A spectrum of novel NPHS1 and NPHS2 gene mutations in Pediatric Nephrotic syndrome patients from Pakistan

被引：0
|
作者：
Abid, Aiysha [1 ]
Khalique, Shagufta [1 ]
Shahid, Saba [1 ]
Lanewala, Ali [1 ]
Mubarak, Muhammad [1 ]
Hashmi, Seema [1 ]
Masood, Tariq [2 ]
Kazi, Javed [1 ]
Hafeez, Farkhanda [2 ]
Mehdi, S. Qasim [1 ]
机构：
[1] Sindh Inst Urol & Transplantat, Karachi, Pakistan
[2] Children Hosp, Lahore, Pakistan
来源：
PEDIATRIC NEPHROLOGY | 2013年 / 28卷 / 08期
关键词：
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：1461 / 1461
页数：1
相关论文
共 50 条
  • [1] A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan
    Abid, Aiysha
    Khaliq, Shagufta
    Shahid, Saba
    Lanewala, Ali
    Mubarak, Mohammad
    Hashmi, Seema
    Kazi, Javed
    Masood, Tahir
    Hafeez, Farkhanda
    Naqvi, Syed Ali Anwar
    Rizvi, Syed Adeebul Hasan
    Mehdi, Syed Qasim
    [J]. GENE, 2012, 502 (02) : 133 - 137
  • [2] NPHS1 AND NPHS2 MUTATIONS IN CHILDREN WITH NEPHROTIC SYNDROME
    Kandratsenka, Aksana
    Bialkevich, Hanna
    Kazyra, Ina
    Nikitchenko, Natallia
    Yatskiu, Hanna
    Goncharova, Roza
    [J]. PEDIATRIC NEPHROLOGY, 2023, 38 : S167 - S167
  • [3] NPHS1 and NPHS2 Gene Mutations in Chinese Children With Sporadic Nephrotic Syndrome
    Jianhua Mao
    Yang Zhang
    Lizhong Du
    Yuwen Dai
    Weizhong Gu
    Ai'Min Liu
    Shiqiang Shang
    Li Liang
    [J]. Pediatric Research, 2007, 61 : 117 - 122
  • [4] NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome
    Mao, Jianhua
    Zhang, Yang
    Du, Lizhong
    Dai, Yuwen
    Gu, Weizhong
    Liu, Ai'min
    Shang, Shiqiang
    Liang, Li
    [J]. PEDIATRIC RESEARCH, 2007, 61 (01) : 117 - 122
  • [5] A descriptive study of NPHS1 and NPHS2 mutations in children with congenital nephrotic syndrome
    Amr, Khalda
    El-Bassyouni, Hala T.
    Rabie, Eman
    Selim, Abeer
    Zaki, Moushira E.
    Alazem, Eman Abobakr Abd
    El-Shaer, Shereen
    Rady, Sahar
    Salah, Doaa M.
    [J]. GENE REPORTS, 2020, 20
  • [6] Association Between NPHS1 and NPHS2 Gene Variants Nephrotic Syndrome in Children
    Hashemi, Mohammad
    Sadeghi-Bojd, Simin
    Rahmania, Khaled
    Eskandari-Nasab, Ebrahim
    [J]. IRANIAN JOURNAL OF KIDNEY DISEASES, 2015, 9 (01) : 25 - 30
  • [7] NPHS1 AND NPHS2 MUTATIONS IN CONGENITAL AND LATE-ONSET CHILDHOOD NEPHROTIC SYNDROME
    Lozupone, S.
    Tummolo, A.
    Aceto, G.
    Francioso, G.
    Gigante, M.
    Gesualdo, L.
    Messina, G.
    De Palo, T.
    Penza, R.
    [J]. PEDIATRIC NEPHROLOGY, 2009, 24 (09) : 1805 - 1805
  • [8] Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria
    Caridi, G
    Bertelli, R
    Perfumo, F
    Ghiggeri, GM
    [J]. KIDNEY INTERNATIONAL, 2004, 66 (04) : 1715 - 1716
  • [9] Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome
    Abid, Aiysha
    Shahid, Saba
    Shakoor, Madiha
    Lanewala, Ali A.
    Hashmi, Seema
    Khaliq, Shagufta
    [J]. FRONTIERS IN GENETICS, 2018, 9
  • [10] Clinical Features and Long-Term Outcome of Nephrotic Syndrome Associated with Heterozygous NPHS1 and NPHS2 Mutations
    Caridi, Gianluca
    Gigante, Maddalena
    Ravani, Pietro
    Trivelli, Antonella
    Barbano, Giancarlo
    Scolari, Francesco
    Dagnino, Monica
    Murer, Luisa
    Murtas, Corrado
    Edefonti, Alberto
    Allegri, Landino
    Amore, Alessandro
    Coppo, Rosanna
    Emma, Francesco
    De Palo, Tommaso
    Penza, Rosa
    Gesualdo, Loreto
    Ghiggeri, Gian Marco
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 4 (06): : 1065 - 1072
12345