Sex-related neurologic diseases. Hunter's disease. Lesch-Nyhan syndrome
Nieto Barrera, M.
Anales Espanoles de Pediatria 21(Suppl 20): 47-50
1984
ISSN/ISBN: 0302-4342 PMID: 6440462 Document Number: 233896
Document emailed within 1 workday
Related Documents
Tancredi, F.; Giliberti, P. 1976: The Lesch-Nyhan syndrome Minerva Pediatrica 28(31): 1891-1900Hernández Nieto, L. 1994: Lesch-Nyhan syndrome Medicina Clinica 102(18): 699-700
Warzok, R.; Schwesinger, G.; Knapp, A.; Seidlitz, F. 1982: Neuropathological findings in Lesch-Nyhan syndrome Zentralblatt für Allgemeine Pathologie U. Pathologische Anatomie 126(1-2): 95-104
Burkhardt, W.C.; Jackson, J.F.; Clement, E.G.; Sherline, D.M. 1978: Prenatal diagnosis of the Lesch-Nyhan syndrome Journal of Reproductive Medicine 21(3): 169-170
Félix Acevedo, D.; Fajardo Ramíerez, C.; Fernández Herrer, E. 1977: Lesch-Nyhan syndrome. Report of a case Boletin Medico del Hospital Infantil de Mexico 34(3): 609-618
Schneider, W. 1979: The Lesch-Nyhan syndrome as a rare cause of hemolytic anemia Acta Medica Austriaca 6(5): 202-203
Vranjesević, D.; Dukić, A.; Drndarski, I. 1989: Lesch-Nyhan syndrome: the differential diagnosis and actual aspects Neurologija 38(4): 359-366
Künzer, W. 1975: New case of Lesch-Nyhan syndrome. Attempt at treatment using adenine Archives Francaises de Pediatrie 32(3): 293
DeMars, R. 1971: Genetic studies of HG- PRT deficiency and the Lesch-Nyhan syndrome with cultured human cells Federation Proceedings 30(3): 944-955
Lee, W.J.; Lee, H.M.; Chi, C.S.; Yang, M.T.; Lin, H.Y.; Lin, W.H. 1995: Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family Zhonghua Yi Xue Za Zhi 56(6): 359-366
Jinnah, H.A.; Langlais, P.J.; Friedmann, T. 1992: Functional analysis of brain dopamine systems in a genetic mouse model of Lesch-Nyhan syndrome Journal of Pharmacology and Experimental Therapeutics 263(2): 596-607
Trubo, R. 1983: Genetic manipulation with retroviruses may lead to Lesch-Nyhan treatment Medical World News 24(20): 9
Lübbe, L.; Rudolph, M.; Scherneck, S.; Zimmermann, W.; Geissler, E. 1983: Immortalization of human Lesch-Nyhan-fibroblasts following infection with Simian virus 40 Archiv für Geschwulstforschung 53(2): 105-113
Hösli, P.; de BPRUYN, C.H.; Oei, T.L. 1974: Development of micro HG-PRT activity assay: preliminary complementation studies with Lesch-Nyhan cell strains Advances in Experimental Medicine and Biology 41: 811-815
Castro-Gago, M. 1984: Sex-related neurologic diseases. Duchenne muscular dystrophy. Lowe's disease Anales Espanoles de Pediatria 21(Suppl 20): 51-54
O'Neill, J.; Trombley, L.; Gundel, M.; Hunter, T.; Nicklas, J.; De Michelena, M. 2013: Identificación de una nueva mutación como causa del síndrome de Lesch-Nyhan en una familia peruana: utilidad del examen molecular para el consejo genético Revista de Neuro-Psiquiatria 62(1): 20-27
Del Toro-Riera, M. 2007: Follow-up of patients with Hunter syndrome: the Hunter Outcome Survey (HOS) registry Revista de Neurologia 44(Suppl 1): S13-S17
Larrégue, M.; Prigent, F.; Lorette, F.; Bressieux, J.M.; Daniel, F. 1980: Systemic subscapular papulosis: Hunter's sign in Hunter's disease L'Union Medicale du Canada 109(8): 1163-1170
Rodríguez Costa, T.; Gabarrón Llamas, J.; Casas Fernández, C.; Glover López, G.; Puche Mira, A.; Jiménez Cocina, A. 1984: Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families Anales Espanoles de Pediatria 21(Suppl 20): 54-57
Yamagata, S.; Watanabe, H. 1976: Problem of overlapping of collagen diseases with other related diseases or autoimmune diseases--ulcerative colitis and Crohn's disease Nihon Rinsho. Japanese Journal of Clinical Medicine 34(6): 1167-1172