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Authors whose works are in public domain in at least one jurisdiction

List of works by Justyna Paprocka

Angelman syndrome and hypothyroidism - coincidence or unique correlation?

scientific article published in October 2007

Angelman syndrome revisited

scientific article published in September 2007

CDG type Ia and congenital cytomegalovirus infection: two coexisting conditions

scientific article published in January 2009

CDKL5 Deficiency Disorder-A Complex Epileptic Encephalopathy

scientific article published on 17 February 2020

Circadian Profile of Salivary Melatonin Secretion in Hypoxic Ischemic Encephalopathy

scientific article published on 25 September 2020

Clinical and neuropathological picture of ethylmalonic aciduria - diagnostic dilemma

scientific article published on January 1, 2011

Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency

scientific article published on 01 January 2007

Corpus Callosum Agenesis: An Insight into the Etiology and Spectrum of Symptoms

scientific article published on 09 September 2020

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

scientific article published on 25 October 2005

Efficacy and Safety of Melatonin Treatment in Children with Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder-A Review of the Literature

scientific article published on 07 April 2020

FGF12p.Gly112Ser variant as a cause of phenytoin/phenobarbital responsive epilepsy

scientific article published on 10 July 2019

Four-and-one-half years' experience in monitoring of reproducibility of an MR spectroscopy system--application of in vitro results to interpretation of in vivo data.

scientific article published on 8 May 2014

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing

scientific article published on 5 April 2012

Hereditary neuropathy with liability to pressure palsy

scientific article published on 01 January 2006

Hyperammonemia in children: on the crossroad of different disorders

scientific article published on September 2012

Isolated rhomboencephalosynapsis – a rare cerebellar anomaly ⬇️

scientific article published on January 1, 2012

Joubert syndrome and related disorders

scientific article published on July 2012

Leukoencephalopathy with Calcifications and Cysts-The First Polish Patient with Labrune Syndrome

scientific article published on 18 November 2020

Leukoencephalopathy with macrocephaly and mild clinical course

scientific article published in January 2004

Maternal phenylketonuria.

scientific article published in January 2009

Mathematical evaluation of melatonin secretion in hypoxic ischemic encephalopathy

scientific article published on 01 December 2018

Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.

scientific article

Melatonin and Angelman Syndrome: Implications and Mathematical Model of Diurnal Secretion

scientific article published on 12 December 2017

Melatonin and childhood refractory epilepsy--a pilot study.

scientific article published on September 2010

Melatonin in Epilepsy: A New Mathematical Model of Diurnal Secretion

scientific article published on 13 July 2016

Melatonin in Hypoxic-Ischemic Brain Injury in Term and Preterm Babies

scientific article published on 20 February 2019

Melatonin in Tuberous Sclerosis Complex Analysis Using Modern Mathematical Modeling Methods

scientific article

Melatonin-Measurement Methods and the Factors Modifying the Results. A Systematic Review of the Literature

scientific article published on 15 March 2020

Microcephaly in Neurometabolic Diseases

Neuroimaging of Basal Ganglia in Neurometabolic Diseases in Children

scientific article published on 12 November 2020

Neurological picture and 1H MRS in 4 children with hypoparathyroidism

scientific article

Prospects and Limitations Related to the Use of MicroRNA as a Biomarker of Epilepsy in Children: A Systematic Review

scientific article published on 04 January 2021

Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci

scientific article published on July 2010

[Back pain in children]

scientific article published on 01 January 2008

[Neurocutaneous melanosis--case report]

scientific article published on 01 January 2004

[Niemann-Pick disease, type A: a case report]

scientific article published on 01 May 2006

[Sudden infant death syndrome--current opinions on etiology and pathogenesis]

scientific article published on 01 January 2009

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