Evaluation of γ-carboline-phenothiazine conjugates as simultaneous NMDA receptor blockers and cholinesterase inhibitors von Schwarthoff, Sigrid, Tischer, Nicolas, Sager, Henrike, Schätz, Bianca, Rohrbach, Marius M., Raztsou, Ihar, Robaa, Dina, Gaube, Friedemann, Arndt, Hans-Dieter, Winckler, Thomas

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A cohort of 17 patients with kyphoscoliotic Ehlers–Danlos syndrome caused by biallelic mutations in FKBP14: expansion of the clinical and mutational spectrum and description of the... von Giunta, Cecilia, Baumann, Matthias, Fauth, Christine, Lindert, Uschi, Abdalla, Ebtesam M., Brady, Angela F., Collins, James, Dastgir, Jahannaz, Donkervoort, Sandra, Ghali, Neeti, Johnson, Diana S., Kariminejad, Ariana, Koch, Johannes, Kraenzlin, Marius, Lahiri, Nayana, Lozic, Bernarda, Manzur, Adnan Y., Morton, Jenny E.V., Pilch, Jacek, Pollitt, Rebecca C., Schreiber, Gudrun, Shannon, Nora L., Sobey, Glenda, Vandersteen, Anthony, van Dijk, Fleur S., Witsch-Baumgartner, Martina, Zschocke, Johannes, Pope, F. Michael, Bönnemann, Carsten G., Rohrbach, Marianne

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Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype von Abdalla, Ebtesam M., Rohrbach, Marianne, Bürer, Céline, Kraenzlin, Marius, El-Tayeby, Hazem, Elbelbesy, Mervat F., Nabil, Amira, Giunta, Cecilia

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Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype von Abdalla, Ebtesam M, Rohrbach, Marianne, Bürer, Céline, Kraenzlin, Marius, El-Tayeby, Hazem, Elbelbesy, Mervat F, Nabil, Amira, Giunta, Cecilia

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A cohort of 17 patients with kyphoscoliotic Ehlers-Danlos syndrome caused by biallelic mutations in FKBP14: expansion of the clinical and mutational spectrum and description of the... von Giunta, Cecilia, Baumann, Matthias, Fauth, Christine, Lindert, Uschi, Abdalla, Ebtesam M, Brady, Angela F, Collins, James, Dastgir, Jahannaz, Donkervoort, Sandra, Ghali, Neeti, Johnson, Diana S, Kariminejad, Ariana, Koch, Johannes, Kraenzlin, Marius, Lahiri, Nayana, Lozic, Bernarda, Manzur, Adnan Y, Morton, Jenny E V, Pilch, Jacek, Pollitt, Rebecca C, Schreiber, Gudrun, Shannon, Nora L, Sobey, Glenda, Vandersteen, Anthony, van Dijk, Fleur S, Witsch-Baumgartner, Martina, Zschocke, Johannes, Pope, F Michael, Bönnemann, Carsten G, Rohrbach, Marianne

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Ostéogenèse imparfaite: manifestations cliniques, diagnostic et prise en charge de l’enfance à l’âge adulte von Bonafé, Luisa, Giunta, Cecilia, Hasler, Carol C, Janner, Marco, Kränzlin, Marius, Link, Bianca, Meier, Christian, Ramseier, Leonard E, Rohrbach, Marianne, Unger, Sheila

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