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Respiratory Medicine|January 30, 2016
The efficacy of fluticasone furoate administered in the morning or evening is comparable in patients with persistent asthmaR D Kempsford, J Bal, A Baines, et al.
Medycyna Wieku Rozwojowego|October 27, 2001
[Analysis of hearing impairment causes in molecular diagnosis of deafness]E Nowakowska-Szyrwinska, L Sobieszczanska-Radoszewska, E Matejuk-Studzinska, et al.
Human Genetics|October 1, 1989
Different haplotypes for cystic fibrosis-linked DNA polymorphisms in Polish and Dutch populationsD Maciejko, J Bal, T Mazurczak, et al.
European Journal of Neurology|June 2, 2007
Clinical characteristics of carriers of a GAG deletion in the DYT1 gene amongst Polish patients with primary dystoniaK Szczaluba, M Jurek, M Milewski, et al.
American Journal of Medical Genetics|July 12, 1996
Frequency of Fra X syndrome among institutionalized mentally retarded males in PolandT Mazurczak, E Bocian, M Milewski, et al.
Medycyna Wieku Rozwojowego|July 27, 2000
[Mutations causing hereditary hyperphenylalaninemia]C Zekanowski, M Nowacka, B Cabalska, et al.
Skeletal Radiology|August 1, 1995
Chondrosarcoma in a patient with relapsing polychondritisH R Fransen, F A Ramon, A M De Schepper, et al.
Neurology|November 4, 2006
Genotype-phenotype associations for ARX gene duplication in X-linked mental retardationK Szczaluba, M Nawara, K Poirier, et al.
Acta Biochimica Polonica|January 1, 1996
Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndromeM Milewski, M Zygulska, J Bal, et al.
The British Journal of Dermatology|December 29, 2015
Amelioration of junctional epidermolysis bullosa due to exon skippingC Kowalewski, J Bremer, A Gostynski, et al.
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