Mistreatment of university students most common during medical studies

gan Rautio, Arja, Sunnari, Vappu, Nuutinen, Matti, Laitala, Marja
Cyhoeddwyd 2005

IL-10 polymorphisms +434T/C, +504G/T, and -2849C/T may predispose to tubulointersititial nephritis and uveitis in pediatric population

gan Rytkönen, Sari, Ritari, Jarmo, Peräsaari, Juha, Saarela, Ville, Nuutinen, Matti, Jahnukainen, Timo
Cyhoeddwyd yn PLoS One (2019)

Growth Hormone Therapy Is Safe and Effective in Patients with Lysinuric Protein Intolerance

gan Niinikoski, Harri, Lapatto, Risto, Nuutinen, Matti, Tanner, Laura, Simell, Olli, Näntö-Salonen, Kirsti
Cyhoeddwyd 2011

HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study

gan Koskela, Mikael, Nihtilä, Julia, Ylinen, Elisa, Kolho, Kaija-Leena, Nuutinen, Matti, Ritari, Jarmo, Jahnukainen, Timo
Cyhoeddwyd yn Pediatr Nephrol (2021)

Novel OCRL mutations in patients with Dent-2 disease

gan Böckenhauer, Detlef, Bökenkamp, Arend, Nuutinen, Matti, Unwin, Robert, van't Hoff, William, Sirimanna, Tony, Vrljicak, Kristina, Ludwig, Michael
Cyhoeddwyd yn J Pediatr Genet (2012)

Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings

gan Koskela, Mikael, Ylinen, Elisa, Autio-Harmainen, Helena, Tokola, Heikki, Heikkilä, Päivi, Lohi, Jouko, Jalanko, Hannu, Nuutinen, Matti, Jahnukainen, Timo
Cyhoeddwyd yn Pediatr Nephrol (2019)

Hemolytic uremic syndrome caused by Shiga toxin–producing Escherichia coli in children: incidence, risk factors, and clinical outcome

gan Ylinen, Elisa, Salmenlinna, Saara, Halkilahti, Jani, Jahnukainen, Timo, Korhonen, Linda, Virkkala, Tiia, Rimhanen-Finne, Ruska, Nuutinen, Matti, Kataja, Janne, Arikoski, Pekka, Linkosalo, Laura, Bai, Xiangning, Matussek, Andreas, Jalanko, Hannu, Saxén, Harri
Cyhoeddwyd yn Pediatr Nephrol (2020)

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

gan O’Toole, John F., Liu, Yangjian, Davis, Erica E., Westlake, Christopher J., Attanasio, Massimo, Otto, Edgar A., Seelow, Dominik, Nurnberg, Gudrun, Becker, Christian, Nuutinen, Matti, Kärppä, Mikko, Ignatius, Jaakko, Uusimaa, Johanna, Pakanen, Salla, Jaakkola, Elisa, van den Heuvel, Lambertus P., Fehrenbach, Henry, Wiggins, Roger, Goyal, Meera, Zhou, Weibin, Wolf, Matthias T.F., Wise, Eric, Helou, Juliana, Allen, Susan J., Murga-Zamalloa, Carlos A., Ashraf, Shazia, Chaki, Moumita, Heeringa, Saskia, Chernin, Gil, Hoskins, Bethan E., Chaib, Hassan, Gleeson, Joseph, Kusakabe, Takehiro, Suzuki, Takako, Isaac, R. Elwyn, Quarmby, Lynne M., Tennant, Bryan, Fujioka, Hisashi, Tuominen, Hannu, Hassinen, Ilmo, Lohi, Hellevi, van Houten, Judith L., Rotig, Agnes, Sayer, John A., Rolinski, Boris, Freisinger, Peter, Madhavan, Sethu M., Herzer, Martina, Madignier, Florence, Prokisch, Holger, Nurnberg, Peter, Jackson, Peter K., Khanna, Hemant, Katsanis, Nicholas, Hildebrandt, Friedhelm
Cyhoeddwyd 2010

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

gan O’Toole, John F., Liu, Yangjian, Davis, Erica E., Westlake, Christopher J., Attanasio, Massimo, Otto, Edgar A., Seelow, Dominik, Nurnberg, Gudrun, Becker, Christian, Nuutinen, Matti, Kärppä, Mikko, Ignatius, Jaakko, Uusimaa, Johanna, Pakanen, Salla, Jaakkola, Elisa, van den Heuvel, Lambertus P., Fehrenbach, Henry, Wiggins, Roger, Goyal, Meera, Zhou, Weibin, Wolf, Matthias T.F., Wise, Eric, Helou, Juliana, Allen, Susan J., Murga-Zamalloa, Carlos A., Ashraf, Shazia, Chaki, Moumita, Heeringa, Saskia, Chernin, Gil, Hoskins, Bethan E., Chaib, Hassan, Gleeson, Joseph, Kusakabe, Takehiro, Suzuki, Takako, Isaac, R. Elwyn, Quarmby, Lynne M., Tennant, Bryan, Fujioka, Hisashi, Tuominen, Hannu, Hassinen, Ilmo, Lohi, Hellevi, van Houten, Judith L., Rotig, Agnes, Sayer, John A., Rolinski, Boris, Freisinger, Peter, Madhavan, Sethu M., Herzer, Martina, Madignier, Florence, Prokisch, Holger, Nurnberg, Peter, Jackson, Peter, Khanna, Hemant, Katsanis, Nicholas, Hildebrandt, Friedhelm
Cyhoeddwyd 2010