Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Annette Weichselbaum"'
Autor:
Marcus Weitz, Jan Kern, Peter Huppke, Ruxandra Iancu Ferfoglia, Klaus-Peter Wandinger, Elisabeth Probst-Müller, Steffen Syrbe, Tilman Polster, Ingo Borggraefe, Annette Weichselbaum, Robert Steinfeld, Andreas Ziegler, Julien Bally, Silvia Schmid, Christian G. Bien, Frank Leypoldt, Susi Strozzi, Georg M. Stettner, Corinna I. Bien
Publikováno v:
Neurology. 94:e2290-e2301
ObjectiveTo delineate autoimmune disease in association with contactin-associated protein 2 (CASPR2) antibodies in childhood, we reviewed the clinical phenotype of children with CASPR2 antibodies.MethodsRetrospective assessment of patients recruited
Autor:
Susanne R. Kerscher, Louise L. Schweizer, Thomas Nägele, Martin U. Schuhmann, Karin Haas-Lude, Annette Weichselbaum
Publikováno v:
European Journal of Paediatric Neurology. 23:571-580
Regular measurement of ventricular size is important in children with hydrocephalus. After closure of the fontanelle this is currently addressed by repetitive cranial MRI or CT imaging, coming along with risks of anaesthesia or radiation. As the thir
Autor:
Laura V Sainz, Andrea Bevot, Annette Weichselbaum, Martin U. Schuhmann, Julian Zipfel, Susanne R. Kerscher
Publikováno v:
Child's Nervous System. 35:251-256
External hydrocephalus (eHC) is commonly defined as a subtype of infant “hydrocephalus” consisting of macrocepahly associated with enlarged subarachnoid space and no or mild ventriculomegaly. This status is thought to be related to impaired CSF a
Autor:
Katalin Scherer, Alexander Grimm, Natalie Deininger, Katrin Rupprich, Mari Rossi, Ute Grasshoff, Bianca Flores, Eric Delpire, Annette Weichselbaum, Joohyun Park, Tobias B. Haack, Hanna Kuepper, Maren Rautenberg, Marc Sturm
BackgroundCharcot-Marie-Tooth disease (CMT) is a clinically and genetically heterogeneous disorder of the peripheral nervous system. Biallelic variants in SLC12A6 have been associated with autosomal-recessive hereditary motor and sensory neuropathy w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93402b1cf6f927a8ce9f09293f05ef0f
https://www.ncbi.nlm.nih.gov/pubmed/31439721
https://www.ncbi.nlm.nih.gov/pubmed/31439721
Autor:
Martin Ebinger, Thomas Nägele, Martin U. Schuhmann, Michael Alber, Annette Weichselbaum, Janine Magg
Publikováno v:
Neuropediatrics. 51(2)
Unilateral sensorineural hearing loss is a common symptom of vestibular schwannomas in adolescent patients with neurofibromatosis type 2 or sporadic vestibular schwannomas and is often the initial clinical feature. While rare cases of sensorineural i
Autor:
Annette Weichselbaum
Publikováno v:
Monatsschrift Kinderheilkunde. 164:913-928
Die Symptome von Tumoren des kindlichen Zentralnervensystems (ZNS) hangen v. a. von der Lokalisation, jedoch auch vom Wachstumsverhalten des Tumors sowie von Alter und Entwicklungsstand des Kindes ab. Es kann zwischen Symptomen eines erhohten intrakr
Autor:
Annette Weichselbaum, Janine Magg, Ingeborg Krägeloh-Mann, Tobias B. Haack, Rebecca Buchert-Lo
Publikováno v:
Abstracts of the 44th Annual Meeting of the Society for Neuropediatrics.
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 32(3)
Intracranial sylvian arachnoid cysts are often asymptomatic lesions. We present a 16-year-old female patient with progressive loss of vision together with an unusual visual field defect on the left eye accompanied by headache. A left frontotemporal s
Autor:
Karin Schaeferhoff, Tanja Benkert, Martin Kehrer, Annette Weichselbaum, Ute Grasshoff, Thomas Liehr, Andreas Tzschach, Michael Bonin, Sylke Singer
Publikováno v:
American journal of medical genetics. Part A. (3)
Isolated interstitial duplications of chromosome band 1q25 are apparently very rare; no patients with detailed molecular and clinical characterization of duplications restricted to this region have been published to date. We report on a 9-year-old gi
Autor:
Claudia Sommer, Rainald Mössner, Christine M. Freitag, Klaus-Peter Lesch, Martin Marziniak, Annette Weichselbaum, Jobst Meyer
Publikováno v:
Headache. 45(2)
Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura. Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurre