Primary Coq10 Deficiency: Clinical Spectrum and Genotype-phenotype Correlations

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

Primary Coq10 Deficiency: Clinical Spectrum and Genotype-phenotype Correlations

Stefania Drovandi
, Beata S. Lipska-zietkiewicz
, Fatih Ozaltin
, Francesco Emma
, Bora Gulhan
, Olivia Boyer
, Agnes Trautmann
, Qian Shen
, Jia Rao
, Korbinian M. Riedhammer
, Julia Hoefele
, Sarah L. Stenton
, Alexej Tsygin
, Kar-Hui Ng
, Svitlana Fomina
, Elisa Benetti
, Aurelle Manon
, Larisa Prikhodina
, Anne M. Schijvens
, Monsoureh Tabatabaeifar

Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Cuihua Liu, Shuzhen Sun, Fang Deng, Xiaowen Wang, Caroline Rousset-rouviere, Malgorzata Stanczyk, Irena Balasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus Benz, Saeed Talebi, Hong Xu, Nakysa Hooman, Gema Ariceta, Franz Schaefer

Araştırma sonucu: Dergiye katkı › Toplantı Özeti › bilirkişi

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	3445-3446
Sayfa sayısı	2
Dergi	Pediatric Nephrology
Hacim	36
Basın numarası	10
Yayın durumu	Yayınlandı - Eki 2021

Diger dosyalar ve linkler

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Bundan alıntı yap

Drovandi, S., Lipska-zietkiewicz, B. S., Ozaltin, F., Emma, F., Gulhan, B., Boyer, O., Trautmann, A., Shen, Q., Rao, J., Riedhammer, K. M., Hoefele, J., Stenton, S. L., Tsygin, A., Ng, K.-H., Fomina, S., Benetti, E., Manon, A., Prikhodina, L., Schijvens, A. M., ... Schaefer, F. (2021). Primary Coq10 Deficiency: Clinical Spectrum and Genotype-phenotype Correlations. Pediatric Nephrology, 36(10), 3445-3446.

@article{c1e1bc02910943609501ee914f854346,

title = "Primary Coq10 Deficiency: Clinical Spectrum and Genotype-phenotype Correlations",

author = "Stefania Drovandi and Lipska-zietkiewicz, \{Beata S.\} and Fatih Ozaltin and Francesco Emma and Bora Gulhan and Olivia Boyer and Agnes Trautmann and Qian Shen and Jia Rao and Riedhammer, \{Korbinian M.\} and Julia Hoefele and Stenton, \{Sarah L.\} and Alexej Tsygin and Kar-Hui Ng and Svitlana Fomina and Elisa Benetti and Aurelle Manon and Larisa Prikhodina and Schijvens, \{Anne M.\} and Monsoureh Tabatabaeifar and Maciej Jankowski and Sergey Baiko and Jianhua Mao and Chunyue Feng and Cuihua Liu and Shuzhen Sun and Fang Deng and Xiaowen Wang and Caroline Rousset-rouviere and Malgorzata Stanczyk and Irena Balasz-Chmielewska and Marc Fila and Durkan, \{Anne M.\} and Levart, \{Tanja Kersnik\} and Ismail Dursun and Nasrin Esfandiar and Dorothea Haas and Anna Bjerre and Ali Anarat and Marcus Benz and Saeed Talebi and Hong Xu and Nakysa Hooman and Gema Ariceta and Franz Schaefer",

year = "2021",

month = oct,

language = "English",

volume = "36",

pages = "3445--3446",

journal = "Pediatric Nephrology",

issn = "0931-041X",

publisher = "Springer Science and Business Media Deutschland GmbH",

number = "10",

}

Drovandi, S, Lipska-zietkiewicz, BS, Ozaltin, F, Emma, F, Gulhan, B, Boyer, O, Trautmann, A, Shen, Q, Rao, J, Riedhammer, KM, Hoefele, J, Stenton, SL, Tsygin, A, Ng, K-H, Fomina, S, Benetti, E, Manon, A, Prikhodina, L, Schijvens, AM, Tabatabaeifar, M, Jankowski, M, Baiko, S, Mao, J, Feng, C, Liu, C, Sun, S, Deng, F, Wang, X, Rousset-rouviere, C, Stanczyk, M, Balasz-Chmielewska, I, Fila, M, Durkan, AM, Levart, TK, Dursun, I, Esfandiar, N, Haas, D, Bjerre, A, Anarat, A, Benz, M, Talebi, S, Xu, H, Hooman, N, Ariceta, G & Schaefer, F 2021, 'Primary Coq10 Deficiency: Clinical Spectrum and Genotype-phenotype Correlations', Pediatric Nephrology, hac. 36, no. 10, pp. 3445-3446.

TY - JOUR

T1 - Primary Coq10 Deficiency

T2 - Clinical Spectrum and Genotype-phenotype Correlations

AU - Drovandi, Stefania

AU - Lipska-zietkiewicz, Beata S.

AU - Ozaltin, Fatih

AU - Emma, Francesco

AU - Gulhan, Bora

AU - Boyer, Olivia

AU - Trautmann, Agnes

AU - Shen, Qian

AU - Rao, Jia

AU - Riedhammer, Korbinian M.

AU - Hoefele, Julia

AU - Stenton, Sarah L.

AU - Tsygin, Alexej

AU - Ng, Kar-Hui

AU - Fomina, Svitlana

AU - Benetti, Elisa

AU - Manon, Aurelle

AU - Prikhodina, Larisa

AU - Schijvens, Anne M.

AU - Tabatabaeifar, Monsoureh

AU - Jankowski, Maciej

AU - Baiko, Sergey

AU - Mao, Jianhua

AU - Feng, Chunyue

AU - Liu, Cuihua

AU - Sun, Shuzhen

AU - Deng, Fang

AU - Wang, Xiaowen

AU - Rousset-rouviere, Caroline

AU - Stanczyk, Malgorzata

AU - Balasz-Chmielewska, Irena

AU - Fila, Marc

AU - Durkan, Anne M.

AU - Levart, Tanja Kersnik

AU - Dursun, Ismail

AU - Esfandiar, Nasrin

AU - Haas, Dorothea

AU - Bjerre, Anna

AU - Anarat, Ali

AU - Benz, Marcus

AU - Talebi, Saeed

AU - Xu, Hong

AU - Hooman, Nakysa

AU - Ariceta, Gema

AU - Schaefer, Franz

PY - 2021/10

Y1 - 2021/10

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:000696562600492&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 0931-041X

VL - 36

SP - 3445

EP - 3446

JO - Pediatric Nephrology

JF - Pediatric Nephrology

IS - 10

ER -