Publications by authors named "Uta Tacke"

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Cerebral palsy: an update on its early detection.
Mijna Hadders-Algra, Uta Tacke, Joachim Pietz, Heike Philippi

Lancet· December 2026

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Infants' General Movements Were Not Affected by Exposure to Maternal Severe Acute Respiratory Syndrome Coronavirus 2 Infections.
Kathrin Neumayr, Katharina Lippert, A Sebastian Schroeder, Vinzenz G Eck, Uta Tacke

Acta Paediatr· December 2025

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Using large language models to extract information from pediatric clinical reports.
Katharina Danhauser, Yingding Wang, Christoph Klein, Uta Tacke, Larissa Mantoan, Moritz Tacke

PLOS Digit Health· July 2025

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Predictive value of the General Movements Assessment and Standardized Infant NeuroDevelopmental Assessment in infants at high risk of neurodevelopmental disorders.
Mijna Hadders-Algra, Uta Tacke, Joachim Pietz, André Rupp, Heike Philippi

Dev Med Child Neurol· October 2024

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Neurological soft signs in adolescents are associated with brain structure.
Elena M Bonke, Michaela V Bonfert, Stefan M Hillmann, Johanna Seitz-Holland, Malo Gaubert, Uta Tacke

Cereb Cortex· April 2023

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Neurological soft signs are associated with reduced medial-lateral postural control in adolescent athletes.
Elena M Bonke, Amanda Clauwaert, Stefan M Hillmann, Uta Tacke, Caroline Seer

J Neurol Sci· February 2023

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Standardized Infant NeuroDevelopmental Assessment developmental and socio-emotional scales: reliability and predictive value in an at-risk population.
Mijna Hadders-Algra, Uta Tacke, Joachim Pietz, André Rupp, Heike Philippi

Dev Med Child Neurol· July 2020

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[Analysis of motor development within the first year of life: 3-D motion tracking without markers for early detection of developmental disorders].
Carmen Parisi, Nikolas Hesse, Uta Tacke, Sergi Pujades Rocamora, Astrid Blaschek

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz· July 2020

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General Movement Assessment from videos of computed 3D infant body models is equally effective compared to conventional RGB video rating.
A Sebastian Schroeder, Nikolas Hesse, Raphael Weinberger, Uta Tacke, Lucia Gerstl

Early Hum Dev· May 2020

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Reliability and predictive validity of the Standardized Infant NeuroDevelopmental Assessment neurological scale.
Mijna Hadders-Algra, Uta Tacke, Joachim Pietz, André Rupp, Heike Philippi

Dev Med Child Neurol· June 2019

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Group A Streptococcal Suppurative Arthritis and Osteomyelitis of the Shoulder With Brachial Plexus Palsy in a Newborn.
Alexa Dierig, Nicole Ritz, Uta Tacke, Ulrich Heininger

Pediatr Infect Dis J· October 2016

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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, Marcin Szynkiewicz, Gabriella M A Forte, Uta Tacke

Am J Med Genet A· February 2015

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Epilepsy in Aicardi-Goutières syndrome.
Georgia Ramantani, Louis G Maillard, Thomas Bast, Ralf A Husain, Pascal Niggemann, Uta Tacke

Eur J Paediatr Neurol· January 2014

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Microdeletion 5q14.3 and anomalies of brain development.
Alrun Hotz, Yorck Hellenbroich, Jürgen Sperner, Michaela Linder-Lucht, Uta Tacke

Am J Med Genet A· September 2013

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Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.
Ingrid Bartsch, Kirstin Sandrock, Francois Lanza, Paquita Nurden, Ina Hainmann, Uta Tacke

Thromb Haemost· September 2011

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Congenital ocular malformations (lens subluxation, pupillary displacement, cataract, myopia) and classic galactosaemia associated with Q188R and /or G1391A mutations.
Dieter Schmidt, Yoon S Shin, Claudia Auw-Haedrich, Uta Tacke

Acta Ophthalmol· August 2011

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Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany.
Martin Lindner, Gwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, Karl O Schwab, Uta Tacke

Orphanet J Rare Dis· June 2011

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Neurosurgical treatment strategies in childhood craniopharyngiomas: is less more?
Tilman Schubert, Michael Trippel, Uta Tacke, Vera van Velthoven, Vera Gumpp

Childs Nerv Syst· November 2009

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Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Gillian Rice, Teresa Patrick, Rekha Parmar, Claire F Taylor, Alec Aeby, Uta Tacke

Am J Hum Genet· October 2007

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Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
Yanick J Crow, Andrea Leitch, Bruce E Hayward, Anna Garner, Rekha Parmar, Uta Tacke

Nat Genet· August 2006

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Mutations in antiquitin in individuals with pyridoxine-dependent seizures.
Philippa B Mills, Eduard Struys, Cornelis Jakobs, Barbara Plecko, Peter Baxter, Uta Tacke

Nat Med· March 2006

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The development of childhood asthma: lessons from the German Multicentre Allergy Study (MAS).
Susanne Lau, Renate Nickel, Bodo Niggemann, Christoph Grüber, Christine Sommerfeld, Uta Tacke

Paediatr Respir Rev· September 2002

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