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Results:
1-9
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Results: 9
Authors:
Prengler, M
Sturt, N
Krywawych, S
Surtees, R
Liesner, R
Kirkham, F
Citation: M. Prengler et al., Homozygous thermolabile variant of the methylenetetrahydrofolate reductasegene: a potential risk factor for hyperhomocysteinaemia, CVD, and stroke in childhood, DEVELOP MED, 43(4), 2001, pp. 220-225
Authors:
Rodriguez, D
Gauthier, F
Bertini, E
Bugiani, M
Brenner, M
N'guyen, S
Goizet, C
Gelot, A
Surtees, R
Pedespan, JM
Hernandorena, X
Troncoso, M
Uziel, G
Messing, A
Ponsot, G
Pham-Dinh, D
Dautigny, A
Boespflug-Tanguy, O
Citation: D. Rodriguez et al., Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation, AM J HU GEN, 69(5), 2001, pp. 1134-1140
Authors:
Wilson, CJ
Wood, NW
Leonard, JV
Surtees, R
Rahman, S
Citation: Cj. Wilson et al., Mitochondrial DNA point mutation T9176C in Leigh syndrome, J CHILD NEU, 15(12), 2000, pp. 830-833
Authors:
Surtees, R
Citation: R. Surtees, Inherited ion channel disorders, EUR J PED, 159, 2000, pp. S199-S203
Authors:
Surtees, R
Blau, N
Citation: R. Surtees et N. Blau, The neurochemistry of phenylketonuria, EUR J PED, 159, 2000, pp. S109-S113
Authors:
Wilmshurst, JM
Surtees, R
Cox, T
Robinson, RO
Citation: Jm. Wilmshurst et al., Cerebellar ataxia, anterior horn cell disease, learning difficulties, and dystonia: A new syndrome., DEVELOP MED, 42(11), 2000, pp. 775-779
Authors:
Dobbie, M
Crawley, J
Waruiru, C
Marsh, K
Surtees, R
Citation: M. Dobbie et al., Cerebrospinal fluid studies in children with cerebral malaria: An excitotoxic mechanism?, AM J TROP M, 62(2), 2000, pp. 284-290
Authors:
Surtees, R
Citation: R. Surtees, Inborn errors of neurotransmitter receptors, J INH MET D, 22(4), 1999, pp. 374-380
Authors:
Robinson, R
McCarthy, GT
Bandmann, O
Dobbie, M
Surtees, R
Wood, NW
Citation: R. Robinson et al., GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness, J NE NE PSY, 66(1), 1999, pp. 86-89
Risultati:
1-9
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