K Weigt-Usinger

University Hospital of Bern — Switzerland

Medicine · Health Sciences

8h-index273citations33works0.02yr avg
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Research Topics

Nitric Oxide and Endothelin Effects(4), Muscle Physiology and Disorders(4), Metabolism and Genetic Disorders(4), Infant Development and Preterm Care(4), Glaucoma and retinal disorders(3)

Publications33 total

Retinal layer segmentation in a cohort of healthy children via optical coherence tomography
PLoS ONE·2022· 10 citedOpen Access
Retinal Layer Segmentation In A Cohort Of Healthy Children Via Optical Coherence Tomography
2022· 3 citedOpen Access
Impact of Hippotherapy on Gross Motor Function and Quality of Life in Children with Bilateral Cerebral Palsy: A Randomized Open-Label Crossover Study
Neuropediatrics·2018· 53 cited
Homoarginine (hArg) and asymmetric dimethylarginine (ADMA) in short stature children without and with growth hormone deficiency: hArg and ADMA are involved differently in growth in the childhood
Amino Acids·2015· 19 cited
The l-arginine/NO pathway, homoarginine, and nitrite-dependent renal carbonic anhydrase activity in young people with type 1 diabetes mellitus
Amino Acids·2015· 24 cited
The l-arginine/NO pathway and homoarginine are altered in Duchenne muscular dystrophy and improved by glucocorticoids
Amino Acids·2015· 41 cited
Biosynthesis of homoarginine (hArg) and asymmetric dimethylarginine (ADMA) from acutely and chronically administered free l-arginine in humans
Amino Acids·2015· 46 cited
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Neuropediatrics·2015
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Neuropediatrics·2015
Long Survival in Leigh Syndrome: New Cases and Review of Literature
Neuropediatrics·2014· 21 cited
Das DDAH/ADMA/NO-System bei Kindern und Jugendlichen mit Diabetes mellitus Typ 1
Diabetologie und Stoffwechsel·2014
Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene - a dietetic attempt
Neuropediatrics·2013
Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene
Neuropediatrics·2013
A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography
Neuropediatrics·2013
Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency
Neuropediatrics·2013
Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)
Neuropediatrics·2013
Visual impairment - differential diagnoses
Neuropediatrics·2013
Pediatric Herpes Simplex Virus Encephalitis
Journal of Child Neurology·2013· 56 cited
New mutation in TSC1-gene in a sporadic case with initially mild phenotype
Neuropediatrics·2012
Neurocognitive testing of very low birth weight infants at an age of 4 years
Neuropediatrics·2012
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Frequent Co-authors

Thomas Lücke(24), Charlotte Thiels(11), T. Lücke(8), Matthias Vorgerd(6), Arslan Arinc Kayacelebi(4), Kristine Chobanyan-Jürgens(4), Dimitrios Tsikas(4), Irina Hörster(4), Christina Carmann(4), Cornelia Köhler(4), Christoph M. Heyer(4), Gabriele Dekomien(4), A Weitkämper(4), Thomas Opladen(3), Ulrike Schara(3), Bibiana Beckmann(3), Eggert Lilienthal(3), Helmut Neumann(3), Ch. Thiels(3), Norbert Teig(3)