نتائج البحث - Kamsteeg, Erik-Jan
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Reply: A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia; and Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar at... حسب Eidhof, Ilse, Baets, Jonathan, Kamsteeg, Erik-Jan, Schenck, Annette, van de Warrenburg, Bart P
منشور في 2020نص -
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Coenzyme Q10 deficiency due to a COQ4 gene defect causes childhood-onset spinocerebellar ataxia and stroke-like episodes حسب Bosch, Annet M., Kamsteeg, Erik-Jan, Rodenburg, Richard J., van Deutekom, Arend W., Buis, Dennis R., Engelen, Marc, Cobben, Jan-Maarten
منشور في 2018نص -
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Short-chain ubiquitination mediates the regulated endocytosis of the aquaporin-2 water channel حسب Kamsteeg, Erik-Jan, Hendriks, Giel, Boone, Michelle, Konings, Irene B. M., Oorschot, Viola, van der Sluijs, Peter, Klumperman, Judith, Deen, Peter M. T.
منشور في 2006نص -
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Biallelic Variants in the COLGALT1 Gene Causes Severe Congenital Porencephaly: A Case Report حسب Teunissen, Mariel W.A., Kamsteeg, Erik-Jan, Sallevelt, Suzanne C.E.H., Pennings, Maartje, Bauer, Noel J.C., Vermeulen, R. Jeroen, Nicolai, Joost
منشور في 2021نص -
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Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus حسب Kamsteeg, Erik-Jan, Bichet, Daniel G., Konings, Irene B.M., Nivet, Hubert, Lonergan, Michelle, Arthus, Marie-Françoise, van Os, Carel H., Deen, Peter M.T.
منشور في 2003نص -
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Robust and accurate detection and sizing of repeats within the DMPK gene using a novel TP-PCR test حسب Leferink, Maike, Wong, Daphne P. W., Cai, Shiwei, Yeo, Minli, Ho, Jocelin, Lian, Mulias, Kamsteeg, Erik-Jan, Chong, Samuel S., Haer-Wigman, Lonneke, Guan, Ming
منشور في 2019نص -
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Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 حسب Kamsteeg, Erik-Jan, Kress, Wolfram, Catalli, Claudio, Hertz, Jens M, Witsch-Baumgartner, Martina, Buckley, Michael F, van Engelen, Baziel G M, Schwartz, Marianne, Scheffer, Hans
منشور في 2012نص -
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De novo BK channel variant causes epilepsy by affecting voltage gating but not Ca(2+) sensitivity حسب Li, Xia, Poschmann, Sibylle, Chen, Qiuyun, Fazeli, Walid, Oundjian, Nelly Jouayed, Snoeijen-Schouwenaars, Francesca M., Fricke, Oliver, Kamsteeg, Erik-Jan, Willemsen, Marjolein, Wang, Qing Kenneth
منشور في 2018نص -
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Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders حسب van de Warrenburg, Bart P, Schouten, Meyke I, de Bot, Susanne T, Vermeer, Sascha, Meijer, Rowdy, Pennings, Maartje, Gilissen, Christian, Willemsen, Michèl AAP, Scheffer, Hans, Kamsteeg, Erik-Jan
منشور في 2016نص -
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Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders حسب van de Warrenburg, Bart P, Schouten, Meyke I, de Bot, Susanne T, Vermeer, Sascha, Meijer, Rowdy, Pennings, Maartje, Gilissen, Christian, Willemsen, Michèl AAP, Scheffer, Hans, Kamsteeg, Erik-Jan
منشور في 2017نص -
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GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia حسب Eidhof, Ilse, Baets, Jonathan, Kamsteeg, Erik-Jan, Deconinck, Tine, van Ninhuijs, Lisa, Martin, Jean-Jacques, Schüle, Rebecca, Züchner, Stephan, De Jonghe, Peter, Schenck, Annette, van de Warrenburg, Bart P
منشور في 2018نص -
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LIP5 Interacts with Aquaporin 2 and Facilitates Its Lysosomal Degradation حسب van Balkom, Bas W.M., Boone, Michelle, Hendriks, Giel, Kamsteeg, Erik-Jan, Robben, Joris H., Stronks, H. Christiaan, van der Voorde, Anne, van Herp, Francois, van der Sluijs, Peter, Deen, Peter M.T.
منشور في 2009نص -
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Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome حسب Willemsen, Michèl A, Vissers, Lisenka ELM, Verbeek, Marcel M, van Bon, Bregje W, Geuer, Sinje, Gilissen, Christian, Klepper, Joerg, Kwint, Michael P, Leen, Wilhelmina G, Pennings, Maartje, Wevers, Ron A, Veltman, Joris A, Kamsteeg, Erik-Jan
منشور في 2017نص