Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Nephrotic Syndrome and LAMB2[original query] |
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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2). Pediatrics 2007 Apr 119 (4): e907-19. Hinkes Bernward G, Mucha Bettina, Vlangos Christopher N, Gbadegesin Rasheed, Liu Jinhong, Hasselbacher Katrin, Hangan Daniela, Ozaltin Fatih, Zenker Martin, Hildebrandt Friedhelm, |
Eye involvement in children with primary focal segmental glomerulosclerosis. Pediatric nephrology (Berlin, Germany) 2008 Mar 23 (3): 421-7. Ozaltin Fatih, Heeringa Saskia, Poyraz Ceren Erdogan, Bilginer Yelda, Kadayifcilar Sibel, Besbas Nesrin, Topaloglu Rezan, Ozen Seza, Hildebrandt Friedhelm, Bakkaloglu Ays |
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. Journal of the American Society of Nephrology : JASN 2010 Jul 21 (7): 1209-17. Machuca Eduardo, Benoit Geneviève, Nevo Fabien, Tête Marie-Josèphe, Gribouval Olivier, Pawtowski Audrey, Brandström Per, Loirat Chantal, Niaudet Patrick, Gubler Marie-Claire, Antignac Corin |
Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience. Bosnian journal of basic medical sciences / Udruz?enje basic?nih mediciniskih znanosti = Association of Basic Medical Sciences 2014 May 14 (2): 89-93. Bi?czak-Kuleta Agnieszka, Rubik Jacek, Litwin Mieczys?aw, Ryder Ma?gorzata, Lewandowska Klaudyna, Taryma-Le?niak Olga, Clark Jeremy S, Grenda Ryszard, Ciechanowicz Andrz |
Whole-exome sequencing reveals genetic variants associated with chronic kidney disease characterized by tubulointerstitial damages in North Central Region, Sri Lanka. Environmental health and preventive medicine 2015 Sep 20 (5): 354-9. Nanayakkara Shanika, Senevirathna Stmld, Parahitiyawa Nipuna B, Abeysekera Tilak, Chandrajith Rohana, Ratnatunga Neelakanthi, Hitomi Toshiaki, Kobayashi Hatasu, Harada Kouji H, Koizumi Ak |
Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2015 Aug 30 (8): 1279-87. Cil Onur, Besbas Nesrin, Duzova Ali, Topaloglu Rezan, Peco-Anti? Amira, Korkmaz Emine, Ozaltin Fat |
Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome. Frontiers in genetics 2018 9 214. Abid Aiysha, Shahid Saba, Shakoor Madiha, Lanewala Ali A, Hashmi Seema, Khaliq Shaguf |
Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome. BMC nephrology 2018 12 19 (1): 382. Li Guo-Min, Cao Qi, Shen Qian, Sun Li, Zhai Yi-Hui, Liu Hai-Mei, An Yu, Xu Ho |
A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
Kidney podocyte-associated gene polymorphisms affect tacrolimus concentration in pediatric patients with refractory nephrotic syndrome. The pharmacogenomics journal 2020 Jan . Mo Xiaolan, Li Jiali, Liu Yunfeng, Liao Xin, Tan Mei, Chen Yilu, He Fan, He Yanling, Li Yingjie, Huang M |
Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome. Molecular biology reports 2021 Sep . Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya |
Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India. Indian pediatrics 2021 5 58 (5): 445-451. Joshi Aditi, Sinha Aditi, Sharma Aakanksha, Shamim Uzma, Uppilli Bharathram, Sharma Pooja, Zahra Sana, Parveen Shaista, Mathur Aradhana, Chandan Monica, Tewari Prachi, Khandelwal Priyanka, Hari Pankaj, Mukerji Mitali, Faruq Mohammed, Bagga Arvind, |
Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa. European journal of pediatrics 2022 Oct 181 (10): 3595-3606. Nandlal Louansha, Winkler Cheryl A, Bhimma Rajendra, Cho Sungkweon, Nelson George W, Haripershad Sudesh, Naicker Thajasvar |
Molecular Genetic Testing for Kidney Disorders During the COVID-19 Pandemic. Delaware journal of public health 2022 5 7 (5): 24-27. Kirwin Susan M, Robbins Katherine M, Vinette Kathleen M B, Hirata Lee, Gripp Karen W, Funanage Vicky |
Tacrolimus pharmacokinetics in pediatric nephrotic syndrome: A combination of population pharmacokinetic modelling and machine learning approaches to improve individual prediction. Frontiers in pharmacology 2022 12 13 942129. Huang Qiongbo, Lin Xiaobin, Wang Yang, Chen Xiujuan, Zheng Wei, Zhong Xiaoli, Shang Dewei, Huang Min, Gao Xia, Deng Hui, Li Jiali, Zeng Fangling, Mo Xiaol |
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