首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
CLINICAL AND GENETIC HETEROGENEITY IN CHARCOT-MARIE-TOOTH NEUROPATHY TYPE 2 PATIENTS FROM TURKEY
被引:0
|
作者
:
Parman, Y.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Parman, Y.
[
1
]
Durmus, H.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Durmus, H.
[
1
]
Deymeer, F.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Deymeer, F.
[
1
]
Oflazer-Serdaroglu, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Oflazer-Serdaroglu, P.
[
1
]
Battaloglu, E.
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Battaloglu, E.
[
2
]
机构
:
[1]
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
[2]
Bogazici Univ, Istanbul, Turkey
来源
:
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
|
2017年
/ 22卷
/ 03期
关键词
:
D O I
:
暂无
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
引用
收藏
页码:355 / 355
页数:1
相关论文
共 50 条
[21]
AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH NEUROPATHY
Espinos, Carmen
论文数:
0
引用数:
0
h-index:
0
机构:
CIBERER, Unit 732, Valencia, Spain
CIBERER, Unit 732, Valencia, Spain
Espinos, Carmen
Calpena, Eduardo
论文数:
0
引用数:
0
h-index:
0
机构:
CIBERER, Unit 732, Valencia, Spain
CSIC, IBV, Unit Genet & Mol Med, Valencia, Spain
CIBERER, Unit 732, Valencia, Spain
Calpena, Eduardo
Martinez-Rubio, Dolores
论文数:
0
引用数:
0
h-index:
0
机构:
CIBERER, Unit 732, Valencia, Spain
CSIC, IBV, Unit Genet & Mol Med, Valencia, Spain
CIBERER, Unit 732, Valencia, Spain
Martinez-Rubio, Dolores
Lupo, Vincenzo
论文数:
0
引用数:
0
h-index:
0
机构:
CIBERER, Unit 732, Valencia, Spain
CSIC, IBV, Unit Genet & Mol Med, Valencia, Spain
CIBERER, Unit 732, Valencia, Spain
Lupo, Vincenzo
NEURODEGENERATIVE DISEASES,
2012,
724
: 61
-
75
[22]
LINKAGE OF THE GENE FOR CHARCOT-MARIE-TOOTH NEUROPATHY
NICHOLSON, GA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
NICHOLSON, GA
MESTEROVIC, N
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
MESTEROVIC, N
ROSS, DA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
ROSS, DA
BLOCK, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
BLOCK, J
MCLEOD, JG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT MED,SYDNEY,NSW 2006,AUSTRALIA
MCLEOD, JG
CYTOGENETICS AND CELL GENETICS,
1989,
51
(1-4):
: 1052
-
1053
[23]
ANTENATAL TESTING FOR CHARCOT-MARIE-TOOTH NEUROPATHY
NICHOLSON, GA
论文数:
0
引用数:
0
h-index:
0
机构:
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
NICHOLSON, GA
KENNERSON, M
论文数:
0
引用数:
0
h-index:
0
机构:
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
KENNERSON, M
MORGAN, G
论文数:
0
引用数:
0
h-index:
0
机构:
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
MORGAN, G
MCDONALD, B
论文数:
0
引用数:
0
h-index:
0
机构:
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
MCDONALD, B
KERR, B
论文数:
0
引用数:
0
h-index:
0
机构:
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
PRINCE WALES CHILDRENS HOSP,RANDWICK,NSW 2031,AUSTRALIA
KERR, B
MEDICAL JOURNAL OF AUSTRALIA,
1992,
156
(08)
: 579
-
579
[24]
Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages
论文数:
引用数:
h-index:
机构:
Candayan, Ayse
Parman, Yesim
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Med Sch, Istanbul, Turkey
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Parman, Yesim
Battaloglu, Esra
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Battaloglu, Esra
BALKAN MEDICAL JOURNAL,
2022,
39
(01)
: 3
-
11
[25]
Molecular analysis of Russian patients with Charcot-Marie-Tooth neuropathy
Mersiyanova, I
论文数:
0
引用数:
0
h-index:
0
机构:
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Mersiyanova, I
Dadali, EL
论文数:
0
引用数:
0
h-index:
0
机构:
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Dadali, EL
Perepelov, AV
论文数:
0
引用数:
0
h-index:
0
机构:
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Perepelov, AV
Evgrafov, OV
论文数:
0
引用数:
0
h-index:
0
机构:
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Russian Acad Med Sci, Med Genet Res Ctr, Moscow, Russia
Evgrafov, OV
EUROPEAN JOURNAL OF HUMAN GENETICS,
1998,
6
: 148
-
148
[26]
European guidelines for the molecular genetic diagnostics of the Charcot-Marie-Tooth neuropathy
Rautenstrauss, Bernd
论文数:
0
引用数:
0
h-index:
0
机构:
Med Genet Zentrum, D-80336 Munich, Germany
Med Genet Zentrum, D-80336 Munich, Germany
Rautenstrauss, Bernd
Nelis, Eva
论文数:
0
引用数:
0
h-index:
0
机构:
Med Genet Zentrum, D-80336 Munich, Germany
Med Genet Zentrum, D-80336 Munich, Germany
Nelis, Eva
MEDIZINISCHE GENETIK,
2009,
21
(04)
: 543
-
554
[27]
Mitochondrial GTPase mitofusin 2 mutations in Korean patients with Charcot-Marie-Tooth neuropathy type 2
Cho, H-J
论文数:
0
引用数:
0
h-index:
0
机构:
Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med, Seoul 135710, South Korea
Cho, H-J
Sung, D. H.
论文数:
0
引用数:
0
h-index:
0
机构:
Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med, Seoul 135710, South Korea
Sung, D. H.
Kim, B. J.
论文数:
0
引用数:
0
h-index:
0
机构:
Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med, Seoul 135710, South Korea
Kim, B. J.
Ki, C-S
论文数:
0
引用数:
0
h-index:
0
机构:
Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med, Seoul 135710, South Korea
Ki, C-S
CLINICAL GENETICS,
2007,
71
(03)
: 267
-
272
[28]
CHARCOT-MARIE-TOOTH DISEASE IN TURKEY: CLINICAL AND GENETIC FINDINGS FROM A SINGLE-CENTRE EXPERIENCE
Akcay, Halil Ibrahim
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Akcay, Halil Ibrahim
Durmus, Hacer
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Durmus, Hacer
Deymeer, Feza
论文数:
0
引用数:
0
h-index:
0
机构:
Mem Sisli Hosp, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Deymeer, Feza
Serdaroglu, Piraye
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Sch Med, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Serdaroglu, Piraye
Sivaci, Merve
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Biol & Mol Genet, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Sivaci, Merve
Candayan, Ayse
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Biol & Mol Genet, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Candayan, Ayse
Battaloglu, Esra
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Biol & Mol Genet, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Battaloglu, Esra
Parman, Yesim
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Istanbul Fac Med, Dept Neurol, Istanbul, Turkey
Parman, Yesim
NEUROLOGY,
2017,
88
[29]
CHARCOT-MARIE-TOOTH DISEASE IN TURKEY: CLINICAL AND GENETIC FINDINGS FROM A SINGLE-CENTRE EXPERIENCE
Akcay, H., I
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Akcay, H., I
Durmus, H.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Durmus, H.
Deymeer, F.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Deymeer, F.
Oflazer-Serdaroglu, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Oflazer-Serdaroglu, P.
Sivaci, M.
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Sivaci, M.
Candayan, A.
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Candayan, A.
Battaloglu, E.
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Battaloglu, E.
Parman, Y.
论文数:
0
引用数:
0
h-index:
0
机构:
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey
Parman, Y.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM,
2016,
21
(03)
: 230
-
231
[30]
Charcot-Marie-tooth polyneuropathy: Duplication, gene dosage, and genetic heterogeneity
Lupski, JR
论文数:
0
引用数:
0
h-index:
0
机构:
Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
Lupski, JR
PEDIATRIC RESEARCH,
1999,
45
(02)
: 159
-
165
←
1
2
3
4
5
→