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Results:
1-7
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Results: 7
Authors:
Higgins, JJ
Loveless, JM
Goswami, S
Nee, LE
Cozzo, C
De Biase, A
Rosen, DR
Citation: Jj. Higgins et al., An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia, NEUROLOGY, 56(11), 2001, pp. 1482-1485
Authors:
Higgins, JJ
Kluetzman, K
Berciano, J
Combarros, O
Loveless, JM
Citation: Jj. Higgins et al., Posterior column ataxia and retinitis pigmentosa: A distinct clinical and genetic disorder, MOVEMENT D, 15(3), 2000, pp. 575-578
Authors:
Higgins, JJ
Rosen, DR
Loveless, JM
Clyman, JC
Grau, MJ
Citation: Jj. Higgins et al., A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter, NEUROLOGY, 55(3), 2000, pp. 335-340
Authors:
Higgins, JJ
Loveless, JM
Jankovic, J
Patel, PI
Citation: Jj. Higgins et al., Evidence that a gene for essential tremor maps to chromosome 2p in four families (vol 13, pg 972, 1998), MOVEMENT D, 14(1), 1999, pp. 200-200
Authors:
Higgins, JJ
Adler, RL
Loveless, JM
Citation: Jj. Higgins et al., Mutational analysis of the tau gene in progressive supranuclear palsy, NEUROLOGY, 53(7), 1999, pp. 1421-1424
Authors:
Higgins, JJ
Litvan, I
Nee, LE
Loveless, JM
Citation: Jj. Higgins et al., A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration, NEUROLOGY, 52(2), 1999, pp. 404-406
Authors:
Higgins, JJ
Morton, DH
Loveless, JM
Citation: Jj. Higgins et al., Posterior column ataxia with retinitis pigmentosa (AXPC1) maps to chromosome lq31-q32, NEUROLOGY, 52(1), 1999, pp. 146-150
Risultati:
1-7
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