Adde Adde

Adde Adde


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 July 2010 in Developmental Medicine & Child Neurology
Verified
Journal Article
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AAAdde Adde
Adde Adde
JHJorunn L Helbostad
Jorunn L Helbostad
AJAlexander Refsum Jensenius
Alexander Refsum Jensenius
GTGunnar Taraldsen
Gunnar Taraldsen
KGKristine H Grunewaldt
Kristine H Grunewaldt
RSRagnhild Støen
Ragnhild Støen

1 September 2009 in Early Human Development
Verified
Journal Article
Closed access
AAAdde Adde
Adde Adde
JHJorunn L. Helbostad
Jorunn L. Helbostad
AJAlexander Refsum Jensenius
Alexander Refsum Jensenius
GTGunnar Taraldsen
Gunnar Taraldsen
RSRagnhild Støen
Ragnhild Støen

18 December 2019 in Journal of Clinical Medicine
Verified
Journal Article
Open access
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EIEspen Alexander Fürst Ihlen
Espen Alexander Fürst Ihlen
RSRagnhild Stoen
Ragnhild Stoen
LBLynn Boswell
Lynn Boswell
RDRaye-Ann Odegaard DeRegnier
Raye-Ann Odegaard DeRegnier
TFToril Fjørtoft
Toril Fjørtoft
AAAdde Adde
Adde Adde
Background: Early identification of cerebral palsy (CP) during infancy will provide opportunities for early therapies and treatments. The aim of the present study was to present a novel machine-learning model, the Computer-based Infant Movement Assessment (CIMA) model, for clinically feasible early CP prediction based on infant video recordings. Methods: The CIMA model was designed to assess the proportion (%) of CP risk-related movements using a time–frequency decomposition of the movement trajectories of the infant’s body parts. The CIMA model was developed and tested on video recordings from a cohort of 377 high-risk infants at 9–15 weeks corrected age to predict CP status and motor function (ambulatory vs. non-ambulatory) at mean 3.7 years age. The performance of the model was compared with results of the general movement assessment (GMA) and neonatal imaging. Results: The CIMA model had sensitivity (92.7%) and specificity (81.6%), which was comparable to observational GMA or neonatal cerebral imaging for the prediction of CP. Infants later found to have non-ambulatory CP had significantly more CP risk-related movements (median: 92.8%, p = 0.02) compared with those with ambulatory CP (median: 72.7%). Conclusion: The CIMA model may be a clinically feasible alternative to observational GMA.

11 July 2022 in JAMA Network Open
Verified
Journal Article
Open access
PDF file
DGDaniel Groos
Daniel Groos
AAAdde Adde
Adde Adde
SASindre Aubert
Sindre Aubert
LBLynn Boswell
Lynn Boswell
RRRaye-Ann de Regnier
Raye-Ann de Regnier
RSRagnhild Støen
Ragnhild Støen
Cerebral palsy (CP) is the most common physical disability in children, producing functional limitation and co-occurring impairments1 (eg, pain, musculoskeletal deformities, seizures, and communication and sleep disorders) because of injury to the developing brain.2 Cerebral palsy is typically diagnosed between ages 12 and 24 months, and milder forms of CP may be diagnosed even later in childhood.3,4 Early identification of infants with a high risk of CP is important to provide targeted follow-up and interventions during infancy when neuroplasticity is high,5,6 improve access to community services to minimize complications,7 and reassure parents of infants at high risk if their children are unlikely to develop CP.8

1 January 2007 in Early Human Development
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Journal Article
Closed access
AAAdde Adde
Adde Adde
MRMarite Rygg
Marite Rygg
KLKristin Lossius
Kristin Lossius
GØGunn Kristin Øberg
Gunn Kristin Øberg
RSRagnhild Støen
Ragnhild Støen

1 July 2014 in Research in Developmental Disabilities
Verified
Journal Article
Closed access
RSRannei Sæther
Rannei Sæther
Jorunn HelbostadJorunn Helbostad
Jorunn Helbostad
AAAdde Adde
Adde Adde
SBSiri Brændvik
Siri Brændvik
SLStian Lydersen
Stian Lydersen
TVTorstein Vik
Torstein Vik