Knut Brockmann

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 17

Top Venues

Journal of clinical medicine

Orphanet journal of rare diseases

Proceedings (Baylor University. Medical Center)

Biomedicines

This page only lists publications with an associated author ORCID identifier.

Publications

Marina Zeldovich, Leonie Krol, Inga K Koerte, Katrin Cunitz, Matthias Kieslich, Marlene Henrich, Knut Brockmann, Anna Buchheim, Michael Lendt, Christian Auer, Axel Neu, Joenna Driemeyer, Ulrike Wartemann, Claudius Thomé, Daniel Pinggera, Steffen Berweck, Michaela V Bonfert, Joachim Suss, Holger Muehlan, Nicole von Steinbüchel
A short scale to measure health-related quality of life after traumatic brain injury in children and adolescents (QOLIBRI-OS-KID/ADO): psychometric properties and German reference values. Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation (2024)
Simone Schröder, Gökhan Yigit, Yun Li, Janine Altmüller, Hans-Martin Büttel, Barbara Fiedler, Christoph Kretzschmar, Peter Nürnberg, Jürgen Seeger, Valentina Serpieri, Enza Maria Valente, Bernd Wollnik, Eugen Boltshauser, Knut Brockmann
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued. Orphanet journal of rare diseases 18 (1) (2023)
Knut Brockmann, Silke Kaulfuß
Moebius syndrome and gastroschisis-The second case of a rare association. American journal of medical genetics. Part A (2023)
Simone Schröder, Gökhan Yigit, Yun Li, Janine Altmüller, Hans-Martin Büttel, Barbara Fiedler, Christoph Kretzschmar, Peter Nürnberg, Jürgen Seeger, Valentina Serpieri, Enza Maria Valente, Bernd Wollnik, Eugen Boltshauser, Knut Brockmann
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued. Orphanet journal of rare diseases 18 (1) (2023)
Katrin Cunitz, Ivana Holloway, Anne Harzendorf, Sven Greving, Marina Zeldovich, Ugne Krenz, Dagmar Timmermann, Inga K Koerte, Michaela Veronika Bonfert, Steffen Berweck, Matthias Kieslich, Knut Brockmann, Maike Roediger, Anna Buchheim, Nada Andelic, Michael Lendt, Michael Staebler, Holger Muehlan, Nicole von Steinbuechel
Health-Related Quality of Life after Pediatric Traumatic Brain Injury: A Quantitative Comparison between Children's and Parents' Perspectives of the QOLIBRI-KID/ADO Questionnaire. Journal of clinical medicine 12 (23) (2023)
Simone Schröder, Gökhan Yigit, Yun Li, Janine Altmüller, Hans-Martin Büttel, Barbara Fiedler, Christoph Kretzschmar, Peter Nürnberg, Jürgen Seeger, Valentina Serpieri, Enza Maria Valente, Bernd Wollnik, Eugen Boltshauser, Knut Brockmann
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued. Orphanet journal of rare diseases 18 (1) (2023)
Simone Schröder, Gökhan Yigit, Yun Li, Janine Altmüller, Hans-Martin Büttel, Barbara Fiedler, Christoph Kretzschmar, Peter Nürnberg, Jürgen Seeger, Valentina Serpieri, Enza Maria Valente, Bernd Wollnik, Eugen Boltshauser, Knut Brockmann
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued. Orphanet journal of rare diseases 18 (1) (2023)
Fabian Bockhop, Marina Zeldovich, Sven Greving, Ugne Krenz, Katrin Cunitz, Dagmar Timmermann, Elena M Bonke, Michaela Veronika Bonfert, Inga K Koerte, Matthias Kieslich, Maike Roediger, Michael Staebler, Steffen Berweck, Thomas Paul, Knut Brockmann, Philine Rojczyk, Anna Buchheim, Nicole von Steinbuechel
Psychometric Properties of the German Version of the Rivermead Post-Concussion Symptoms Questionnaire in Adolescents after Traumatic Brain Injury and Their Proxies. Journal of clinical medicine 12 (1) (2022)
Gabriel Cassinelli Petersen, Mitra Amirkhizi, Knut Brockmann, Payam Dibaj
Hemifacial spasm through changes of cerebrospinal fluid pressure in idiopathic intracranial hypertension. Proceedings (Baylor University. Medical Center) 36 (1) (2022)
Gabriel Cassinelli Petersen, Mitra Amirkhizi, Knut Brockmann, Payam Dibaj
Hemifacial spasm through changes of cerebrospinal fluid pressure in idiopathic intracranial hypertension. Proceedings (Baylor University. Medical Center) 36 (1) (2022)
Dagmar Timmermann, Ugne Krenz, Silke Schmidt, Michael Lendt, Christel Salewski, Knut Brockmann, Nicole von Steinbüchel
Health-Related Quality of Life after Pediatric Traumatic Brain Injury: A Qualitative Comparison of Perspectives of Children and Adolescents after TBI and a Comparison Group without a History of TBI. Journal of clinical medicine 11 (22) (2022)
Fabian Bockhop, Marina Zeldovich, Sven Greving, Ugne Krenz, Katrin Cunitz, Dagmar Timmermann, Elena M Bonke, Michaela Veronika Bonfert, Inga K Koerte, Matthias Kieslich, Maike Roediger, Michael Staebler, Steffen Berweck, Thomas Paul, Knut Brockmann, Philine Rojczyk, Anna Buchheim, Nicole von Steinbuechel
Psychometric Properties of the German Version of the Rivermead Post-Concussion Symptoms Questionnaire in Adolescents after Traumatic Brain Injury and Their Proxies. Journal of clinical medicine 12 (1) (2022)
Fabian Bockhop, Marina Zeldovich, Sven Greving, Ugne Krenz, Katrin Cunitz, Dagmar Timmermann, Elena M Bonke, Michaela Veronika Bonfert, Inga K Koerte, Matthias Kieslich, Maike Roediger, Michael Staebler, Steffen Berweck, Thomas Paul, Knut Brockmann, Philine Rojczyk, Anna Buchheim, Nicole von Steinbuechel
Psychometric Properties of the German Version of the Rivermead Post-Concussion Symptoms Questionnaire in Adolescents after Traumatic Brain Injury and Their Proxies. Journal of clinical medicine 12 (1) (2022)
Gökhan Yigit, Ruth Sheffer, Muhannad Daana, Yun Li, Emrah Kaygusuz, Hagar Mor-Shakad, Janine Altmüller, Peter Nürnberg, Liza Douiev, Silke Kaulfuss, Peter Burfeind, Bernd Wollnik, Knut Brockmann
Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state. Journal of medical genetics (2021)
Jan Henje Döring, Afshin Saffari, Thomas Bast, Knut Brockmann, Laura Ehrhardt, Walid Fazeli, Wibke G Janzarik, Gerhard Kluger, Hiltrud Muhle, Rikke Steensjerre Moller, Konrad Platzer, Joana Larupa Dos Santos, Iben Bache, Astrid Bertsche, Michaela Bonfert, Ingo Borggräfe, Philip J Broser, Alexandre N Datta, Trine Bjørg Hammer, Hans Hartmann, Anette Hasse-Wittmer, Marco Henneke, Hermann Kühne, Johannes R Lemke, Oliver Maier, Eva Matzker, Andreas Merkenschlager, Joachim Opp, Steffi Patzer, Kevin Rostasy, Birgit Stark, Adam Strzelczyk, Celina von Stülpnagel, Yvonne Weber, Markus Wolff, Birgit Zirn, Georg Friedrich Hoffmann, Stefan Kölker, Steffen Syrbe
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood. Biomedicines 8 (11) (2020)
Simone Schröder, Yun Li, Gökhan Yigit, Janine Altmüller, Ingrid Bader, Andrea Bevot, Saskia Biskup, Steffi Dreha-Kulaczewski, G Christoph Korenke, Raimund Kottke, Johannes A Mayr, Martin Preisel, Sandra P Toelle, Sarah Wente-Schulz, Saskia B Wortmann, Heidi Hahn, Eugen Boltshauser, Anja Uhmann, Bernd Wollnik, Knut Brockmann
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia. Genetics in medicine : official journal of the American College of Medical Genetics 23 (2) (2020)
Sarah Wente, Simone Schröder, Johannes Buckard, Hans-Martin Büttel, Florian von Deimling, Wilfried Diener, Martin Häussler, Susanne Hübschle, Silvia Kinder, Gerhard Kurlemann, Christoph Kretzschmar, Michael Lingen, Wiebke Maroske, Dirk Mundt, Iciar Sánchez-Albisua, Jürgen Seeger, Sandra P Toelle, Eugen Boltshauser, Knut Brockmann
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study. Orphanet journal of rare diseases 11 (1) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Knut Brockmann