H. Dmeńska

发表

Common Variable Immune Deficiency in Children—Clinical Characteristics Varies Depending on Defect in Peripheral B Cell Maturation

B. Wolska-Kuśnierz, E. Heropolitanska-Pliszka, M. Pac, 2013, Journal of Clinical Immunology.

Organization of Patient Management and Fungal Epidemiology in Cystic Fibrosis

V. Chrenkova, N. Kondori, R. Cantón, 2017, Mycopathologia.

Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

E. Ziętkiewicz, M. Witt, K. Grzela, 2019, Journal of Medical Genetics.

Mutations in Radial Spoke Head Genes and Ultrastructural Cilia Defects in East-European Cohort of Primary Ciliary Dyskinesia Patients

E. Ziętkiewicz, M. Witt, A. Pogorzelski, 2012, PloS one.

Progressive bronchiectasis and CMC in a patient with STAT1 GOF - a rare case of primary immunodeficiency.

M. Pac, B. Pietrucha, B. Piątosa, 2020, Advances in respiratory medicine.

Novel de novo large deletion in cystic fibrosis transmembrane conductance regulator gene results in a severe cystic fibrosis phenotype.

A. Sobczyńska-Tomaszewska, A. Norek, M. Jurek, 2011, The Journal of pediatrics.

Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss.

M. Krawczyński, M. Witt, H. Dmeńska, 2004, Journal of applied genetics.

Interstitial Lung Disease in Children With Selected Primary Immunodeficiency Disorders—A Multicenter Observational Study

M. Pronicki, I. Wojsyk-Banaszak, K. Grzela, 2020, Frontiers in Immunology.

Common Variable Immune Deficiency in Children—Clinical Characteristics Varies Depending on Defect in Peripheral B Cell Maturation

B. Wolska-Kuśnierz, M. Pac, E. Bernatowska, 2013, Journal of Clinical Immunology.