Search Results - Tabatabaeifar, Mansoureh
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1
Oral coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency by Drovandi, Stefania (Author) , Lipska-Ziętkiewicz, Beata S. (Author) , Ozaltin, Fatih (Author) , Emma, Francesco (Author) , Gulhan, Bora (Author) , Boyer, Olivia (Author) , Trautmann, Agnes (Author) , Xu, Hong (Author) , Shen, Qian (Author) , Rao, Jia (Author) , Riedhammer, Korbinian M. (Author) , Heemann, Uwe (Author) , Hoefele, Julia (Author) , Stenton, Sarah L. (Author) , Tsygin, Alexey N. (Author) , Ng, Kar-Hui (Author) , Fomina, Svitlana (Author) , Benetti, Elisa (Author) , Aurelle, Manon (Author) , Prikhodina, Larisa (Author) , Schreuder, Michiel F. (Author) , Tabatabaeifar, Mansoureh (Author) , Jankowski, Maciej (Author) , Baiko, Sergey (Author) , Mao, Jianhua (Author) , Feng, Chunyue (Author) , Liu, Cuihua (Author) , Sun, Shuzhen (Author) , Deng, Fang (Author) , Wang, Xiaowen (Author) , Clavé, Stéphanie (Author) , Stańczyk, Małgorzata (Author) , Bałasz-Chmielewska, Irena (Author) , Fila, Marc (Author) , Durkan, Anne M. (Author) , Levart, Tanja Kersnik (Author) , Dursun, Ismail (Author) , Esfandiar, Nasrin (Author) , Haas, Dorothea (Author) , Bjerre, Anna (Author) , Anarat, Ali (Author) , Benz, Marcus R. (Author) , Talebi, Saeed (Author) , Hooman, Nakysa (Author) , Ariceta, Gema (Author) , Serna Higuita, Lina Maria (Author) , Schaefer, Franz (Author) , Gheissari, Alaleh (Author) , Nigmatullina, Nazym (Author) , Tkaczyk, Marcin (Author) , Borzecka, Halina (Author) , Bogdanovic, Radovan (Author) , Mir, Sevgi (Author) , Klopstock, Thomas (Author) , Prokisch, Holger (Author) , Kornblum, Cornelia (Author) , Liu, Cui-Hua (Author) , Sun, Shu-Zhen (Author) , Dong, Yang (Author) , Wang, Xiao-Wen (Author) , Luan, Jiang-Wei (Author) ,
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2
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy by Drovandi, Stefania (Author) , Lipska-Ziętkiewicz, Beata S. (Author) , Ozaltin, Fatih (Author) , Emma, Francesco (Author) , Gulhan, Bora (Author) , Boyer, Olivia (Author) , Trautmann, Agnes (Author) , Ziętkiewicz, Szymon (Author) , Xu, Hong (Author) , Shen, Qian (Author) , Rao, Jia (Author) , Riedhammer, Korbinian M. (Author) , Heemann, Uwe (Author) , Hoefele, Julia (Author) , Stenton, Sarah L. (Author) , Tsygin, Alexey N. (Author) , Ng, Kar-Hui (Author) , Fomina, Svitlana (Author) , Benetti, Elisa (Author) , Aurelle, Manon (Author) , Prikhodina, Larisa (Author) , Schijvens, Anne M. (Author) , Tabatabaeifar, Mansoureh (Author) , Jankowski, Maciej (Author) , Baiko, Sergey (Author) , Mao, Jianhua (Author) , Feng, Chunyue (Author) , Deng, Fang (Author) , Rousset-Rouviere, Caroline (Author) , Stańczyk, Małgorzata (Author) , Bałasz-Chmielewska, Irena (Author) , Fila, Marc (Author) , Durkan, Anne M. (Author) , Levart, Tanja Kersnik (Author) , Dursun, Ismail (Author) , Esfandiar, Nasrin (Author) , Haas, Dorothea (Author) , Bjerre, Anna (Author) , Anarat, Ali (Author) , Benz, Marcus R. (Author) , Talebi, Saeed (Author) , Hooman, Nakysa (Author) , Ariceta, Gema (Author) , Schaefer, Franz (Author) ,
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3
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation i... by Tabatabaeifar, Mansoureh (Author) , Fluhr, Theresa Leonie (Author) , Syring, Hanna (Author) , Göhring, Gudrun (Author) , Schaefer, Franz (Author) , Jung-Klawitter, Sabine (Author) ,
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4
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... by Fluhr, Theresa (Author) , Tabatabaeifar, Mansoureh (Author) , Syring, Hanna (Author) , Göhring, Gudrun (Author) , Schaefer, Franz (Author) , Jung-Klawitter, Sabine (Author) ,
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5
Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT) by Neirijnck, Yasmine (Author) , Reginensi, Antoine (Author) , Tabatabaeifar, Mansoureh (Author) , Schaefer, Franz (Author) ,
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An inducible mouse model of podocin-mutation-related nephrotic syndrome by Tabatabaeifar, Mansoureh (Author) , Wlodkowski, Tanja (Author) , Simić, Ivana (Author) , Denc, Helga (Author) , Moyers, John Julius (Author) , Brühl, Barbara (Author) , Schaefer, Franz (Author) ,
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7
ADCK4-Associated glomerulopathy causes Adolescence-Onset FSGS by Kahraman, Emine (Author) , Lipska-Ziętkiewicz, Beata S. (Author) , Boyer, Olivia (Author) , Gribouval, Olivier (Author) , Fourrage, Cecile (Author) , Tabatabaeifar, Mansoureh (Author) , Schnaidt, Sven (Author) , Gucer, Safak (Author) , Kaymaz, Figen (Author) , Arici, Mustafa (Author) , Dinckan, Ayhan (Author) , Mir, Sevgi (Author) , Bayazit, Aysun K. (Author) , Emre, Sevinc (Author) , Balat, Ayse (Author) , Rees, Lesley (Author) , Shroff, Rukshana (Author) , Bergmann, Carsten (Author) , Mourani, Chebl (Author) , Antignac, Corinne (Author) , Ozaltin, Fatih (Author) , Schaefer, Franz (Author) , Consortium, the PodoNet (Author) ,
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8
Animal models of nephrotic syndrome by Simić, Ivana (Author) , Tabatabaeifar, Mansoureh (Author) , Schaefer, Franz (Author) ,
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9
Mutation in BMP4 and its functional antagonists GREM1 and CRIM1 associate with abnormal kidney development in humans by Tabatabaeifar, Mansoureh (Author)
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Related Subjects
mitochondria
Animal models of disease
CAKUT
COQ2
COQ6
COQ8B
CoQ
CoQ supplementation therapy
ESKD
Fibrosis
Glomeruli
Kidneys
Knock-in
Knock-out
Mouse
Mouse models
Phenotypes
Proteinuria
Renal failure
Sox11
Steroid-resistant nephrotic syndrome
Zebrafish
coenzyme Q
coenzyme Q deficiency
coenzyme Q10
duplex kidneys
end-stage kidney disease
familial nephropathy
focal segmental glomerulosclerosis
genetic kidney disease