Rates for tic disorders and obsessive compulsive symptomatology in families of children and adolescents with Gilles de la Tourette syndrome von Hebebrand, Johannes, Klug, Birgit, Fimmers, Rolf, Seuchter, Susanne A., Wettke-Schäfer, Roswitha, Deget, Felicitas, Camps, Astrid, Lisch, Sonja, Hebebrand, Kathrin, Von Gontard, Alexander, Lehmkuhl, Gerd, Poustka, Fritz, Schmidt, Martin, Baur, Max P., Remschmidt, Helmut

Volltext

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients von KLAUCK, S. M, MÜNSTERMANN, E, BIEBER-MARTIG, B, RÜHL, D, LISCH, S, SCHMÖTZER, G, POUSTKA, A, POUSTKA, F

Volltext

No association between length of the (CAG) n repeat of the huntington's disease gene and tourette's syndrome von Hebebrand, Johannes, Nöthen, Markus M., Klug, Birgit, Wettke-Schäfer, Roswitha, Camps, Astrid, Lisch, Sonja, Hemmer, Susanne, von Gontard, Alexander, Poustka, Fritz, Lehmkuhl, Gerd, Schmidt, Martin, Propping, Peter, Remschmidt, Helmut

Volltext

Association analysis of the dopamine D 2 receptor gene in Tourette's syndrome using the haplotype relative risk method von Nöthen, Markus M., Hebebrand, Johannes, Knapp, Michael, Hebebrand, Kathrin, Camps, Astrid, von Gontard, Alexander, Wettke‐Schäfer, Roswitha, Lisch, Sonja, Cichon, Sven, Poustka, Fritz, Schmidt, Martin, Lehmkuhl, Gerd, Remschmidt, Helmut, Propping, Peter

Volltext

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method von Nöthen, Markus M., Hebebrand, Johannes, Knapp, Michael, Hebebrand, Kathrin, Camps, Astrid, von Gontard, Alexander, Wettke-Schäfer, Roswitha, Lisch, Sonja, Cichon, Sven, Poustka, Fritz, Schmidt, Martin, Lehmkuhl, Gerd, Remschmidt, Helmut, Propping, Peter

Volltext

NF1 mutation analysis using a combined heteroduplex/SSCP approach von Abernathy, Corinne R., Rasmussen, Sonja A., Stalker, Heather J., Zori, Roberto, Driscoll, Daniel J., Williams, Charles A., Kousseff, Boris G., Wallace, Margaret R.

Volltext

Gene clustering and copy number variation in alkaloid metabolic pathways of opium poppy von Li, Qiushi, Ramasamy, Sukanya, Singh, Pooja, Hagel, Jillian M., Dunemann, Sonja M., Chen, Xue, Chen, Rongji, Yu, Lisa, Tucker, Joseph E., Facchini, Peter J., Yeaman, Sam

Volltext

Structural and biochemical consequences of NF1 associated nontruncating mutations in the Sec14-PH module of neurofibromin von Welti, Stefan, Kühn, Sonja, D'Angelo, Igor, Brügger, Britta, Kaufmann, Dieter, Scheffzek, Klaus

Volltext

Functional Impact of the G279S Substitution in the Adenosine A1-Receptor (A1R-G279S7.44), a Mutation Associated with Parkinson’s Disease von Nasrollahi-Shirazi, Shahrooz, Szöllösi, Daniel, Yang, Qiong, Muratspahic, Edin, El-Kasaby, Ali, Sucic, Sonja, Stockner, Thomas, Nanoff, Christian, Freissmuth, Michael

Volltext

Promoter methylation of DNA damage repair (DDR) genes in human tumor entities: RBBP8 / CtIP is almost exclusively methylated in bladder cancer von Mijnes, Jolein, Veeck, Jürgen, Gaisa, Nadine T, Burghardt, Eduard, de Ruijter, Tim C, Gostek, Sonja, Dahl, Edgar, Pfister, David, Schmid, Sebastian C, Knüchel, Ruth, Rose, Michael

Volltext

A novel GSN variant outside the G2 calcium‐binding domain associated with Amyloidosis of the Finnish type von Mullany, Sean, Souzeau, Emmanuelle, Klebe, Sonja, Zhou, Tiger, Knight, Lachlan S. W., Qassim, Ayub, Berry, Ella C., Marshall, Henry, Hussey, Matthew, Dubowsky, Andrew, Breen, James, Hassall, Mark M., Mills, Richard A., Craig, Jamie E., Siggs, Owen M.

Volltext

Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort von Souzeau, Emmanuelle, Siggs, Owen M., Mullany, Sean, Schmidt, Joshua M., Hassall, Mark M., Dubowsky, Andrew, Chappell, Angela, Breen, James, Bae, Haae, Nicholl, Jillian, Hadler, Johanna, Kearns, Lisa S., Staffieri, Sandra E., Hewitt, Alex W., Mackey, David A., Gupta, Aanchal, Burdon, Kathryn P., Klebe, Sonja, Craig, Jamie E., Mills, Richard A.

Volltext

Epigenetic Differentiation of Natural Populations of Lilium bosniacum Associated with Contrasting Habitat Conditions von Zoldoš, Vlatka, Biruš, Ivan, Muratovic, Edina, Šatovic, Zlatko, Vojta, Aleksandar, Robin, Odile, Pustahija, Fatima, Bogunic, Faruk, Vicic Bockor, Vedrana, Siljak-Yakovlev, Sonja

Volltext

Mikrobieller Plastikabbau im Meer: die Suche nach dem Unwahrscheinlichen von Oberbeckmann, Sonja, Markert, Stephanie, Labrenz, Matthias

Volltext

Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1 von Rasmussen, Sonja A., Overman, Jennifer, Thomson, Susanne A.M., Colman, Steven D., Abernathy, Corinne R., Trimpert, Rachael E., Moose, Rebecca, Virdi, Gurinder, Roux, Kyle, Bauer, Mislen, Rojiani, Amyn M., Maria, Bernard L., Muir, David, Wallace, Margaret R.

Volltext

Neurofibromatosis segmentaria, a propósito de un caso von Ocampo, Juan David Dufflart, Barragan, Yonatan Armendariz, Gómez, Daniela Ruiz, Corral, Claudia Ileana Sáenz, Caire, Sonia Toussaint, Memije, Maria Elisa Vega

Volltext

NEITMANN, SONJA "Von der Grafschaft Mark nach Livland. Ritterbrüder aus Westfalen im livländischen Deutschen Orden" (Book Review) von Boockmann, Hartmut

Volltext

Lyrik und Autobiographik von Klimek, Sonja

Volltext

Culture of cytogenetically abnormal Schwann cells from benign and malignant NF1 tumors von Wallace, Margaret R., Rasmussen, Sonja A., Lim, Ingrid T., Gray, Brian A., Zori, Roberto T., Muir, David

Volltext

Wie Sie die aktuellen Leitlinien in der Praxis umsetzen von Finsterer, Stefan, Weyerbrock, Sonja, Basler, Markus, Mühling, Holger, Silber, Sigmund

Volltext