Beata Kazmierczak
Warsaw, MZ 02097, Poland
Last Updated: 09/26/2026
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Found 14 publications
Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-Associated Optic Neuritis - A Case Report and Literature Review.
Journal: International medical case reports journal
Published: February 02, 2024
The hidden role of the Sigma1 receptor in muscle cells.
Journal: Journal of receptor and signal transduction research
Published: February 15, 2020
Simpson-Golabi-Behmel syndrome in a 39-year-old male patient with suspected acromegaly-A case study.
Simpson-Golabi-Behmel syndrome in a 39-year-old male patient with suspected acromegaly-A case study.
Journal: American journal of medical genetics. Part A
Published: April 17, 2018
Validation of qPCR reference genes in lymphocytes from patients with amyotrophic lateral sclerosis.
Journal: PloS one
Published: June 23, 2016
Clinical Outcomes after Uncomplicated Cataract Surgery with Implantation of the Tecnis Toric Intraocular Lens.
Journal: Journal of ophthalmology
Published: November 20, 2015
Targeting the expression of glutathione- and sulfate-dependent detoxification enzymes in HepG2 cells by oxygen in minimal and amino acid enriched medium.
Journal: Experimental and molecular pathology
Published: November 04, 2015
GSTP1 Polymorphisms and their Association with Glutathione Transferase and Peroxidase Activities in Patients with Motor Neuron Disease.
Journal: CNS & neurological disorders drug targets
Published: May 25, 2015
Aquaporin-4: A novel diagnostic biomarker for seronegative neuromyelitis optica.
Journal: Multiple sclerosis (Houndmills, Basingstoke, England)
Published: March 04, 2015
Alteration of Motor Protein Expression Involved in Bidirectional Transport in Peripheral Blood Mononuclear Cells of Patients with Amyotrophic Lateral Sclerosis.
Journal: Neuro-degenerative diseases
Published: February 12, 2015
Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: August 01, 2013
Dynactin Deficiency in the CNS of Humans with Sporadic ALS and Mice with Genetically Determined Motor Neuron Degeneration.
Journal: Neurochemical research
Published: April 22, 2013
SMN1 gene duplications are more frequent in patients with progressive muscular atrophy.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: March 13, 2013
Last Updated: 09/26/2026