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Nicole Heußinger

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
2020 · Joerg Klepper, Cigdem Akman, et al. · Epilepsia Open · 296
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Expression of the Epstein–Barr virus (EBV)‐encoded latent membrane protein 2A (LMP2A) in EBV‐associated nasopharyngeal carcinoma
2004 · Nicole Heussinger, Maike Büttner, et al. · The Journal of Pathology · 103
Oligoclonal bands predict multiple sclerosis in children with optic neuritis
2015 · Nicole Heussinger, Evangelos Kontopantelis, et al. · Annals of Neurology · 76
PRRT2-related disorders: further PKD and ICCA cases and review of the literature
2013 · Felicitas Becker, Julian Schubert, et al. · Journal of Neurology · 74
10 patients, 10 years – Long term follow-up of cardiovascular risk factors in Glut1 deficiency treated with ketogenic diet therapies: A prospective, multicenter case series
2017 · Nicole Heussinger, Adela Della Marina, et al. · Clinical Nutrition · 46
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Predicting multiple sclerosis following isolated optic neuritis in children
2013 · N. Heussinger, E. Kontopantelis, et al. · European Journal of Neurology · 28
Expression of Epstein–Barr virus (EBV)-encoded latent membrane proteins and STAT3 activation in nasopharyngeal carcinoma
2006 · Maike Buettner, Nicole Heussinger, et al. · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · 22
Paroxysmal Nonepileptic Events in Glut1 Deficiency
2016 · Joerg Klepper, Baerbel Leiendecker, et al. · Movement Disorders Clinical Practice · 19
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Ultrasound-guided neuronavigation improves safety of ventricular catheter insertion in preterm infants
2012 · Nicole Heussinger, Ilker Y. Eyüpoglu, et al. · Brain and Development · 16
Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity
2016 · Nicole Heussinger, Marc Saake, et al. · Pediatric Neurology · 13
Make Bayley III Scores Comparable between United States and German Norms—Development of Conversion Equations
2022 · Pauline Kosmann, Annett Blaeser, et al. · Neuropediatrics · 6
Severe Hypertriglyceridemia in Glut1D on Ketogenic Diet
2016 · Baerbel Leiendecker, Nicole Heussinger, et al. · Neuropediatrics · 6
Mechanography in children: pediatric references in postural control.
2022 · Franziska Pilz, Katharina Vill, et al. · PubMed Central · 3
Gastrointestinally mediated food allergy causing Spondyloarthritis-like disease
2020 · M Raithel, S Finzel, et al. · Archives of Clinical Gastroenterology · 3
The Presence of MRZ Reactions Improves the Prediction of Multiple Sclerosis in Children with Optic Neuritis
2025 · Franziska Kauth, Sophie Chen, et al. · Children · 1
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WDR45-Associated BPAN: A Rare Cause for Infantile-Onset Seizures and Expressive Language Disorder in a 26-Month-Old Girl
2021 · N. Greulich, A. Abicht, et al. · Neuropediatrics · 1
Pädiatrische Neurologie - Neuropädiatrie
2025 · Maria Abel, Lucia Abela, et al.
Presence of a Positive MRZ Reaction Improves the Predictions of Multiple Sclerosis in Children with Optic Neuritis
2024 · F. Kauth, N. Heussinger, et al. · Neuropediatrics
FV 330. Have We Done Wrong? Long-Term Follow-up of Cardiovascular Risk Factors in Glut1-Deficiency Treated with Ketogenic Diet Therapies
2018 · Nicole Heußinger, Adela Marina, et al. · Neuropediatrics
Paroxysmal Events in Glut1 Deficiency
2016 · N. Heussinger, B. Leiendecker, et al. · Neuropediatrics
Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases
2016 · E. Salamano, P. Freisinger, et al. · Neuropediatrics
Enterovirus Induced Opsoclonus-Myoclonus Syndrome in a 16-Month-Old Girl
2016 · N. Greulich, J. Klepper, et al. · Neuropediatrics
OP64 – 2760: Oligoclonal bands predict multiple sclerosis in children with isolated optic neuritis
2015 · N. Heussinger, E. Kontopantelis, et al. · European Journal of Paediatric Neurology
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
2015 · N. Heußinger, E. Kontopantelis, et al. · Neuropediatrics
Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene
2015 · N. Greulich, J. Klepper, et al. · Neuropediatrics
Works count: 31
Citation count: 713
H-index: 10
I10-index: 10
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