Interstitial pulmonary fibrosis in children
Majewska-Zalewska, H.
Pneumonologia Polska 45(3): 229-238
1977
ISSN/ISBN: 0376-4761 PMID: 558606 Document Number: 124066
Document emailed within 1 workday
Related Documents
Skovránek, J.; First, T.; Zapletal, A. 1988: Echocardiographic findings in children and adolescents with idiopathic interstitial pulmonary fibrosis Ceskoslovenska Pediatrie 43(3): 139-144Croft, P.R.; Racz, M.I.; Bloch, J.D.; Palmer, C.H. 2005: Autopsy confirmation of severe pulmonary interstitial fibrosis secondary to Munchausen syndrome presenting as cystic fibrosis Journal of Forensic Sciences 50(5): 1194-1198
Májský, A.; Copová, M.; Houstĕk, J. 1986: HLA and diffuse interstitial pulmonary fibrosis Ceskoslovenska Pediatrie 41(6): 319-320
Kondoh, Y.; Kaneko, M.; Tanaka, H.; Nakashima, Y.; Miyatake, H.; Shindoh, J.; Isogai, T.; Suzuki, K.; Taki, F.; Yamaki, K. 1990: Desquamative interstitial pneumonia-like changes in idiopathic pulmonary fibrosis Nihon Kyobu Shikkan Gakkai Zasshi 28(9): 1245-1251
Brune, J.; Wiesendanger, T.; Moulin, G.; Rousset, H.; Serin, D. 1973: Diffuse interstitial pulmonary fibrosis in collagen diseases Le Poumon et le Coeur 29(5): 635-641
Huang, L.Y. 1980: Diffuse pulmonary interstitial fibrosis--report of a case Zhonghua Nei Ke Za Zhi 19(6): 422-424
Laval, P.; Feliciano, J.M.; Kleisbauer, J.P.; Poirier, R. 1973: Value of functional respiratory exploration in the course of diffuse interstitial pulmonary fibrosis Le Poumon et le Coeur 29(5): 597-602
Bariffi, F.; Sanduzzi, A. 1984: Recent findings on the pathogenesis of diffuse interstitial pulmonary fibrosis Archivio Monaldi Per la Tisiologia E le Malattie Dell'apparato Respiratorio 39(3): 183-190
Samánek, M.; Ruth, C.; Zapletal, Z.; Paul, T. 1974: Regional ventilation in patients with idiopathic interstitial pulmonary fibrosis Ceskoslovenska Pediatrie 29(7): 373-375
Hosoda, Y.; Yoshida, S.; Mimori, T.; Toguchi, T.; Inada, S.; Tomii, M.; Yamagata, H.; Akizuki, M.; Abe, T. 1981: Polymyositis associated with interstitial pulmonary fibrosis and glomerulonephritis. A report of two autopsy cases Ryumachi 21 Suppl: 183-188
Popov, N.; Strumeliev, S. 1982: Diffuse idiopathic interstitial pulmonary fibrosis (Hamman-Rich syndrome) Vutreshni Bolesti 21(6): 96-101
Popov, N.; Strumeliev, S. 1982: Diffuse idiopathic interstitial pulmonary fibrosis (Hamman-Rich syndrome) Vutreshni Bolesti 21(6): 96-101
Szymańska, D. 1971: Diffuse interstitial idiopathic pulmonary fibrosis in the light of pathomorphological studies Gruzlica i Choroby Pluc; Tuberculosis et Pneumonologia 39(3): 187-193
Poudenx, M.; Otto, J.; Rotomondo, C.; Ferrari, E.; Lemoigne-Marsol, F.; Blaive, B. 1991: Increase of carbohydrate antigen 19-9 in 7 cases of primary diffuse interstitial pulmonary fibrosis Presse Medicale 20(42): 2161
Popova, E.N.; Lebedeva, M.V.; Ponomarev, A.B.; Popova, I.A.; Fomin, V.V. 2014: Interstitial pulmonary fibrosis: the role of angiogenic factors, the inhibitory pathways of progression Terapevticheskii Arkhiv 86(8): 23-28
Homma, Y. 1981: Experimental models of lung diseases pulmonary fibrosis (idiopathic interstitial pneumonia) Nihon Kyobu Shikkan Gakkai Zasshi 19(11): 813-819
Fischer, E.; Thiele, A.; Stierle, H.E.; Lang, B. 1995: Anti-Jo-1 antibodies: specific autoantibodies for polymyositis with interstitial pulmonary fibrosis. 2 case reports Zeitschrift für Rheumatologie 54(3): 171-177
Fehr, A.; Baghdady, S.; Ghaleb, R.; Maklad, S. 2018: Transthoracic Ultrasound in the Detection of Interstitial Pulmonary Fibrosis in Patients with Rheumatic Connective Tissue Diseases Bulletin of the Hospital for Joint Disease 76(3): 156-160
Shishido, M.; Ichiki, H.; Yano, M.; Toda, K.; Ohtsuki, Y. 1992: A case of idiopathic pulmonary fibrosis with histology of usual interstitial pneumonia that responded to pulse therapy followed by combined immunosuppression with prednisolone and azathioprine Nihon Kyobu Shikkan Gakkai Zasshi 30(12): 2139-2145
Pesci, A.; Bertorelli, G.; Manganelli, P. 1986: Differentiation between idiopathic pulmonary fibrosis and interstitial pneumonia associated with collagen vascular diseases by comparison of the ratio of OKT4+ cells and OKT8+ in BALF T-lymphocytes European Journal of Respiratory Diseases 68(2): 155-156