E Rowińska

Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases

Ewa Pronicka, Elżbieta Ciara, Paulina Halat et al. · Journal of Applied Genetics · 2017 · 92 citations · Full text

Molecular background of polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome in a Polish population: novel <i>AIRE</i> mutations and an estimate of disease prevalence

Bartosz Stolarski, Ewa Pronicka, L Korniszewski et al. · Clinical Genetics · 2006 · 77 citations

Genetics, Immunodeficiencies, Genetic Epidemiology +19

Infection of the pleura by Aspergillus fumigatus

P Krakówka, E Rowińska, H Halweg · Thorax · 1970 · 48 citations · Full text

Diagnostic Mycology, Pathogenic Microbiology, Interventional Pulmonology +17

Persistent hypercalciuria and elevated 25-hydroxyvitamin D 3 in children with infantile hypercalcaemia

Ewa Pronicka, E Rowińska, H Kulczycka et al. · Pediatric Nephrology · 1997 · 46 citations

Inherited Metabolic Disease, Clinical Nutrition, Pediatrics +7

X-linked hypophosphatemia in Polish patients. 2. Analysis of clinical features and genotype-phenotype correlation.

Ewa Popowska, Ewa Pronicka, Anna Sułek et al. · PubMed · 2001 · 18 citations