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21篇 您的检索式：作者名="Finnila S"

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	题名	作者	年代	出处	被引量
1	A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL显示文摘	Finnila S Tuisku S Herva R	2001	J Mol Med2001，79，11：	1
2	Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat显示文摘	Sajanti J Bjorkstrand AS Finnila S	1999	Biochem Biophys Acta1999，1454，3：	1
3	Phylogenetic network for European mtDNA 显示文摘	Finnila S Lehtonen MS Majamaa K	2001	Am J Hum Genet2001，68，6：	1
4	A novel mitochondrial DNA mutation and a mutation in tbe Notch3 gene in a patient with myopathy and CADASIL显示文摘	Finnila S Tuisku S Herva R	2001	J Mol Med (Berl)2001，79，11：	1
5	Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia显示文摘	Autere J Moilanen JS Finnila S	2004	Human genetics2004，115，1：	1
6	Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat显示文摘	Sajanti J Bjorkstrand AS Finnila S	1999	Biochim Biophys Acta1999，1454，3：	1
7	Cytoskeletal structure in cells harboring two mutations:R133C in NOTCH3 and 5650G > A in mitoehondrial DNA显示文摘	Annunen-Rasila J Karppa M Finnila S	2007	Mitochondrion2007，7，：	1
8	Chromosome 19q13and multiple sclerosis susceptibility in Finland:a linkage and two-stage association study显示文摘	Reunanen K Finnila S Laaksonen M	2002	J Neuroimmunol2002，126，12：	1
9	Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat 显示文摘	Sajanti J Bjorkstrand AS Finnila S	1999	Biochim Biophys Acta1999，1454，：	1
10	Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy显示文摘	Remes A M Finnila S Mononen H	2004	Neurology2004，63，2：	1
11	Phylogenetic Network for European mtDNA显示文摘	FINNILA S LEHTONEN M S MAJAMAA K	2001	Am J Hum Genet2001，68，6：	1
12	Hereditary dementia with intraeerebral hemorrhages and cerebral amyloid angiopathy显示文摘	Remes AM Finnila S Mononen H	2004	Neu- rology2004，63，2：	1
13	Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat显示文摘	Sajanti J Bjorkstrand AS Finnila S	1999	Biochim Biophys Aeta1999，1454，3：	1
14	Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformationsensitive gel electrophoresis显示文摘	Hassinen IE Ala-Kokko L	2000	Am J Hum Genet2000，66，3：	1
15	Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations 显示文摘	Finnila S Hassinen IE Majamaa K	1999	Mutat Res1999，406，24：	1
16	Mitochondrial DNA polymorphisms at risk factors for Parkinson's disease and Parkin- son's disease dementia显示文摘	Autere J Moilanen J S Finnila S	2004	Hum Genet2004，115，：	1
17	Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat 显示文摘	Sajanti J Bjorkstrand AS Finnila S	1999	Biochim Biophys Acta1999，1454，3：	1
18	Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy 显示文摘	Remes AM Finnila S Mononen H	2004	Neurology2004，63，2：	1
19	Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations显示文摘	Finnila S Ilmo E Hassinen KM	1999	Mutation Research Genomics1999，406，24：	1
20	A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL显示文摘	Finnila S Tuisku S Herva R	2001	J Mol Med2001，79，11：	1

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