Marschik, Peter B.

[["dc.bibliographiccitation.firstpage","107"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Early Human Development"],["dc.bibliographiccitation.lastpage","114"],["dc.bibliographiccitation.volume","83"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Garzarolli, Bettina"],["dc.contributor.author","Prechtl, Heinz F. R."],["dc.date.accessioned","2020-06-23T08:52:55Z"],["dc.date.available","2020-06-23T08:52:55Z"],["dc.date.issued","2007"],["dc.description.abstract","Background Obstetrical and neonatal complications and/or an adverse parenting environment are risk factors for language impairment, but little is known about their effects on early word production (late talking). Aims To determine obstetrical and neonatal risk factors in children with delayed word production; to assess the influence of the parenting environment on word production; to determine whether the toddler's vocabulary competence is related to his/her social competence; to document the neurodevelopmental outcome at the late preschool age. Study design Prospective follow-up study. Based on word production at 18 months, children were retrospectively classified into consistent or transient late talkers and controls. Subjects Full-term infants, N = 30 (mean GA 40.3 ± 1.1 weeks, mean birth weight 3577 ± 267 g) were assessed at 18 and 24 months; and 5 years and 7 months. Methods Austrian Communicative Development Inventories; Bayley Scales of Infant Development; Griffiths Developmental Scales. Outcome measures Peabody Picture Vocabulary Test; Kaufman Assessment Battery for Children; Touwen's neurological examination. Results and Conclusions Lower Apgar scores and the need for neonatal intensive care were associated with delayed word production. The parents' educational and vocational levels were lower in late talkers. Early vocabulary competence correlated with social competence. With regard to the prediction of lexical and cognitive outcomes, late talkers did not differ from controls. Minor neurological dysfunctions (MND) were seen in nearly half of the late talkers and indicate the necessity to follow these children into school age, when MND might become more obvious and literacy can be assessed."],["dc.identifier.doi","10.1016/j.earlhumdev.2006.05.009"],["dc.identifier.isi","WOS:000244597100006"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66609"],["dc.identifier.url","http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000244597100006&KeyUID=WOS:000244597100006"],["dc.language.iso","en"],["dc.relation.issn","0378-3782"],["dc.title","Events at early development: Are they associated with early word production and neurodevelopmental abilities at the preschool age?"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1616"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Journal of Clinical Medicine"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Bos, Arend F."],["dc.contributor.author","Krieber-Tomantschger, Magdalena"],["dc.contributor.author","Alvarado, Elsa"],["dc.contributor.author","Barbosa, Vanessa M."],["dc.contributor.author","Bertoncelli, Natascia"],["dc.contributor.author","Burger, Marlette"],["dc.contributor.author","Chorna, Olena"],["dc.contributor.author","Del Secco, Sabrina"],["dc.contributor.author","DeRegnier, Raye-Ann"],["dc.contributor.author","Hüning, Britta"],["dc.contributor.author","Ko, Jooyeon"],["dc.contributor.author","Lucaccioni, Laura"],["dc.contributor.author","Maeda, Tomoki"],["dc.contributor.author","Marchi, Viviana"],["dc.contributor.author","Martín, Erika"],["dc.contributor.author","Morgan, Catherine"],["dc.contributor.author","Mutlu, Akmer"],["dc.contributor.author","Nogolová, Alice"],["dc.contributor.author","Pansy, Jasmin"],["dc.contributor.author","Peyton, Colleen"],["dc.contributor.author","Pokorny, Florian B."],["dc.contributor.author","Prinsloo, Lucia R."],["dc.contributor.author","Ricci, Eileen"],["dc.contributor.author","Saini, Lokesh"],["dc.contributor.author","Scheuchenegger, Anna"],["dc.contributor.author","Silva, Cinthia R. D."],["dc.contributor.author","Soloveichick, Marina"],["dc.contributor.author","Spittle, Alicia J."],["dc.contributor.author","Toldo, Moreno"],["dc.contributor.author","Utsch, Fabiana"],["dc.contributor.author","van Zyl, Jeanetta"],["dc.contributor.author","Viñals, Carlos"],["dc.contributor.author","Wang, Jun"],["dc.contributor.author","Yang, Hong"],["dc.contributor.author","Yardımcı-Lokmanoğlu, Bilge N."],["dc.contributor.author","Cioni, Giovanni"],["dc.contributor.author","Ferrari, Fabrizio"],["dc.contributor.author","Guzzetta, Andrea"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2020-12-10T18:47:11Z"],["dc.date.available","2020-12-10T18:47:11Z"],["dc.date.issued","2019"],["dc.description.sponsorship","Bill and Melinda Gates Foundation"],["dc.description.sponsorship","Oesterreichische Nationalbank"],["dc.description.sponsorship","Fondazione Pierfranco e Luisa Mariani"],["dc.description.sponsorship","Shanghai Municipal Commission of Health and Family Planning"],["dc.identifier.doi","10.3390/jcm8101616"],["dc.identifier.eissn","2077-0383"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17109"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/78676"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.publisher","MDPI"],["dc.relation.eissn","2077-0383"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Cerebral Palsy: Early Markers of Clinical Phenotype and Functional Outcome"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","95"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.lastpage","108"],["dc.bibliographiccitation.volume","82"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Roche, Laura"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Krieber, Magdalena"],["dc.contributor.author","McLay, Laurie"],["dc.contributor.author","Bölte, Sven"],["dc.contributor.author","Poustka, Luise"],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Gugatschka, Markus"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2020-06-03T07:28:14Z"],["dc.date.available","2020-06-03T07:28:14Z"],["dc.date.issued","2018"],["dc.description.abstract","ackground Responding to one’s own name (RtN) has been reported as atypical in children with developmental disorders, yet comparative studies on RtN across syndromes are rare. Aims We aim to (a) overview the literature on RtN in different developmental disorders during the first 24 months of life, and (b) report comparative data on RtN across syndromes. Methods and procedures In Part 1, a literature search, focusing on RtN in children during the first 24 months of life with developmental disorders, identified 23 relevant studies. In Part 2, RtN was assessed utilizing retrospective video analysis for infants later diagnosed with ASD, RTT, or FXS, and typically developing peers. Outcomes and results Given a variety of methodologies and instruments applied to assess RtN, 21/23 studies identified RtN as atypical in infants with a developmental disorder. We observed four different developmental trajectories of RtN in ASD, RTT, PSV, and FXS from 9 to 24 months of age. Between-group differences became more distinctive with age. Conclusions and implications RtN may be a potential parameter of interest in a comprehensive early detection model characterising age-specific neurofunctional biomarkers associated with specific disorders, and contribute to early identification."],["dc.identifier.doi","10.1016/j.ridd.2018.04.004"],["dc.identifier.pmid","29655507"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66133"],["dc.language.iso","en"],["dc.relation.issn","0891-4222"],["dc.title","Response to name and its value for the early detection of developmental disorders: Insights from autism spectrum disorder, Rett syndrome, and fragile X syndrome. A perspectives paper"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","6"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Kindheit und Entwicklung"],["dc.bibliographiccitation.lastpage","14"],["dc.bibliographiccitation.volume","30"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Zhang, Dajie"],["dc.contributor.author","Marschik, Peter B."],["dc.date.accessioned","2021-04-14T08:30:20Z"],["dc.date.available","2021-04-14T08:30:20Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1026/0942-5403/a000323"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83193"],["dc.language.iso","de"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","2190-6246"],["dc.relation.issn","0942-5403"],["dc.title","Die Bedeutung fötaler und neonataler Motorik für die kindliche Entwicklung und die Früherkennung von Entwicklungsstörungen"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","355"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Developmental Neurorehabilitation"],["dc.bibliographiccitation.lastpage","357"],["dc.bibliographiccitation.volume","14"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Einspieler, Christa"],["dc.date.accessioned","2020-06-22T06:39:00Z"],["dc.date.available","2020-06-22T06:39:00Z"],["dc.date.issued","2011"],["dc.identifier.doi","10.3109/17518423.2011.604355"],["dc.identifier.pmid","22136120"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66581"],["dc.language.iso","en"],["dc.relation.eissn","1751-8431"],["dc.relation.issn","1751-8423"],["dc.title","Methodological note: Video analysis of the early development of Rett syndrome—one method for many disciplines"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","837"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Early Human Development"],["dc.bibliographiccitation.lastpage","843"],["dc.bibliographiccitation.volume","88"],["dc.contributor.author","Yang, Hong"],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Shi, Wei"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Wang, Yi"],["dc.contributor.author","Cao, Yun"],["dc.contributor.author","Li, Hui"],["dc.contributor.author","Liao, Yuan-Gui"],["dc.contributor.author","Shao, Xiao-Mei"],["dc.date.accessioned","2020-06-18T08:09:01Z"],["dc.date.available","2020-06-18T08:09:01Z"],["dc.date.issued","2012"],["dc.description.abstract","Background A deviant motor behaviour at age 3 to 5 months is predictive of cerebral palsy (CP). Particular features of the early motor repertoire even proved predictive of the degree of functional limitations as classified on the Gross Motor Function Classification System (GMFCS) in children with CP, born preterm. Aims We aimed to determine whether an association between the early motor repertoire and the GMFCS also holds true for children born at term. Study design Longitudinal study. Subjects 79 infants (60 boys and 19 girls; 47 infants born at term; video recorded for the assessment of movements and posture at age 9 to 20 weeks postterm age) who developed CP. Outcome measures The GMFCS was applied at age 2 to 5 years. Results Motor optimality at age 3 to 5 months showed a significant correlation with functional mobility and activity limitation as classified on the GMFCS at age 2 to 5 years in both children born at term (Spearman rho = − 0.66, p < 0.001) and born preterm (rho = − 0.37, p < 0.05). Infants born preterm were more likely to show normal movement patterns than infants born at term. A normal posture and an abnormal, jerky (yet not monotonous) movement character resulted in better levels of function and mobility. With the exception of one, none of the infants showed fidgety movements. A cramped-synchronised movement character, repetitive opening and closing of the mouth, and abnormal finger postures characterised children who would show a poor self-mobility later. Conclusions Assessing the quality of motor performance at 9 to 20 weeks postterm age (irrespective of the gestational age) improves our ability to predict later functional limitations in children with CP."],["dc.identifier.doi","10.1016/j.earlhumdev.2012.06.004"],["dc.identifier.pmid","22795821"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66472"],["dc.language.iso","en"],["dc.relation.issn","0378-3782"],["dc.title","Cerebral palsy in children: movements and postures during early infancy, dependent on preterm vs. full term birth"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","58"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Developmental Neurorehabilitation"],["dc.bibliographiccitation.lastpage","66"],["dc.bibliographiccitation.volume","16"],["dc.contributor.author","Hinton, Rebecca"],["dc.contributor.author","Budimirovic, Dejan B."],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Talisa, Victor B."],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Gipson, Tatjana"],["dc.contributor.author","Johnston, Michael V."],["dc.date.accessioned","2020-05-19T11:13:55Z"],["dc.date.available","2020-05-19T11:13:55Z"],["dc.date.issued","2013"],["dc.description.abstract","Objective: This study examined features of early language and motor milestones in children with fragile X syndrome (FXS) and contrasted these features with a diagnosis of Autism Spectrum Disorder (ASD) later in life in these children. Methods: We retrospectively examined parental report of age of onset for walking and first words for primarily boys with FXS, both with ASD (FXS + ASD) and FXS-only. The diagnosis of ASD was established by DSM-IV criteria, which were complemented by the ADOS. The age of onset was analyzed as a continuous and categorical variable, which were compared to the upper limit of typically developing children. Results: Individuals with FXS-only are more delayed in the onset of first words than first walks. The finding represents a pattern suggesting a continuum as robustly demonstrated in individuals with FXS + ASD vs. FXS-only. Conclusion: Our results support validity of FXS + ASD co-morbidity as a distinct phenotype in individuals with FXS."],["dc.identifier.doi","10.3109/17518423.2012.704414"],["dc.identifier.pmid","23249372"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65583"],["dc.language.iso","en"],["dc.relation.eissn","1751-8431"],["dc.relation.issn","1751-8423"],["dc.title","Parental reports on early language and motor milestones in fragile X syndrome with and without autism spectrum disorders"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","73"],["dc.bibliographiccitation.journal","Developmental Neurorehabilitation"],["dc.bibliographiccitation.lastpage","74"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Einspieler, Christa"],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Enzinger, Christian"],["dc.contributor.author","Bölte, Sven"],["dc.date.accessioned","2020-05-18T13:26:00Z"],["dc.date.available","2020-05-18T13:26:00Z"],["dc.date.issued","2015"],["dc.identifier.doi","10.3109/17518423.2014.916362"],["dc.identifier.pmid","24840633"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65533"],["dc.language.iso","en"],["dc.relation.issn","1751-8423"],["dc.relation.issn","1751-8431"],["dc.title","The interdisciplinary quest for behavioral biomarkers pinpointing developmental disorders"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3133"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Research in Developmental Disabilities"],["dc.bibliographiccitation.lastpage","3138"],["dc.bibliographiccitation.volume","34"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Sigafoos, Jeff"],["dc.contributor.author","Tager-Flusberg, H."],["dc.contributor.author","Kaufmann, W. E."],["dc.contributor.author","Grossmann, T."],["dc.contributor.author","Einspieler, Christa"],["dc.date.accessioned","2020-05-20T13:08:42Z"],["dc.date.available","2020-05-20T13:08:42Z"],["dc.date.issued","2013"],["dc.description.abstract","Rett syndrome (RTT) is a severe neurological disorder characterized by a developmental regression in motor and speech-language domains. There is, however, limited research on socio-communicative development of affected children before the onset of regression. We analyzed audio–video recordings made by parents of six 9- to 12-month old girls later diagnosed with typical RTT, applying the Inventory of Potential Communicative Acts (IPCA) to identify early communicative forms and functions. Each girl used at least one communicative form (e.g., body movement, eye gaze, or vocalizations) to gain attention and answer, but none were observed to make choices or request information. Varying numbers of children were observed to perform other communicative functions according to the IPCA including social convention, rejecting or requesting an object. Non-verbal forms (e.g., reaching, moving closer, eye contact, smiling) were more common than non-linguistic verbal forms (e.g., unspecified vocalizations, pleasure vocalizations, crying). (Pre-)linguistic verbal forms (e.g., canonical or variegated babbling, proto-words) were not used for communicative purposes. These data suggest that atypical developmental patterns in the socio-communicative domain are evident prior to regression in young individuals later diagnosed with RTT."],["dc.identifier.doi","10.1016/j.ridd.2013.06.040"],["dc.identifier.pmid","23891731"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65631"],["dc.language.iso","en"],["dc.relation.issn","0891-4222"],["dc.title","Early socio-communicative forms and functions in typical Rett syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","284"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Developmental Neurorehabilitation"],["dc.bibliographiccitation.lastpage","290"],["dc.bibliographiccitation.volume","17"],["dc.contributor.author","Marschik, Peter B."],["dc.contributor.author","Vollmann, Ralf"],["dc.contributor.author","Bartl-Pokorny, Katrin D."],["dc.contributor.author","Green, Vanessa A."],["dc.contributor.author","van der Meer, Larah"],["dc.contributor.author","Wolin, Thomas"],["dc.contributor.author","Einspieler, Christa"],["dc.date.accessioned","2020-06-23T07:42:30Z"],["dc.date.available","2020-06-23T07:42:30Z"],["dc.date.issued","2014"],["dc.description.abstract","Objective: We assessed various aspects of speech-language and communicative functions of an individual with the preserved speech variant of Rett syndrome (RTT) to describe her developmental profile over a period of 11 years. Methods: For this study, we incorporated the following data resources and methods to assess speech-language and communicative functions during pre-, peri- and post-regressional development: retrospective video analyses, medical history data, parental checklists and diaries, standardized tests on vocabulary and grammar, spontaneous speech samples and picture stories to elicit narrative competences. Results: Despite achieving speech-language milestones, atypical behaviours were present at all times. We observed a unique developmental speech-language trajectory (including the RTT typical regression) affecting all linguistic and socio-communicative sub-domains in the receptive as well as the expressive modality. Conclusion: Future research should take into consideration a potentially considerable discordance between formal and functional language use by interpreting communicative acts on a more cautionary note."],["dc.identifier.doi","10.3109/17518423.2013.783139"],["dc.identifier.pmid","23870013"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66596"],["dc.language.iso","en"],["dc.relation.eissn","1751-8431"],["dc.relation.issn","1751-8423"],["dc.title","Developmental profile of speech-language and communicative functions in an individual with the preserved speech variant of Rett syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dspace.entity.type","Publication"]]