نتائج البحث - "Agnes Trautmann"

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)
Scientia

مصطلحات 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

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

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, 604-612

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b84c27b3e90b69a46a805c20918a32ef
http://hdl.handle.net/10852/100389

6

Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children

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

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Management of children with congenital nephrotic syndrome: challenging treatment paradigms

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