Ceroid neuronal lipofuscinosis (CLN) is a rare group of autosomal recessive neurodegenerative diseases that cause developmental delay and seizures. Herein, we present a case of a 7-year-old girl who referred for magnetic resonance imaging (MRI) following cognitive impairment and seizures. MRI was performed demonstrating some usual findings, and, surprisingly, a normal-sized cerebellum. This case draws attention to not hold to just the classical imaging presentation in order to suspect some leukodystrophy
AIM: To characterize the phenotypic profile of a cohort of children affected with CLN5, a rare form ...
The clinical traits of Kufs disease (KD) type B (CLN13), an adult-onset neuronal ceroid lipofuscinos...
AbstractIn childhood the neuronal ceroid lipofuscinoses (NCL) are the most frequent lysosomal diseas...
Ceroid neuronal lipofuscinosis (CLN) is a rare group of autosomal recessive neurodegenerative diseas...
Abstract Background Neuronal ceroid lipofuscinosis (NCLs) are lysosomal storage disorders characteri...
AIM: Late infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease is a rare neurodegenerative...
The neuronal ceroid lipofuscinoses are a heterogeneous group of inherited degenerative disorders of ...
Neuronal ceroid lipofuscinoses are the most common neurodegenerative childhood-onset disorders chara...
Clinical picture of neuronal ceroid lipofuscinosis with late infantile onset (LINCL) is characterize...
The neuronal ceroid lipofuscinoses (NCL) are heterogeneous neurodegenerative disorders with typical ...
WOS: 000264889000024PubMed ID: 19201763The neuronal ceroid lipofuscinoses (NCLs), the most common ne...
2 p.Introduction: Neuronal ceroid lipofuscinosis (NCL), inherited neurodegenerative diseases of all...
CLN8 is a ubiquitously expressed membrane-spanning protein that localizes primarily in the ER, with ...
Neuronal ceroid lipofuscinoses (NCLs) are relatively common storage diseases of childhood and early ...
Neuronal ceroid lipofuscinoses (NCLs), also referred as “Batten disease”, are a group of thirteen ra...
AIM: To characterize the phenotypic profile of a cohort of children affected with CLN5, a rare form ...
The clinical traits of Kufs disease (KD) type B (CLN13), an adult-onset neuronal ceroid lipofuscinos...
AbstractIn childhood the neuronal ceroid lipofuscinoses (NCL) are the most frequent lysosomal diseas...
Ceroid neuronal lipofuscinosis (CLN) is a rare group of autosomal recessive neurodegenerative diseas...
Abstract Background Neuronal ceroid lipofuscinosis (NCLs) are lysosomal storage disorders characteri...
AIM: Late infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease is a rare neurodegenerative...
The neuronal ceroid lipofuscinoses are a heterogeneous group of inherited degenerative disorders of ...
Neuronal ceroid lipofuscinoses are the most common neurodegenerative childhood-onset disorders chara...
Clinical picture of neuronal ceroid lipofuscinosis with late infantile onset (LINCL) is characterize...
The neuronal ceroid lipofuscinoses (NCL) are heterogeneous neurodegenerative disorders with typical ...
WOS: 000264889000024PubMed ID: 19201763The neuronal ceroid lipofuscinoses (NCLs), the most common ne...
2 p.Introduction: Neuronal ceroid lipofuscinosis (NCL), inherited neurodegenerative diseases of all...
CLN8 is a ubiquitously expressed membrane-spanning protein that localizes primarily in the ER, with ...
Neuronal ceroid lipofuscinoses (NCLs) are relatively common storage diseases of childhood and early ...
Neuronal ceroid lipofuscinoses (NCLs), also referred as “Batten disease”, are a group of thirteen ra...
AIM: To characterize the phenotypic profile of a cohort of children affected with CLN5, a rare form ...
The clinical traits of Kufs disease (KD) type B (CLN13), an adult-onset neuronal ceroid lipofuscinos...
AbstractIn childhood the neuronal ceroid lipofuscinoses (NCL) are the most frequent lysosomal diseas...