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Physical Characterization and Innate Immunogenicity of Aggregated Intravenous Immunoglobulin (IGIV) in an In Vitro Cell-Based Model

Pharmaceutical research, 2016-07, Vol.33 (7), p.1736-1751

2016

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An international collaborative study to establish the WHO 1st international standard for alpha-1-antitrypsin

Vox sanguinis, 2011-07, Vol.101 (1), p.83-89

2011

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Do Immunological Profiles of the Cerebrospinal Fluid Correlate with Disease Severity in Multiple Sclerosis? (P02.095)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P02-P02.095

2012

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O3-6 Carrier-state of the T allele of 677C > T polymorphism in MTHFR gene increases the risk of ischemic stroke in Polish boys

European journal of paediatric neurology, 2009, Vol.13, p.S6-S6

2009

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Agenesis of Corpus Callosum: Clinical Description and Etiology

Journal of child neurology, 2000-06, Vol.15 (6), p.401-405

2000

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Do children with Adams-Oliver syndrome require endocrine follow-up? New information on the phenotype and management

Clinical genetics, 2010-09, Vol.78 (3), p.227-235

2010

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Tolerable risk guidelines

ISA transactions, 2001-01, Vol.40 (4), p.391-399

Marszal, Edward M

2001

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Difficulties in differentiation of Parry-Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome

Child's nervous system, 2006-04, Vol.22 (4), p.409-415

2006

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Characterization of differences in isoelectric focusing behavior of alpha-proteinase inhibitor products

Transfusion (Philadelphia, Pa.), 2006-05, Vol.46 (5), p.872-3; author reply 874

2006

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Characterization of Therapeutic Proteins

Protein Therapeutics, 2017, Vol.21, p.69-121

2017

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A Novel Mode of Polymerization of alpha sub(1)-Proteinase Inhibitor

The Journal of biological chemistry, 2003-05, Vol.278 (22), p.19611-19618

2003

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Platelet and intestinal 5-HT sub(2A) receptor mRNA in autistic spectrum disorders - results of a pilot study

Acta neurobiologiae experimentalis, 2010-01, Vol.70 (2), p.232-238

2010

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Artificial intelligence advancements applied in off-the-shelf controllers

Process safety progress, 2002-06, Vol.21 (2), p.97-101

Marszal, Edward M.

2002

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Melatonin and childhood refractory epilepsy

European journal of paediatric neurology, 2008, Vol.12, p.S42-S42

2008

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Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts

Biochimie, 1997-07, Vol.79 (7), p.439-448

1997

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Comparison of safety integrity level selection methods an utilization of risk based approaches

Process safety progress, 1999, Vol.18 (4), p.189-194

1999

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ADEM – evolution of the clinical and radiological presentation

European journal of paediatric neurology, 2008, Vol.12, p.S72-S72

2008

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Parsonage – Turner syndrome in juvenile patients

European journal of paediatric neurology, 2008, Vol.12, p.S55-S55

2008

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Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency

Folia neuropathologica, 2007, Vol.45 (4), p.213-219

2007

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White matter abnormalities in siblings with Goldberg Shprintzen syndrome

European journal of paediatric neurology, 2008, Vol.12, p.S47-S47

2008

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Polymorphism of gene encoding transporting protein MDR1 and frequency of CYP3A5 SNPs in patients with cryptogenic partial epilepsy – preliminary results

European journal of paediatric neurology, 2008, Vol.12, p.S39-S39

2008

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Hereditary neuropathy with liability to pressure palsy

Folia neuropathologica, 2006, Vol.44 (4), p.290-294

2006

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Lipid raft disease? A new severe congenital myopathy

Folia neuropathologica, 2007, Vol.45 (4), p.242-246

2007

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The cerebral form of toxocarosis in a seven-year-old patient

Folia neuropathologica, 2006, Vol.44 (1), p.72-76

2006

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Friedreich's ataxia

Journal of child neurology, 2002-05, Vol.17 (5), p.315-319

2002

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Physical Characterization and Innate Immunogenicity of Aggregated Intravenous Immunoglobulin (IGIV) in an In Vitro Cell-Based Model

An international collaborative study to establish the WHO 1st international standard for alpha-1-antitrypsin

Do Immunological Profiles of the Cerebrospinal Fluid Correlate with Disease Severity in Multiple Sclerosis? (P02.095)

O3-6 Carrier-state of the T allele of 677C > T polymorphism in MTHFR gene increases the risk of ischemic stroke in Polish boys

Agenesis of Corpus Callosum: Clinical Description and Etiology

Do children with Adams-Oliver syndrome require endocrine follow-up? New information on the phenotype and management

Tolerable risk guidelines

Difficulties in differentiation of Parry-Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome

Characterization of differences in isoelectric focusing behavior of alpha-proteinase inhibitor products

Characterization of Therapeutic Proteins

A Novel Mode of Polymerization of alpha sub(1)-Proteinase Inhibitor

Platelet and intestinal 5-HT sub(2A) receptor mRNA in autistic spectrum disorders - results of a pilot study

Artificial intelligence advancements applied in off-the-shelf controllers

Melatonin and childhood refractory epilepsy

Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts

Comparison of safety integrity level selection methods an utilization of risk based approaches

ADEM – evolution of the clinical and radiological presentation

Parsonage – Turner syndrome in juvenile patients

Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency

White matter abnormalities in siblings with Goldberg Shprintzen syndrome

Polymorphism of gene encoding transporting protein MDR1 and frequency of CYP3A5 SNPs in patients with cryptogenic partial epilepsy – preliminary results

Hereditary neuropathy with liability to pressure palsy

Lipid raft disease? A new severe congenital myopathy

The cerebral form of toxocarosis in a seven-year-old patient

Friedreich's ataxia

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