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24篇 您的检索式：作者名="Andreu AL"

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	题名	作者	年代	出处	被引量
1	Familial multiple symmetric lipomatosis assoeiated with the A8344G mutation of mitochondrial DNA显示文摘	Gamez J Playan A Andreu AL	1998	Neurology1998，51，1：	1
2	Radiological manifestations oF pulmmary tuberculosis 显示文摘	Andreu J Caceres J Pallisa E el al	2004	Eur J Radiol2004，51，2：	1
3	Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA 显示文摘	Andreu AL Hanna MG Reichmann H	1999	N Engl J Med1999，341，14：	1
4	Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene显示文摘	Andreu AL Tanji K Bruno C	1999	Ann Neurol1999，45，6：	1
5	Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA显示文摘	Andreu AL Hanna MG Reiehmann H	1999	N Eng J Med1999，341，：	1
6	Infantile encephalopathy associated with the MELAS A3243G mutation显示文摘	Sue CM Bruno C Andreu AL	1999	J Pediatr1999，134，6：	1
7	Group B streptococcicausing neonatal infections in barcelona are a stable clonalpopulation: 18-year surveillance显示文摘	Martins ER Andreu A Correia P ei al	2011	J Clin Microbiol2011，49，8：	1
8	Sequence analysis of the entire mitochondrial genome in Parkinson's disease显示文摘	Vives- Bauza C Andreu AL Manfredi G	2002	Biochem Biophys Res Commun2002，290，：	1
9	Mutations in mitochondrial DNA as a cause of exercise intolerance显示文摘	DiMauro S Andreu AL	2001	Ann Med2001，33，：	1
10	Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy显示文摘	Andreu AL Bruno C Shanske S	1998	Neurology1998，51，11：	1
11	A Nonsense mutation(G15059A)in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria显示文摘	Andreu AL Bruno C Dunne TC	1999	Ann Neurol1999，45，1：	1
12	Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA显示文摘	Andreu AL Hanna MG Reichmann H	1999	N Engl J Med1999，341，14：	1
13	Infantile encephalopathy associated with the MELAS A3243G mutation 显示文摘	Sue CM Bruno C Andreu AL	1999	J Pediatr1999，134，6：	1
14	Current classification of mitochondrial disor- ders 显示文摘	Andreu AL DiMauro S	2003	J Neurol2003，250，12：	1
15	Myophosphorylase deficiency ( glycogenosis type V, McArdle disease) 显示文摘	Dimaur S Andreu AL Bruno C	2002	Curr Mol Med2002，2，2：	1
16	Familial muhiple symmet- ric lipomalosis associated with the A8344G mutation of mitochon- drial DNA显示文摘	Gamez J Playan A Andreu AL	1998	Neurology1998，51，1：	1
17	Mutations in mtDNA:are we scraping the bottle of the barrel 显示文摘	Di-Mauro S Andreu AL	2000	Brain Pathol2000，10，3：	1
18	Familial multiple symmetri-clipomatosis associated with the A8344G mutation of mitochondriaDNA显示文摘	Gamez J Playan A Andreu AL	1998	Neurology1998，51，1：	1
19	Reduced mitochondrial DNA transcription in senescent rat heart显示文摘	Andreu AL Arbos MA Perez-Martos A	1998	Biochem Biophys Res Commun1998，252，3：	1
20	Myophosphorylase deficiency (glycogenosis type V; McArdle disease)显示文摘	Dimaur S Andreu AL Bruno C	2002	Curr Mol Med2002，2，：	1

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