endothelin receptor antagonist bosentan in patients with pulmonary arterial hypertension: a 1-year follow-up studyOlivier Sitbon
Service de Pneumologie Réanimation Respiratoire, Hopital Antoine Beclere, 157, Avenue de la Porte Trivaux, F 92141 Clamart Cedex, France
Chest 124:247-54. 2003..We report on the long-term safety and efficacy of bosentan treatment in patients with pulmonary arterial hypertension (PAH)...
Pulmonary arterial hypertensionKelly M Chin
Department of Internal Medicine, Division of Pulmonary and Critical Care, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA
J Am Coll Cardiol 51:1527-38. 2008..The purpose of this review is to describe the current state of evidence for the diagnosis, prognosis, and treatment of the patient with PAH...
Defining appropriate outcome measures in pulmonary arterial hypertension related to systemic sclerosis: a Delphi consensus study with cluster analysisOliver Distler
University Hospital Zurich, Zurich, Switzerland
Arthritis Rheum 59:867-75. 2008..The aim of the present study was to establish an expert consensus regarding which outcome measures are most appropriate for clinical trials in PAH-SSc...
Addition of sildenafil to long-term intravenous epoprostenol therapy in patients with pulmonary arterial hypertension: a randomized trialGerald Simonneau
Service de Pneumologie, Hopital Antoine Beclere, Universite Paris Sud, Clamart, France
Ann Intern Med 149:521-30. 2008..Oral sildenafil and intravenous epoprostenol have independently been shown to be effective in patients with pulmonary arterial hypertension...
Favorable effects of inhaled treprostinil in severe pulmonary hypertension: results from randomized controlled pilot studiesRobert Voswinckel
Department of Internal Medicine, University Hospital Giessen, Giessen, Germany
J Am Coll Cardiol 48:1672-81. 2006..CONCLUSIONS: Inhaled treprostinil exerts sustained pulmonary vasodilation with excellent tolerability at relatively low doses and may be inhaled in a few breaths...
Epoprostenol therapy as a bridge to pulmonary thromboendarterectomy for chronic thromboembolic pulmonary hypertensionKim M Kerr
Chest 123:319-20. 2003
Inhaled iloprost for severe pulmonary hypertensionHorst Olschewski
Department of Internal Medicine II, University Clinic, Giessen, Germany
N Engl J Med 347:322-9. 2002..CONCLUSIONS: Inhaled iloprost is an effective therapy for patients with severe pulmonary hypertension...
Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in patients with pulmonary arterial hypertension: a double-blind, randomized, placebo-controlled trialGerald Simonneau
Division of Pulmonary and Critical Care Medicine, Antoine Beclere Hospital, Clamart, Paris Sud University, Clamart, France
Am J Respir Crit Care Med 165:800-4. 2002..We conclude that chronic subcutaneous infusion of treprostinil is an effective treatment with an acceptable safety profile in patients with pulmonary arterial hypertension...
Comparative analysis of clinical trials and evidence-based treatment algorithm in pulmonary arterial hypertensionNazzareno Galie
Institute of Cardiology, University of Bologna, Bologna, Italy
J Am Coll Cardiol 43:81S-88S. 2004..Combination therapy can be attempted in selected cases. Both balloon atrial septostomy and lung transplantation are indicated for refractory patients or where medical treatment is unavailable...
Ambrisentan for the treatment of pulmonary arterial hypertension: results of the ambrisentan in pulmonary arterial hypertension, randomized, double-blind, placebo-controlled, multicenter, efficacy (ARIES) study 1 and 2Nazzareno Galie
Institute of Cardiology, University of Bologna, Via Massarenti, 9, 40138 Bologna, Italy
Circulation 117:3010-9. 2008..Ambrisentan is a propanoic acid-based, A-selective endothelin receptor antagonist for the once-daily treatment of pulmonary arterial hypertension...
Ambrisentan therapy for pulmonary arterial hypertensionNazzareno Galie
University of Bologna, Bologna, Italy
J Am Coll Cardiol 46:529-35. 2005..The purpose of this study was to examine the efficacy and safety of four doses of ambrisentan, an oral endothelin type A receptor-selective antagonist, in patients with pulmonary arterial hypertension (PAH)...
Sildenafil citrate therapy for pulmonary arterial hypertensionNazzareno Galie
Institute of Cardiology, University of Bologna, Bologna, Italy
N Engl J Med 353:2148-57. 2005....
Epoprostenol and nesiritide in pulmonary hypertensionLewis J Rubin
Chest 127:1870. 2005
Chronic thromboembolic pulmonary hypertensionMarius M Hoeper
Department of Respiratory Medicine, Hannover Medical School, 30623 Hannover, Germany
Circulation 113:2011-20. 2006
Randomized study of adding inhaled iloprost to existing bosentan in pulmonary arterial hypertensionVallerie V McLaughlin
The University of Michigan Health System, Ann Arbor, Michigan, USA
Am J Respir Crit Care Med 174:1257-63. 2006..Small, open-label studies suggest that combinations of existing therapies may be effective for pulmonary arterial hypertension (PAH)...
Pathogenesis of pulmonary arterial hypertension: the need for multiple hitsJason X-J Yuan
Circulation 111:534-8. 2005
Endothelin-1 and the pulmonary vascular response to altitude: a new therapeutic target?Lewis J Rubin
Circulation 114:1350-1. 2006
Treprostinil, a prostacyclin analogue, in pulmonary arterial hypertension associated with connective tissue diseaseRonald J Oudiz
Research and Education Institute, Harbor UCLA Medical Center, Torrance, CA 90502, USA
Chest 126:420-7. 2004..To assess the efficacy and safety of continuous subcutaneous infusion of treprostinil, a stable prostacyclin analogue, for treating pulmonary arterial hypertension (PAH) in patients with connective tissue disease (CTD)...
Right ventricular function and failure: report of a National Heart, Lung, and Blood Institute working group on cellular and molecular mechanisms of right heart failureNorbert F Voelkel
Pulmonary Hypertension Center, University of Colorado at Denver and Health Sciences Center, 4200 E Ninth Ave, MC: C272, Denver, CO 80262, USA
Circulation 114:1883-91. 2006
Complications of right heart catheterization procedures in patients with pulmonary hypertension in experienced centersMarius M Hoeper
Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany
J Am Coll Cardiol 48:2546-52. 2006..This study sought to assess the risks associated with right heart catheter procedures in patients with pulmonary hypertension...
Differential effects of stable prostacyclin analogs on smooth muscle proliferation and cyclic AMP generation in human pulmonary arteryLucie H Clapp
Centre for Clinical Pharmacology, Department of Medicine, University College London, Rayne Institute 4th Floor, 5 University Street, London W1C 6JJ, United Kingdom
Am J Respir Cell Mol Biol 26:194-201. 2002..Thus, PGI(2) analogs potently inhibit proliferation of human pulmonary artery, probably via a cAMP-dependent pathway, although cAMP elevation in itself is not a good predictor of antiproliferative potency...
Sildenafil for enhanced performance at high altitude?Lewis J Rubin
Ann Intern Med 141:233-5. 2004
New treatments for pulmonary arterial hypertensionMarius M Hoeper
Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany
Am J Respir Crit Care Med 165:1209-16. 2002
Management following pulmonary thromboendarterectomy: experience versus evidenceNick H S Kim
Crit Care Med 33:2132-3. 2005
Therapy of pulmonary hypertension: the evolution from vasodilators to antiproliferative agentsLewis J Rubin
Am J Respir Crit Care Med 166:1308-9. 2002
Efficacy and safety of treprostinil: an epoprostenol analog for primary pulmonary hypertensionVallerie V McLaughlin
Rush Presbyterian St Luke s Medical Center, Chicago, Illinois 60612, USA
J Cardiovasc Pharmacol 41:293-9. 2003..Subcutaneous treprostinil has favorable hemodynamic effects when given acutely and in the short term. Treprostinil can be given safely to an ambulatory patient with a novel subcutaneous delivery pump system...
Clinical classification of pulmonary hypertensionGerald Simonneau
Department of Pulmonary and Critical Medicine, University of Paris Sud, Paris, France
J Am Coll Cardiol 43:5S-12S. 2004....
Temporal trends and drug exposures in pulmonary hypertension: an American experienceAlexander M Walker
Harvard School of Public Health, Boston, MA, USA
Am Heart J 152:521-6. 2006..We also studied whether use of anorexigens and other drugs differed among patients with pulmonary hypertension of different etiologies...
BMPR2 mutation and outcome in pulmonary arterial hypertension: clinical relevance to physicians and patientsLewis J Rubin
Am J Respir Crit Care Med 177:1300-1. 2008
Sildenafil for pulmonary arterial hypertension associated with connective tissue diseaseDavid B Badesch
Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA
J Rheumatol 34:2417-22. 2007..The phosphodiesterase-5 inhibitor sildenafil citrate enhances vasodilatation, has antiproliferative effects, and is effective in the treatment of PAH. We examined the efficacy and safety of oral sildenafil in patients with PAH-CTD...
