Research output per year
Research output per year
Personal profile
Expertise
Clinical expertise: neurology, pediatric neurology, (neuro)metabolic disorders, primary neurotransmitter disorders, hereditary movement disorders
Research expertise: primary neurotransmitter disorders (aromatic l-amino acid decarboxylase deficiency; tyrosine hydroxylase deficiency, dopamine beta hydroxylase deficiency, tetrahydrobiopterin disorders), movement disorders
External positions
PhD Candidate Primary Neurotransmitter Disorders, Radboud University Nijmegen Medical Centre
1 Jun 2009 → …Fingerprint
Dive into the research topics where Tessa Wassenberg is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Clinical presentation and long-term follow-up of dopamine beta hydroxylase deficiency
Wassenberg, T., Deinum, J., van Ittersum, F. J., Kamsteeg, E-J., Pennings, M., Verbeek, M. M., Wevers, R. A., van Albada, M. E., Kema, I. P., Versmissen, J., van den Meiracker, T., Lenders, J. W. M., Monnens, L. & Willemsen, M. A., May 2021, In : Journal of Inherited Metabolic Disease. 44, 3, p. 554-565 12 p.Research output: Contribution to journal › Article
1 Citation (Scopus) -
Hypocalcemia as a Cause of Complex Febrile Seizures in a Toddler
Meesters, K., Wassenberg, T. & Vanbesien, J., 14 Jul 2021, In : Case reports in pediatrics. 2021, 4 p., 1798741.Research output: Contribution to journal › Article
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Novel Protein Biomarkers of Monoamine Metabolism Defects Correlate with Disease Severity
Tristán-Noguero, A., Borràs, E., Molero-Luis, M., Wassenberg, T., Peters, T., Verbeek, M. M., Willemsen, M., Opladen, T., Jeltsch, K., Pons, R., Thony, B., Horvath, G., Yapici, Z., Friedman, J., Hyland, K., Agosta, G. E., López-Laso, E., Artuch, R., Sabidó, E. & García-Cazorla, À., Mar 2021, In : Movement Disorders : Official Journal of the Movement Disorder Society. 36, 3, p. 690-703 14 p.Research output: Contribution to journal › Article
1 Citation (Scopus) -
Autosomal dominant GCH1 mutations causing spastic paraplegia at disease onset
Wassenberg, T., Schouten, M. I., Helmich, R. C., Willemsen, M. A. A. P., Kamsteeg, E-J. & van de Warrenburg, B. P. C., May 2020, In : Parkinsonism & Related Disorders. 74, p. 12-15 4 p.Research output: Contribution to journal › Article
6 Citations (Scopus) -
Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies
International Working Group on Neurotransmitter related disorders (iNTD), 26 May 2020, In : Orphanet Journal of Rare Diseases. 15, 1, 30 p., 126.Research output: Contribution to journal › Article
25 Citations (Scopus)
Activities
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Virtual EPNS Training Course
Tessa Wassenberg (Participant)14 Apr 2021 → 15 Apr 2021Activity: Participating in or organising an event › Participation in conference
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Virtual EPNS Training Course
Tessa Wassenberg (Participant)12 Apr 2021 → 13 Apr 2021Activity: Participating in or organising an event › Participation in conference
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Primary Neurotransmitter Disorders, what a pediatrician needs to know
Tessa Wassenberg (Speaker)12 Sep 2020Activity: Talk or presentation › Talk or presentation at a conference
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Endo-ERN: webinar on Prader Willi Syndrome
Tessa Wassenberg (Participant)20 Sep 2020Activity: Participating in or organising an event › Participation in conference
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European Neurofibromatosis Meeting 2020, virtual meeting
Tessa Wassenberg (Participant)10 Dec 2020 → 11 Dec 2020Activity: Participating in or organising an event › Participation in conference