Rac1 as a potential therapeutic target for chemo-radioresistant head and neck squamous cell carcinomas (HNSCC)
Skvortsov, S, Dudás, J, Eichberger, P, Witsch-Baumgartner, M, Loeffler-Ragg, J, Pritz, C, Schartinger, V H, Maier, H, Hall, J, Debbage, P, Riechelmann, H, Lukas, P, Skvortsova, I
Published in British journal of cancer (27.05.2014)
Published in British journal of cancer (27.05.2014)
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Journal Article
Seasonality at the clinical onset of type 1 diabetes—Lessons from the SWEET database
Gerasimidi Vazeou, A., Kordonouri, O., Witsch, M., Hermann, J.M., Forsander, G., de Beaufort, C., Veeze, H.J., Maffeis, C., Cherubini, V., Cinek, O., Piccini, B., Holl, R.W., Danne, T.
Published in Pediatric diabetes (01.10.2016)
Published in Pediatric diabetes (01.10.2016)
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Journal Article
Risk of recurrent severe hypoglycemia remains associated with a past history of severe hypoglycemia up to 4 years: Results from a large prospective contemporary pediatric cohort of the DPV initiative
Pacaud, D, Hermann, JM, Karges, B, Rosenbauer, J, Danne, T, Dürr, R, Herbst, A, Lindauer, S, Müther, S, Pötzsch, S, Raile, K, Witsch, M, Holl, RW
Published in Pediatric diabetes (01.05.2018)
Published in Pediatric diabetes (01.05.2018)
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Journal Article
Characterization of large deletions in the DHCR7 gene
Lanthaler, B., Hinderhofer, K., Maas, B., Haas, D., Sawyer, H., Burton-Jones, S., Carter, K., Suri, M., Witsch-Baumgartner, M.
Published in Clinical genetics (01.08.2015)
Published in Clinical genetics (01.08.2015)
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Journal Article
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome
Witsch-Baumgartner, M, Gruber, M, Kraft, H G, Rossi, M, Clayton, P, Giros, M, Haas, D, Kelley, R I, Krajewska-Walasek, M, Utermann, G
Published in Journal of medical genetics (01.08.2004)
Published in Journal of medical genetics (01.08.2004)
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Journal Article
VP25.06: Anophthalmia due to a novel mutation in the SOX2 gene
Nanda, M., Gellen, J., Csapo, B., Eisnecker, K., Greimel, P., Duba, H., Pölsler, L., Witsch‐Baumgartner, M., Kampelmuhler, E., Klaritsch, P.
Published in Ultrasound in obstetrics & gynecology (01.10.2020)
Published in Ultrasound in obstetrics & gynecology (01.10.2020)
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Journal Article
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey
Kalb, S, Caglayan, AO, Degerliyurt, A, Schmid, S, Ceylaner, S, Hatipoglu, N, Hinderhofer, K, Rehder, H, Kurtoglu, S, Ceylaner, G, Zschocke, J, Witsch-Baumgartner, M
Published in Clinical genetics (01.06.2012)
Published in Clinical genetics (01.06.2012)
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Journal Article
Andrological findings in infertile men with two (biallelic) CFTR mutations: results of a multicentre study in Germany and Austria comprising 71 patients
Rudnik-Schöneborn, S, Messner, M, Vockel, M, Wirleitner, B, Pinggera, G -M, Witsch-Baumgartner, M, Murtinger, M, Kliesch, S, Swoboda, M, Sänger, N, Zschocke, J, Tüttelmann, F
Published in Human reproduction (Oxford) (18.02.2021)
Published in Human reproduction (Oxford) (18.02.2021)
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Journal Article
Guidelines for the genetic diagnosis of hereditary recurrent fevers
Shinar, Y, Obici, L, Aksentijevich, I, Bennetts, B, Austrup, F, Ceccherini, I, Costa, J M, De Leener, A, Gattorno, M, Kania, U, Kone-Paut, I, Lezer, S, Livneh, A, Moix, I, Nishikomori, R, Ozen, S, Phylactou, L, Risom, L, Rowczenio, D, Sarkisian, T, van Gijn, M E, Witsch-Baumgartner, M, Morris, M, Hoffman, H M, Touitou, I
Published in Annals of the Rheumatic Diseases (01.10.2012)
Published in Annals of the Rheumatic Diseases (01.10.2012)
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Journal Article
Book Review
Immunological evidence for the presence of plant homologues of the actin- related protein Arp3 in tobacco and maize: subcellular localization to actin-enriched pit fields and emerging root hairs
Van Gestel, K, Slegers, H, Von Witsch, M, Samaj, J, Baluska, F, Verbelen, J-P
Published in Protoplasma (01.09.2003)
Published in Protoplasma (01.09.2003)
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Journal Article
Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy
Witsch-Baumgartner, M., Clayton, P., Clusellas, N., Haas, D., Kelley, R.I., Krajewska-Walasek, M., Lechner, S., Rossi, M., Zschocke, J., Utermann, G.
Published in Human mutation (01.04.2005)
Published in Human mutation (01.04.2005)
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Journal Article
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations
Witsch-Baumgartner, M, Ciara, E, Löffler, J, Menzel, H J, Seedorf, U, Burn, J, Gillessen-Kaesbach, G, Hoffmann, G F, Fitzky, B U, Mundy, H, Clayton, P, Kelley, R I, Krajewska-Walasek, M, Utermann, G
Published in European journal of human genetics : EJHG (01.01.2001)
Published in European journal of human genetics : EJHG (01.01.2001)
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Journal Article
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome
Ciara, E, Nowaczyk, MJM, Witsch-Baumgartner, M, Malunowicz, E, Popowska, E, Jezela-Stanek, A, Piotrowicz, M, Waye, JS, Utermann, G, Krajewska-Walasek, M
Published in Clinical genetics (01.12.2004)
Published in Clinical genetics (01.12.2004)
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Journal Article
The SWEET Project 10-Year Benchmarking in 19 Countries Worldwide Is Associated with Improved HbA1c and Increased Use of Diabetes Technology in Youth with Type 1 Diabetes
Gerhardsson, Peter, Schwandt, Anke, Witsch, Michael, Kordonouri, Olga, Svensson, Jannet, Forsander, Gun, Battelino, Tadej, Veeze, Henk, Danne, Thomas
Published in Diabetes technology & therapeutics (01.07.2021)
Published in Diabetes technology & therapeutics (01.07.2021)
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Journal Article
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations
Witsch-Baumgartner, M, Schwentner, I, Gruber, M, Benlian, P, Bertranpetit, J, Bieth, E, Chevy, F, Clusellas, N, Estivill, X, Gasparini, G, Giros, M, Kelley, R I, Krajewska-Walasek, M, Menzel, J, Miettinen, T, Ogorelkova, M, Rossi, M, Scala, I, Schinzel, A, Schmidt, K, Schönitzer, D, Seemanova, E, Sperling, K, Syrrou, M, Talmud, P J, Wollnik, B, Krawczak, M, Labuda, D, Utermann, G
Published in Journal of medical genetics (01.04.2008)
Published in Journal of medical genetics (01.04.2008)
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Journal Article
The COVID-19 Pandemic Affects Seasonality, With Increasing Cases of New-Onset Type 1 Diabetes in Children, From the Worldwide SWEET Registry
Reschke, Felix, Lanzinger, Stefanie, Herczeg, Vivien, Prahalad, Priya, Schiaffini, Riccardo, Mul, Dick, Clapin, Helen, Zabeen, Bedowra, Pelicand, Julie, Phillip, Moshe, Limbert, Catarina, Danne, Thomas
Published in Diabetes care (01.11.2022)
Published in Diabetes care (01.11.2022)
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Journal Article
Mutational Spectrum in the Δ7-Sterol Reductase Gene and Genotype-Phenotype Correlation in 84 Patients with Smith-Lemli-Opitz Syndrome
Witsch-Baumgartner, M., Fitzky, B.U., Ogorelkova, M., Kraft, H.G., Moebius, F.F., Glossmann, H., Seedorf, U., Gillessen-Kaesbach, G., Hoffmann, G.F., Clayton, P., Kelley, R.I., Utermann, G.
Published in American journal of human genetics (2000)
Published in American journal of human genetics (2000)
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Journal Article
Profilin is associated with the plasma membrane in microspores and pollen
von Witsch, Matthias, Baluška, František, Staiger, Christopher J., Volkmann, Dieter
Published in European journal of cell biology (01.12.1998)
Published in European journal of cell biology (01.12.1998)
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