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Journal of the Peripheral Nervous System : JPNS|December 15, 2015
Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?Anna Potulska-Chromik, Barbara Ryniewicz, Karolina Aragon-Gawinska, et al.Neurologia I Neurochirurgia Polska|December 3, 2025
SIGMAR1 gene-related neuromuscular disorders - what do we know?Maciej Kalita, Maria Jędrzejowska, Anna Potulska-Chromik, et al.Journal of Clinical Medicine|March 3, 2021
Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy PatientsAnna Potulska-Chromik, Maria Jędrzejowska, Monika Gos, et al.Folia Neuropathologica|January 16, 2013
Charcot-Marie-Tooth type 1C disease coexisting with progressive multiple sclerosis: a study of an overlapping syndromeAnna Potulska-Chromik, Elena Sinkiewicz-Darol, Anna Kostera-Pruszczyk, et al.Frontiers in Neurology|February 7, 2022
Corrigendum: Pediatric CIDP: Diagnosis and Management. A Single-Center ExperienceMałgorzata Łukawska, Anna Potulska-Chromik, Marta Lipowska, et al.Journal of Applied Genetics|August 17, 2024
Expanding TBCE-related phenotype-novel variant causing rigid spine, eosinophilia, neutropenia, and nocturnal hypoxemiaMagdalena Badura-Stronka, Adam Sebastian Hirschfeld, Evgenia Globa, et al.Frontiers in Neurology|July 19, 2021
Pediatric CIDP: Diagnosis and Management. A Single-Center ExperienceMałgorzata Łukawska, Anna Potulska-Chromik, Marta Lipowska, et al.Journal of the Peripheral Nervous System : JPNS|November 19, 2014
Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot-Marie-Tooth diseaseAnna Kostera-Pruszczyk, Joanna Kosinska, Agnieszka Pollak, et al.Journal of Child Neurology|July 2, 2026
Neuromuscular Symptoms of ORAI1-Related ImmunodeficiencyMaria Jędrzejowska, Anna Potulska-Chromik, Karolina Czeczko, et al.Plos One|December 27, 2014
Two desmin gene mutations associated with myofibrillar myopathies in Polish familiesJakub Piotr Fichna, Justyna Karolczak, Anna Potulska-Chromik, et al.Pageof 5