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	有本地全文	6篇
	有全文链接	4篇

出版年度

	2022	1篇
	2018	1篇
	2017	2篇
	2016	4篇
	2015	2篇

作者

	Leila Mehdizadeh Fanid	9篇
	Mina Adampourezare	3篇
	Mohammad Ali HosseinpourFeizi	3篇
	SeyedGholamreza Noorazar	3篇
	A Eslami	2篇

	Hasan Shahrokhi	2篇
	Hassan Shahrokhi	2篇
	Mina Adampour Zare	2篇
	Mina Adampurzare	2篇
	Mohamad Ali Hosseinpour Feizi	2篇
	Mohammad Ali Hosseinpour Feizi	2篇
	Mortaza Bonyadi	2篇
	Adel Abdi	1篇
	Asghar Arfaie	1篇
	Azam Hosein nejad	1篇
	Habibeh Barzegar	1篇
	Khalil Esmaeilpour	1篇
	Leila Mehdizadeh Fanid	1篇
	Maryam Parvizi Aghdam	1篇
	Narges Zeinalzadeh	1篇
	Nava Khalilinejad	1篇
	Seyed Mahmoud Tabatabaei	1篇
	Shahrokh Amiri	1篇

来源期刊

International Journal of Pediatrics

10篇

学科主题

医学、卫生

10篇

语种

英文

10篇

国别/地区

伊朗

10篇

检索条件:"( ( 高级检索(( ((AU:(("Leila Mehdizadeh Fanid")))) )) ) )"

共 10 条记录

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1.An Association Analysis of Reelin Gene (RELN) Exon 22 (G/C), Rs.362691, Polymorphism with Autism Spectrum Disorder among Iranian-Azeri Population

作　　者：Leila Mehdizadeh Fanid ;Mohammad Ali Hosseinpour Feizi ;Mina Adampour Zare 等

出　　处：International Journal of Pediatrics. 2016 ;4(7):2027-2033.

出版社：Mashhad University of Medical Sciences

文章 ID：181215100

文章详细全文下载
2.Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

作　　者：Leila Mehdizadeh Fanid ;Hassan Shahrokhi ;Mina Adampourezare 等

出　　处：International Journal of Pediatrics. 2015 ;3(6.1):1065-1071.

出版社：Mashhad University of Medical Sciences

文章 ID：179929805

文章详细全文下载
3.The Association of DRD2 Gene TaqI Polymorphism with Attention Deficit Hyperactivity Disorder a Population Sample of Iranian Azeri-children

作　　者：Leila Mehdizadeh Fanid ;Mina Adampurzare ;SeyedGholamreza Noorazar 等

出　　处：International Journal of Pediatrics. 2016 ;4(5):1803-1807.

出版社：Mashhad University of Medical Sciences

文章 ID：179930595

文章详细全文下载
4.Evaluating Sleep Disorders amongst Children with Attention Deficit/ Hyperactivity Disorder (ADHD)

作　　者：Khalil Esmaeilpour ;Leila Mehdizadeh Fanid ;Azam Hosein nejad

出　　处：International Journal of Pediatrics. 2017 ;5(10):5907-5917.doi:10.22038/ijp.2017.25322.2149

出版社：Mashhad University of Medical Sciences

文章 ID：200298482

文章详细全文下载
5.Study of Polymorphism of the DRD2 Gene (-141C Ins/Del, rs1799732) with Attention Deficit Hyperactivity Disorder a Population Sample of Children in Iranian-Azeri

作　　者：Leila Mehdizadeh Fanid ;Mina Adampourezare ;Mohammad Ali HosseinpourFeizi 等

出　　处：International Journal of Pediatrics. 2017 ;5(3):4569-4574.doi:10.22038/ijp.2016.21049.1764

出版社：Mashhad University of Medical Sciences

文章 ID：197614607

文章详细全文下载
6.The Survey of DBH Gene Polymorphism Rs5320 in Children with Attention Deficit Hyperactivity Disorder (ADHD)

作　　者：Shahrokh Amiri ;Seyed Mahmoud Tabatabaei ;Asghar Arfaie 等

出　　处：International Journal of Pediatrics. 2018 ;6(9):8177-8184.doi:10.22038/ijp.2018.29296.2566

出版社：Mashhad University of Medical Sciences

文章 ID：218165541

文章详细全文下载
7.An Association Analysis of Reelin Gene (RELN) Exon 22 (G/C), Rs.362691, Polymorphism with Autism Spectrum Disorder among Iranian-Azeri Population

作　　者：Leila Mehdizadeh Fanid ;Mohammad Ali Hosseinpour Feizi ;Mina Adampour Zare 等

出　　处：International Journal of Pediatrics. 2016 ;4(7):2027-2033.doi:10.22038/ijp.2016.6856

出版社：Mashhad University of Medical Sciences

文章 ID：218535061

文章详细
8.The Association of DRD2 Gene TaqI Polymorphism with Attention Deficit Hyperactivity Disorder a Population Sample of Iranian Azeri-children

作　　者：Leila Mehdizadeh Fanid ;Mina Adampurzare ;SeyedGholamreza Noorazar 等

出　　处：International Journal of Pediatrics. 2016 ;4(5):1803-1807.doi:10.22038/ijp.2016.6726

出版社：Mashhad University of Medical Sciences

文章 ID：218535128

文章详细
9.Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

作　　者：Leila Mehdizadeh Fanid ;Hassan Shahrokhi ;Mina Adampourezare 等

出　　处：International Journal of Pediatrics. 2015 ;3(6.1):1065-1071.doi:10.22038/ijp.2015.5668

出版社：Mashhad University of Medical Sciences

文章 ID：218535198

文章详细
10.Polymorphism of dopamine transporter gene 3'-UTR VNTR in Iranian Azeri Turkish patients with ADHD

作　　者：Adel Abdi ;Narges Zeinalzadeh ;Leila Mehdizadeh Fanid 等

出　　处：International Journal of Pediatrics. 2022 ;10(2):15466-15473.doi:10.22038/ijp.2022.59297.4621

出版社：Mashhad University of Medical Sciences

文章 ID：1038408905

文章详细

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