Artigo Revisado por pares

DSP-01 conversion from PLS to ALS: a Dutch cohort study

2024; Taylor & Francis; Volume: 25; Issue: sup1 Linguagem: Inglês

10.1080/21678421.2024.2403307

ISSN

2167-9223

Tópico(s)

Neurogenetic and Muscular Disorders Research

Resumo

AcknowledgmentsEditorial support was provided by p-value communications.AcknowledgmentsThe authors thank Irene Brody, VMD, PhD, of p-value communications, Cedar Knolls, NJ, USA, for providing medical writing support. Editorial support was also provided by p-value communications.AcknowledgmentsWe thank all participants and the ALS community for taking part in this study.AcknowledgementsWe thank all the patients with ALS who participated in this study. We also thank all the physicians and staff who participated in the Japanese Consortium for Amyotrophic Lateral Sclerosis research (JaCALS).AcknowledgementsWe thank patients, investigators and member-sites' personnel of NEALS, PRO-ACT, PRO-ACE, and ALS/MND Natural History consortia.AcknowledgmentsThe authors thank all study participants.AcknowledgmentsThe authors thank Irene Brody, VMD, PhD, of p-value communications, Cedar Knolls, NJ, USA, for providing medical writing support. Editorial support was also provided by p-value communications.AcknowledgmentsThe authors thank Irene Brody, VMD, PhD, of p-value communications, Cedar Knolls, NJ, USA, for providing medical writing support. Editorial support was also provided by p-value communications.

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