S. Dominique

发表

Systemic sclerosis and exposure to heavy metals: A case control study of 100 patients and 300 controls.

A. Cailleux, M. Bubenheim, I. Marie, 2017, Autoimmunity reviews.

Progressive multifocal leukoencephalopathy in patients with sarcoidosis

F. Ducray, C. Broussolle, P. Sève, 2014, Neurology.

In vivo probe-based confocal laser endomicroscopy in amiodarone-related pneumonia

G. Bourg-Heckly, J. Vergnon, L. Thiberville, 2012, European Respiratory Journal.

Cyclophosphamide added to glucocorticoids in acute exacerbation of idiopathic pulmonary fibrosis (EXAFIP): a randomised, double-blind, placebo-controlled, phase 3 trial.

P. Brillet, S. Leroy, L. Plantier, 2021, The Lancet. Respiratory medicine.

Interstitial lung disease in primary Sjögren's syndrome.

I. Marie, H. Lévesque, A. Smail, 2017, Autoimmunity reviews.

Clinical manifestations and outcome of anti-PL7 positive patients with antisynthetase syndrome.

O. Decaux, E. Hachulla, J. Ménard, 2013, European journal of internal medicine.

Interstitial Lung Disease in Anti–Jo‐1 Patients With Antisynthetase Syndrome

L. Mouthon, E. Hachulla, J. Ménard, 2013, Arthritis care & research.

Comparison of long-term outcome between anti-Jo1- and anti-PL7/PL12 positive patients with antisynthetase syndrome.

O. Decaux, L. Mouthon, J. Ménard, 2012, Autoimmunity reviews.

Short-term and long-term outcome of anti-Jo1-positive patients with anti-Ro52 antibody.

L. Mouthon, J. Ménard, I. Marie, 2012, Seminars in arthritis and rheumatism.

Rituximab therapy for refractory interstitial lung disease related to antisynthetase syndrome.

J. Ménard, I. Marie, H. Lévesque, 2012, Respiratory medicine.

Short-term and long-term outcomes of interstitial lung disease in polymyositis and dermatomyositis: a series of 107 patients.

L. Mouthon, J. Ménard, I. Marie, 2011, Arthritis and rheumatism.

Interstitial lung disease in polymyositis and dermatomyositis.

E. Hachulla, I. Marie, H. Lévesque, 2002, Arthritis and rheumatism.

Pleuroparenchymal fibroelastosis after allogeneic hematopoietic stem cell transplantation

S. Leroy, M. Reynaud‐Gaubert, G. Socié, 2019, Bone Marrow Transplantation.

Anti‐IgE Monoclonal Antibody (Omalizumab) in Refractory and Relapsing Eosinophilic Granulomatosis With Polyangiitis (Churg‐Strauss): Data on Seventeen Patients

V. Cottin, L. Mouthon, A. Coste, 2016, Arthritis & rheumatology.

AGER -429T/C Is Associated with an Increased Lung Disease Severity in Cystic Fibrosis

P. Böelle, P. Reix, J. Dalphin, 2012, PloS one.

Evidence that Langerhans cells in adult pulmonary Langerhans cell histiocytosis are mature dendritic cells: importance of the cytokine microenvironment.

P. Soler, A. Hance, A. Bergeron, 1999, Journal of immunology.

Serial computed tomography and lung function testing in pulmonary Langerhans’ cell histiocytosis

S. Chevret, C. de Bazelaire, B. Crestani, 2012, European Respiratory Journal.

Physiologic Determinants of Exercise Capacity in Pulmonary Langerhans Cell Histiocytosis: A Multidimensional Analysis

J. Giovannelli, B. Wallaert, O. Le Rouzic, 2017, PloS one.

Large granular lymphocyte leukemia and pre-capillary pulmonary hypertension.

M. Humbert, O. Decaux, C. Chabanne, 2020, Chest.

Pharmacokinetics and safety of tobramycin administered by the PARI eFlow rapid nebulizer in cystic fibrosis.

S. Leroy, J. Kovarik, L. Mély, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[Churg-Strauss syndrome relapse when antileucotriene in taggered].

C. Picard, H. Bérard, S. Dominique, 2005, La Revue de medecine interne.

Bronchoalveolar Lavage Fluid

A. Hance, S. Dominique, F. Bouchonnet, 2020, Definitions.

The natural history of adult pulmonary Langerhans cell histiocytosis: a prospective multicentre study

S. Chevret, B. Wallaert, D. Valeyre, 2015, Orphanet Journal of Rare Diseases.

[Sarcoidosis simulating a pulmonary veno-occlusive disease].

F. Portier, J. Muir, L. Thiberville, 1991, Revue des maladies respiratoires.

[Pulmonary involvement in systemic scleroderma. Part II. Isolated pulmonary arterial hypertension, bronchopulmonary cancer, alveolar hemorrhage].

I. Marie, H. Lévesque, H. Courtois, 1999, La Revue de medecine interne.

Association of occupational exposure with features of systemic sclerosis.

M. Bubenheim, J. Ménard, I. Marie, 2015, Journal of the American Academy of Dermatology.

Prospective study to evaluate the association between systemic sclerosis and occupational exposure and review of the literature.

A. Cailleux, M. Bubenheim, I. Marie, 2014, Autoimmunity reviews.

Functional outcome and prognostic factors in anti-Jo1 patients with antisynthetase syndrome

E. Hachulla, J. Ménard, I. Marie, 2013, Arthritis Research & Therapy.

First Description of Azole-Resistant Aspergillus fumigatus Due to TR46/Y121F/T289A Mutation in France

P. Le Pape, J. Meis, G. Gargala, 2015, Antimicrobial Agents and Chemotherapy.

Real-Life Safety and Effectiveness of Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis.

D. Caimmi, A. Didier, S. Leroy, 2020, American journal of respiratory and critical care medicine.

Real-life initiation of lumacaftor/ivacaftor combination in adults with cystic fibrosis homozygous for the Phe508del CFTR mutation and severe lung disease.

S. Leroy, P. Burgel, D. Grenet, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Retrospective observational study of French patients with cystic fibrosis and a Gly551Asp-CFTR mutation after 1 and 2years of treatment with ivacaftor in a real-world setting.

A. Munck, L. Mély, V. David, 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Gastrointestinal mucosal abnormalities using videocapsule endoscopy in systemic sclerosis

P. Ducrotte, M. Antonietti, E. Hachulla, 2014, Alimentary pharmacology & therapeutics.

High frequency of voriconazole-related phototoxicity in cystic fibrosis patients

S. Rondeau, C. Marguet, L. Couderc, 2012, European Respiratory Journal.

Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome: Molecular, Cellular, and Clinical Features From a French National Survey

A. Fischer, C. Bodemer, J. Casanova, 2012, Medicine.

Microbiologic contamination study of nebulizers after aerosol therapy in patients with cystic fibrosis.

J. Lemeland, F. Brémont, J. Derelle, 2000, American journal of infection control.

Paternity in men with cystic fibrosis: a retrospective survey in France.

I. Durieu, G. Bellis, M. de Braekeleer, 2006, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Plasma 5-fluorouracil and α-fluoro-β-alanin accumulation in lung cancer patients treated with continuous infusion of cisplatin and 5-fluorouracil

L. Thiberville, G. Bastian, M. Richard, 2004, Cancer Chemotherapy and Pharmacology.

Regulator of telomere length 1 (RTEL1) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes

P. Revy, P. Dieudé, A. Cazes, 2019, European Respiratory Journal.

[Association of sarcoidosis and Takayasu's arteritis: an additional case report].

I. Marie, H. Lévesque, S. Dominique, 2005, La Revue de medecine interne.

Effect of one-year lumacaftor-ivacaftor treatment on glucose tolerance abnormalities in cystic fibrosis patients.

I. Durieu, L. Kessler, S. Touzet, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Confocal fluorescence endomicroscopy of the human airways.

Mathieu Salaün, Luc Thiberville, Samy Lachkar, 2009, Proceedings of the American Thoracic Society.

Budesonide/Formoterol for bronchiolitis obliterans after hematopoietic stem cell transplantation.

S. Chevret, M. Robin, E. Bergot, 2015, American journal of respiratory and critical care medicine.

In vivo probe‐based confocal laser endomicroscopy in chronic interstitial lung diseases: Specific descriptors and correlation with chest CT

Mathieu Salaün, Luc Thiberville, Stéphane Dominique, 2019, Respirology.

Human in vivo fluorescence microimaging of the alveolar ducts and sacs during bronchoscopy

G. Bourg-Heckly, L. Thiberville, G. Bourg-Heckly, 2009, European Respiratory Journal.

Extrathoracic investigation in adult patients with isolated pulmonary langerhans cell histiocytosis

L. Vercellino, S. Chevret, B. Wallaert, 2016, Orphanet Journal of Rare Diseases.

Vinblastine chemotherapy in adult patients with langerhans cell histiocytosis: a multicenter retrospective study

S. Chevret, V. Cottin, A. Aouba, 2017, Orphanet Journal of Rare Diseases.

Cystic fibrosis and AA amyloidosis: a survey in the French cystic fibrosis network

S. Leroy, A. Clément, D. Grenet, 2014, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Esophageal involvement and pulmonary manifestations in systemic sclerosis.

P. Ducrotte, I. Marie, H. Lévesque, 2001, Arthritis and rheumatism.

Management of male infertility due to congenital bilateral absence of vas deferens should not ignore the diagnosis of cystic fibrosis

N. Rives, L. Sibert, B. Macé, 2012, Andrologia.

Intense paraneoplastic neutrophilic leukemoid reaction related to a G‐CSF‐Secreting lung sarcoma

F. Jardin, L. Thiberville, H. Tilly, 2005, American journal of hematology.

THU0484 Impact of TNF Antagonists on the Joint Manifestations of Sarcoidosis

O. Vittecoq, V. Goeb, O. Vittecoq, 2013 .

[Acute respiratory distress syndrome due to pneumonitis following intrathecal methotrexate administration].

H. Tilly, N. Contentin, S. Dominique, 2003, Revue des maladies respiratoires.

Nebulised liposomal amphotericin-B as maintenance therapy in allergic bronchopulmonary aspergillosis: a randomised, multicentre trial

D. Caillaud, F. Laurent, S. Ragot, 2021, European Respiratory Journal.

Virtual Bronchoscopy Planner and Radial-EBUS Guided Biopsy for Organizing Pneumonia Diagnosis

L. Thiberville, F. Guisier, S. Dominique, 2021, Journal of clinical medicine.

Spectrum and Prognosis of Antineutrophil Cytoplasmic Antibody–associated Vasculitis-related Bronchiectasis: Data from 61 Patients

I. Annesi-Maesano, P. Brillet, V. Cottin, 2019, The Journal of Rheumatology.

Relevance of 3D Cholangiography and Transient Elastography to Assess Cystic Fibrosis-Associated Liver Disease?

C. Lemaître, G. Savoye, C. Savoye-Collet, 2016, Canadian respiratory journal.

Panniculitis in a Woman With Opportunistic Pulmonary Coinfection by Pneumocystis jirovecii and Cryptococcus neoformans: 18F-FDG PET/CT Revealing the Infection and Assessing Treatment Response.

P. Courville, P. Vera, A. Duval-Modeste, 2020, Clinical nuclear medicine.

Outcome of anti-PL12 positive patients with antisynthetase syndrome.

O. Decaux, I. Marie, S. Jouneau, 2013, Presse medicale.

In vivo probe-based confocal laser endomicroscopy in chronic diffuse parenchymal lung diseases

L. Thiberville, G. Zalcman, V. Jounieaux, 2012 .

Pulmonary Artery Obstruction and Giant Cell Arteritis

J. Gligorov, S. Dominique, P. Chassagne, 1995, Annals of Internal Medicine.

[The transition in cystic fibrosis care: an adult physician's point of view].

S. Dominique, C. Leguillon, B. Masseline, 2007, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Real-life initiation of lumacaftor/ivacaftor combination in adults with cystic fibrosis homozygous for the Phe508del CFTR mutation and severe lung disease.

S. Leroy, P. Burgel, D. Grenet, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Anti‐IgE Monoclonal Antibody (Omalizumab) in Refractory and Relapsing Eosinophilic Granulomatosis With Polyangiitis (Churg‐Strauss): Data on Seventeen Patients

V. Cottin, L. Mouthon, A. Coste, 2016, Arthritis & rheumatology.

Interstitial lung disease in primary Sjögren's syndrome.

S. Dominique, J. Schmidt, F. Roca, 2017, Autoimmunity reviews.

Plasma 5-fluorouracil and alpha-fluoro-beta-alanin accumulation in lung cancer patients treated with continuous infusion of cisplatin and 5-fluorouracil.

L. Thiberville, G. Bastian, M. Richard, 1994, Cancer chemotherapy and pharmacology.

Management of male infertility due to congenital bilateral absence of vas deferens should not ignore the diagnosis of cystic fibrosis

S. Dominique, V. Grzegorczyk, Louis Sibert, 2012, Andrologia.