Kamila Wyrozumska-Zur

Krakow, MA, Poland

Last Updated: 09/26/2026

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Found 18 publications

Leukodystrophy associated with a mutation in the ERLIN2 gene.

Leukodystrophy associated with a mutation in the ERLIN2 gene.

Journal: Neurologia i neurochirurgia polska

Published: July 08, 2026

Severe hypersensitivity reaction during tofersen therapy in amyotrophic lateral sclerosis associated with the rare SOD1 p.Val120Phe mutation.

Severe hypersensitivity reaction during tofersen therapy in amyotrophic lateral sclerosis associated with the rare SOD1 p.Val120Phe mutation.

Journal: Neurologia i neurochirurgia polska

Published: July 06, 2026

Highlighting the CSF1R mutational spectrum: c.2549C>T variant in late-onset leukoencephalopathy mimicking multiple sclerosis.

Highlighting the CSF1R mutational spectrum: c.2549C>T variant in late-onset leukoencephalopathy mimicking multiple sclerosis.

Journal: Neurologia i neurochirurgia polska

Published: May 23, 2026

Multiple sclerosis in patients with rheumatoid arthritis: a nationwide, pilot study from Poland based on health care claims (2009-2021).

Multiple sclerosis in patients with rheumatoid arthritis: a nationwide, pilot study from Poland based on health care claims (2009-2021).

Journal: Polish archives of internal medicine

Published: January 07, 2026

Hematopoietic Stem Cell Transplantation for CSF1R-Related Disorder: A Longitudinal Study of Efficacy and Safety.

Hematopoietic Stem Cell Transplantation for CSF1R-Related Disorder: A Longitudinal Study of Efficacy and Safety.

Journal: Journal of movement disorders

Published: January 06, 2026

Hematopoietic Stem Cell Transplantation for CSF1R-Related Disorder: A Longitudinal Study of Efficacy and Safety.

Hematopoietic Stem Cell Transplantation for CSF1R-Related Disorder: A Longitudinal Study of Efficacy and Safety.

Journal: Journal of movement disorders

Published: January 06, 2026

A case of an ALS patient with an SQSTM1 mutation - implications for the p62/NF-κB/Nrf2/autophagy pathways in the selection of individualised therapeutic strategies: a preliminary report.

A case of an ALS patient with an SQSTM1 mutation - implications for the p62/NF-κB/Nrf2/autophagy pathways in the selection of individualised therapeutic strategies: a preliminary report.

Journal: Folia medica Cracoviensia

Published: December 17, 2025

Impact of interferon-β and dimethyl fumarate on nonlinear dynamical characteristics of electroencephalogram signatures in patients with multiple sclerosis.

Impact of interferon-β and dimethyl fumarate on nonlinear dynamical characteristics of electroencephalogram signatures in patients with multiple sclerosis.

Journal: Frontiers in neuroinformatics

Published: October 29, 2024

Academic Motivation and Quality of Life of Polish Medical Students.

Academic Motivation and Quality of Life of Polish Medical Students.

Journal: Folia medica Cracoviensia

Published: April 05, 2024

HSPB1 mutation causing distal Hereditary Motor Neuropathy type 2B in a Polish family.

HSPB1 mutation causing distal Hereditary Motor Neuropathy type 2B in a Polish family.

Journal: Folia medica Cracoviensia

Published: April 05, 2024

Hematopoietic Stem Cell Transplantation in CSF1R-Related Leukoencephalopathy: Retrospective Study on Predictors of Outcomes.

Hematopoietic Stem Cell Transplantation in CSF1R-Related Leukoencephalopathy: Retrospective Study on Predictors of Outcomes.

Journal: Pharmaceutics

Published: October 30, 2022

The First Allogeneic Hematopoietic Stem Cell Transplantation in a Polish Patient with Adult-Onset Leukoencephalopathy with Spheroids and Pigmented Glia.

The First Allogeneic Hematopoietic Stem Cell Transplantation in a Polish Patient with Adult-Onset Leukoencephalopathy with Spheroids and Pigmented Glia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: March 14, 2022

Showing 1-12 of 18

Last Updated: 09/26/2026