Back

dr. A.M. van Eerde

dr. A.M. van Eerde

Associate Professor - medical

Show full profile

Research Output (85)

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract

Münch Johannes, Engesser Marie, Schönauer Ria, Hamm J Austin, Hartig Christin, Hantmann Elena, Akay Gulsen, Pehlivan Davut, Mitani Tadahiro, Akdemir Zeynep Coban, Tüysüz Beyhan, Shirakawa Toshihiko, Dateki Sumito, Claus Laura R, van Eerde Albertien M, Smol Thomas, Devisme Louise, Franquet Hélène, Attié-Bitach Tania, Wagner Timo, Bergmann Carsten, Höhn Anne Kathrin, Shril Shirlee, Pollack Ari, Wegner Tara, Scott Abbey, Paolucci Sarah, Buchan Jillian, Gabriel George C, Posey Jennifer E, Lupski James R, Petit Florence, McCarthy Andrew A, Pazour Gregory J, Lo Cecilia W, Popp Bernt, Halbritter Jan, 25 Feb 2022, In: Kidney International. 101 , p. 1039-1053 15 p.

Review of genetic testing in kidney disease patients:Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups

Claus Laura R, Snoek Rozemarijn, Knoers Nine V A M, van Eerde Albertien M 2022, In: American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 190 , p. 358-376 19 p.

Guidelines for Genetic Testing and Management of Alport Syndrome

Savige Judy, Lipska-Zietkiewicz Beata S, Watson Elizabeth, Hertz Jens Michael, Deltas Constantinos, Mari Francesca, Hilbert Pascale, Plevova Pavlina, Byers Peter, Cerkauskaite Agne, Gregory Martin, Cerkauskiene Rimante, Ljubanovic Danica Galesic, Becherucci Francesca, Errichiello Carmela, Massella Laura, Aiello Valeria, Lennon Rachel, Hopkinson Louise, Koziell Ania, Lungu Adrian, Rothe Hansjorg Martin, Hoefele Julia, Zacchia Miriam, Martic Tamara Nikuseva, Gupta Asheeta, van Eerde Albertien, Gear Susie, Landini Samuela, Palazzo Viviana, Al-Rabadi Laith, Claes Kathleen, Corveleyn Anniek, Van Hoof Evelien, van Geel Micheel, Williams Maggie, Ashton Emma, Belge Hendica, Ars Elisabet, Bierzynska Agnieszka, Gangemi Concetta, Renieri Alessandra, Storey Helen, Flinter Frances 20 Dec 2021, In: Clinical Journal of the American Society of Nephrology. 17 , p. 143-154 12 p.

An update on the use of tolvaptan for autosomal dominant polycystic kidney disease:consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International

Müller Roman-Ulrich, Messchendorp A Lianne, Birn Henrik, Capasso Giovambattista, Gall Emilie Cornec-Le, Devuyst Olivier, van Eerde Albertien, Guirchon Patrick, Harris Tess, Hoorn Ewout J, Knoers Nine V A M, Korst Uwe, Mekahli Djalila, Meur Yannick Le, Nijenhuis Tom, Ong Albert C M, Sayer John A, Schaefer Franz, Servais Aude, Tesar Vladimir, Torra Roser, Walsh Stephen B, Gansevoort Ron T 19 Nov 2021, In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 37 , p. 825-839 15 p.

Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA

Viering Daan, Schlingmann Karl-Peter, Hureaux Marguerite, Nijenhuis Tom, Mallett Andrew, Chan Melanie, van Beek Andre, van Eerde Albertien, Coulibaly Jean-Marie, Vallet Marion, Decramer Stéphane, Pelletier Solenne, Klaus Günter, Kömhoff Martin, Beetz Rolf, Patel Chirag, Shenoy Mohan, Steenbergen Eric, Anderson Glenn, Bongers Ernie, Bergmann Carsten, Panneman Daan, Rodenburg Richard, Kleta Robert, Houillier Pascal, Konrad Martin, Vargas-Poussou Rosa, Bockenhauer Detlef, de Baaij Jeroen 4 Oct 2021, In: Journal of the American Society of Nephrology. 33 , p. 305-325 21 p.

Genetics-first approach improves diagnostics of ESKD patients <50 years old

Snoek Rozemarijn, van Jaarsveld Richard H, Nguyen Tri Q, Peters Edith D J, Elferink Martin G, Ernst Robert F, Rookmaaker Maarten B, Lilien Marc R, Spierings Eric, Goldschmeding Roel, Knoers Nine V A M, van der Zwaag Bert, van Zuilen Arjan D, van Eerde Albertien M 11 Dec 2020, In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 37 , p. 349-357 9 p.

Preimplantation genetic testing for monogenic kidney disease

Snoek Rozemarijn, Stokman Marijn F, Lichtenbelt Klaske D, van Tilborg Theodora C, Simcox Cindy E, Paulussen Aimée D C, Dreesen Jos C M F, van Reekum Franka, Lely A Titia, Knoers Nine V A M, de Die-Smulders Christine E M, van Eerde Albertien M 27 Aug 2020, In: Clinical Journal of the American Society of Nephrology. 15 , p. 1279-1286 8 p.

Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease

Huynh Vinh T, Audrézet Marie-Pierre, Sayer John A, Ong Albert C, Lefevre Siriane, Le Brun Valoris, Després Aurore, Senum Sarah R, Chebib Fouad T, Barroso-Gil Miguel, Patel Chirag, Mallett Andrew J, Goel Himanshu, Mallawaarachchi Amali C, Van Eerde Albertien M, Ponlot Eléonore, Kribs Marc, Le Meur Yannick, Harris Peter C, Cornec-Le Gall Emilie, Aug 2020, In: Kidney International. 98 , p. 476-487 12 p.

PRE-IMPLANTATION GENETIC TESTING FOR MONOGENIC KIDNEY DISEASE: TWENTY-FIVE YEAR EXPERIENCE IN THE NETHERLANDS

Snoek R., Stokman Marijn F., Lichtenbelt Klaske D., Simcox Cindy E., Van Tilborg Theodora C., Paulussen Aimee D. C., Dreessen Jos C. M. F., Van Reekum Franka, Knoers Nine, De Die-Smulders Christine, Van Eerde Albertien M. Jun 2020, In: Nephrology Dialysis Transplantation. 35 , p. 346-346

Pregnancy in Advanced Kidney Disease:Clinical Practice Considerations on a Challenging Combination

Snoek Rozemarijn, van der Graaf Rieke, Meinderts Jildau R, van Reekum Franka, Bloemenkamp Kitty W M, Knoers Nine V A M, van Eerde Albertien M, Lely A Titia 1 Apr 2020, In: Nephron. 144 , p. 185-189 5 p.

Thank you for your review!

Has this information helped you?

Please tell us why, so that we can improve our website.

Contact

Afspraken

Praktisch

hetwkz.nl uses cookies

This website uses cookies This website displays videos from, among others, YouTube. Such parties place cookies (third-party cookies). If you do not want these cookies, you can indicate that here. We also place cookies ourselves to improve our site.

Read more about the cookie policy

Agree No, rather not