Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
Kratz, C P, Franke, L, Peters, H, Kohlschmidt, N, Kazmierczak, B, Finckh, U, Bier, A, Eichhorn, B, Blank, C, Kraus, C, Kohlhase, J, Pauli, S, Wildhardt, G, Kutsche, K, Auber, B, Christmann, A, Bachmann, N, Mitter, D, Cremer, F W, Mayer, K, Daumer-Haas, C, Nevinny-Stickel-Hinzpeter, C, Oeffner, F, Schlüter, G, Gencik, M, Überlacker, B, Lissewski, C, Schanze, I, Greene, M H, Spix, C, Zenker, M
Published in British journal of cancer (14.04.2015)
Published in British journal of cancer (14.04.2015)
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Journal Article
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Kortüm, Fanny, Das, Soma, Flindt, Max, Morris-Rosendahl, Deborah J, Stefanova, Irina, Goldstein, Amy, Horn, Denise, Klopocki, Eva, Kluger, Gerhard, Martin, Peter, Rauch, Anita, Roumer, Agathe, Saitta, Sulagna, Walsh, Laurence E, Wieczorek, Dagmar, Uyanik, Gökhan, Kutsche, Kerstin, Dobyns, William B
Published in Journal of medical genetics (01.06.2011)
Published in Journal of medical genetics (01.06.2011)
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Journal Article
Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci
Chilian, B, Abdollahpour, H, Bierhals, T, Haltrich, I, Fekete, G, Nagel, I, Rosenberger, G, Kutsche, K
Published in Clinical genetics (01.12.2013)
Published in Clinical genetics (01.12.2013)
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Journal Article
Structure–function–behavior relationship in estrogen-induced synaptic plasticity
Vierk, R., Bayer, J., Freitag, S., Muhia, M., Kutsche, K., Wolbers, T., Kneussel, M., Sommer, T., Rune, G.M.
Published in Hormones and behavior (01.08.2015)
Published in Hormones and behavior (01.08.2015)
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Journal Article
Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body
Harms, F.L., Nampoothiri, S., Kortüm, F., Thomas, J., Panicker, V.V., Alawi, M., Altmüller, J., Yesodharan, D., Kutsche, K.
Published in British journal of dermatology (1951) (01.11.2018)
Published in British journal of dermatology (1951) (01.11.2018)
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Journal Article
Sea-Anemone Toxin ATX-II Elicits A-Fiber-Dependent Pain and Enhances Resurgent and Persistent Sodium Currents in Large Sensory Neurons
Klinger, Alexandra B, Eberhardt, Mirjam, Link, Andrea S, Namer, Barbara, Kutsche, Lisa K, Schuy, E Theresa, Sittl, Ruth, Hoffmann, Tali, Alzheimer, Christian, Huth, Tobias, Carr, Richard W, Lampert, Angelika
Published in Molecular pain (15.09.2012)
Published in Molecular pain (15.09.2012)
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Journal Article
Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation
Sheikhzadeh, S., Sondermann, C., Rybczynski, M., Habermann, C.R., Brockstaedt, L., Keyser, B., Kaemmerer, H., Mir, T., Staebler, A., Robinson, P.N., Kutsche, K., Berger, J., Blankenberg, S., von Kodolitsch, Y.
Published in Clinical genetics (01.09.2014)
Published in Clinical genetics (01.09.2014)
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Journal Article
Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic features
Lozić, B, Ljubković, J, Pandurić, D Gabrić, Saltvig, I, Kutsche, K, Krželj, V, Zemunik, T
Published in Brazilian journal of medical and biological research (01.12.2012)
Published in Brazilian journal of medical and biological research (01.12.2012)
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Journal Article
Dural ectasia in Loeys-Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation
Sheikhzadeh, S., Brockstaedt, L., Habermann, C.R., Sondermann, C., Bannas, P., Mir, T.S., Staebler, A., Seidel, H., Keyser, B., Arslan-Kirchner, M., Kutsche, K., Berger, J., Blankenberg, S., von Kodolitsch, Y.
Published in Clinical genetics (01.12.2014)
Published in Clinical genetics (01.12.2014)
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Journal Article
Refining the phenotype of α-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly
Morris-Rosendahl, DJ, Najm, J, Lachmeijer, AMA, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C, Omran, H, Kraus, U, Van der Knaap, MS, Schuierer, G, Kutsche, K, Uyanik, G
Published in Clinical genetics (01.11.2008)
Published in Clinical genetics (01.11.2008)
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Journal Article
Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly
Morris-Rosendahl, D J, Najm, J, Lachmeijer, A M A, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C, Omran, H, Kraus, U, Van der Knaap, M S, Schuierer, G, Kutsche, K, Uyanik, G
Published in Clinical genetics (01.11.2008)
Published in Clinical genetics (01.11.2008)
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Journal Article
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome
Schulz, AL, Albrecht, B, Arici, C, Van Der Burgt, I, Buske, A, Gillessen-Kaesbach, G, Heller, R, Horn, D, Hübner, CA, Korenke, GC, König, R, Kress, W, Krüger, G, Meinecke, P, Mücke, J, Plecko, B, Rossier, E, Schinzel, A, Schulze, A, Seemanova, E, Seidel, H, Spranger, S, Tuysuz, B, Uhrig, S, Wieczorek, D, Kutsche, K, Zenker, M
Published in Clinical genetics (01.01.2008)
Published in Clinical genetics (01.01.2008)
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Journal Article
Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8
Schmidt, T., Bierhals, T., Kortüm, F., Bartels, I., Liehr, T., Burfeind, P., Shoukier, M., Frank, V., Bergmann, C., Kutsche, K.
Published in Cytogenetic and genome research (01.01.2014)
Published in Cytogenetic and genome research (01.01.2014)
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Journal Article
237 The Association of Pain Scores and Vital Signs in the Emergency Department
Betcher, J, Kutsche, K, Ebadi-Tehrani, M, Springsteen, C, Phu, J, Jones, J.S
Published in Annals of emergency medicine (2011)
Published in Annals of emergency medicine (2011)
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Journal Article
Induced Neurons for the Study of Neurodegenerative and Neurodevelopmental Disorders
Sauter, Evelyn J., Kutsche, Lisa K., Klapper, Simon D., Busskamp, Volker
Published in Fragile-X Syndrome (2019)
Published in Fragile-X Syndrome (2019)
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Book Chapter
Journal Article
Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies
Kortüm, F., Chyrek, M., Fuchs, S., Albrecht, B., Gillessen-Kaesbach, G., Mütze, U., Seemanova, E., Tinschert, S., Wieczorek, D., Rosenberger, G., Kutsche, K.
Published in Molecular syndromology (01.12.2011)
Published in Molecular syndromology (01.12.2011)
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Journal Article
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis
Kutsche, Lisa K., Gysi, Deisy M., Fallmann, Joerg, Lenk, Kerstin, Petri, Rebecca, Swiersy, Anka, Klapper, Simon D., Pircs, Karolina, Khattak, Shahryar, Stadler, Peter F., Jakobsson, Johan, Nowick, Katja, Busskamp, Volker
Published in Cell systems (24.10.2018)
Published in Cell systems (24.10.2018)
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Journal Article
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp
Kutsche, K., Werner, W., Bartsch, O., von der Wense, A., Meinecke, P., Gal, A.
Published in Cytogenetic and Genome Research (01.01.2002)
Published in Cytogenetic and Genome Research (01.01.2002)
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Journal Article