Maciej Jankowski

Medical University of Gdańsk

H指数:4

被引数:170

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Triglyceride/HDL-cholesterol ratio as a predictor for treatment-related severe hypertriglyceridemia in children with lymphoid malignancies

甘油三酯/高密度脂蛋白胆固醇比值作为儿童淋巴肿瘤患者治疗相关严重高甘油三酯血症的预测因子

Scientific Reports

IF3.9

2026-07-020

Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin

HUMAN MUTATION

IF3.7

2024-03-210

OAAI

Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency

KIDNEY INTERNATIONAL

IF12.6

2022-09-0133

Drovandi, Stefania; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Emma, Francesco; Gulhan, Bora; Boyer, Olivia; Trautmann, Agnes; Xu, Hong; Shen, Qian; Rao, Jia; Riedhammer, Korbinian M.; Heemann, Uwe; Hoefele, Julia; Stenton, Sarah L.; Tsygin, Alexey N.; Ng, Kar-Hui; Fomina, Svitlana; Benetti, Elisa; Aurelle, Manon; Prikhodina, Larisa; Schreuder, Michiel F.; Tabatabaeifar, Mansoureh; Jankowski, Maciej; Baiko, Sergey; Mao, Jianhua; Feng, Chunyue; Liu, Cuihua; Sun, Shuzhen; Deng, Fang; Wang, Xiaowen; Clave, Stephanie; Stanczyk, Malgorzata; Balasz-Chmielewska, Irena; Fila, Marc; Durkan, Anne M.; Levart, Tanja Kersnik; Dursun, Ismail; Esfandiar, Nasrin; Haas, Dorothea; Bjerre, Anna; Anarat, Ali; Benz, Marcus R.; Talebi, Saeed; Hooman, Nakysa; Ariceta, Gema; Schaefer, Franz

Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

KIDNEY INTERNATIONAL

IF12.6

2022-09-0126

Drovandi, Stefania; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Emma, Francesco; Gulhan, Bora; Boyer, Olivia; Trautmann, Agnes; Zietkiewicz, Szymon; Xu, Hong; Shen, Qian; Rao, Jia; Riedhammer, Korbinian M.; Heemann, Uwe; Hoefele, Julia; Stenton, Sarah L.; Tsygin, Alexey N.; Ng, Kar-Hui; Fomina, Svitlana; Benetti, Elisa; Aurelle, Manon; Prikhodina, Larisa; Schijvens, Anne M.; Tabatabaeifar, Mansoureh; Jankowski, Maciej; Baiko, Sergey; Mao, Jianhua; Feng, Chunyue; Deng, Fang; Rousset-Rouviere, Caroline; Stanczyk, Malgorzata; Balasz-Chmielewska, Irena; Fila, Marc; Durkan, Anne M.; Levart, Tanja Kersnik; Dursun, Ismail; Esfandiar, Nasrin; Haas, Dorothea; Bjerre, Anna; Anarat, Ali; Benz, Marcus R.; Talebi, Saeed; Hooman, Nakysa; Ariceta, Gema; Serna Higuita, Lina Maria; Schaefer, Franz; Trautmann, Agnes; Tabatabaeifar, Mansoureh; Gheissari, Alaleh; Hooman, Nakysa; Benetti, Elisa; Emma, Francesco; Nigmatullina, Nazym; Tkaczyk, Marcin; Borzecka, Halina; Tsygin, Alexey N.; Prikhodina, Larisa; Bogdanovic, Radovan; Mir, Sevgi; Fomina, Svitlana; Klopstock, Thomas; Prokisch, Holger; Kornblum, Cornelia; Liu, Cui-Hua; Sun, Shu-Zhen; Dong, Yang; Wang, Xiao-Wen; Luan, Jiang-Wei; Schaefer, Franz

Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife

KIDNEY INTERNATIONAL

IF12.6

2021-06-0123

OAAI

Zurowska, Aleksandra M.; Bielska, Olga; Daca-Roszak, Patrycja; Jankowski, Maciej; Szczepanska, Maria; Roszkowska-Bjanid, Dagmara; Kuzma-Mroczkowska, Elzbieta; Panczyk-Tomaszewska, Malgorzata; Moczulska, Anna; Drozdz, Dorota; Hadjipanagi, Despina; Deltas, Constantinos; Ostalska-Nowicka, Danuta; Rabiega, Alina; Taraszkiewicz, Janina; Taranta-Janusz, Katarzyna; Wieczorkiewicz-Plaza, Anna; Jobs, Katarzyna; Mews, Judyta; Musial, Kinga; Jakubowska, Anna; Nosek, Hanna; Jander, Anna E.; Koutsofti, Constantina; Stanislawska-Sachadyn, Anna; Kuleszo, Dominka; Zietkiewicz, Ewa; Lipska-Zietkiewicz, Beata S.

Maciej Jankowski

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