Browsing Universitätsbibliographie by Title

Now showing items 12440-12459 of 63055

De la escritura científica a la conversación coloquial adolescente : El caso de tipo

Mihatsch, Wiltrud (2018)
De la fécondation croisée entre le LEI et le DÉRom

Reinhardt, Jan (2012)
De la jouissance au "jouis-sens" : le jeu de mots dans l'œuvre de Jacques Derrida

Wocke, Brendon (2017)
De la supplique à l'admonition : la critique du pouvoir royal dans l'affaire de la celle Saint-Josse

Pezé, Warren (2019)
De motu animalium : Griechisch - Deutsch = Über die Bewegung der Lebewesen

Corcilius, Klaus (2018)
De nova lipogenesis in health and disease

Kalbacher, Hubert (2014)
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects

Grimmel, Mona; Haack, Tobias (2020)
De novo design of a four-fold symmetric TIM-barrel protein with atomic-level accuracy

Höcker, Birte; Feldmeier, Kaspar Konrad (2016)
De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies

Grimmel, Mona; Sturm, Marc; Beck-Wödl, Stefanie; Haack, Tobias (2018)
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy

Buena Atienza, Elena; Baumann, Britta; Zobor, Ditta; Weisschuh, Nicole; Kohl, Susanne; Wissinger, Bernd (2016)
De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function

Synofzik, Matthis Benjamin; Harmuth, Florian; Gburek-Augustat, Janina; Krägeloh-Mann, Ingeborg; Bauer, Peter; Schüle-Freyer, Rebecca (2018)
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Hedrich, Ulrike B. S.; Synofzik, Matthis Benjamin; Detert, Katja; Wolff, Markus; Maljevic, Snezana; Lerche, Holger; Müller, Stephan Tobias; Löffler, Heidrun; Schöls, Ludger; Schüle-Freyer, Rebecca; Weber, Yvonne G. (2015)
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Weber, Yvonne G.; Lerche, Holger (2013)
De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents

Klingel, Karin (2021)
De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome

Gabriel, Heinz (2019)
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome

Sturm, Marc
De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)

Karle, Kathrin Nora; Biskup, Saskia; Schweitzer, Katherine Johanna; Bauer, Peter; Bender, Benjamin; Schüle-Freyer, Rebecca; Schöls, Ludger; Krüger, Rejko; Nägele, Thomas (2013)
De novo mutations in PDE1 0A cause childhood-onset chorea with bilateral striatal lesions

Wiethoff, Sarah (2016)
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Lauerer, Robert J.; Bahr, Jacqueline C.; Schwarz, Niklas; Goldmann, Eva; Hedrich, Ulrike B. S.; Lerche, Holger; Uysal, Betül (2018)
De novo sensitization during subcutaneous allergen specific immunotherapy - an analysis of 51 cases of SCIT and 33 symptomatically treated controls

Becker, Sven (2020)

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