Neuronal ceroid-lipofuscinoses: The current status
- 31 July 1992
- journal article
- review article
- Published by Elsevier in Brain & Development
- Vol. 14 (4), 203-211
- https://doi.org/10.1016/s0387-7604(12)80231-2
Abstract
No abstract availableKeywords
This publication has 62 references indexed in Scilit:
- Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villiPrenatal Diagnosis, 1990
- Intraepidermal morphologic manifestations in lysosomal diseasesBrain & Development, 1989
- Neuronal ceroid-lipofuscinoses in childhoodBrain & Development, 1988
- ULTRASTRUCTURAL STUDIES OF THE RETINA IN INFANTILE NEURONAL CEROID-LIPOFUSCINOSISRetina, 1988
- Diagnosis and treatment of typical and atypical forms of lipopigment storage disordersAmerican Journal of Medical Genetics, 1988
- Therapeutic modification of membrane lipid abnormalities in juvenile neuronal ceroid-lipofuscinosis (Batten disease)American Journal of Medical Genetics, 1988
- Bibliography on ceroid-lipofuscinosesAmerican Journal of Medical Genetics, 1988
- Sanfilippo Disease, Type A with some Features of Ceroid LipofuscinosisNeuropediatrics, 1985
- Neuronal ceroid lipofuscinosis and arthropathy: a family study.Journal of Medical Genetics, 1981
- Loss of pigment-laden stellate cells: A severe alteration of the isocortex in juvenile neuronal ceroid-lipofuscinosisActa Neuropathologica, 1978