Reply to: Viability of diffusion tensor imaging for assessing retrochiasmatic involvement in Kearns-Sayre syndrome remains elusive
Neuroradiology
.
2020 Feb;62(2):133-134.
doi: 10.1007/s00234-019-02344-4.
Epub 2019 Dec 14.
Authors
Maria Camilla Rossi-Espagnet
1
2
,
Stefano Pro
3
,
Diego Martinelli
4
,
Daria Diodato
5
,
Antonio Napolitano
6
,
Daniela Longo
7
Affiliations
1
Neuroradiology Unit, Imaging Department, Bambino Gesù Children's Hospital, Piazza Sant'Onofrio 4, IRCCS, 00100, Rome, Italy.
[email protected]
.
2
NESMOS Department, Sant'Andrea Hospital, Sapienza University, Rome, Italy.
[email protected]
.
3
Neurology Unity, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
4
Division of Metabolism and Research Unit of Metabolic Biochemistry, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
5
Unit of Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
6
Medical Physics Department, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
7
Neuroradiology Unit, Imaging Department, Bambino Gesù Children's Hospital, Piazza Sant'Onofrio 4, IRCCS, 00100, Rome, Italy.
PMID:
31838563
DOI:
10.1007/s00234-019-02344-4
No abstract available
Publication types
Letter
Comment
MeSH terms
Diffusion Tensor Imaging
Humans
Kearns-Sayre Syndrome*