Clinical, Electrophysiological, Imaging, and Ultrastructural Description in 68 Patients With Neuronal Ceroid Lipofuscinoses and Its Subtypes-Reference-Cited by-同舟云学术

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Clinical, Electrophysiological, Imaging, and Ultrastructural Description in 68 Patients With Neuronal Ceroid Lipofuscinoses and Its Subtypes

Published:2014-01 Issue:1 Volume:50 Page:85-95
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Jadav Rakesh H.,Sinha Sanjib,Yasha T.C.,Aravinda H.,Gayathri N.,Rao S.,Bindu P.S.,Satishchandra P.

Publisher

Elsevier BV

Subject

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

Reference52 articles.

1. Analysis of NCL proteins from an evolutionary standpoint;Muzaffar;Curr Genom,2008

2. The neuronal ceroid-lipofuscinoses. Recent advances;Goebel;Brain Pathol,1998

3. Neuronal ceroid-lipofuscinosis: preferential metabolic alterations in thalamus and posterior association cortex demonstrated by PET;De Volder;J Neurol Neurosurg Psychol,1990

4. Neuronal ceroid lipofuscinoses in childhood;Santavuori;Neurol Sci,2000

5. Neuroradiological findings (MRS, MRI, SPECT) in infantile neuronal ceroid lipofuscinosis (CLN1 Infantile) at different stages of the disease;Vanhanen;Neuropediatrics,2004

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