维普期刊资源整合服务平台（V6.5）

35篇 您的检索式：作者名="Parisi MA"

选中清除导出查看参考文献查看引证文献引用追踪共2页首页上一页第1页下一页末页 /2 跳转

	题名	作者	年代	出处	被引量
1	Genetics of Hirschsprung disease显示文摘	Parisi MA Kapur RP	2000	CUff Opin Pediatr2000，12，6：	1
2	Phenylketonuria scientific review conference: state of the science and fu- ture research needs显示文摘	Camp K_M Parisi MA Acosta PB	2014	Mol Genet Metab2014，112，2：	1
3	Phenylketonuria scientific review conference: state of the science and future research needs 显示文摘	Camp KM Parisi MA Acosta PB	2014	Mol Genet Metab2014，112，2：	1
4	The influence of body mass index and low-grade systemic inflammation on thyroid hormone abnormalities inpatients with type 2 diabetes显示文摘	Moura Neto A Parisi MC Tambascia MA	2013	Endocr J2013，60，7：	1
5	Clinical and molecular features of Joubert syndrome and related disorders显示文摘	Parisi MA	2009	Am J Ned Genet C Semin Ned Genet2009，151，：	1
6	Human malformations of the midbrain and hindbrain: review and proposed classification scheme显示文摘	Parisi MA Dobyns WB	2003	Mol Genet Metab2003，80，1：	1
7	Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease? 显示文摘	Parisi MA Kapur RP Neilson I	2002	Am J Med Genet2002，108，1：	1
8	Erythropoietin prevents cognition impairment induced by transient brain ischemia in gerbils 显示文摘	Catania MA Marciano MC Parisi A	2002	Eur J Pharmacol2002，437，3：	1
9	Genetic background modifies intestinal pseudo-obstruction and the expression of a reporter gene in Hox 11L1/mice 显示文摘	Parisi MA Baldessari AE Iida MH	2003	Gastroenterology2003，125，5：	1
10	Joubert syndrome (and related disorders)显示文摘	Parisi MA Doherty D Chance PF		0，，05：	1
11	Erythropoietin prevents cognition impairment induced by transient brain ischemia in gerbils显示文摘	Catania MA Marciano MC Parisi A	2002	Eur J Pharmacol2002，437，：	1
12	Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas显示文摘	Ligon AH Moore SD Parisi MA	2005	Am J Hum Genet2005，76，2：	1
13	Human malformations of the midbrain and hindbrain:review and proposed classification scheme显示文摘	Parisi MA Dobyns WB	2003	Mol Genet Metabol2003，80，：	1
14	Ocular application of nerve growth factor protects degenerating retinal ganglion cells in a rat model of glaucoma显示文摘	Colafrancesco V Parisi V Sposato V Rossi S Russo MA Coassin M		0，，2：	1
15	Similarity of human mitochondrial transcription factor 1 to high mobility group proteins显示文摘	Parisi MA Clayton DA		0，，5008：	1
16	Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease 显示文摘	Kapur RP Neilson I	2002	Am J Med Genet2002，108，1：	1
17	Clinical and molecular features of Joubert syndrome and related disorders显示文摘	Parisi MA	2009	Am J Med Genet C Semin Med Genet2009，151，4：	1
18	CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal bodyprotein CEP290显示文摘	Gorden NT Arts HH Parisi MA	2008	Am J Hum Genet2008，83，5：	1
19	CC2D2A is mutated in Joubert syndrome and interacts with the eiliopathy-associated basal body protein CEP290 显示文摘	Gorden NT1 Arts HH Parisi MA	2008	Am J Hum Genet2008，83，5：	1
20	Genetics of Hirschsprungs disease显示文摘	Parisi MA Kapur RP	2000	Curr Opin Pediatr2000，12，6：	1

返回顶部每页显示：

共2页首页上一页第1页下一页末页 /2 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示