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43篇 您的检索式：作者名="GABREELS"

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	题名	作者	年代	出处	被引量
1	A second common mutation in the methylenetetrahydrofolate reductase gene:anodelitional risk factor for neural tube defects显示文摘	Vander Put NMJ Gabreels F Stevens EMB	1998	Am J Hum Gene1998，62，：	1
2	Age - related changes of neuron - specific enolase, S - 100 protein, and myelin basic protein concentrations in cerebrospinal fluid显示文摘	Van Engelen BG Lamers KJ Gabreels FJ	1992	Clin Chem1992，38，：	1
3	A Second common mutation in the methylenetetrahydrofolate reductase gene:an additional risk factor for neural-tube defects显示文摘	van der Put NM Gabreels F Stevens EM	1998	Am J Hum Genet1998，62，5：	1
4	A new leukoencephalopathy with vanishing white matter 显示文摘	van der Knaap MS Barth PG Gabreels FJM	1997	Neurology1997，48，：	1
5	A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? 显示文摘	Van der Put NM Gabreels F Stevens EM	1998	Am J Hum Genet1998，62，5：	1
6	A second common mutation in the methylenetetrahydrofolate reductase gene:an additional risk factor for neural-tube defects 显示文摘	Van der Put NM Gabreels F Stevens EM	1998	Am J Hum Genet1998，62，5：	1
7	A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects显示文摘	Van der Put N M J Gabreels F Stevens E M B	1998	Am J Hum Genet1998，62，：	1
8	Towards a standardised assessment procedure for developmental apraxia of speech 显示文摘	Thoonen G Maassen B Gabreels F	1997	Eur J Disord Commun1997，32，1：	1
9	A second common mutation in the methylenetetrahydrofolate reductase gene:an additional risk factor for neural-tube defeets?显示文摘	VAN DER PUT N M GABREELS F STEVENS E M	1998	Am J Hun Genet1998，62，5：	1
10	Study on the gene and phenotypic characterization of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q-23-q33显示文摘	Gabreels Gesten A van Beersum S Eshuis L	2001	J Neurol Neurosurg Psychiatry2001，66，：	1
11	Occupational exposure and fects of the central nervous system in offspring显示文摘	Roeleveld N Zlelhuls GA Gabreels F	1990	British J Industrial Med1990，47，：	1
12	Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders 显示文摘	Lamers KJ van Engelen BG Gabreels FJ	1995	Acta Neurol Scand1995，92，3：	1
13	Age-related changes of neuron-specific enolase,S-100 protein, and myelin basic protein concentrations incerebrospinal fluid显示文摘	Van Engelen BG Lamers KJB Gabreels FJM	1992	Clin Chem1992，38，6：	1
14	A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural tube defects 显示文摘	NATHALIE M J PUT V D GABREELS F	1998	Am J Hum Genet1998，62，：	1
15	Clinical symptoms ofadult metachromatic leukodystrophy and arysulfatase A pseudodeficiency显示文摘	Hageman AT Gabreels F J de Jong JG	1995	Arch Neurol1995，52，4：	1
16	A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome显示文摘	De Vries DD Van Engelen BG Gabreeles FJ	1993	Ann Neuro11993，34，：	1
17	The vasopressin precursor is not processed in the hypothalamus of Wolfram syndrome patients with diabetes insipidus:evidence for the involvement of PC2 and 7B2显示文摘	Gabreels BA Swaab DF de Klejjn DP	1998	J Clin Endocrinol Metab1998，83，：	1
18	Sensory exonopathy in hereditary disal spinal muscular atrophy显示文摘	Frequin ST Gabreels FJ Gabreels-Festen AAWM	1991	Clini Neurol Neurosurg1991，93，：	1
19	A second common mu-tation in the methylenettrahydrofolate reducase gene:an additional riskfactor for neural-tube defects显示文摘	van der Put NM Gabreels F Stevens EM	1998	Am J Hum Genet1998，62，：	1
20	A second common mutation in the methyienetrtrahydrofolate reductase gene: an additional risk factor for neural-tube defects显示文摘	van der Put NM Gabreels F Stevens EM	1998	Am J Hum Genet1998，62，5：	1

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