-
1دورية أكاديمية
المؤلفون: Agnes Trautmann, Beata S. Lipska-Ziętkiewicz, Franz Schaefer
المصدر: Frontiers in Pediatrics, Vol 6 (2018)
مصطلحات موضوعية: SRNS, nephrotic syndrome, NPHS2, WT1, steroid resistant nephrotic syndrome, Pediatrics, RJ1-570
وصف الملف: electronic resource
-
2دورية أكاديمية
المؤلفون: Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, Olivier Gribouval, Szymon Ziętkiewicz, Jameela A Kari, Mohamed A Shalaby, Fatih Ozaltin, Jiri Dusek, Anette Melk, Aysun K Bayazit, Laura Massella, Lidia Hyla-Klekot, Sandra Habbig, Astrid Godron, Maria Szczepańska, Beata Bieniaś, Dorota Drożdż, Rasha Odeh, Wioletta Jarmużek, Katarzyna Zachwieja, Agnes Trautmann, Corinne Antignac, Franz Schaefer, PodoNet Consortium
المصدر: PLoS ONE, Vol 12, Iss 8, p e0180926 (2017)
وصف الملف: electronic resource
-
3
المؤلفون: Agnes Trautmann, Kjell Tullus
المصدر: Pediatric Kidney Disease ISBN: 9783031116643
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::cc40cb66737cc79a43002c185c5b8680
https://doi.org/10.1007/978-3-031-11665-0_49 -
4
المؤلفون: Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Szymon Ziętkiewicz, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Anne M. Schijvens, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Fang Deng, Caroline Rousset-Rouviere, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan
المساهمون: Institut Català de la Salut, [Drovandi S] Division of Pediatric Nephrology, Center for Pediatrics and Adolescent Medicine, University of Heidelberg, Heidelberg, Germany. Division of Nephrology, Dialysis and Transplantation, Department of Internal Medicine, Ospedale Policlinico San Martino and University of Genoa, Genoa, Italy. Division of Nephrology, Dialysis, Transplantation, Giannina Gaslini Children's Hospital, Genoa, Italy. [Lipska-Ziętkiewicz BS] Rare Diseases Centre, Medical University of Gdańsk, Gdańsk, Poland. Department of Biology and Medical Genetics, Clinical Genetics Unit, Medical University of Gdańsk, Gdańsk, Poland. [Ozaltin F, Gulhan B] Division of Pediatric Nephrology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey. [Emma F] Department of Pediatric Subspecialties, Division of Nephrology and Dialysis, Bambino Gesù Childrens Hospital, IRCCS, Rome, Italy. [Boyer O] APHP, Necker-Enfants Malades Hospital, Pediatric Nephrology, MARHEA and SNI Reference Centers, Paris, France. Imagine Institute, Paris University, Paris, France. [Ariceta G] Servei de Nefrologia Pediàtrica, Vall d'Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus
المصدر: Kidney Int. 102, 592-603 (2022)
Scientiaمصطلحات موضوعية: técnicas de investigación::técnicas genéticas::estudios de asociación genética [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Mitochondrial Diseases, Muscle Weakness, Nephrotic Syndrome, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Ubiquinone, Mitocondris - Malalties - Aspectes genètics, enfermedades urogenitales masculinas::enfermedades urológicas::enfermedades renales::nefrosis::síndrome nefrótico [ENFERMEDADES], Male Urogenital Diseases::Urologic Diseases::Kidney Diseases::Nephrosis::Nephrotic Syndrome [DISEASES], Nutritional and Metabolic Diseases::Metabolic Diseases::Mitochondrial Diseases [DISEASES], Ronyons - Malalties - Aspectes genètics, Coenzyme Q10, Mitochondria, Steroid-resistant Nephrotic Syndrome, Nephrology, Mutation, Other subheadings::Other subheadings::/genetics [Other subheadings], Humans, Ataxia, Steroids, Investigative Techniques::Genetic Techniques::Genetic Association Studies [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], enfermedades nutricionales y metabólicas::enfermedades metabólicas::enfermedades mitocondriales [ENFERMEDADES], Genetic Association Studies
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e1e37391fef1cc876f8e121f4381fe
http://hdl.handle.net/10852/99032 -
5
المؤلفون: Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Michiel F. Schreuder, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Cuihua Liu, Shuzhen Sun, Fang Deng, Xiaowen Wang, Stéphanie Clavé, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan
المصدر: Kidney International, 102, 3, pp. 604-612
Kidney Int. 102, 604-612 (2022)
Kidney International, 102, 604-612مصطلحات موضوعية: Mitochondrial Diseases, Muscle Weakness, Nephrotic Syndrome, Ubiquinone, Coq2, Coq6, Coq8b, Coq(10) Supplementation Therapy, Eskd, Coenzyme Q(10) Deficiency, Genetic Kidney Disease, Hereditary, Kidney Survival, Outcome, Proteinuria Reduction, Kidney, Proteinuria, Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11], Nephrology, Dietary Supplements, Mutation, Humans, Ataxia, Steroids
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b84c27b3e90b69a46a805c20918a32ef
http://hdl.handle.net/10852/100389 -
6
المؤلفون: Fatih Ozaltin, Ayse Balat, Bassam Saeed, Radovan Bogdanovic, Giuseppe Remuzzi, Marta Azocar, Franz Schaefer, Beata S. Lipska-Ziętkiewicz, Salim Caliskan, Ozlem Erdogan, Jun Oh, Maria Szczepańska, Anette Melk, Katharina Hees, Kibriya Fidan, Esra Baskin, Elzbieta Kuzma-Mroczkowska, Sevgi Mir, Dusan Paripovic, Hagen Staude, Halina Borzecka, Agnieszka Firszt-Adamczyk, Dorota Drozdz, Augustina Jankauskiene, Eva Simkova, Sven Schnaidt, Bruno Ranchin, Luisa Murer, Jutta Gellermann, Alexandra Zurowska, Monica Bodria, Alaleh Gheisari, Alev Yilmaz, Agnes Trautmann, Anna Wasilewska, Mieczysław Litwin, Helena Jardim, Lina Maria Serna Higuita, Ali Anarat, Nikoleta Printza, Francesco Emma, Marcin Tkaczyk
المساهمون: Çocuk Sağlığı ve Hastalıkları, Ege Üniversitesi, Çukurova Üniversitesi
المصدر: Journal of the American Society of Nephrology. 28:3055-3065
مصطلحات موضوعية: medicine.medical_specialty, Nephrotic Syndrome, PODOCIN, Adolescent, CYCLOSPORINE-A, medicine.medical_treatment, 030232 urology & nephrology, 030204 cardiovascular system & hematology, Gastroenterology, FOCAL SEGMENTAL GLOMERULOSCLEROSIS, 03 medical and health sciences, 0302 clinical medicine, Clinical Research, Internal medicine, CYCLOPHOSPHAMIDE, Biopsy, medicine, Humans, Child, Survival rate, SPECTRUM, Proteinuria, medicine.diagnostic_test, MUTATIONS, Proportional hazards model, business.industry, Infant, KIDNEY-DISEASE, Immunosuppression, General Medicine, Urology & Nephrology, medicine.disease, Survival Analysis, Steroid-resistant nephrotic syndrome, Calcineurin, Nephrology, Child, Preschool, Kidney Failure, Chronic, TRIAL, medicine.symptom, business, Nephrotic syndrome, Immunosuppressive Agents, Follow-Up Studies
وصف الملف: text/plain; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d9c2ab8268eb137330d9447bfc6e6b2
https://doi.org/10.1681/asn.2016101121 -
7
المؤلفون: Valerie Said Conti, Detlef Bockenhauer, Mesiha Ekim, Enrico Vidal, Ali Duzova, Nikoleta Printza, Tuula Hölttä, Fabio Paglialonga, Gema Ariceta, Augustina Jankauskiene, Claus Peter Schmitt, Enrico Verrina, Christoph Aufricht, Rukshana Shroff, Constantinos J. Stefanidis, Ismail Dursun, Hazel Webb, Maria do Sameiro Faria, Agnes Trautmann, Justine Bacchetta, Elisa Ylinen, Aysun Karabay Bayazit, Karel Vondrak, Rumeysa Yasemin Cicek, Stephanie Dufek, Daniela Iancu, Günter Klaus, Andrea Pasini, Harika Alpay, Alberto Edefonti, Sevcan A. Bakkaloglu, Argyroula Zampetoglou
المساهمون: Dufek, Stephanie, Holtta, Tuula, Trautmann, Agnes, Ylinen, Elisa, Alpay, Harika, Ariceta, Gema, Aufricht, Christoph, Bacchetta, Justine, Bakkaloglu, Sevcan A., Bayazit, Aysun, Cicek, Rumeysa Yasemin, Dursun, Ismail, Duzova, Ali, Ekim, Mesiha, Iancu, Daniela, Jankauskiene, Augustina, Klaus, Guenter, Paglialonga, Fabio, Pasini, Andrea, Printza, Nikoleta, Conti, Valerie Said, Faria, Maria do Sameiro, Schmitt, Claus Peter, Stefanidis, Constantinos J., Verrina, Enrico, Vidal, Enrico, Vondrak, Karel, Webb, Hazel, Zampetoglou, Argyroula, Bockenhauer, Detlef, Edefonti, Alberto, Shroff, Rukshana, Çukurova Üniversitesi
المصدر: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 34(8)
مصطلحات موضوعية: Nephrology, Male, Nephrotic Syndrome, NPHS1, medicine.medical_treatment, congenital nephrotic syndrome, 030232 urology & nephrology, 030204 cardiovascular system & hematology, Nephrectomy, Pediatrics, 0302 clinical medicine, Interquartile range, STEROID-RESISTANT, Prospective Studies, GLOMERULAR PROTEIN, Prospective cohort study, Child, Congenital nephrotic syndrome, bilateral nephrectomies, management approach, genotype–phenotype correlation, 3. Good health, Europe, Proteinuria, Child, Preschool, SURVIVAL, GENOTYPE/PHENOTYPE CORRELATIONS, Female, NEPHRIN, medicine.medical_specialty, DIFFUSE MESANGIAL SCLEROSIS, genotype-phenotype correlation, 03 medical and health sciences, Internal medicine, Albumins, Sepsis, medicine, Humans, Dialysis, Retrospective Studies, Transplantation, MUTATIONS, business.industry, 1ST YEAR, Infant, Membrane Proteins, Thrombosis, medicine.disease, LIFE, management approach, NPHS1, Mutation, business, Nephrotic syndrome
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd13eaca158d895c6e696d7792534ea5
https://pubmed.ncbi.nlm.nih.gov/30215773 -
8
المؤلفون: Fatih Ozaltin, Salim Caliskan, Ali Anarat, Alev Yilmaz, Harald Mischak, Augustina Jankauskiene, Agnes Trautmann, Petra Zürbig, Dusan Paripovic, Franz Schaefer
المصدر: Nephrology Dialysis Transplantation. 33:i630-i630
مصطلحات موضوعية: 03 medical and health sciences, Transplantation, 0302 clinical medicine, Nephrology, business.industry, 030232 urology & nephrology, Cancer research, Medicine, Biomarker (medicine), 030204 cardiovascular system & hematology, business, Steroid-resistant nephrotic syndrome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::ed0ba4d2e024f8451dd7b7cca647a350
https://doi.org/10.1093/ndt/gfy104.suo035 -
9
المؤلفون: Audrey O. Segal, Sudarsana De, Aoife M. Waters, Agnes Trautmann, Christoph Licht, Elizabeth A. Harvey
المصدر: Pediatric Nephrology. 25:97-104
مصطلحات موضوعية: Nephrology, medicine.medical_specialty, medicine.medical_treatment, Blood Component Transfusion, Peritoneal dialysis, Plasma, Recurrence, Internal medicine, Atypical hemolytic uremic syndrome, medicine, Humans, Infusions, Intravenous, Intensive care medicine, Atypical Hemolytic Uremic Syndrome, business.industry, Infant, Plasmapheresis, Eculizumab, medicine.disease, Combined Modality Therapy, Transplantation, Complement Factor H, Factor H, Hemolytic-Uremic Syndrome, Mutation, Pediatrics, Perinatology and Child Health, Paroxysmal nocturnal hemoglobinuria, Prednisone, Female, business, Peritoneal Dialysis, medicine.drug
-
10
المؤلفون: Stephanie Dufek, Enrico Vidal, Andrea Pasini, Tuula Hölttä, Agnes Trautmann, Constantinos J. Stefanidis, Alberto Edefonti, Claus Peter Schmitt, Argyroula Zampetoglou, Rukshana Shroff, Elisa Ylinen
المصدر: Nephrology Dialysis Transplantation. 32:iii738-iii738
مصطلحات موضوعية: 03 medical and health sciences, Transplantation, Pediatrics, medicine.medical_specialty, 0302 clinical medicine, Nephrology, business.industry, 030232 urology & nephrology, medicine, 030204 cardiovascular system & hematology, medicine.disease, business, Congenital nephrotic syndrome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::1898ab6f1a36242227798d6dabae9223
https://doi.org/10.1093/ndt/gfx183