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Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder.
Fu R, Ceballos-Picot I, Torres RJ, Larovere LE, Yamada Y, Nguyen KV, Hegde M, Visser JE, Schretlen DJ, Nyhan WL, Puig JG, O'Neill PJ, Jinnah HA; Lesch-Nyhan Disease International Study Group. Fu R, et al. Among authors: jinnah ha. Brain. 2014 May;137(Pt 5):1282-303. doi: 10.1093/brain/awt202. Epub 2013 Aug 22. Brain. 2014. PMID: 23975452 Free PMC article. Review.
Animal models of Lesch-Nyhan syndrome.
Jinnah HA, Gage FH, Friedmann T. Jinnah HA, et al. Brain Res Bull. 1990 Sep;25(3):467-75. doi: 10.1016/0361-9230(90)90239-v. Brain Res Bull. 1990. PMID: 2292045 Review.
Lesch-Nyhan disease and the basal ganglia.
Visser JE, Bär PR, Jinnah HA. Visser JE, et al. Among authors: jinnah ha. Brain Res Brain Res Rev. 2000 Apr;32(2-3):449-75. doi: 10.1016/s0165-0173(99)00094-6. Brain Res Brain Res Rev. 2000. PMID: 10760551 Free article. Review.
Ocular motor dysfunction in Lesch-Nyhan disease.
Jinnah HA, Lewis RF, Visser JE, Eddey GE, Barabas G, Harris JC. Jinnah HA, et al. Pediatr Neurol. 2001 Mar;24(3):200-4. doi: 10.1016/s0887-8994(00)00265-4. Pediatr Neurol. 2001. PMID: 11301220
The spectrum of mutations causing HPRT deficiency: an update.
Jinnah HA, Harris JC, Nyhan WL, O'Neill JP. Jinnah HA, et al. Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1153-60. doi: 10.1081/NCN-200027400. Nucleosides Nucleotides Nucleic Acids. 2004. PMID: 15571220
The motor disorder of classic Lesch-Nyhan disease.
Visser JE, Harris JC, Barabas G, Eddey GE, Jinnah HA. Visser JE, et al. Among authors: jinnah ha. Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1161-4. doi: 10.1081/NCN-200027432. Nucleosides Nucleotides Nucleic Acids. 2004. PMID: 15571221
324 results