BACKGROUND Lesch-Nyhan disease (LND) is an X-chromosomal disorder of purine metabolism characterized by hyperuricemia, dystonia, and self-mutilation, leading to an extremely high burden of disease in affected patients and families. Although allopurinol therapy can control hyperuricemia, it has no effect on self-mutilation and neurological symptoms. Single reports describe a beneficial effect of S-adenosylmethionine (SAM) on the neurological symptoms, which motivated us to evaluate this alternative treatment. METHODS We performed a double-blind placebo-controlled trial to analyze the effects of SAM on self-mutilation attempts in a male patient affected by LND. The trial lasted for 282 days and comprised three alternating verum and p...
OBJECTIVE: A systematic review on S-adenosylmethionine (SAMe) for treatment of neuropsychiatric cond...
Self-mutilation is a serious clinical problem. In humans self-mutilation is a characteristic of the ...
Lesch-Nyhan Disease (LND) is a rare X-linked genetic disease with hypoxanthine-guanine phosphoribosy...
BACKGROUND Lesch-Nyhan disease (LND) is an X-chromosomal disorder of purine metabolism characteri...
BACKGROUND: Lesch-Nyhan disease (LND) is an X-chromosomal disorder of purine metabolism characterize...
Background: Lesch-Nyhan disease (LND) is a rare X-linked recessive neurogenetic disorder caused by d...
Background, rationale, and methods . Lesch-Nyhan disease is a rare, X-linked disorder due to hypoxan...
Lesch-Nyhan disease (LND) is a rare X-linked genetic disorder, with complete hypoxanthine-guanine ph...
Lesch–Nyhan syndrome (LNS) is a rare genetic condition resulting from an inherited disorder of purin...
Lesch-Nyhan syndrome (LNS), first described in 1964 by Lesch and Nyhan, is a rare X-linked genetic d...
Lesch-Nyhan Syndrome is a rare X- linked disease due to absence of HPRT enzyme. It leads to hyperuri...
This paper describes Lesch-Nyhan syndrome in a 1-year-old boy. This X-linked recessive error of puri...
Item does not contain fulltextLesch-Nyhan disease is a neurogenetic disorder caused by deficiency of...
Contains fulltext : 51161.pdf (publisher's version ) (Open Access)Lesch-Nyhan dise...
S-adenosyl-L-methionine (SAMe) has been shown to increase hepatocyte membrane fluidity thereby relie...
OBJECTIVE: A systematic review on S-adenosylmethionine (SAMe) for treatment of neuropsychiatric cond...
Self-mutilation is a serious clinical problem. In humans self-mutilation is a characteristic of the ...
Lesch-Nyhan Disease (LND) is a rare X-linked genetic disease with hypoxanthine-guanine phosphoribosy...
BACKGROUND Lesch-Nyhan disease (LND) is an X-chromosomal disorder of purine metabolism characteri...
BACKGROUND: Lesch-Nyhan disease (LND) is an X-chromosomal disorder of purine metabolism characterize...
Background: Lesch-Nyhan disease (LND) is a rare X-linked recessive neurogenetic disorder caused by d...
Background, rationale, and methods . Lesch-Nyhan disease is a rare, X-linked disorder due to hypoxan...
Lesch-Nyhan disease (LND) is a rare X-linked genetic disorder, with complete hypoxanthine-guanine ph...
Lesch–Nyhan syndrome (LNS) is a rare genetic condition resulting from an inherited disorder of purin...
Lesch-Nyhan syndrome (LNS), first described in 1964 by Lesch and Nyhan, is a rare X-linked genetic d...
Lesch-Nyhan Syndrome is a rare X- linked disease due to absence of HPRT enzyme. It leads to hyperuri...
This paper describes Lesch-Nyhan syndrome in a 1-year-old boy. This X-linked recessive error of puri...
Item does not contain fulltextLesch-Nyhan disease is a neurogenetic disorder caused by deficiency of...
Contains fulltext : 51161.pdf (publisher's version ) (Open Access)Lesch-Nyhan dise...
S-adenosyl-L-methionine (SAMe) has been shown to increase hepatocyte membrane fluidity thereby relie...
OBJECTIVE: A systematic review on S-adenosylmethionine (SAMe) for treatment of neuropsychiatric cond...
Self-mutilation is a serious clinical problem. In humans self-mutilation is a characteristic of the ...
Lesch-Nyhan Disease (LND) is a rare X-linked genetic disease with hypoxanthine-guanine phosphoribosy...