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Instytut Matki i Dziecka: Warszawa, PL

1998-02-01 to present (Klinika Neurologii Dzieci i Młodzieży)
Employment
Source: Self-asserted source
Iwona Terczyńska

Works (32)

Neuroimaging results, short-term assessment of psychomotor development and the risk of autism spectrum disorder in extremely premature infants (≤28 GA) - a prospective cohort study (preliminary report).

Developmental period medicine
2018 | Journal article
WOSUID:

MEDLINE:29641420

Contributors: Rutkowska, Magdalena; Bekiesinska-Figatowska, Monika; Kmita, Grazyna; Terczynska, Iwona; Polak, Katarzyna; Kalisiak, Marcin; Prazmowska, Dorota; Kiepura, Eliza; Szkudlinska-Pawlak, Sylwia; Seroczynska, Malgorzata et al.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Comprehensive genomic analysis of patients with disorders of cerebral cortical development.

European journal of human genetics : EJHG
2018-04 | Journal article
Contributors: Wiszniewski W; Gawlinski P; Gambin T; Bekiesinska-Figatowska M; Obersztyn E; Antczak-Marach D; Akdemir ZHC; Harel T; Karaca E; Jurek M et al.
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central
grade
Preferred source (of 2)‎

Neuroimaging results, short-term assessment of psychomotor development and the risk of autism spectrum disorder in extremely premature infants (≤28 GA) - a prospective cohort study (preliminary report).

Developmental period medicine
2018-01 | Journal article
Contributors: Rutkowska M; Bekiesińska-Figatowska M; Kmita G; Terczyńska I; Polak K; Kalisiak M; Prażmowska D; Kiepura E; Szkudlińska-Pawlak S; Seroczyńska M et al.
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central

INTRATHECAL INFUSION OF AUTOLOGIC ADIPOSE DERIVED REGENERATIVE CELLS (ADRC) IN AN AUTOIMMUNE DETERMINED REFRACTORY EPILEPSY IN CHILDREN

Epilepsia
2017 | Journal article
WOSUID:

WOS:000417566600393

Contributors: Szczepanik, E.; Mierzewska, H.; Antczak-Marach, D.; Figiel-Dazbrowska, A.; Miszkurka, Z. Zalewska; Kruk, M.; Terczynska, I.; Tryfon, J.; Krzesniak, N.; Sawicka, E. et al.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

DUPLICATIONS OF THE SLC9A6 GENE CAUSE SYNDROMIC INTELLECTUAL DISABILITY WITH STATUS EPILEPTICUS DURING SLOW-WAVE SLEEP A NEW TYPE OF GENE MUTATIONS INVOLVING THE NHE6 DYSFUNCTION IN ESES

Epilepsia
2016 | Journal article
WOSUID:

WOS:000425754400337

Contributors: Dorota, Hoffman-Zacharska D.; Rzonca, S.; Charzewska, A.; Posmyk, R.; Terczynska, I; Kutkowska-Kazmierczak, A.; Bartnik, M.; Szczepanik, E.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

GLUCOSE TRANSPORTER DEFICIENCY TYPE 1 (GLUT1-DS) DUE TO GENE SLC2A1 MUTATIONS - HOW OFTEN EPILEPTIC PATIENTS DISPLAY MOVEMENT DISORDERS. EXPERIENCE FROM ONE POLISH MEDICAL CENTRE

Epilepsia
2016 | Journal article
WOSUID:

WOS:000425754400297

Contributors: Szczepanik, E.; Terczynska, I; Jurek, M.; Kruk, M.; Rudzka-Dybala, M.; Antczak-Marach, D.; Lipiec, A.; Dorota, Hoffman-Zacharska D.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Magnetic resonance imaging of neonates in the magnetic resonance compatible incubator.

Archives of medical science : AMS
2016-08 | Journal article
Contributors: Bekiesińska-Figatowska M; Helwich E; Rutkowska M; Stankiewicz J; Terczyńska I
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central
grade
Preferred source (of 2)‎

[Patterns of the EEG records in children with West Syndrome].

Przeglad lekarski
2015 | Journal article
WOSUID:

MEDLINE:27012133

Contributors: Rudzka-Dybala, Mariola; Szczepanik, Elzbieta; Terczynska, Iwona
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Glucose transporter type 1 deficiency due to SLC2A1 gene mutations--a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review.

Developmental period medicine
2015 | Journal article
WOSUID:

MEDLINE:26982753

Contributors: Szczepanik, Elzbieta; Terczynska, Iwona; Kruk, Malgorzata; Lipiec, Agata; Dudko, Ewa; Tryfon, Jolanta; Jurek, Marta; Hoffman-Zacharska, Dorota
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Glucose transporter type 1 deficiency due to SLC2A1 gene mutations--a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review.

Developmental period medicine
2015-10 | Journal article
Contributors: Szczepanik E; Terczyńska I; Kruk M; Lipiec A; Dudko E; Tryfon J; Jurek M; Hoffman-Zacharska D
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central

From focal epilepsy to Dravet syndrome--Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit.

Neurologia i neurochirurgia polska
2015-06 | Journal article
Contributors: Hoffman-Zacharska D; Szczepanik E; Terczynska I; Goszczanska-Ciuchta A; Zalewska-Miszkurka Z; Tataj R; Bal J
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central
grade
Preferred source (of 2)‎

[Patterns of the EEG records in children with West Syndrome].

Przeglad lekarski
2015-01 | Journal article
Contributors: Rudzka-Dybała M; Szczepanik E; Terczyńska I
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central

Genetic epilepsies with febrile seizures plus: clinical spectrum of Polish patients with SCN1A mutation - preliminary report.

Developmental period medicine
2014 | Journal article
WOSUID:

MEDLINE:25874779

Contributors: Terczynska, Iwona; Szczepanik, Elzbieta; Duszyc, Kinga; Gorka, Paulina; Tataj, Renata; Hoffman-Zacharska, Dorota
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

T1174S SCN1A MUTATION IS ASSOCIATED WITH SEIZURE AND MIGRAINE - MAY IT ALSO CHANGE THE EPILEPTIC ENCEPHALOPATHIES' COURSE?

Epilepsia
2014 | Journal article
WOSUID:

WOS:000337979300230

Contributors: Hoffman-Zacharska, D.; Terczynska, I; Gorka, P.; Winczewska-Wiktor, A.; Steinborn, B.; Mazurczak, T.; Goral, J.; Charzewska, A.; Tataj, R.; Szczepanik, E.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Genetic epilepsies with febrile seizures plus: clinical spectrum of Polish patients with SCN1A mutation - preliminary report.

Developmental period medicine
2014-10 | Journal article
Contributors: Terczyńska I; Szczepanik E; Duszyc K; Górka P; Tataj R; Hoffman-Zacharska D
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central

Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance.

Journal of applied genetics
2014-09 | Journal article
Contributors: Duszyc K; Terczynska I; Hoffman-Zacharska D
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central
grade
Preferred source (of 2)‎

CLINICAL VARIABILITY RESULTING FROM THE MUTATIONS AT THE P. ARG1596 RESIDUE IN THE SCN1A GENE

Epilepsia
2012 | Journal article
WOSUID:

WOS:000308875900127

Contributors: Hoffman-Zacharska, D.; Szczepanik, E.; Tataj, R.; Terczynska, I.; Goszczanska-Ciuchta, A.; Zalewska-Miszkura, Z.; Antczak-Marach, D.; Bal, J.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

MUTATIONS IN CDKL5 AS A CAUSE OF EARLY ONSET EPILEPSY

Epilepsia
2012 | Journal article
WOSUID:

WOS:000308875900004

Contributors: Gos, M.; Hoffman-Zacharska, D.; Bartnik, M.; Derwinska, K.; Terczynska, I.; Mazurkiewicz, H.; Mazurczak, T.; Stankiewicz, P.; Szczepanik, E.; Bocian, E. et al.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

SEVERE PATTERN-SENSITIVITY IN A GIRL WITH DRAVET SYNDROME, DUE TO MICRODELETION IN LOCUS 2Q24.3. A CASE REPORT

Epilepsia
2012 | Journal article
WOSUID:

WOS:000308875900813

Contributors: Szczepanik, E.; Hoffman-Zacharska, D.; Anetta, A. Jeziorek; Terczynska, I.; Bal, J.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
2012-07 | Journal article
Contributors: Bartnik M; Szczepanik E; Derwińska K; Wiśniowiecka-Kowalnik B; Gambin T; Sykulski M; Ziemkiewicz K; Kędzior M; Gos M; Hoffman-Zacharska D et al.
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central
grade
Preferred source (of 2)‎

Identification of CNVs in children with neurodevelopmental disorders using oligonucleotide array-CGH

Chromosome Research
2011 | Journal article
WOSUID:

WOS:000411870600114

Contributors: Bartnik, Magdalena; Derwinska, Katarzyna; Nowakowska, Beata; Wisniowiecka-Kowalnik, Barbara; Obersztyn, Ewa; Szczaluba, Krzysztof; Kutkowska-Kazmierczk, Anna; Klapecki, Jakub; Szczepanik, Elzbieta; Mazurczak, Tomasz et al.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

SCN1A-RELATED SPECTRUM OF FOCAL EPILEPSY WITH FEBRILE SEIZURES PLUS IN POLISH FAMILY

Epilepsia
2011 | Journal article
WOSUID:

WOS:000294217200208

Contributors: Szczepanik, E.; Goszczanska-Ciuchta, A.; Hoffman-Zacharska, D.; Terczynska, I
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

SPECTRUM AND FREQUENCY OF SCN1A MUTATIONS IN DRAVET SYNDROME PATIENTS: THE FIRST ATTEMPT OF MOLECULAR DIAGNOSTIC IN POLAND

Epilepsia
2011 | Journal article
WOSUID:

WOS:000294217200302

Contributors: Hoffman-Zacharska, D.; Terczynska, I; Tataj, R.; Szczepanik, E.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females.

Genetics in medicine : official journal of the American College of Medical Genetics
2011-05 | Journal article
Contributors: Bartnik M; Derwińska K; Gos M; Obersztyn E; Kołodziejska KE; Erez A; Szpecht-Potocka A; Fang P; Terczyńska I; Mierzewska H et al.
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central
grade
Preferred source (of 2)‎

[Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2].

Przeglad lekarski
2010 | Journal article
WOSUID:

MEDLINE:21387820

Contributors: Terczynska, Iwona; Mierzewska, Hanna; Szczepanik, Elibieta; Antczak-Marach, Dorota
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Neurosurgical treatment of drug-resistant epilepsy on the basis of a fusion of MRI and SPECT images - case report.

Polish journal of radiology
2010 | Journal article
WOSUID:

MEDLINE:22802792

Contributors: Jurkiewicz, Elzbieta; Bekiesinska-Figatowska, Monika; Misko, Jolanta; Kaminska, Anna; Kwiatkowski, Stanislaw; Terczynska, Iwona
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Neurosurgical treatment of drug-resistant epilepsy on the basis of a fusion of MRI and SPECT images - case report.

Polish journal of radiology
2010-07 | Journal article
Contributors: Jurkiewicz E; Bekiesińska-Figatowska M; Miśko J; Kamińska A; Kwiatkowski S; Terczyńska I
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central

[Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2].

Przeglad lekarski
2010-01 | Journal article
Contributors: Terczyńska I; Mierzewska H; Szczepanik E; Antczak-Marach D
Source: Self-asserted source
Iwona Terczyńska via Europe PubMed Central

Juvenile myoclonic epilepsy-clinical course depending on the age of seizure onset

Journal of the Neurological Sciences
2009 | Journal article
WOSUID:

WOS:000272521300890

Contributors: Szczepanik, E.; Terczynska, I.; Antczak-Marach, D.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Symptomatic epilepsy in the course of polymicrogyria in one of the set of monozygous twins

Epilepsia
2007 | Journal article
WOSUID:

WOS:000253978700555

Contributors: Szczepanik, E.; Antczak-Marach, D.; Terczynska, I; Tryfon, J.; Hoffman-Zacharska, D.; Poski, R.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Idiopathic generalised epilepsy: Nonpharmacological factors influence on juvenile myoclonic epilepsy

Epilepsia
2006 | Journal article
WOSUID:

WOS:000243021800649

Contributors: Mazurczak, T.; Terczynska, I.; Antczak-Marach, D.; Jeziorek, A.; Szymanska, K.; Tryfon, J.; Hoffman-Zacharska, D.; Szczepanik, E.
Source: Self-asserted source
Iwona Terczyńska via ResearcherID

Benign myoclonic epilepsy of infancy followed by juvenile myoclonic epilepsy: A case report

Epilepsia
2005 | Journal article
WOSUID:

WOS:000231885301206

Contributors: Szczepanik, E; Hoffman-Zacharska, D; Antczak-Marach, D; Terczynska, I
Source: Self-asserted source
Iwona Terczyńska via ResearcherID