Bibliografia UJ CM

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Simone Sanna-Cherchi, Kamal Khan, Rik Westland, Priya Krithivasan, Lorraine Fievet, Hila Milo Rasouly, Juliana Ionita-Laza, Valentina P. Capone, David A. Fasel, Krzysztof Kiryluk, Sitharthan Kamalakaran, Monica Bodria, Edgar A. Otto, Matthew G. Sampson, Christopher E. Gillies, Virginia Vega-Warner, Katarina Vukojevic, Igor Pediaditakis, Gabriel S. Makar, Adele Mitrotti, Miguel Verbitsky, Jeremiah Martino, Qingxue Liu, Young-Ji Na, Vinicio Goj, Gianluigi Ardissino, Maddalena Gigante, Loreto Gesualdo, Magdalena Janezcko [Janeczko], Marcin Zaniew, Cathy Lee Mendelsohn, Shirlee Shril, Friedhelm Hildebrandt, Joanna A.E. van Wijk, Adela Arapovic, Marijan Saraga, Landino Allegri, Claudia Izzi, Francesco Scolari, Velibor Tasic, Gian Marco Ghiggeri, Anna Latos-Bielenska, Anna Materna-Kiryluk, Shrikant Mane, David B. Goldstein, Richard P. Lifton, Nicholas Katsanis, Erica E. Davis, Ali G. Gharavi.
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
American Journal of Human Genetics
2017 : Vol. 101, nr 5, s. 789-802
Autor korespondencyjny: Simone Sanna-Cherchi, Erica E Davis.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 8.855
Adres url:
Streszczenie w PubMed:
DOI:
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Beata S. Lipska, Paraskevas Iatropoulos, Ramona Maranta, Gianluca Caridi, Fatih Ozaltin, Ali Anarat, Ayse Balat, Jutta Gellermann, Agnes Trautmann, Ozlem Erdogan, Bassam Saeed, Sevinc Emre, Radovan Bogdanovic, Marta Azocar, Irena Balasz-Chmielewska, Elisa Benetti, Salim Caliskan, Sevgi Mir, Anette Melk, Pelin Ertan, Esra Baskin, Helena Jardim, Tinatin Davitaia, Anna Wasielewska, Dorota Drozdz, Maria Szczepanska, Augustina Jankauskiene, Lina Maria Serna Higuita, Gianluigi Ardissino, Ozan Ozkaya, Elzbieta Kuzma-Mroczkowska, Oguz Soylemezoglu, Bruno Ranchin, Anna Medynska, Marcin Tkaczyk, Amira Peco-Antic, Ipek Akil, Tomasz Jarmolinski, Agnieszka Firszt-Adamczyk, Jiri Dusek, Giacomo D. Simonetti, Faysal Gok, Alaleh Gheissari, Francesco Emma, Rafael T. Krmar, Michel Fischbach, Nikoleta Printza, Eva Simkova, Caterina Mele, Gian Marco Ghiggeri, Franz Schaefer.
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Kidney International
2013 : Vol. 84, nr 1, s. 206-213, il., bibliogr. 37 poz.
p-ISSN: 0085-2538
AZ
ORG
AIF
IF: 8.520
Adres url:
Streszczenie w PubMed:
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Claus Peter Schmitt, Gianluigi Ardissino, Sara Testa, Aldo Claris-Appiani, Otto Mehls, European Study Group on Vitamin D in Children with Renal Failure.
Growth in children with chronic renal failure on intermittent versus daily calcitriol.
Pediatric Nephrology
2003 : Vol. 18, nr 5, s. 440-444, il., bibliogr. 29 poz., abstr.
AZ
ORG
AIF
IF: 1.219
DOI:
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Gianluigi Ardissino, Claus Peter Schmitt, Maria Luisa Bianchi, Valeria Dacco, Aldo Claris-Appiani, Otto Mehls, European Study Group on Vitamin D in Children with Renal Failure.
No difference in intestinal strontium absorption after oral or IV calcitriol in children with secondary hyperparathyroidism.
Kidney International
2000 : Vol. 58, nr 3, s. 981-988, il., bibliogr. 40 poz.
AZ
ORG
AIF
IF: 4.371
Adres url:
DOI:
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