Susi Strozzi
Overview
Explore the profile of Susi Strozzi including associated specialties, affiliations and a list of published articles.
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9
Citations
233
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Recent Articles
1.
Syrbe S, Stettner G, Bally J, Borggraefe I, Bien C, Iancu Ferfoglia R, et al.
Neurology
. 2020 May;
94(22):e2290-e2301.
PMID: 32424051
Objective: To delineate autoimmune disease in association with contactin-associated protein 2 (CASPR2) antibodies in childhood, we reviewed the clinical phenotype of children with CASPR2 antibodies. Methods: Retrospective assessment of patients...
2.
Soleman J, Knorr C, Datta A, Strozzi S, Ramelli G, Mariani L, et al.
Childs Nerv Syst
. 2017 Dec;
34(5):893-900.
PMID: 29255920
Aim: Data concerning the benefit of vagal nerve stimulation (VNS) in children under the age of 12 years is sparse. It was shown that reduction of seizure frequency and duration...
3.
Verma R, Wagner F, Weisstanner C, Strozzi S, Lang M
Acta Radiol Open
. 2015 Dec;
4(12):2058460115617353.
PMID: 26668757
We report a case of a 9-year-old boy presenting with spastic-dystonic movement disorder of the right arm. MRI showed vast unilateral left-sided polymicrogyria (PMG) with perisylvian, temporal, frontal, and parietal...
4.
Goeggel Simonetti B, Rieubland C, Courage C, Strozzi S, Tschumi S, Gallati S, et al.
Epilepsia
. 2012 Sep;
53(12):2128-34.
PMID: 23016767
Purpose: Sodium channel gene aberrations are associated with a wide range of seizure disorders, particularly Dravet syndrome. They usually consist of missense or truncating gene mutations or deletions. Duplications involving...
5.
Lemke J, Riesch E, Scheurenbrand T, Schubach M, Wilhelm C, Steiner I, et al.
Epilepsia
. 2012 May;
53(8):1387-98.
PMID: 22612257
Purpose: Epilepsies have a highly heterogeneous background with a strong genetic contribution. The variety of unspecific and overlapping syndromic and nonsyndromic phenotypes often hampers a clear clinical diagnosis and prevents...
6.
Wingeier K, Giger E, Strozzi S, Kreis R, Joncourt F, Conrad B, et al.
J Clin Neurosci
. 2010 Nov;
18(1):90-5.
PMID: 21109441
Mutations in the dystrophin gene have long been recognised as a cause of mental retardation. However, for reasons that are unclear, some boys with dystrophin mutations do not show general...
7.
Huber B, Strozzi S, Steinlin M, Aebi C, Fluri S
Eur J Pediatr
. 2009 Sep;
169(4):441-5.
PMID: 19774394
Opsoclonus-myoclonus syndrome (OMS) is a rare acquired movement disorder occurring in all age groups, predominantly in infants. Although the exact pathogenesis is still undefined, there is strong evidence for a...
8.
Hauf M, Wiest R, Nirkko A, Strozzi S, Federspiel A
Epilepsy Res
. 2009 Jan;
83(2-3):265-8.
PMID: 19121924
Multimodal imaging was performed in Rasmussen Encephalitis (RE) during episodes of complex-partial and focal motor status epilepticus including independent component analysis of BOLD-fMRI, arterial spin labeling perfusion imaging and diffusion...
9.
Steinlin M, Klein A, Haas-Lude K, Zafeiriou D, Strozzi S, Muller T, et al.
Eur J Paediatr Neurol
. 2007 Feb;
11(3):146-52.
PMID: 17320436
We report 24 children (14 girls) who presented with the typical neuroimaging findings of pontocerebellar hypoplasia (PCH) to describe the clinical spectrum of type 2. Twenty-one presented with the classical...