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result sql = Liver transplantation as treatment for neurological disorders.
Liver transplantation as treatment for neurological disorders.
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char = m;code = 109
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char = n;code = 110
char = i;code = 105
char = a;code = 97
char = ,;code = 44
char = ;code = 32
char = c;code = 99
char = a;code = 97
char = n;code = 110
char = ;code = 32
char = b;code = 98
char = e;code = 101
char = ;code = 32
char = i;code = 105
char = m;code = 109
char = m;code = 109
char = e;code = 101
char = d;code = 100
char = i;code = 105
char = a;code = 97
char = t;code = 116
char = e;code = 101
char = l;code = 108
char = y;code = 121
char = ;code = 32
char = c;code = 99
char = o;code = 111
char = r;code = 114
char = r;code = 114
char = e;code = 101
char = c;code = 99
char = t;code = 116
char = e;code = 101
char = d;code = 100
char = ;code = 32
char = b;code = 98
char = y;code = 121
char = ;code = 32
char = l;code = 108
char = i;code = 105
char = v;code = 118
char = e;code = 101
char = r;code = 114
char = ;code = 32
char = t;code = 116
char = r;code = 114
char = a;code = 97
char = n;code = 110
char = s;code = 115
char = p;code = 112
char = l;code = 108
char = a;code = 97
char = n;code = 110
char = t;code = 116
char = a;code = 97
char = t;code = 116
char = i;code = 105
char = o;code = 111
char = n;code = 110
char = .;code = 46
char = <;code = 60
char = b;code = 98
char = r;code = 114
char = /;code = 47
char = >;code = 62
result sql = Liver transplantation has been performed for patients with incurable liver diseases but this therapeutic technique can be extended to neurological disorders, such as familial amyloid polyneuropathy and adult-onset type II citrullinemia. An amyloid precursor in familial amyloid polyneuropathy, a variant form of transthyretin, is produced mainly in the liver. After liver transplantation, it has been shown that this amyloid precursor disappears from the sera of patients once progression of the disease has halted. Type II citrullinemia is caused by a deficiency of liver-specific argininosuccinate synthetase activity and shows various neurological manifestations closely resembling those of hepatic encephalopathy, resulting in fatal outcome. All metabolic abnormalities in this disease, which include elevated plasma concentrations of citrulline and ammonia, can be immediately corrected by liver transplantation.

Publication: Expert Rev Neurother 2003 Jul ;3(4)::547-55. :doi: 10.1586/14737175.3.4.547.
Publication Date: 2003 Jul
Study Author(s): Ikeda, Shu-Ichi;Takei, Yo-Ichi;Hashikura, Yasuhiko;
Institution: Third Department of Medicine, Shinshu University School of Medicine, Matsumoto 390-8621, Japan. [email protected]
Shortcut link to this study:
Liver transplantation has been performed for patients with incurable liver diseases but this therapeutic technique can be extended to neurological disorders, such as familial amyloid polyneuropathy and adult-onset type II citrullinemia. An amyloid precursor in familial amyloid polyneuropathy, a variant form of transthyretin, is produced mainly in the liver. After liver transplantation, it has been shown that this amyloid precursor disappears from the sera of patients once progression of the disease has halted. Type II citrullinemia is caused by a deficiency of liver-specific argininosuccinate synthetase activity and shows various neurological manifestations closely resembling those of hepatic encephalopathy, resulting in fatal outcome. All metabolic abnormalities in this disease, which include elevated plasma concentrations of citrulline and ammonia, can be immediately corrected by liver transplantation.
PMID: 19810938

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