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25篇 您的检索式：作者名="Fermo E"

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	题名	作者	年代	出处	被引量
1	Red cell pyruvate kinase deficiency: molecular and clinical aspects 显示文摘	Zanella A Fermo E Bianchi P	2005	Br J Haematol2005，130，1：	1
2	Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family 显示文摘	Gupta N Bianchi P Fermo E	2007	Prenat Diagn2007，27，2：	1
3	Pyruvate kinase deficiency: the genotype-phenotype association 显示文摘	Zanella A Fermo E Bianchi P	2007	Blood Rev2007，21，4：	1
4	Pyruvate kinase deficiency:the genotype-phenotype association显示文摘	Zanella A Fermo E Bianchi P	2007	Blood Bey2007，21，4：	1
5	Diagnostic power of laboratory tests for hereditary sphero-cytosis:a comparison study in 150 patients grouped according to molecular and clinical characteristics显示文摘	Bianchi P Fermo E Vercellati C	2012	Hematologica2012，97，4：	1
6	Hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency:a biochemical,genetic and clinical overview显示文摘	Chiarelli LR Fermo E Zanella A	2006	Hematology2006，11，1：	1
7	Red cell pyruvate ki-nase deficiency : molecular and clinical aspects 显示文摘	ZANELLA A FERMO E BIANCHI P	2005	Br J Haematol2005，130，1：	1
8	Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations 显示文摘	ZANELLA A BIANCHI P FERMO E	2006	Br J Haematol2006，133，：	1
9	Heredi-tary pyrimidine 5-nucleotidase deficiency:from genet-ics to clinical manifestations 显示文摘	ZANELLA A BIANCHI P FERMO E	2006	Br J Haematol2006，133，：	1
10	Congenital dyserythropoietic anemia type Ⅱ(CDA-Ⅱ)is caused by mutations in the SEC23B gene显示文摘	Bianchi P Fermo E Vercellati C		0，，：	1
11	Congenital dyser- ythropoietic anemia type Ⅱ (CDAIIY is caused by mutations in the SEC23B gene显示文摘	Bianchi P Fermo E Vereellati C	2009	Hum Mutat2009，30，9：	1
12	Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemia显示文摘	Chiarelli LR Bianchi P Fermo E	2005	Blood2005，105，8：	1
13	Hereditary red cell membrane defects: diagnostic and clinical aspects 显示文摘	BARCELLINI W BIANCHI P FERMO E	2011	131ood Transfus2011，9，3：	1
14	Diagnostic power of labora- tory tests for hereditary spherocytosis: a comparison study in 150 pa- tients grouped according to molecular and clinical characteristics 显示文摘	Bianchi P Fermo E Vercellati C	2012	Haematologica2012，97，4：	1
15	Immunoregulatory cytokine polymorphisms in Italian patients affected by paroxysmal nocturnal haemoglobinuria and aplastic anaemia显示文摘	Fermo E Bianchi P Barcellini W	2004	Eur J Immunogenet2004，31，6：	1
16	Red cell pyruvate kinase deficiency:molecular and clinical aspects显示文摘	Zanella A Fermo E Bianchi P	2005	Br J Hematol2005，130，1：	1
17	Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family显示文摘	Gupta N Bianchi P Fermo E	2007	Prenat Diagn2007，27，2：	1
18	Pyruvate kinase deficiency:the genotype-phenotype association显示文摘	Zanella A Fermo E Bianchi P	2007	Blood Rev2007，21，4：	1
19	Clinical and molecular aspects of 23 patients affected by paroxysmal nocturnal hemoglobinuria显示文摘	BOSCHETTI C FERMO E BIANCHI P	2004	Am J Hematol2004，77，1：	1
20	Serum amino acid analysis with pre-column derivatization: comparison of the O-phthaldialdehyde and N,N-diethyl-2,4-dinitro-5-fluroaniline methods显示文摘	Fermo Vecchi E D E	1990	J Chrom1990，534，：	1

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