A. Van Der Ploeg - Rotterdam, The Netherlands

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论文共 44 篇作者统计合作学者相似作者

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COMET: Patient-reported outcome measures in patients with late-onset Pompe disease after 145 weeks' avalglucosidase alfa

A. Toscano, P. Kishnani, J. Diaz-Manera, H. Kushlaf, S. Ladha, T. Mozaffar, V. Straub,A. Van der Ploeg, P. Clemens, J. Day, S. Illarioshkin, M. Roberts,

EUROPEAN JOURNAL OF NEUROLOGY (2023): 209-210

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Neurofilament light as a biomarker for involvement of the brain in classic infantile Pompe patients

M. Mackenbach, J. van den Dorpel,N. van der Beek, E. Willemse,D. Rizopoulos,C. Teunissen,A. van der Ploeg,J. van den Hout

NEUROMUSCULAR DISORDERS (2022): S77-S77

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Serum Neurofilament Light Chain Levels Associate With Central Nervous System Involvement In Pompe

A. Carrasco-Rozas, H. Van Den Hout, D. Natera,L. Martin-Aguilar,J. Alonso Perez, I. Ditters,L. Querol,W. Pijnappel,A. Nascimento,A. Van Der Ploeg,J. Diaz Manera

EUROPEAN JOURNAL OF NEUROLOGY（2021）

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Neo-Ext: Skeletal Muscle % Fat In Late-Onset Pompe Disease After Long-Term Avalglucosidase Alfa (3-Point Dixon Mri)

P. Carlier,J. Vissing,J. Diaz Manera,R. Barohn,B. Byrne, O. Goker-Alpan, P. Kishnani,S. Ladha, P. Laforet, K. Mengel,L. Pena,S. Sacconi,

EUROPEAN JOURNAL OF NEUROLOGY（2021）

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Respiratory Function and Ambulation Status Assessments of Late-onset Pompe Disease Patients with and without the Common IVS1 Variant from the Pompe Registry

B. Schoser, M. -A. Abbott,T. Mongini,D. Stockton, R. Araujo,A. Van der Ploeg

EUROPEAN JOURNAL OF NEUROLOGY（2020）

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P.71The emerging phenotype in long-term enzyme-treated classic infantile Pompe patients: severe distal muscle weakness

J. van den Dorpel, E. Poelman, L. Harlaar,H. Kooten, L. van der Giessen,P. van Doorn,A. van der Ploeg,J. van den Hout,N. van der Beek

Neuromuscular Disorders（2019）

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P.72Optimizing long-term outcome in classic infantile Pompe patients: effects of higher dosing and immunomodulation

E. Poelman, J. van den Dorpel,M. Hoogeveen-Westerveld,J. van den Hout, L. van der Giessen,N. van der Beek, W. Pijnappel,A. van der Ploeg

Neuromuscular Disorders（2019）

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G.P.12 – Childhood Pompe disease: Clinical spectrum and genotype in 31 children

F Van Spronsen,Jaak Jaeken,M E Rubiogozalbo, J Van Der Meijden,M A A P Willemsen, Martina Baethmann, R H Lachmann,C Van Capelle,Eugen Mengel,Thomas Voit,Helen Michelakakis, J Van Der Hout,

Neuromuscular Disordersno. SUPnan (2015): S190-S190

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T.P.24: Alglucosidase alfa reduces lysosomal glycogen in skeletal muscle biopsies of patients with late-onset Pompe disease (LOPD)

B.L. Thurberg,A. van der Ploeg, J.T. Kissel, B. Schoser, A. Pestronk, R.J. Barohn, O. Goker-Alpan, T. Mozaffar, L.D.M. Pena, Z. Simmons, V. Straub,P. Young,

Neuromuscular Disordersno. 9-10 (2014): 871-872

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A higher dose of enzyme therapy in patients with classic infantile Pompe disease seems to improve ventilator-free survival and motor function

C van Gelder,I Plug,M Kroos, A Reuser,A van der Ploeg

BMC Musculoskeletal Disorders（2013）

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