Muenke syndrome: An international multicenter natural history study
Kruszka, Paul, Addissie, Yonit A., Yarnell, Colin M. P., Hadley, Donald W., Guillen Sacoto, Maria J., Platte, Petra, Paelecke, Yvonne, Collmann, Hartmut, Snow, Nicole, Schweitzer, Tilmann, Boyadjiev, Simeon A., Aravidis, Christos, Hall, Samantha E., Mulliken, John B., Roscioli, Tony, Muenke, Maximilian
Published in American journal of medical genetics. Part A (01.04.2016)
Published in American journal of medical genetics. Part A (01.04.2016)
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Journal Article
Executive Function and Adaptive Behavior in Muenke Syndrome
Yarnell, Colin M.P., BA, Addissie, Yonit A., BA, Hadley, Donald W., MS, Guillen Sacoto, Maria J., MD, Agochukwu, Nneamaka B., MD, Hart, Rachel A., BS, Wiggs, Edythe A., PhD, Platte, Petra, PhD, Paelecke, Yvonne, PhD, Collmann, Hartmut, MD, Schweitzer, Tilmann, MD, Kruszka, Paul, MD, MPH, Muenke, Maximilian, MD
Published in The Journal of pediatrics (01.08.2015)
Published in The Journal of pediatrics (01.08.2015)
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Journal Article
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon‐like craniosynostosis
Keupp, Katharina, Li, Yun, Vargel, Ibrahim, Hoischen, Alexander, Richardson, Rebecca, Neveling, Kornelia, Alanay, Yasemin, Uz, Elif, Elcioğlu, Nursel, Rachwalski, Martin, Kamaci, Soner, Tunçbilek, Gökhan, Akin, Burcu, Grötzinger, Joachim, Konas, Ersoy, Mavili, Emin, Müller‐Newen, Gerhard, Collmann, Hartmut, Roscioli, Tony, Buckley, Michael F., Yigit, Gökhan, Gilissen, Christian, Kress, Wolfram, Veltman, Joris, Hammerschmidt, Matthias, Akarsu, Nurten A., Wollnik, Bernd
Published in Molecular genetics & genomic medicine (01.11.2013)
Published in Molecular genetics & genomic medicine (01.11.2013)
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Journal Article
Surgical management of tethered spinal cord in adults: report of 54 cases
Hüttmann, S, Krauss, J, Collmann, H, Sörensen, N, Roosen, K
Published in Journal of neurosurgery (01.10.2001)
Published in Journal of neurosurgery (01.10.2001)
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Journal Article
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
KRESS, Wolfram, SCHROPP, Christian, PAHNKE, Jan, TRUSEN, Andreas, SÖRENSEN, Niels, KRAUSS, Jürgen, COLLMANN, Hartmut, LIEB, Gabriele, PETERSEN, Birgit, BÜSSE-RATZKA, Maria, KUNZ, Jürgen, REINHART, Edeltraut, SCHÄFER, Wolf-Dieter, SOLD, Johanna, HOPPE, Florian
Published in European journal of human genetics : EJHG (01.01.2006)
Published in European journal of human genetics : EJHG (01.01.2006)
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Journal Article
Friedrich Weickmann (1913-1983): some reminiscences
Nisch, Gunther, Collmann, Hartmut
Published in Journal of neurological surgery. Part A, Central European neurosurgery (01.01.2015)
Published in Journal of neurological surgery. Part A, Central European neurosurgery (01.01.2015)
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Journal Article
Patient-specific biodegradable implant in pediatric craniofacial surgery
Linz, Christian, Collmann, Hartmut, Kübler, Alexander, Böhm, Hartmut, Schweitzer, Tilmann
Published in Journal of cranio-maxillo-facial surgery (01.08.2017)
Published in Journal of cranio-maxillo-facial surgery (01.08.2017)
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Journal Article
Occipital plagiocephaly: unilateral lambdoid synostosis versus positional plagiocephaly
Linz, Christian, Collmann, Hartmut, Meyer-Marcotty, Philipp, Böhm, Hartmut, Krauß, Jürgen, Müller-Richter, Urs D, Ernestus, Ralf-Ingo, Wirbelauer, Johannes, Kübler, Alexander C, Schweitzer, Tilmann
Published in Archives of disease in childhood (01.02.2015)
Published in Archives of disease in childhood (01.02.2015)
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Journal Article
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
Kress, Wolfram, Schropp, Christian, Lieb, Gabriele, Petersen, Birgit, Büsse-Ratzka, Maria, Kunz, Jürgen, Reinhart, Edeltraut, Schäfer, Wolf-Dieter, Sold, Johanna, Hoppe, Florian, Pahnke, Jan, Trusen, Andreas, Sörensen, Niels, Krauss, Jürgen, Collmann, Hartmut
Published in European journal of human genetics : EJHG (01.01.2006)
Published in European journal of human genetics : EJHG (01.01.2006)
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Journal Article
Mutations in the interleukin receptor IL 11 RA cause autosomal recessive Crouzon‐like craniosynostosis
Keupp, Katharina, Li, Yun, Vargel, Ibrahim, Hoischen, Alexander, Richardson, Rebecca, Neveling, Kornelia, Alanay, Yasemin, Uz, Elif, Elcioğlu, Nursel, Rachwalski, Martin, Kamaci, Soner, Tunçbilek, Gökhan, Akin, Burcu, Grötzinger, Joachim, Konas, Ersoy, Mavili, Emin, Müller‐Newen, Gerhard, Collmann, Hartmut, Roscioli, Tony, Buckley, Michael F., Yigit, Gökhan, Gilissen, Christian, Kress, Wolfram, Veltman, Joris, Hammerschmidt, Matthias, Akarsu, Nurten A., Wollnik, Bernd
Published in Molecular genetics & genomic medicine (01.11.2013)
Published in Molecular genetics & genomic medicine (01.11.2013)
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Journal Article
A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly
Steinberger, D, Collmann, H, Schmalenberger, B, Müller, U
Published in Journal of medical genetics (01.05.1997)
Published in Journal of medical genetics (01.05.1997)
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Journal Article
Standardized evaluation and documentation of findings in patients with craniosynostosis
Jünger, Thies Hendrik, Reicherts, Monika, Steinberger, Daniela, Collmann, Hartmut, Kotrikova, Bibiana, Zöller, Joachim, Howaldt, Hans-Peter
Published in Journal of cranio-maxillo-facial surgery (01.02.2001)
Published in Journal of cranio-maxillo-facial surgery (01.02.2001)
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Journal Article