Ph. Camus (Dijon, France), A. Morais (Maia, Portugal)
Clinical features of lymphangioleiomyomatosis complicated by renal angiomyolipomas
Y. Mizushina, M. Bando, T. Hosono, N. Mato, T. Nakaya, Y. Ishii, H. Yamasawa, Y. Sugiyama (Shimotsuke, Japan)
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Clinical course in hypersensitivity pneumonitis: a review of 38 cases
M. J. Ribeiro, D. Moniz, A. C. Mendes, A. Bugalho de Almeida (Lisbon, Portugal)
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Pulmonary Langerhans histiocytosis: clinical, radiological and functional pattern in spontaneous remission
C. Russo, F. Lassandro, E. Carpentieri, G. Rea, A. A. Stanziola, M. Sofia (Naples, Italy)
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Relation between NYHA functional degree of dyspnea and static and dynamic lung compliance in patients with interstitial pneumopathies
M. D. R. Rodriguez Moreno, M. A. Guzman Ubeda, A. Romero Ortiz, M. T. Miranda Leon, I. Rodriguez Moreno (Granada, Spain)
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Clinical-pathologic study on small airways in patients with idiopathic interstitial pneumonia
L. P. Zhang, H. P. DAI, C. Q. Xia, M. L. Jin, P. Wei (Beijing, China)
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What is the role of hypoxaemia, 6-minute walk test, diffusion capacity, pulmonary arterial hypertension in diffuse interstitial lung diseases?
N. Demir Firat, A. Merzi Ozturk, T. Kaya, D. Karnak, O. Kayacan (Ankara, Turkey)
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Clinical and pathological features of 13 adult patients with pulmonary Langerhans‘ cell histiocytosis
F. S. Oymak, N. Tutar, H. Buyukoglan, M. Bilgin, S. Balkanli, E. Mavili, R. Demir, I. Gulmez (Kayseri, Turkey)
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Manifestation of idiopathic chronic eosinophilic pneumonia
E. Danila, J. Norkuniene, R. Nargela, E. Zurauskas, B. Satkauskas, R. Aleksoniene (Vilnius, Lithuania)
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Cryptogenic organising pneumonia – just a manifestation of community acquired pneumonia? A retrospective analysis from 1995 to 2004
A. Dittrich, W. R. Guschall, G. Liebetrau (Lostau, Neuruppin, Germany)
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Clinical and radiological findings in patients with silicosis based on ILO classification
A. Fakharian, S. Kahkoii, M. Nikoonia, S. Salehpour, M. Bolursaz, M. Masjedi (Tehran, Islamic Republic Of Iran)
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Bronchiolitis obliterans organizing pneumonia. A report of 10 cases
F. Guedes, T. Shiang, M. C. Brito, S. Neves (V N Gaia, Portugal)
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Pulmonary alveolar proteinosis therapy success with combined lavage procedures: a case report
N. Demir Firat, A. Ciledag, P. Akin Kabalak, D. Karnak, S. Erekul, O. Kayacan (Ankara, Turkey)
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Clinical features of cryptogenic organising pneumonia in Chinese population
H. Chu, S. Ren, X. Yi (Shanghai, China)
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Pulmonary alveolar proteinosis: report of two cases
D. Tas, E. Kunter, Z. Kucukodaci, O. Ayten, Z. Kartaloglu (Istanbul, Turkey)
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Pulmonary Langerhans cell histiocytosis – analysis of factors influencing the course of the disease
E. Radzikowska, E. Wiatr, R. Langfort, I. Bestry, P. Remiszewski (Warsaw, Poland)
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Diagnosis of idiopathic pulmonary fibrosis: from guidelines to clinical practice
R. Lazor, J. F. Vodoz, T. Geiser, M. Riederer, T. Rochat, L. P. Nicod (Lausanne, Bern, Burgdorf, Genève, Switzerland)
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Pulmonary thromboembolism associated with interstitial pneumonia
M. Furuiye, M. Tamaoka, Y. Miyazaki, Y. Ohtani, N. Inase, Y. Yoshizawa (Tokyo, Japan)
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Importance of unrecognised exposure to avian antigen in chronic bird-related hypersensitivity pneumonitis
N. Inase, Y. Ohtani, Y. Miyazaki, Y. Yoshizawa (Tokyo, Japan)
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Pulmonary haemosiderosis in children: report of 10 cases
R. Boukari, C. Kaddache, L. Smati, K. N. Benhalla, O. Redjala, S. Hannouz, M. Baghriche (Blida, Algiers, Algeria)
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Idiopathic pulmonary haemosiderosis in children –cases with long survival
E. C. Bica, D. Bulucea, R. Diaconu (Craiova, Romania)
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