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Clinical Genetics|September 1, 1996
A cystic fibrosis patient homozygous for 621 + 1G-->T mutation has a severe pulmonary disease, mild pancreatic insufficiency and a gastro-esophageal refluxM Witt, A Pogorzelski, J Zebrak, et al.Pediatria Polska|April 1, 1995
[Broncho-pulmonary complications due to aspiration of foreign bodies by children]A Pogorzelski, J Zebrak, J Pawlik, et al.European Journal of Medical Research|February 17, 2010
Idiopathic pulmonary hemosiderosis in a 9-year-old girlE Kamienska, T Urasinski, A Gawlikowska-Sroka, et al.Otolaryngologia Polska = the Polish Otolaryngology|January 1, 1995
[Problems with treatment in patients with tongue and/or floor of the mouth neoplasms]W Domka, A Pogorzelski, T Wiewiórska, et al.Pneumonologia I Alergologia Polska|September 25, 1999
[Frequency of mutations and genotypes of the CFTR gene in cystic fibrosis adults in Poland]M Witt, A Pogorzelski, J Bal, et al.Otolaryngologia Polska = the Polish Otolaryngology|January 1, 1995
[The point of view of otolaryngologist and head and neck surgeon on thyroid diseases]A Betkowski, A Pogorzelski, K Gotkowska, et al.Journal of Applied Genetics|October 18, 2003
Effect of genotype on selected clinical features of Polish cystic fibrosis adultsL Majka, A Pogorzelski, W Młynarczyk, et al.Pediatric Pulmonology|April 23, 1999
Alveolar macrophages of children suffering from recurrent infections of respiratory tract are less efficient in eliminating apoptotic neutrophilsJ Pryjma, J Kaszuba-Zwoinska, J Pawlik, et al.Otolaryngologia Polska = the Polish Otolaryngology|August 29, 2000
[The recurrent laryngeal nerve paralysis as a complication after thyroid surgery]B Wedrychowicz, D Szuber, A Betkowski, et al.Clinical Genetics|March 25, 2000
Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosisJ Zebrak, B Skuza, A Pogorzelski, et al.Pageof 3