Gardiner RM[au] - Search Results

Year	Number of Results
1978	2
1979	4
1980	7
1983	1
1985	1
1986	1
1987	3
1988	4
1989	6
1990	5
1991	3
1992	1
1993	7
1994	4
1995	6
1996	7
1997	10
1998	7
1999	11
2000	6
2001	4
2002	7
2003	3
2004	1
2005	1
2006	3
2008	3
2009	3
2015	1
2022	0

1

Genes and epilepsy.

Gardiner RM. Gardiner RM. J Med Genet. 1990 Sep;27(9):537-44. doi: 10.1136/jmg.27.9.537. J Med Genet. 1990. PMID: 2231646 Free PMC article. Review. No abstract available.

2

Genetic analysis of Batten disease.

Gardiner RM. Gardiner RM. J Inherit Metab Dis. 1993;16(4):787-90. doi: 10.1007/BF00711910. J Inherit Metab Dis. 1993. PMID: 8412021 Review.

3

The epilepsies.

Rees M, Gardiner RM. Rees M, et al. Among authors: gardiner rm. Baillieres Clin Neurol. 1994 Aug;3(2):297-313. Baillieres Clin Neurol. 1994. PMID: 7952849 Review.

4

The molecular genetic basis of the neuronal ceroid lipofuscinoses.

Gardiner RM. Gardiner RM. Neurol Sci. 2000;21(3 Suppl):S15-9. doi: 10.1007/s100720070035. Neurol Sci. 2000. PMID: 11073223 Review.

5

Impact of our understanding of the genetic aetiology of epilepsy.

Gardiner RM. Gardiner RM. J Neurol. 2000 May;247(5):327-34. doi: 10.1007/s004150050598. J Neurol. 2000. PMID: 10896263 Review.

6

Human forms of neuronal ceroid-lipofuscinosis (Batten disease): consensus on diagnostic criteria, Hamburg 1992.

Kohlschütter A, Gardiner RM, Goebel HH. Kohlschütter A, et al. Among authors: gardiner rm. J Inherit Metab Dis. 1993;16(2):241-4. doi: 10.1007/BF00710254. J Inherit Metab Dis. 1993. PMID: 8411970 Review. No abstract available.

7

Transport of amino acids across the blood-brain barrier: implications for treatment of maternal phenylketonuria.

Gardiner RM. Gardiner RM. J Inherit Metab Dis. 1990;13(4):627-33. doi: 10.1007/BF01799517. J Inherit Metab Dis. 1990. PMID: 2122125 Review.

8

Studies of the lethargic (lh/lh) mouse model of absence seizures: regulatory mechanisms and identification of the lh gene.

Hosford DA, Lin FH, Wang Y, Caddick SJ, Rees M, Parkinson NJ, Barclay J, Cox RD, Gardiner RM, Hosford DA, Denton P, Wang Y, Seldin MF, Chen B. Hosford DA, et al. Among authors: gardiner rm. Adv Neurol. 1999;79:239-52. Adv Neurol. 1999. PMID: 10514818 Review.

9

Prenatal diagnosis of Batten's disease.

Munroe PB, Rapola J, Mitchison HM, Mustonen A, Mole SE, Gardiner RM, Jarvela I. Munroe PB, et al. Among authors: gardiner rm. Lancet. 1996 Apr 13;347(9007):1014-5. doi: 10.1016/s0140-6736(96)90148-8. Lancet. 1996. PMID: 8606564

10

The molecular genetic bases of the progressive myoclonus epilepsies.

Serratosa JM, Gardiner RM, Lehesjoki AE, Pennacchio LA, Myers RM. Serratosa JM, et al. Among authors: gardiner rm. Adv Neurol. 1999;79:383-98. Adv Neurol. 1999. PMID: 10514828 Review.

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