Conversion to dementia in mild cognitive impairment is associated with decline of N -actylaspartate and creatine as revealed by magnetic resonance spectroscopy von Pilatus, Ulrich, Lais, Christoph, Rochmont, Anna du Mesnil de, Kratzsch, Tillmann, Frölich, Lutz, Maurer, Konrad, Zanella, Friedhelm E, Lanfermann, Heinrich, Pantel, Johannes

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Spot urine iodine levels below the WHO recommendation are not related to impaired thyroid function in healthy children and adolescents von Wallborn, Tillmann, Vogel, Mandy, Kneuer, Antje, Thamm, Michael, Dittrich, Katalin, Kiess, Wieland, Kratzsch, Jürgen

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Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation von Kruis, Tassilo, Klammt, Jürgen, Galli-Tsinopoulou, Assimina, Wallborn, Tillmann, Schlicke, Marina, Müller, Eva, Kratzsch, Jürgen, Körner, Antje, Odeh, Rasha, Kiess, Wieland, Pfäffle, Roland

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A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal... von Wallborn, Tillmann, Wüller, Stefan, Klammt, Jürgen, Kruis, Tassilo, Kratzsch, Jürgen, Schmidt, Gabriele, Schlicke, Marina, Müller, Eva, Schmitz van de Leur, Hildegard, Kiess, Wieland, Pfäffle, Roland

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Clinical and functional characterization of a patient carrying a compound heterozygous pericentrin mutation and a heterozygous IGF1 receptor mutation von Müller, Eva, Dunstheimer, Desiree, Klammt, Jürgen, Friebe, Daniela, Kiess, Wieland, Kratzsch, Jürgen, Kruis, Tassilo, Laue, Sandy, Pfäffle, Roland, Wallborn, Tillmann, Heidemann, Peter H

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A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal... von Wallborn, Tillmann, Wüller, Stefan, Klammt, Jürgen, Kruis, Tassilo, Kratzsch, Jürgen, Schmidt, Gabriele, Schlicke, Marina, Müller, Eva, Schmitz van de Leur, Hildegard, Kiess, Wieland, Pfäffle, Roland

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Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation von Kruis, Tassilo, Klammt, Jürgen, Galli-Tsinopoulou, Assimina, Wallborn, Tillmann, Schlicke, Marina, Müller, Eva, Kratzsch, Jürgen, Körner, Antje, Odeh, Rasha, Kiess, Wieland, Pfäffle, Roland

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A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal... von Wallborn, Tillmann, Wüller, Stefan, Klammt, Jürgen, Kruis, Tassilo, Kratzsch, Jürgen, Schmidt, Gabriele, Schlicke, Marina, Müller, Eva, Schmitz van de Leur, Hildegard, Kiess, Wieland, Pfäffle, Roland

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Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation von Kruis, Tassilo, Klammt, Jürgen, Galli-Tsinopoulou, Assimina, Wallborn, Tillmann, Schlicke, Marina, Müller, Eva, Kratzsch, Jürgen, Körner, Antje, Odeh, Rasha, Kiess, Wieland, Pfäffle, Roland

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