A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
Arcos-Burgos, M, Jain, M, Acosta, M T, Shively, S, Stanescu, H, Wallis, D, Domené, S, Vélez, J I, Karkera, J D, Balog, J, Berg, K, Kleta, R, Gahl, W A, Roessler, E, Long, R, Lie, J, Pineda, D, Londoño, A C, Palacio, J D, Arbelaez, A, Lopera, F, Elia, J, Hakonarson, H, Johansson, S, Knappskog, P M, Haavik, J, Ribases, M, Cormand, B, Bayes, M, Casas, M, Ramos-Quiroga, J A, Hervas, A, Maher, B S, Faraone, S V, Seitz, C, Freitag, C M, Palmason, H, Meyer, J, Romanos, M, Walitza, S, Hemminger, U, Warnke, A, Romanos, J, Renner, T, Jacob, C, Lesch, K-P, Swanson, J, Vortmeyer, A, Bailey-Wilson, J E, Castellanos, F X, Muenke, M
Published in Molecular psychiatry (01.11.2010)
Published in Molecular psychiatry (01.11.2010)
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Journal Article
Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis
Nibali, L, Medlar, A, Stanescu, H, Kleta, R, Darbar, U, Donos, N
Published in Oral diseases (01.01.2013)
Published in Oral diseases (01.01.2013)
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Journal Article
Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005
Brooks, BP, Kleta, R, Stuart, C, Tuchman, M, Jeong, A, Stergiopoulos, SG, Bei, T, Bjornson, B, Russell, L, Chanoine, J-P, Tsagarakis, S, Kalsner, LR, Stratakis, CA
Published in Clinical genetics (01.09.2005)
Published in Clinical genetics (01.09.2005)
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Journal Article
Antenatal Bartter's syndrome: why is this not a lethal condition?
Bockenhauer, D., Cruwys, M., Kleta, R., Halperin, L.F., Wildgoose, P., Souma, T., Nukiwa, N., Cheema-Dhadli, S., Chong, C.K., Kamel, K.S., Davids, M.R., Halperin, M.L.
Published in QJM : An International Journal of Medicine (01.12.2008)
Published in QJM : An International Journal of Medicine (01.12.2008)
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Journal Article
Deletion in MEFV resulting in the loss of p.M694 residue as the cause of autosomal dominant familial Mediterranean fever in North Western European Caucasians - a case series and genetic exploration
Rowczenio, D, Iancu, D, Trojer, H, Gilbertson, J, Gillmore, J, Wechalekar, A, Tekman, M, Stanescu, H, Kleta, R, Lane, T, Hawkins, P, Lachmann, H
Published in Pediatric rheumatology online journal (28.09.2015)
Published in Pediatric rheumatology online journal (28.09.2015)
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Journal Article
New Treatment Options for Bartter's Syndrome
Kleta, Robert, Basoglu, Candan, Kuwertz-Bröking, Eberhard
Published in The New England journal of medicine (31.08.2000)
Published in The New England journal of medicine (31.08.2000)
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Journal Article
P090 Epilepsy, Ataxia, Sensorineural deafness, Tubulopathy and KCNJ10 mutations
Arora, R, Cross, H, Feather, S, Stanescu, H.C, Zdebik, A.A, van't Hoff, W, Dobbie, A, Warth, R, Sheridan, E, Kleta, R, Bockenhauer, D
Published in European journal of paediatric neurology (2009)
Published in European journal of paediatric neurology (2009)
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Journal Article
022 Genetic investigations in renal tubulopathies
Bockenhauer, D, Ashton, E, W Van’tHoff, Hayes, W, Kleta, R
Published in Archives of disease in childhood (01.12.2018)
Published in Archives of disease in childhood (01.12.2018)
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Journal Article
Familial hypomagnesemia-hypercalciuria in 2 siblings
Kuwertz-Bröking, E, Fründ, S, Bulla, M, Kleta, R, August, C, Kisters, K
Published in Clinical nephrology (01.08.2001)
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Published in Clinical nephrology (01.08.2001)
Journal Article
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1
Enerbäck, Sven, Nilsson, Daniel, Edwards, Noel, Heglind, Mikael, Alkanderi, Sumaya, Ashton, Emma, Deeb, Asma, Kokash, Feras E B, Bakhsh, Abdul R A, Van't Hoff, William, Walsh, Stephen B, D'Arco, Felice, Daryadel, Arezoo, Bourgeois, Soline, Wagner, Carsten A, Kleta, Robert, Bockenhauer, Detlef, Sayer, John A
Published in Journal of the American Society of Nephrology (01.03.2018)
Published in Journal of the American Society of Nephrology (01.03.2018)
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Journal Article
Treatment and long-term outcome in primary distal renal tubular acidosis
Lopez-Garcia, Sergio Camilo, Emma, Francesco, Walsh, Stephen B, Fila, Marc, Hooman, Nakysa, Zaniew, Marcin, Bertholet-Thomas, Aurélia, Colussi, Giacomo, Burgmaier, Kathrin, Levtchenko, Elena, Sharma, Jyoti, Singhal, Jyoti, Soliman, Neveen A, Ariceta, Gema, Basu, Biswanath, Murer, Luisa, Tasic, Velibor, Tsygin, Alexey, Decramer, Stéphane, Gil-Peña, Helena, Koster-Kamphuis, Linda, La Scola, Claudio, Gellermann, Jutta, Konrad, Martin, Lilien, Marc, Francisco, Telma, Tramma, Despoina, Trnka, Peter, Yüksel, Selçuk, Caruso, Maria Rosa, Chromek, Milan, Ekinci, Zelal, Gambaro, Giovanni, Kari, Jameela A, König, Jens, Taroni, Francesca, Thumfart, Julia, Trepiccione, Francesco, Winding, Louise, Wühl, Elke, Ağbaş, Ayşe, Belkevich, Anna, Vargas-Poussou, Rosa, Blanchard, Anne, Conti, Giovanni, Boyer, Olivia, Dursun, Ismail, Pınarbaşı, Ayşe Seda, Melek, Engin, Miglinas, Marius, Novo, Robert, Mallett, Andrew, Milosevic, Danko, Szczepanska, Maria, Wente, Sarah, Cheong, Hae Il, Sinha, Rajiv, Gucev, Zoran, Dufek, Stephanie, Iancu, Daniela, Kleta, Robert, Schaefer, Franz, Bockenhauer, Detlef
Published in Nephrology, dialysis, transplantation (01.06.2019)
Published in Nephrology, dialysis, transplantation (01.06.2019)
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Journal Article
Horseshoe kidney and Turner syndrome [Letters and Replies]
Kleta, Robert, Brämswig, Jürgen H., Nahm, Anne‐Maria, Ritz, Eberhard
Published in Nephrology, dialysis, transplantation (01.07.2000)
Published in Nephrology, dialysis, transplantation (01.07.2000)
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Journal Article
Unexpected electrophysiological effects of D-19575, a new cytostatic drug
Kleta, R, Burckhardt, B C, Wolff, N A, Schlatter, E
Published in Nephrology, dialysis, transplantation (1999)
Published in Nephrology, dialysis, transplantation (1999)
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Journal Article
cGMP-activating peptides do not regulate electrogenic electrolyte transport in principal cells of rat CCD
Schlatter, E, Cermak, R, Forssmann, W G, Hirsch, J R, Kleta, R, Kuhn, M, Sun, D, Schafer, J A
Published in American journal of physiology. Renal physiology (01.12.1996)
Published in American journal of physiology. Renal physiology (01.12.1996)
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Journal Article
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1
Siitonen, Maija, Börjesson-Hanson, Anne, Pöyhönen, Minna, Ora, Ari, Pasanen, Petra, Bras, Jose, Kern, Silke, Kern, Jürgen, Andersen, Oluf, Stanescu, Horia, Kleta, Robert, Baumann, Marc, Kalaria, Rajesh, Kalimo, Hannu, Singleton, Andy, Hardy, John, Viitanen, Matti, Myllykangas, Liisa, Guerreiro, Rita
Published in Brain (London, England : 1878) (01.05.2017)
Published in Brain (London, England : 1878) (01.05.2017)
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Journal Article