Auflistung nach Autor "Alber, Michael Wolfgang Hans-Peter"

Anzeige der Dokumente 1-19 von 19

A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis

Alber, Michael Wolfgang Hans-Peter (2015)
A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability

Reith, Milda; Zeltner, Lena; Witt, Dennis; Zuleger, Theresia; Bornemann, Antje; Ruf, Susanne; Stingl, Katarina; Weisschuh, Nicole; Schäferhoff, Karin; Haack, Tobias; Alber, Michael Wolfgang Hans-Peter; Schöls, Ludger (2022)
An Association between External Hydrocephalus in Infants and Reversible Collapse of the Venous Sinuses

Alber, Michael Wolfgang Hans-Peter; Schuhmann, Martin Ulrich (2014)
Comparison of Different Tractography Algorithms and Validation by Intraoperative Stimulation in a Child with a Brain Tumor

Klose, Uwe; Wilke, Marko; Küpper, Hanna; Gröschel, Samuel; Alber, Michael Wolfgang Hans-Peter; Schuhmann, Martin Ulrich (2015)
Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis

Alber, Michael Wolfgang Hans-Peter; Kranz, Julia (2019)
Fetal suppression burst pattern in Ohtahara syndrome visualized by fetal magnetoencephalography

Wacker-Gußmann, Annette; Alber, Michael Wolfgang Hans-Peter; Abele, Harald; Goelz, Rangmar (2013)
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants

Alber, Michael Wolfgang Hans-Peter (2022)
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect

Alber, Michael Wolfgang Hans-Peter (2018)
Long-term clinical course and treatment outcomes of individuals with Nodding Syndrome

Kegele, Josua; Lerche, Holger; Alber, Michael Wolfgang Hans-Peter (2024)
Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Lorenzen, Anna; Wilke, Marko; Bornemann, Antje; Ernemann, Ulrike; Rona, Sabine; Alber, Michael Wolfgang Hans-Peter; Milian, Monika Ramona (2016)
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Alber, Michael Wolfgang Hans-Peter; Ruf, Susanne; Wolff, Markus; Becker, Felicitas; Weber, Yvonne G.; Lerche, Holger; Biskup, Saskia (2013)
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Alber, Michael Wolfgang Hans-Peter (2012)
Rituximab, IVIg, and Tetracosactide (ACTH1-24) Combination Immunotherapy (""RITE-CI"") for Pediatric Opsoclonus-Myoclonus Syndrome : Immunomarkers and Clinical Observations

Alber, Michael Wolfgang Hans-Peter (2018)
Targeted next generation sequencing as a diagnostic tool in epileptic disorders

Alber, Michael Wolfgang Hans-Peter; Wolff, Markus; Rona, Sabine; Synofzik, Matthis; Becker, Felicitas; Weber, Yvonne G.; Lerche, Holger (2012)
The Multiple Sclerosis Inventory of Cognition for Adolescents (MUSICADO) : A brief screening instrument to assess cognitive dysfunction, fatigue and loss of health-related quality of life in pediatric-onset multiple sclerosis

Alber, Michael Wolfgang Hans-Peter; Kranz, Julia (2019)
The phenotype of SCN8A developmental and epileptic encephalopathy

Wolff, Markus; Alber, Michael Wolfgang Hans-Peter (2018)
Transtemporal Ultrasound (US) Assessment of Third Ventricle Diameter (TVD): Comparison of US and MRI TVD in Pediatric Patients

Kerscher, Susanne Regina; Schweizer, Louise L.; Nägele, Thomas; Bevot, Andrea; Alber, Michael Wolfgang Hans-Peter; Schuhmann, Martin Ulrich (2020)
Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics

Alber, Michael Wolfgang Hans-Peter (2022)
Unilateral Hearing Loss Due to Cochlear Nerve Involvement as Isolated Symptom of a Primary Medulloblastoma

Weichselbaum, Annette; Ebinger, Martin; Magg, Janine; Nägele, Thomas; Alber, Michael Wolfgang Hans-Peter; Schuhmann, Martin Ulrich (2020)

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Auflistung nach Autor "Alber, Michael Wolfgang Hans-Peter"

Auflistung nach Autor "Alber, Michael Wolfgang Hans-Peter"

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