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Nucleus (Austin, Tex.)|April 11, 2018
Clinical aspects of Emery-Dreifuss muscular dystrophyAgnieszka Madej-PilarczykMedycyna Wieku Rozwojowego|October 10, 2006
[Hutchinson-Gilford progeria in the light of contemporary genetics]Agnieszka Madej-PilarczykInternational Journal of Occupational Medicine and Environmental Health|May 20, 2014
Professional activity of Emery-Dreifuss muscular dystrophy patients in PolandAgnieszka Madej-PilarczykClinical Neuropathology|August 9, 2013
Is mutation p.Arg168Gly in TPM3 gene responsible for Type 1 fiber hypoplasia and cap structure formation?Anna Fidzianska, Agnieszka Madej-Pilarczyk, Irena Hausmanowa-PetrusewiczNeuropediatrics|March 19, 2013
Morphologic and clinical aspects of Danon disease in a patient with a mutation c.137G > A in the LAMP-2 geneAnna Fidzianska, Agnieszka Madej-Pilarczyk, Ewa Walczak, et al.Folia Neuropathologica|December 31, 2013
Might prepatterned acetylcholine-receptor clusters on surface myotubes be a sign of neuromuscular-junction maturation failure?Anna Fidziańska, Maria Jędrzejowska, Agnieszka Madej-Pilarczyk, et al.Polski Merkuriusz Lekarski : Organ Polskiego Towarzystwa Lekarskiego|April 18, 2002
[Low-symptomatic pheochromocytoma]Agnieszka Madej, Marek Czarkowski, Maciej Skórski, et al.Orphanet Journal of Rare Diseases|May 21, 2026
Longitudinal study of somatic development in Polish patients with Silver-Russell syndrome reveals that chest-to-head proportion as a new clinical indicator for the syndromeAnna Świąder-Leśniak, Dorota Jurkiewicz, Agnieszka Madej-Pilarczyk, et al.Neurologia I Neurochirurgia Polska|January 8, 2010
Emery-Dreifuss dystrophy: a 4-year follow-up on a laminopathy of special interestIrena Hausmanowa-Petrusewicz, Agnieszka Madej-Pilarczyk, Michał Marchel, et al.Pageof 4