Longitudinal analysis of anthropometric measures over 5 years in patients with Friedreich ataxia in the <scp>EFACTS</scp> natural history study

Significant anthropometric abnormalities were identified, with underweight and short stature prevalent in children and overweight in adults. These findings highlight the need for regular nutritional monitoring and interventions to manage underweight in children and promote healthy weight in adults.

Authors

Institutions

Publication Details

Journal
European Journal of Neurology
Published
2025-01-01
DOI
https://doi.org/10.1111/ene.70011
Citations
1
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.91

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Longitudinal analysis of anthropometric measures over 5 years in patients with Friedreich ataxia in the EFACTS natural history study

Myriam Rai, Stella A. Glasmacher, Imis Dogan, Ana Sofia Costa et al.
1 citations
European Journal of Neurology
Genetic Neurodegenerative Diseases
0.91
article

Longitudinal analysis of anthropometric measures over 5 years in patients with Friedreich ataxia in the EFACTS natural history study

Myriam Rai, Stella A. Glasmacher, Imis Dogan, Ana Sofia Costa, Claire Didszun, Wolfgang Nachbauer, Claire Ewenczyk, Lorenzo Nanetti, Thomas Klopstock, Jörg B. Schulz, Caterina Mariotti, Kathrin Reetz, Zofia Fleszar, Michael Parkinson, Kerstin Konrad, Paola Giunti, Sylvia Boesch, Marcus Grobe‐Einsler, Claudia Stendel, Ludger J. Schöls, Francisco Javier Rodríguez de Rivera Garrido, Massimo Pandolfo, Thomas Klockgether, Ilaria Giordano, Alexandra Durr, Sara Annabelle Schawohl
article en
1 citations

Abstract

Significant anthropometric abnormalities were identified, with underweight and short stature prevalent in children and overweight in adults. These findings highlight the need for regular nutritional monitoring and interventions to manage underweight in children and promote healthy weight in adults.

European Journal of NeurologyVol. 32(1)
Centre National de la Recherche Scientifique (FR), Université Libre de Bruxelles (BE), Innsbruck Medical University (AT), Inserm (FR), Forschungszentrum Jülich (DE), University Hospital Bonn (DE), Hospital Universitario La Paz (ES), German Center for Neurodegenerative Diseases (DE), Sorbonne Université (FR), Munich Cluster for Systems Neurology (DE), Friedrich Baur Stiftung (DE), Friedreich's Ataxia Research Alliance (US), Hertie Institute for Clinical Brain Research (DE), National Hospital for Neurology and Neurosurgery (GB), Institut du Cerveau (FR), Fondazione IRCCS Istituto Neurologico Carlo Besta (IT), University College London (GB), University of Tübingen (DE), Ludwig-Maximilians-Universität München (DE), RWTH Aachen University (DE)
Biogen, Voyager Therapeutics, European Commission, RWTH Aachen University
Zero hunger
Openalex Percentile: Top 32%
Genetic Neurodegenerative Diseases
0.91
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.