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Gadolinium Brain Deposition after Macrocyclic Gadolinium Administration: A Pediatric Case-Control Study

Radiology, 2017-10, Vol.285 (1), p.223-230

2017

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NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

American journal of human genetics, 2016-10, Vol.99 (4), p.894-902

2016

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Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration

Brain (London, England : 1878), 2020-01, Vol.143 (1), p.94-111

2020

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Treatment with long-acting lanreotide autogel in early infancy in patients with severe neonatal hyperinsulinism

Orphanet journal of rare diseases, 2017-06, Vol.12 (1), p.108-108, Article 108

2017

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Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities

American journal of human genetics, 2020-02, Vol.106 (2), p.246-255

2020

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“shortCardiac” — An open-source framework for fast and standardized assessment of cardiac function

SoftwareX, 2023-07, Vol.23, p.101453, Article 101453

2023

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Fluorescence optical imaging and musculoskeletal ultrasonography in juvenile idiopathic polyarticular disease before and during antirheumatic treatment - a multicenter non-interventional diagnostic evaluation

Arthritis research & therapy, 2017-06, Vol.19 (1), p.147-147, Article 147

2017

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Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders

Antioxidants, 2023-03, Vol.12 (3), p.718

2023

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Deep Learning-Based Post-Processing of Real-Time MRI to Assess and Quantify Dynamic Wrist Movement in Health and Disease

Diagnostics (Basel), 2021-06, Vol.11 (6), p.1077

2021

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EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosum

Metabolic brain disease, 2016-06, Vol.31 (3), p.717-721

2016

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Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene

Pediatric neurology, 2012-06, Vol.46 (6), p.407-409

2012

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Crossed cerebellar diaschisis after status epilepticus in a young child

Neuropediatrics, 2012-04, Vol.43 (2), p.55-58

2012

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Classical homocystinuria presenting with transient basal ganglia pathology and dystonia

Journal of inherited metabolic disease, 2023-11, Vol.46 (6), p.1206-1208

2023

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MATR3 haploinsufficiency and early-onset neurodegeneration

Brain (London, England : 1878), 2021-10, Vol.144 (9), p.e72-e72

2021

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Häufige Symptome – seltene Differenzialdiagnose: Zervikale Lymphadenopathie, Fieber und unspezifisches Exanthem bei einem 8-jährigen Mädchen

Arthritis + Rheuma, 2020-12, Vol.40 (6), p.449-451

2020

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Real-time MRI: a new tool of radiologic imaging in small children

European journal of pediatrics, 2023-08, Vol.182 (8), p.3405-3417

2023

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RANBP2 Mutation Mimicking Viral Encephalitis

Neuropediatrics, 2022-08, Vol.53 (4), p.301-302

2022

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Spirometry‐based reconstruction of real‐time cardiac MRI: Motion control and quantification of heart–lung interactions

Magnetic resonance in medicine, 2021-11, Vol.86 (5), p.2692-2702

2021

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Entwicklung der Kinder- und Jugendradiologie – Strategiepapier des Vorstands der Gesellschaft für Pädiatrische Radiologie (GPR e. V.)

RöFo : Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebende Verfahren, 2020-06, Vol.192 (6), p.531-536

2020

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Informationen der Gesellschaft für Pädiatrische Radiologie zur Verwendung von gadoliniumhaltigem Kontrastmittel für die Kernspintomografie im Kindes- und Jugendalter

RöFo : Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebende Verfahren, 2017-09, Vol.189 (9), p.817-819

2017

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Dynamic assessment of scapholunate ligament status by real-time magnetic resonance imaging: an exploratory clinical study

Skeletal radiology, 2024-04, Vol.53 (4), p.791-800

2024

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Comparison of cardiac volumetry using real-time MRI during free-breathing with standard cine MRI during breath-hold in children

Pediatric radiology, 2022-07, Vol.52 (8), p.1462-1475

2022

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First experience with real-time magnetic resonance imaging-based investigation of respiratory influence on cardiac function in pediatric congenital heart disease patients with chronic right ventricular volume overload

Pediatric radiology, 2023-12, Vol.53 (13), p.2608-2621

2023

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Screening for non-alcoholic fatty liver disease in children and adolescents with type 1 diabetes mellitus: a cross-sectional analysis

European journal of pediatrics, 2017-04, Vol.176 (4), p.529-536

2017

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Biallelic mutation of human SLC6A6 encoding the taurine transporter TAUT is linked to early retinal degeneration

The FASEB journal, 2019-10, Vol.33 (10), p.11507-11527

2019

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Gadolinium Brain Deposition after Macrocyclic Gadolinium Administration: A Pediatric Case-Control Study

NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration

Treatment with long-acting lanreotide autogel in early infancy in patients with severe neonatal hyperinsulinism

Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities

“shortCardiac” — An open-source framework for fast and standardized assessment of cardiac function

Fluorescence optical imaging and musculoskeletal ultrasonography in juvenile idiopathic polyarticular disease before and during antirheumatic treatment - a multicenter non-interventional diagnostic evaluation

Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders

Deep Learning-Based Post-Processing of Real-Time MRI to Assess and Quantify Dynamic Wrist Movement in Health and Disease

EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosum

Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene

Crossed cerebellar diaschisis after status epilepticus in a young child

Classical homocystinuria presenting with transient basal ganglia pathology and dystonia

MATR3 haploinsufficiency and early-onset neurodegeneration

Häufige Symptome – seltene Differenzialdiagnose: Zervikale Lymphadenopathie, Fieber und unspezifisches Exanthem bei einem 8-jährigen Mädchen

Real-time MRI: a new tool of radiologic imaging in small children

RANBP2 Mutation Mimicking Viral Encephalitis

Spirometry‐based reconstruction of real‐time cardiac MRI: Motion control and quantification of heart–lung interactions

Entwicklung der Kinder- und Jugendradiologie – Strategiepapier des Vorstands der Gesellschaft für Pädiatrische Radiologie (GPR e. V.)

Informationen der Gesellschaft für Pädiatrische Radiologie zur Verwendung von gadoliniumhaltigem Kontrastmittel für die Kernspintomografie im Kindes- und Jugendalter

Dynamic assessment of scapholunate ligament status by real-time magnetic resonance imaging: an exploratory clinical study

Comparison of cardiac volumetry using real-time MRI during free-breathing with standard cine MRI during breath-hold in children

First experience with real-time magnetic resonance imaging-based investigation of respiratory influence on cardiac function in pediatric congenital heart disease patients with chronic right ventricular volume overload

Screening for non-alcoholic fatty liver disease in children and adolescents with type 1 diabetes mellitus: a cross-sectional analysis

Biallelic mutation of human SLC6A6 encoding the taurine transporter TAUT is linked to early retinal degeneration

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