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Tessa Wassenberg
Tessa Wassenberg
PhD candidate, Neurology Resident, Radboudumc Nijmegen
Verified email at radboudumc.nl
Title
Cited by
Cited by
Year
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency
L Brun, LH Ngu, WT Keng, GS Ch'Ng, YS Choy, WL Hwu, WT Lee, ...
Neurology 75 (1), 64-71, 2010
1912010
Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency
T Wassenberg, M Molero-Luis, K Jeltsch, GF Hoffmann, B Assmann, ...
Orphanet journal of rare diseases 12 (1), 1-21, 2017
1472017
Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies
T Opladen, E López-Laso, E Cortès-Saladelafont, TS Pearson, HS Sivri, ...
Orphanet journal of rare diseases 15 (1), 1-30, 2020
482020
The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders
T Opladen, E Cortès-Saladelafont, M Mastrangelo, G Horvath, R Pons, ...
Molecular genetics and metabolism reports 9, 61-66, 2016
412016
l-Dopa in dystonia: a modern perspective
RP Maas, T Wassenberg, JP Lin, BPC van de Warrenburg, ...
Neurology 88 (19), 1865-1871, 2017
402017
Urinary dopamine in aromatic L-amino acid decarboxylase deficiency: the unsolved paradox
T Wassenberg, MAAP Willemsen, PBH Geurtz, M Lammens, K Verrijp, ...
Molecular genetics and metabolism 101 (4), 349-356, 2010
382010
Neurodevelopmental outcome in full‐term newborns with refractory neonatal seizures
IA Maartens, T Wassenberg, J Buijs, L Bok, MJK de Kleine, T Katgert, ...
Acta Paediatrica 101 (4), e173-e178, 2012
302012
Non-motor symptoms and quality of life in dopa-responsive dystonia patients
ER Timmers, A Kuiper, M Smit, AL Bartels, DJ Kamphuis, NI Wolf, ...
Parkinsonism & Related Disorders 45, 57-62, 2017
242017
Multi-channel amplitude-integrated EEG characteristics in preterm infants with a normal neurodevelopment at two years of corrected age
HJ Niemarkt, W Jennekens, IA Maartens, T Wassenberg, M van Aken, ...
Early human development 88 (4), 209-216, 2012
232012
Neonatal airway obstruction caused by rapidly growing nasopharyngeal teratoma
IA Maartens, T Wassenberg, FJ Halbertsma, HAM Marres, P Andriessen
Acta Paediatrica 98 (11), 1852-1854, 2009
222009
CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia
A Shetty, Z Gan-Or, S Ashtiani, JA Ruskey, B van de Warrenburg, ...
European Journal of Medical Genetics 62 (12), 103605, 2019
192019
The Paradox of Hyperdopaminuria in Aromatic l-Amino Acid Deficiency Explained
T Wassenberg, LAH Monnens, BPBH Geurtz, RA Wevers, MM Verbeek, ...
JIMD Reports-Case and Research Reports, 2012/1, 39-45, 2011
162011
Autosomal dominant GCH1 mutations causing spastic paraplegia at disease onset
T Wassenberg, MI Schouten, RC Helmich, MAAP Willemsen, ...
Parkinsonism & related disorders 74, 12-15, 2020
132020
Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines
O Kuseyri Hübschmann, G Horvath, E Cortès-Saladelafont, Y Yıldız, ...
Nature communications 12 (1), 1-15, 2021
102021
International Working Group on Neurotransmitter related Disorders (iNTD). Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies
T Opladen, E López-Laso, E Cortès-Saladelafont, TS Pearson, HS Sivri, ...
Orphanet J Rare Dis 15 (1), 126, 2020
102020
Clinical presentation and long‐term follow‐up of dopamine beta hydroxylase deficiency
T Wassenberg, J Deinum, FJ van Ittersum, EJ Kamsteeg, M Pennings, ...
Journal of inherited metabolic disease 44 (3), 554-565, 2021
62021
Novel protein biomarkers of monoamine metabolism defects correlate with disease severity
A Tristán‐Noguero, E Borràs, M Molero‐Luis, T Wassenberg, T Peters, ...
Movement Disorders 36 (3), 690-703, 2021
62021
International Working Group on Neurotransmitter related, d. The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused …
T Opladen, E Cortes-Saladelafont, M Mastrangelo, G Horvath, R Pons, ...
Mol. Genet. Metab. Rep 9, 61-66, 2016
52016
Hypocalcemia as a Cause of Complex Febrile Seizures in a Toddler
K Meesters, T Wassenberg, J Vanbesien
Case reports in pediatrics 2021, 2021
22021
CAPN1: novel mutations expanding the phenotype of hereditary spastic paraparesis.(P6. 039)
A Shetty, S Ashtiani, Z Gan-Or, B Van de Warrenburg, T Wassenberg, ...
Neurology 90 (15 Supplement), 2018
22018
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Articles 1–20