Neuromyelitis optica: evaluation of 871 attacks and 1,153 treatment courses

I Kleiter, A Gahlen, N Borisow, K Fischer… - Annals of …, 2016 - Wiley Online Library
Objective Neuromyelitis optica (NMO) attacks often are severe, are difficult to treat, and
leave residual deficits. Here, we analyzed the frequency, sequence, and efficacy of …

Apheresis therapies for NMOSD attacks: a retrospective study of 207 therapeutic interventions

I Kleiter, A Gahlen, N Borisow, K Fischer… - Neurology …, 2018 - AAN Enterprises
Objective To analyze whether 1 of the 2 apheresis techniques, therapeutic plasma
exchange (PE) or immunoadsorption (IA), is superior in treating neuromyelitis optica …

Immunotherapies in neuromyelitis optica spectrum disorder: efficacy and predictors of response

JP Stellmann, M Krumbholz, T Friede… - Journal of Neurology …, 2017 - jnnp.bmj.com
Objective To analyse predictors for relapses and number of attacks under different
immunotherapies in patients with neuromyelitis optica spectrum disorder (NMOSD). Design …

Influence of female sex and fertile age on neuromyelitis optica spectrum disorders

N Borisow, I Kleiter, A Gahlen… - Multiple Sclerosis …, 2017 - journals.sagepub.com
Background: Gender and age at onset are important epidemiological factors influencing
prevalence, clinical presentation, and treatment response in autoimmune diseases …

Efficacy of glatiramer acetate in neuromyelitis optica spectrum disorder: a multicenter retrospective study

I Ayzenberg, J Schöllhammer, R Hoepner, K Hellwig… - Journal of …, 2016 - Springer
Glatiramer acetate (GA) is an approved therapy for relapsing–remitting multiple sclerosis,
but its efficacy for the prevention of attacks in neuromyelitis optica spectrum disorder …

[HTML][HTML] Cerebrospinal fluid findings in patients with psychotic symptoms—a retrospective analysis

TW Rattay, P Martin, D Vittore, H Hengel, I Cebi… - Scientific reports, 2021 - nature.com
In current international classification systems (ICD-10, DSM5), the diagnostic criteria for
psychotic disorders (eg schizophrenia and schizoaffective disorder) are based on …

[HTML][HTML] Defining diagnostic cutoffs in neurological patients for serum very long chain fatty acids (VLCFA) in genetically confirmed X-Adrenoleukodystrophy

TW Rattay, M Rautenberg, AS Söhn, H Hengel… - Scientific reports, 2020 - nature.com
Abstract X-linked Adrenoleukodystrophy (X-ALD) is caused by mutations in the ABCD1 gene
resulting in the accumulation of very long chain fatty acids (VLCFA). X-ALD is the most …

[HTML][HTML] Confirmation of TACO1 as a Leigh syndrome disease gene in two additional families

Y Oktay, S Güngör, L Zeltner, S Wiethoff… - Journal of …, 2020 - content.iospress.com
Background: In 2009, we identified TACO1 as a novel mitochondrial disease gene in a
single family, however no second family has been described to confirm the role of TACO1 in …

Susceptibility‐Weighted Imaging Reveals Subcortical Iron Deposition in PLA2G6‐associated Neurodegeneration: The “Double Cortex Sign

B Roeben, L Zeltner, GE Hagberg… - Movement …, 2023 - Wiley Online Library
Magnetic resonance imaging (MRI) findings in PLA2G6-associated Neurodegeneration
(PLAN), a “Neurodegeneration with Brain Iron Accumulation”(NBIA) disorder caused by …

[HTML][HTML] Effect of the addition of a mental health specialist for evaluation of undiagnosed patients in centres for rare diseases (ZSE-DUO): a prospective, controlled trial …

H Hebestreit, AM Lapstich, L Brandstetter… - …, 2023 - thelancet.com
Background People with complex symptomatology but unclear diagnosis presenting to a
centre for rare diseases (CRD) may present with mental (co-) morbidity. We hypothesised …