Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-45 |
Sentence |
denotes |
53-year-old man with rapid cognitive decline. |
T1 |
0-45 |
Sentence |
denotes |
53-year-old man with rapid cognitive decline. |
TextSentencer_T2 |
46-205 |
Sentence |
denotes |
Kufs' disease (adult neuronal ceroid lipofuscinosis) is a rare form of neurodegenerative lysosomal storage disease, the genetic basis of which remains obscure. |
T2 |
46-205 |
Sentence |
denotes |
Kufs' disease (adult neuronal ceroid lipofuscinosis) is a rare form of neurodegenerative lysosomal storage disease, the genetic basis of which remains obscure. |
TextSentencer_T3 |
206-428 |
Sentence |
denotes |
We present a case of a 53-year-old man with a long history of adult onset epilepsy who presented with confusion and amnesia, and subsequently underwent rapidly progressive cognitive decline associated with myoclonic jerks. |
T3 |
206-428 |
Sentence |
denotes |
We present a case of a 53-year-old man with a long history of adult onset epilepsy who presented with confusion and amnesia, and subsequently underwent rapidly progressive cognitive decline associated with myoclonic jerks. |
TextSentencer_T4 |
429-482 |
Sentence |
denotes |
The clinical diagnosis was Creutzfeldt Jakob disease. |
T4 |
429-482 |
Sentence |
denotes |
The clinical diagnosis was Creutzfeldt Jakob disease. |
TextSentencer_T5 |
483-626 |
Sentence |
denotes |
However, autopsy brain examination revealed changes of Kufs' disease (Adult onset neuronal ceroid lipofuscinosis, or ANCL, also known as CLN4). |
T5 |
483-626 |
Sentence |
denotes |
However, autopsy brain examination revealed changes of Kufs' disease (Adult onset neuronal ceroid lipofuscinosis, or ANCL, also known as CLN4). |
TextSentencer_T6 |
627-825 |
Sentence |
denotes |
No specific gross abnormalities were found but light microscopic examination revealed widespread neuronal ballooning and histochemical staining showed neuronal accumulation of PAS-positive material. |
T6 |
627-825 |
Sentence |
denotes |
No specific gross abnormalities were found but light microscopic examination revealed widespread neuronal ballooning and histochemical staining showed neuronal accumulation of PAS-positive material. |
TextSentencer_T7 |
826-954 |
Sentence |
denotes |
Ultrastructural examination demonstrated excessive and abnormal lipopigment lysosomes typical of neuronal ceroid lipofuscinosis. |
T7 |
826-954 |
Sentence |
denotes |
Ultrastructural examination demonstrated excessive and abnormal lipopigment lysosomes typical of neuronal ceroid lipofuscinosis. |
TextSentencer_T8 |
955-1104 |
Sentence |
denotes |
The typical clinical and pathologic features of the Kufs' disease are discussed and the classification of neuronal ceroid lipofuscinosis is reviewed. |
T8 |
955-1104 |
Sentence |
denotes |
The typical clinical and pathologic features of the Kufs' disease are discussed and the classification of neuronal ceroid lipofuscinosis is reviewed. |