Genetic basis of hypertrophic cardiomyopathy in children
Rupp, Stefan, Felimban, Moataz, Schänzer, Anne, Schranz, Dietmar, Marschall, Christoph, Zenker, Martin, Logeswaran, Thushiha, Neuhäuser, Christoph, Thul, Josef, Jux, Christian, Hahn, Andreas
Published in Clinical research in cardiology (01.03.2019)
Published in Clinical research in cardiology (01.03.2019)
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A novel SPEG mutation causes non-compaction cardiomyopathy and neuropathy in a floppy infant with centronuclear myopathy
Wang, Haicui, Schänzer, Anne, Kampschulte, Birgit, Daimagüler, Hülya-Sevcan, Logeswaran, Thushiha, Schlierbach, Hannah, Petzinger, Jutta, Ehrhardt, Harald, Hahn, Andreas, Cirak, Sebahattin
Published in Acta neuropathologica communications (29.08.2018)
Published in Acta neuropathologica communications (29.08.2018)
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Journal Article
Long-term neurodevelopmental outcome and serial cerebral magnetic resonance imaging assessment in Fontan patients at school age
Reich, Bettina, Schwan, Sabrina, Heye, Kristina, Logeswaran, Thushiha, Hahn, Andreas, Götschi, Andrea, Held, Ulrike, Wetterling, Kristina, Steger, Celine, Kottke, Raimund, Latal, Beatrice, Knirsch, Walter
Published in European journal of cardio-thoracic surgery (01.08.2023)
Published in European journal of cardio-thoracic surgery (01.08.2023)
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Journal Article
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
Motta, Marialetizia, Sagi-Dain, Lena, Krumbach, Oliver H F, Hahn, Andreas, Peleg, Amir, German, Alina, Lissewski, Christina, Coppola, Simona, Pantaleoni, Francesca, Kocherscheid, Luisa, Altmüller, Franziska, Schanze, Denny, Logeswaran, Thushiha, Chahrokh-Zadeh, Soheyla, Munzig, Anna, Nakhaei-Rad, Saeideh, Cavé, Hélène, Ahmadian, Mohammad R, Tartaglia, Marco, Zenker, Martin
Published in Human molecular genetics (21.07.2020)
Published in Human molecular genetics (21.07.2020)
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Journal Article
Parental Awareness of Oral Health and Nutritional Behavior in Children with Congenital Heart Diseases Compared to Healthy Children
Schulz-Weidner, Nelly, Logeswaran, Thushiha, Schlenz, Maximiliane Amelie, Krämer, Norbert, Bulski, Julia Camilla
Published in International journal of environmental research and public health (27.09.2020)
Published in International journal of environmental research and public health (27.09.2020)
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Journal Article
Evaluation of the Effectiveness of an Interdisciplinary Preventive Oral Hygiene Program for Children with Congenital Heart Disease
Schulz-Weidner, Nelly, Logeswaran, Thushiha, Jux, Christian, Schlenz, Maximiliane Amelie, Krämer, Norbert, Bulski, Julia Camilla
Published in International journal of environmental research and public health (28.03.2021)
Published in International journal of environmental research and public health (28.03.2021)
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Journal Article
Neuromonitoring, neuroimaging, and neurodevelopmental follow-up practices in neonatal congenital heart disease: a European survey
Feldmann, Maria, Hagmann, Cornelia, de Vries, Linda, Disselhoff, Vera, Pushparajah, Kuberan, Logeswaran, Thushiha, Jansen, Nicolaas J G, Breur, Johannes M P J, Knirsch, Walter, Benders, Manon, Counsell, Serena, Reich, Bettina, Latal, Beatrice
Published in Pediatric research (01.01.2023)
Published in Pediatric research (01.01.2023)
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Journal Article
Risk Factors for Perioperative Brain Lesions in Infants With Congenital Heart Disease: A European Collaboration
Bonthrone, Alexandra F, Stegeman, Raymond, Feldmann, Maria, Claessens, Nathalie H P, Nijman, Maaike, Jansen, Nicolaas J G, Nijman, Joppe, Groenendaal, Floris, de Vries, Linda S, Benders, Manon J N L, Haas, Felix, Bekker, Mirielle N, Logeswaran, Thushiha, Reich, Bettina, Kottke, Raimund, Hagmann, Cornelia, Latal, Beatrice, Dave, Hitendu, Simpson, John, Pushparajah, Kuberan, Austin, Conal, Kelly, Christopher J, Arulkumaran, Sophie, Rutherford, Mary A, Counsell, Serena J, Knirsch, Walter, Breur, Johannes M P J
Published in Stroke (1970) (01.12.2022)
Published in Stroke (1970) (01.12.2022)
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Journal Article
Perioperative Brain Injury in Relation to Early Neurodevelopment Among Children with Severe Congenital Heart Disease: Results from a European Collaboration
Neukomm, Astrid, Claessens, Nathalie H.P., Bonthrone, Alexandra F., Stegeman, Raymond, Feldmann, Maria, Nijman, Maaike, Jansen, Nicolaas J.G., Nijman, Joppe, Groenendaal, Floris, de Vries, Linda S., Benders, Manon J.N.L., Breur, Johannes M.P.J., Haas, Felix, Bekker, Mireille N., Logeswaran, Thushiha, Reich, Bettina, Kottke, Raimund, Dave, Hitendu, Simpson, John, Pushparajah, Kuberan, Kelly, Christopher J., Arulkumaran, Sophie, Rutherford, Mary A., Counsell, Serena J., Chew, Andrew, Knirsch, Walter, Sprong, Maaike C.A., van Schooneveld, Monique M., Hagmann, Cornelia, Latal, Beatrice
Published in The Journal of pediatrics (01.03.2024)
Published in The Journal of pediatrics (01.03.2024)
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Journal Article
Symptom‐orientated oral hygiene for children after heart transplantation: Effectiveness of a standardized prophylactic program
Schulz‐Weidner, Nelly, Bulski, Julia C., Siahi‐Benlarbi, Rachida, Bauer, Jürgen, Logeswaran, Thushiha, Jux, Christian, Wetzel, Willi‐Eckhard, Krämer, Norbert
Published in Pediatric transplantation (01.11.2020)
Published in Pediatric transplantation (01.11.2020)
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Journal Article
Neurodevelopmental outcome in hypoplastic left heart syndrome after hybrid procedure
Reich, Bettina, Heye, Kristina N, Wetterling, Kristina, Logeswaran, Thushiha, Hahn, Andreas, Akintürk, Hakan, Jux, Christian, Schranz, Dietmar
Published in Translational pediatrics (01.04.2019)
Published in Translational pediatrics (01.04.2019)
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Journal Article
Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome
Logeswaran, Thushiha, Friedburg, Christoph, Hofmann, Karoline, Akintuerk, Hakan, Biskup, Saskia, Graef, Michael, Rad, Ali, Weber, Axel, Neubauer, Bernd A., Schranz, Dietmar, Bouvagnet, Patrice, Lorenz, Birgit, Hahn, Andreas
Published in American journal of medical genetics. Part A (01.04.2017)
Published in American journal of medical genetics. Part A (01.04.2017)
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Journal Article
Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome
Logeswaran, Thushiha, Friedburg, Christoph, Hofmann, Karoline, Akintuerk, Hakan, Biskup, Saskia, Graef, Michael, Rad, Ali, Weber, Axel, Neubauer, Bernd A., Schranz, Dietmar, Bouvagnet, Patrice, Lorenz, Birgit, Hahn, Andreas
Published in American journal of medical genetics. Part A (01.09.2017)
Published in American journal of medical genetics. Part A (01.09.2017)
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