J-F. Cordier (Lyon, France), T. Peros Golubicic (Zagreb, Croatia)
Treatment of severe pulmonary alveolar proteinosis using inhaled GM-CSF
G. Keir, A. Wells, C. Morgan (London, United Kingdom)
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Association of diffuse alveolar hemorrhage with VKORC1, CYP2C9, and CYP2C19 polymorphisms
P. Wijnen, F. Cox, R. Mostard, O. Bekers, M. Drent (Maastricht, , Oss, Heerlen, Netherlands)
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Doxycicline in the treatment of lymphangioleiomyomatosis
S. Pimenta, P. Medeiros-Jr., B. Baldi, R. Kairalla, C. Carvalho (São Paulo, Brazil)
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Serial CT density in lymphangioleiomyomatosis (LAM)
M. Kokosi, J. Ravenel, C. Strange, M. Investigators (Athens, Greece; Charleston, United States Of America)
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Clinical course and outcome of pulmonary Langerhans‘-cell histiocytosis
N. D. Bakan, D. Kanmaz, G. Camsari, A. Bahadir, G. Özgül, N. Isik, G. Özkan, E. Tuncay, E. Cetinkaya, E. Caglar, A. Gür, S. Altin (Istanbul, Turkey)
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A national French web database for interstitial lung diseases in children
N. Nathan, R. Abou Taam, M. Mahloul, D. Michon, C. Toussaint, J. F. Vibert, J. de Blic, A. Clement (Paris, France)
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Serum CYFRA reflects disease severity of autoimmune pulmonary alveolar proteinosis
T. Arai, Y. Inoue, C. Sugimoto, A. Matsumuro, Y. Iwaki, M. Hirose, M. Kitaichi, M. Akira, S. Hayashi, K. Nakata, M. Sakatani (Sakai, Niigata, Japan)
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Pulmonary amyloidosis: Clinical features in a series of twelve patients
R. Athanazio, S. Rached, A. Cukier, H. Minamoto, C. Carvalho, R. Kairalla (Brazil)
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New mutation associated to the pulmonary alveolar microlithiasis
M. T. Palacio, T. Romero, A. B. García-García, C. Escudero, S. Castillo, U. Estada, I. Piqueras, A. Escribano (Valencia, Barcelona, Spain)
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Chronic eosinophilic pneumonia (CEP): Chest radiographs and CT findings in 71 cases
R. Katsuda, Y. Mochizuki, Y. Nakahara, T. Kawamura, S. Sasaki, H. Okamoto, A. Morimito, H. Tsukamoto, Y. Mizumori, T. Mayumi, T. Miyagawa, H. Tabata, E. Watanabe, T. Yokoyama, T. Goto, K. Mimura (Japan)
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Eosinophilic pulmonary syndromes: Retrospective study of the past 18 years in Coimbra University Hospital
P. G. Ferreira, A. J. Ferreira (Coimbra, Portugal)
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Protein analysis of bronchoalveolar lavage in pulmonary Langerhans-cell histiocytosis by a proteomic approach
P. Rottoli, C. Landi, E. Bargagli, M. G. Perari, A. Prasse, J. Mueller-Quernheim, L. Bini (Siena, Italy; Frieburg, Germany)
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A study on the pulmonary function of patients with chronic eosinophilic pneumonia
Y. Mizumori, Y. Mochiduki, Y. Nakahara, T. Kawamura, S. Shin, H. Okamoto, A. Morimoto, H. Tsukamoto, T. Mayumi, T. Miyagawa, H. Tabata, E. Watanabe, T. Yokoyama, K. Mimura, R. Katsuda (Himeji, Japan)
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Quantitative CT in pulmonary lymphangioleiomyomatosis: Comparison with pulmonary dysfunction
Y. Inoue, M. Akira, M. Hirose, T. Arai, T. Okuma, Y. Iwaki, C. Sugimoto, K. Tachibana, M. Akiko, M. Nakagawa, M. Kitaichi, S. Hayashi, M. Okada, M. Sakatani (Osaka, Japan)
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Clinical evaluation in 14 cases of diffuse alveolar hemorrhage – Relationship between initial findings and prognosis –
Y. Kohashi, Y. Saito, Y. Yoneda, Y. Totani, M. Okazawa, H. Sakakibara (Toyoake, Japan)
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Treatment of pulmonary Langerhans cell histiocytosis with multifocal involvement with vinblastine, prednisolon, mercaptopurine
E. Radzikowska, E. Wiatr, R. Langfort, I. Bestry, P. Rodzinski, A. Jarzebska (Warsaw, Bydgoszcz, Poland)
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Pulmonary alveolar proteinosis, study of 29 cases
A. Fakharian, L. Mansouri, M. Bakhshayesh-Karam, M. R. Masjedi (Tehran, Islamic Republic Of Iran)
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Clinical activity and high-resolution tomography findings in pulmonary Wegener‘s granulomatosis
K. Zycinska, K. Wardyn, T. Zielonka, E. Piotrowsa, A. Bogaczewicz (Warsaw, Poland)
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Interstitial lung diseases in children – Clinical and pathological characteristics
K. Krenke, J. Lange, J. Peradzynska, W. Zagorska, J. Ziolkowski, M. Kulus (Poland)
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131I-labeled lipiodol-induced interstitial pneumonia: A retrospective series of 15 cases
S. Jouneau, E. Vauléon, S. Caulet-Maugendre, E. Polard, A. C. Volatron, C. Meunier, P. Tattevin, E. Garin, J. L. Raoul, P. Delaval (Rennes, France)
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