Time-course of myelination and atrophy on cerebral imaging in 35 patients withPLP1-related disorders

Author:

Sarret Catherine12,Lemaire Jean-Jacques13,Tonduti Davide45,Sontheimer Anna1,Coste Jerome1ORCID,Pereira Bruno16,Feschet Fabien1,Roche Basile1,Boespflug-Tanguy Odile47

Affiliation:

1. Image-Guided Clinical Neuroscience and Connectomics (IGCNC); Clermont University; University of Auvergne; Clermont-Ferrand France

2. Department of Paediatrics; Clermont-Ferrand University Hospital; Clermont-Ferrand France

3. Department of Neurosurgery; Clermont-Ferrand University Hospital; Clermont-Ferrand France

4. Inserm U1141 Paris Diderot Sorbonne University-Paris Cité; DHU PROTECT; Robert Debré Hospital; Paris France

5. Department of Child Neurology; Neurological Institute C. Besta Foundation IRCCS; Milan Italy

6. Biostatistics Unit (DRCI); Clermont-Ferrand University Hospital; Clermont-Ferrand France

7. Department of Child Neurology and Metabolic Diseases; Leukodystrophies Reference Centre; Robert Debré Hospital; Paris France

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Reference22 articles.

1. Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease;Cailloux;Eur J Hum Genet,2000

2. Magnetic resonance imaging pattern recognition in hypomyelinating disorders;Steenweg;Brain,2010

3. Myelination and Retarded Myelination

4. An MRI and MRS study of Pelizaeus-Merzbacher disease;Nezu;Pediatr Neurol,1998

5. MR-revealed myelination in the cerebral corticospinal tract as a marker for Pelizaeus-Merzbacher's disease with proteolipid protein gene duplication;Takanashi;Am J Neuroradiol,1999

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