Five boys with Lesch-Nyhan syndrome and varying degrees of dystonia, chorea, spasticity, ataxia, dysarthria, and mental retardation were studied at the Depts of Neurology and Medicine, Baylor College of Medicine, and Depts of Neurology and Pediatrics, University of Texas Health Science Center, Houston, TX
Lesch-Nyhan syndrome, a rare inborn error of metabolism, is characterized by mental retardation and ...
Background: Lesch-Nyhan disease (LND) is a rare X-linked recessive neurogenetic disorder caused by d...
The pilot study focused on the effective design of adaptive biofeedback equipment for use in the con...
The motor disorder associated with Lesch-Nyhan disease (LND) was studied in a total of 44 patients (...
The A.A. outline the Lesch-Nyhan syndrome describing its natural history, etiology, pathology, anato...
Lesch-Nyhan disease (LND) is caused by deficiency of the purine salvage enzyme hypoxanthine-guanine ...
Item does not contain fulltextLesch-Nyhan disease is a neurogenetic disorder caused by deficiency of...
<p>The rare hereditary diseases encountered in the practice of pediatricians, pediatric neurologists...
Lesch Nyhan Syndrome (LNS) is a rare hereditary disorder with an incidence of 1 in 380,000. It is a ...
Lesch–Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hy...
Lesch–Nyhan Disease (LND) is a rare X-linked recessive metabolic and neurological syndrome due to th...
This paper describes Lesch-Nyhan syndrome in a 1-year-old boy. This X-linked recessive error of puri...
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...
AbstractLesch-Nyhan disease is the most severe or complete phenotype of deficiency in hypoxanthine-g...
Lesch-Nyhan syndrome, a rare inborn error of metabolism, is characterized by mental retardation and ...
Background: Lesch-Nyhan disease (LND) is a rare X-linked recessive neurogenetic disorder caused by d...
The pilot study focused on the effective design of adaptive biofeedback equipment for use in the con...
The motor disorder associated with Lesch-Nyhan disease (LND) was studied in a total of 44 patients (...
The A.A. outline the Lesch-Nyhan syndrome describing its natural history, etiology, pathology, anato...
Lesch-Nyhan disease (LND) is caused by deficiency of the purine salvage enzyme hypoxanthine-guanine ...
Item does not contain fulltextLesch-Nyhan disease is a neurogenetic disorder caused by deficiency of...
<p>The rare hereditary diseases encountered in the practice of pediatricians, pediatric neurologists...
Lesch Nyhan Syndrome (LNS) is a rare hereditary disorder with an incidence of 1 in 380,000. It is a ...
Lesch–Nyhan disease (LND) is a rare X-linked recessive genetic disorder caused by a deficiency of hy...
Lesch–Nyhan Disease (LND) is a rare X-linked recessive metabolic and neurological syndrome due to th...
This paper describes Lesch-Nyhan syndrome in a 1-year-old boy. This X-linked recessive error of puri...
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...
AbstractLesch-Nyhan disease is the most severe or complete phenotype of deficiency in hypoxanthine-g...
Lesch-Nyhan syndrome, a rare inborn error of metabolism, is characterized by mental retardation and ...
Background: Lesch-Nyhan disease (LND) is a rare X-linked recessive neurogenetic disorder caused by d...
The pilot study focused on the effective design of adaptive biofeedback equipment for use in the con...
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