Lista de obras - Magdalena Kuźma-Kozakiewicz

ALS and fertility: does ALS affect number of children patients have?

artículo científico publicado en 2020

Alteration of Motor Protein Expression Involved in Bidirectional Transport in Peripheral Blood Mononuclear Cells of Patients with Amyotrophic Lateral Sclerosis.

artículo científico publicado en 2016

An observational study on quality of life and preferences to sustain life in locked-in state

artículo científico publicado en 2019

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration

artículo científico publicado en 2013

Are we really closer to improving the diagnostic sensitivity in ALS patients with Awaji criteria?

artículo científico publicado en 2014

Author response: An observational study on quality of life and preferences to sustain life in locked-in state

artículo científico publicado en 2020

Biochemical parameters in determination of nutritional status in amyotrophic lateral sclerosis

scientific article published on 02 January 2020

Changes in kinesin expression in the CNS of mice with dynein heavy chain 1 mutation.

artículo científico publicado en 2013

Differences in glutathione S-transferase pi expression in transgenic mice with symptoms of neurodegeneration.

artículo científico publicado en 2011

Does the MUNIX Method Reflect Clinical Dysfunction in Amyotrophic Lateral Sclerosis: A Practical Experience

artículo científico publicado en 2016

Dynactin Deficiency in the CNS of Humans with Sporadic ALS and Mice with Genetically Determined Motor Neuron Degeneration

artículo científico publicado en 2013

Dyslipidemia in patients with amyotrophic lateral sclerosis - a case control retrospective study

artículo científico publicado en 2020

Edaravone in the treatment of amyotrophic lateral sclerosis

artículo científico publicado en 2018

Emotional Lability at Disease Onset Is an Independent Prognostic Factor of Faster Disease Progression in Amyotrophic Lateral Sclerosis

artículo científico publicado en 2020

Existential decision-making in a fatal progressive disease: how much do legal and medical frameworks matter?

artículo científico publicado en 2017

Family history of neurodegenerative disorders in patients with amyotrophic lateral sclerosis: population-based case-control study

scientific article published on 12 March 2020

GSTP1 Polymorphisms and their Association with Glutathione Transferase and Peroxidase Activities in Patients with Motor Neuron Disease.

artículo científico publicado en 2015

Gastrostomy and mechanical ventilation in amyotrophic lateral sclerosis: how best to support the decision-making process?

artículo científico publicado en 2020

Healthcare provision in amyotrophic lateral sclerosis: procedures, queries and pitfalls in Germany and Poland

artículo científico publicado en 2020

Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group

scientific article published on 07 April 2020

Influence of Environment and Lifestyle on Incidence and Progress of Amyotrophic Lateral Sclerosis in A German ALS Population

article

International Survey of ALS Experts about Critical Questions for Assessing Patients with ALS.

artículo científico

Intraspinal Transplantation of the Adipose Tissue-Derived Regenerative Cells in Amyotrophic Lateral Sclerosis in Accordance with the Current Experts' Recommendations: Choosing Optimal Monitoring Tools

artículo científico publicado en 2018

Is cerebrospinal fluid obtained for diagnostic purpose a good material for biomarker studies in amyotrophic lateral sclerosis?

artículo científico publicado en 2014

Kinesin expression in the central nervous system of humans and transgenic hSOD1G93A mice with amyotrophic lateral sclerosis

artículo científico publicado en 2012

Mice with mutation in dynein heavy chain 1 do not share the same tau expression pattern with mice with SOD1-related motor neuron disease

artículo científico publicado en 2011

Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALS

article

Multicentre quality control evaluation of different biomarker candidates for amyotrophic lateral sclerosis

Neurotransplantation in mice: The concorde-like position ensures minimal cell leakage and widespread distribution of cells transplanted into the cisterna magna

artículo científico publicado en 2008

New therapeutic targets for amyotrophic lateral sclerosis

artículo científico publicado en 2010

Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis.

artículo científico publicado en 2014

Positron emission tomography neuroimaging in neurodegenerative diseases: Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis

artículo científico publicado en 2019

Putative founder effect in the Polish, Iranian and United States populations for the L144S SOD1 mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis

scientific article published on 10 August 2020

ROCK-ALS: Protocol for a Randomized, Placebo-Controlled, Double-Blind Phase IIa Trial of Safety, Tolerability and Efficacy of the Rho Kinase (ROCK) Inhibitor Fasudil in Amyotrophic Lateral Sclerosis

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family

artículo científico publicado en 2011

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.

artículo científico publicado en 2013

SMN1 gene duplications are more frequent in patients with progressive muscular atrophy.

artículo científico publicado en 2013

Scintigraphic Evaluation of Mild to Moderate Dysphagia in Motor Neuron Disease.

artículo científico publicado en 2016

Spreading in ALS: The relative impact of upper and lower motor neuron involvement

scientific article published on 18 June 2020

TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients.

artículo científico publicado en 2018

Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis.

artículo científico publicado en 2006

The genetics of amyotrophic lateral sclerosis.

artículo científico publicado en 2009

Therapeutic decisions in ALS patients: cross-cultural differences and clinical implications

scientific article published on 04 May 2018

Validation of qPCR reference genes in lymphocytes from patients with amyotrophic lateral sclerosis

artículo científico publicado en 2017

Lista de obras de Magdalena Kuźma-Kozakiewicz

ALS and fertility: does ALS affect number of children patients have?

Alteration of Motor Protein Expression Involved in Bidirectional Transport in Peripheral Blood Mononuclear Cells of Patients with Amyotrophic Lateral Sclerosis.

An observational study on quality of life and preferences to sustain life in locked-in state

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration

Are we really closer to improving the diagnostic sensitivity in ALS patients with Awaji criteria?

Author response: An observational study on quality of life and preferences to sustain life in locked-in state

Biochemical parameters in determination of nutritional status in amyotrophic lateral sclerosis

Changes in kinesin expression in the CNS of mice with dynein heavy chain 1 mutation.

Differences in glutathione S-transferase pi expression in transgenic mice with symptoms of neurodegeneration.

Does the MUNIX Method Reflect Clinical Dysfunction in Amyotrophic Lateral Sclerosis: A Practical Experience

Dynactin Deficiency in the CNS of Humans with Sporadic ALS and Mice with Genetically Determined Motor Neuron Degeneration

Dyslipidemia in patients with amyotrophic lateral sclerosis - a case control retrospective study

Edaravone in the treatment of amyotrophic lateral sclerosis

Emotional Lability at Disease Onset Is an Independent Prognostic Factor of Faster Disease Progression in Amyotrophic Lateral Sclerosis

Existential decision-making in a fatal progressive disease: how much do legal and medical frameworks matter?

Family history of neurodegenerative disorders in patients with amyotrophic lateral sclerosis: population-based case-control study

GSTP1 Polymorphisms and their Association with Glutathione Transferase and Peroxidase Activities in Patients with Motor Neuron Disease.

Gastrostomy and mechanical ventilation in amyotrophic lateral sclerosis: how best to support the decision-making process?

Healthcare provision in amyotrophic lateral sclerosis: procedures, queries and pitfalls in Germany and Poland

Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group

Influence of Environment and Lifestyle on Incidence and Progress of Amyotrophic Lateral Sclerosis in A German ALS Population

International Survey of ALS Experts about Critical Questions for Assessing Patients with ALS.

Intraspinal Transplantation of the Adipose Tissue-Derived Regenerative Cells in Amyotrophic Lateral Sclerosis in Accordance with the Current Experts' Recommendations: Choosing Optimal Monitoring Tools

Is cerebrospinal fluid obtained for diagnostic purpose a good material for biomarker studies in amyotrophic lateral sclerosis?

Kinesin expression in the central nervous system of humans and transgenic hSOD1G93A mice with amyotrophic lateral sclerosis

Mice with mutation in dynein heavy chain 1 do not share the same tau expression pattern with mice with SOD1-related motor neuron disease

Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALS

Multicentre quality control evaluation of different biomarker candidates for amyotrophic lateral sclerosis

Neurotransplantation in mice: The concorde-like position ensures minimal cell leakage and widespread distribution of cells transplanted into the cisterna magna

New therapeutic targets for amyotrophic lateral sclerosis

Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis.

Positron emission tomography neuroimaging in neurodegenerative diseases: Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis

Putative founder effect in the Polish, Iranian and United States populations for the L144S SOD1 mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis

ROCK-ALS: Protocol for a Randomized, Placebo-Controlled, Double-Blind Phase IIa Trial of Safety, Tolerability and Efficacy of the Rho Kinase (ROCK) Inhibitor Fasudil in Amyotrophic Lateral Sclerosis

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.

SMN1 gene duplications are more frequent in patients with progressive muscular atrophy.

Scintigraphic Evaluation of Mild to Moderate Dysphagia in Motor Neuron Disease.

Spreading in ALS: The relative impact of upper and lower motor neuron involvement

TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients.

Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis.

The genetics of amyotrophic lateral sclerosis.

Therapeutic decisions in ALS patients: cross-cultural differences and clinical implications

Validation of qPCR reference genes in lymphocytes from patients with amyotrophic lateral sclerosis