Background: The Argentinean program was initiated more than a decade ago as the first experience of systematic translational research focused on NCL in Latin America. The aim was to overcome misdiagnoses and underdiagnoses in the region. Subjects: 216 NCL suspected individuals from 8 different countries and their direct family members. Methods: Clinical assessment, enzyme testing, electron microscopy, and DNA screening. Results and discussion: 1) The study confirmed NCL disease in 122 subjects. Phenotypic studies comprised epileptic seizures and movement disorders, ophthalmology, neurophysiology, image analysis, rating scales, enzyme testing, and electron microscopy, carried out under a consensus algorithm; 2) DNA screening and validation o...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are lysosomal storage disorders and together are t...
This article addresses the educational issues associated with rare diseases (RD) and in particular t...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorde...
AbstractBackgroundThe Argentinean program was initiated more than a decade ago as the first experien...
Background: The Argentinean programwas initiatedmore than a decade ago as the first experience of sy...
The Neuronal Ceroid Lipofuscinoses (NCLs), inherited neurodegenerative disorders, are the second mos...
2 p.Introduction: Neuronal ceroid lipofuscinosis (NCL), inherited neurodegenerative diseases of all...
Neuronal ceroid lipofuscinosis (NCL), inheritedneurodegenerative diseases of all ages, presents with...
Abstract Neuronal ceroid lipofuscinosis type 2 (CLN2) disease is a rare autosomal recessive neurodeg...
Background: To review the descriptive epidemiological data on neuronal ceroid lipofuscinoses (NCLs) ...
BACKGROUND: To review the descriptive epidemiological data on neuronal ceroid lipofuscinoses (NCLs) ...
AbstractThe neuronal ceroid lipofuscinoses, collectively called NCLs, are rare and fatal lysosomal s...
Neuronal ceroid lipofuscinoses (NCLs), also referred as “Batten disease”, are a group of thirteen ra...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of rare genetic diseases characterised...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorde...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are lysosomal storage disorders and together are t...
This article addresses the educational issues associated with rare diseases (RD) and in particular t...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorde...
AbstractBackgroundThe Argentinean program was initiated more than a decade ago as the first experien...
Background: The Argentinean programwas initiatedmore than a decade ago as the first experience of sy...
The Neuronal Ceroid Lipofuscinoses (NCLs), inherited neurodegenerative disorders, are the second mos...
2 p.Introduction: Neuronal ceroid lipofuscinosis (NCL), inherited neurodegenerative diseases of all...
Neuronal ceroid lipofuscinosis (NCL), inheritedneurodegenerative diseases of all ages, presents with...
Abstract Neuronal ceroid lipofuscinosis type 2 (CLN2) disease is a rare autosomal recessive neurodeg...
Background: To review the descriptive epidemiological data on neuronal ceroid lipofuscinoses (NCLs) ...
BACKGROUND: To review the descriptive epidemiological data on neuronal ceroid lipofuscinoses (NCLs) ...
AbstractThe neuronal ceroid lipofuscinoses, collectively called NCLs, are rare and fatal lysosomal s...
Neuronal ceroid lipofuscinoses (NCLs), also referred as “Batten disease”, are a group of thirteen ra...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of rare genetic diseases characterised...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorde...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are lysosomal storage disorders and together are t...
This article addresses the educational issues associated with rare diseases (RD) and in particular t...
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorde...