The oculocerebrorenal syndrome of Lowe: an update

Por Bökenkamp, Arend, Ludwig, Michael
Publicado no Pediatr Nephrol (2016)

Clinical utility gene card for: Dent disease (Dent-1 and Dent-2)

Por Ludwig, Michael, Levtchenko, Elena, Bökenkamp, Arend
Publicado em 2014

Clinical utility gene card for: Lowe syndrome

Por Bökenkamp, Arend, Levtchenko, Elena, Recker, Florian, Ludwig, Michael
Publicado no Eur J Hum Genet (2015)

No Impact of the Analytical Method Used for Determining Cystatin C on Estimating Glomerular Filtration Rate in Children

Por Alberer, Martin, Hoefele, Julia, Benz, Marcus R., Bökenkamp, Arend, Weber, Lutz T.
Publicado no Front Pediatr (2017)

A case of tubulointerstitial nephritis in a patient with an influenza H1N1 infection

Por Ashtiani, Niloufar, Mulder, Margot F., van Wijk, Joanna A. E., Bokenkamp, Arend
Publicado em 2012

Recurrent pleural effusion during peritoneal dialysis: question

Por De Dooy, Jozef J. M. I., van Wijk, Joanna A. E., Plötz, Frans B., Bökenkamp, Arend
Publicado em 2007

Recurrent pleural effusion during peritoneal dialysis: answer

Por De Dooy, Jozef J. M. I., van Wijk, Joanna A. E., Plötz, Frans B., Bökenkamp, Arend
Publicado em 2007

Intussusception Presenting with Malignant Hypertension and Lethargy

Por de Vries, Andra, Ashtiani, Nilou, Ahmadi, Nazanin, Bakx, Roel, de Vaate, Annelies Walrave-bij, Bökenkamp, Arend
Publicado em 2013

Prevesical Calcification and Hydronephrosis in a Girl Treated for Vesicoureteral Reflux

Por Kuipers, Sarah, van der Horst, Eric H. J. R., Verbeke, Jonathan I. M. L., Bökenkamp, Arend
Publicado no Glob Pediatr Health (2016)

Comparing cystatin C and creatinine in the diagnosis of pediatric acute renal allograft dysfunction

Por Slort, Pauline R., Ozden, Nergiz, Pape, Lars, Offner, Gisela, Tromp, Wilma F., Wilhelm, Abraham J., Bokenkamp, Arend
Publicado em 2011

Precision of Estimating Equations for GFR in Children with a Solitary Functioning Kidney: The KIMONO Study

Por Westland, Rik, Abraham, Yael, Bökenkamp, Arend, Stoffel-Wagner, Birgit, Schreuder, Michiel F., van Wijk, Joanna A.E.
Publicado em 2013

Novel OCRL mutations in patients with Dent-2 disease

Por Böckenhauer, Detlef, Bökenkamp, Arend, Nuutinen, Matti, Unwin, Robert, van't Hoff, William, Sirimanna, Tony, Vrljicak, Kristina, Ludwig, Michael
Publicado no J Pediatr Genet (2012)

Renal Phenotype in Lowe Syndrome: A Selective Proximal Tubular Dysfunction

Por Bockenhauer, Detlef, Bokenkamp, Arend, van't Hoff, William, Levtchenko, Elena, Kist-van Holthe, Joana E., Tasic, Velibor, Ludwig, Michael
Publicado em 2008

Impact of Gestational Age and Birth Weight on Amikacin Clearance on Day 1 of Life

Por Schreuder, Michiel F., Wilhelm, Abraham J., Bökenkamp, Arend, Timmermans, Simone M.H., Delemarre-van de Waal, Henriette A., van Wijk, Joanna A.E.
Publicado em 2009

Renal Dysfunction and Elevated Blood Pressure in Long-Term Childhood Cancer Survivors

Por Knijnenburg, Sebastiaan L., Jaspers, Monique W., van der Pal, Helena J., Schouten-van Meeteren, Antoinette Y., Bouts, Antonia H., Lieverst, Jan A., Bökenkamp, Arend, Koning, Caro C.E., Oldenburger, Foppe, Wilde, James C.H., van Leeuwen, Flora E., Caron, Huib N., Kremer, Leontien C.
Publicado em 2012

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney

Por Westland, Rik, Verbitsky, Miguel, Vukojevic, Katarina, Perry, Brittany J., Fasel, David A., Zwijnenburg, Petra J.G., Bökenkamp, Arend, Gille, Johan J.P., Saraga-Babic, Mirna, Ghiggeri, Gian Marco, D’Agati, Vivette D., Schreuder, Michiel F., Gharavi, Ali G., van Wijk, Joanna A.E., Sanna-Cherchi, Simone
Publicado no Kidney Int (2015)

Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression

Por Baradaran-Heravi, Alireza, Cho, Kyoung Sang, Tolhuis, Bas, Sanyal, Mrinmoy, Morozova, Olena, Morimoto, Marie, Elizondo, Leah I., Bridgewater, Darren, Lubieniecka, Joanna, Beirnes, Kimberly, Myung, Clara, Leung, Danny, Fam, Hok Khim, Choi, Kunho, Huang, Yan, Dionis, Kira Y., Zonana, Jonathan, Keller, Kory, Stenzel, Peter, Mayfield, Christy, Lücke, Thomas, Bokenkamp, Arend, Marra, Marco A., van Lohuizen, Maarten, Lewis, David B., Shaw, Chad, Boerkoel, Cornelius F.
Publicado em 2012

Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic- and non-genetic contributing factors in 441 families from North America and Europe

Por Reutter, Heiko, Boyadjiev, Simeon A., Gambhir, Lisa, Ebert, Anne-Karoline, Rösch, Wolfgang H., Stein, Raimund, Schröder, Annette, Boemers, Thomas M., Bartels, Enrika, Vogt, Hannes, Utsch, Boris, Müller, Martin, Detlefsen, Birte, Zwink, Nadine, Rogenhofer, Sebastian, Gobet, Rita, Beckers, Goedele M.A, Bökenkamp, Arend, Kajbafzadeh, Abdol-Mohammad, Jaureguizar, Enrique, Draaken, Markus, Lakshmanan, Yegappan, Gearhart, John P., Ludwig, Michael, Nöthen, Markus M., Jenetzky, Ekkehart
Publicado em 2011

Genes in the Ureteric Budding Pathway: Association Study on Vesico-Ureteral Reflux Patients

Por van Eerde, Albertien M., Duran, Karen, van Riel, Els, de Kovel, Carolien G. F., Koeleman, Bobby P. C., Knoers, Nine V. A. M., Renkema, Kirsten Y., van der Horst, Henricus J. R., Bökenkamp, Arend, van Hagen, Johanna M., van den Berg, Leonard H., Wolffenbuttel, Katja P., van den Hoek, Joop, Feitz, Wouter F., de Jong, Tom P. V. M., Giltay, Jacques C., Wijmenga, Cisca
Publicado em 2012

Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

Por Morimoto, Marie, Myung, Clara, Beirnes, Kimberly, Choi, Kunho, Asakura, Yumi, Bokenkamp, Arend, Bonneau, Dominique, Brugnara, Milena, Charrow, Joel, Colin, Estelle, Davis, Amira, Deschenes, Georges, Gentile, Mattia, Giordano, Mario, Gormley, Andrew K., Govender, Rajeshree, Joseph, Mark, Keller, Kory, Lerut, Evelyne, Levtchenko, Elena, Massella, Laura, Mayfield, Christy, Najafian, Behzad, Parham, David, Spranger, Jurgen, Stenzel, Peter, Yis, Uluc, Yu, Zhongxin, Zonana, Jonathan, Hendson, Glenda, Boerkoel, Cornelius F.
Publicado no Orphanet J Rare Dis (2016)