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Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 gene.
Fluhr TL, Tabatabaeifar M, Syring H, Göhring G, Schaefer F, Jung-Klawitter S. Fluhr TL, et al. Among authors: tabatabaeifar m. Stem Cell Res. 2021 Dec;57:102579. doi: 10.1016/j.scr.2021.102579. Epub 2021 Oct 18. Stem Cell Res. 2021. PMID: 34695767 Free article.
Animal models of nephrotic syndrome.
Simic I, Tabatabaeifar M, Schaefer F. Simic I, et al. Among authors: tabatabaeifar m. Pediatr Nephrol. 2013 Nov;28(11):2079-88. doi: 10.1007/s00467-012-2376-5. Epub 2012 Dec 19. Pediatr Nephrol. 2013. PMID: 23250714 Review.
An inducible mouse model of podocin-mutation-related nephrotic syndrome.
Tabatabaeifar M, Wlodkowski T, Simic I, Denc H, Mollet G, Weber S, Moyers JJ, Brühl B, Randles MJ, Lennon R, Antignac C, Schaefer F. Tabatabaeifar M, et al. PLoS One. 2017 Oct 19;12(10):e0186574. doi: 10.1371/journal.pone.0186574. eCollection 2017. PLoS One. 2017. PMID: 29049388 Free PMC article.
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schreuder MF, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Liu C, Sun S, Deng F, Wang X, Clavé S, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G; PodoNet Consortium; mitoNET Consortium; CCGKDD Consortium; Schaefer F. Drovandi S, et al. Among authors: tabatabaeifar m. Kidney Int. 2022 Sep;102(3):604-612. doi: 10.1016/j.kint.2022.04.029. Epub 2022 May 25. Kidney Int. 2022. PMID: 35643375 Free article.
Functional analysis of BMP4 mutations identified in pediatric CAKUT patients.
Tabatabaeifar M, Schlingmann KP, Litwin M, Emre S, Bakkaloglu A, Mehls O, Antignac C, Schaefer F, Weber S; ESCAPE Trial Group. Tabatabaeifar M, et al. Pediatr Nephrol. 2009 Dec;24(12):2361-8. doi: 10.1007/s00467-009-1287-6. Epub 2009 Aug 14. Pediatr Nephrol. 2009. PMID: 19685083
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Ziętkiewicz S, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schijvens AM, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Deng F, Rousset-Rouviere C, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G; PodoNet Consortium; mitoNET Consortium; CCGKDD Consortium; Schaefer F. Drovandi S, et al. Among authors: tabatabaeifar m. Kidney Int. 2022 Sep;102(3):592-603. doi: 10.1016/j.kint.2022.02.040. Epub 2022 Apr 26. Kidney Int. 2022. PMID: 35483523 Free article.
Letter to the Editor: Military Traumatic Brain Injury.
Aarabi B, Amirjamshidi A, Taghipour M, Haghnegahdar A, Farrokhi MR, Kamgarpour A, Alibai E, Safdari M, Abbassioun K, Panahi S, Moein H, Birjandi A, Salehpour F, Tabatabaeifar M. Aarabi B, et al. Among authors: tabatabaeifar m. J Neurotrauma. 2023 Mar;40(5-6):592-594. doi: 10.1089/neu.2022.0381. Epub 2022 Dec 26. J Neurotrauma. 2023. PMID: 36576987 No abstract available.
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