49 research outputs found
Erratum to: ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies
Full text linkSolving unsolved rare neurological diseases-a Solve-RD viewpoint.
Get PDFFunder: Durch Princess Beatrix Muscle Fund Durch Speeren voor Spieren Muscle FundFunder: University of Tübingen Medical Faculty PATE programFunder: European Reference Network for Rare Neurological Diseases | 739510Funder: European Joint Program on Rare Diseases (EJP-RD COFUND-EJP) | 44140962
Assessment of intracranial pressure and ventricular size in pediatric neurosurgery using combined ultrasound measurement of the Optic Nerve Sheath Diameter (ONSD) and Third Ventricle Diameter (TVD)
No full textFibrolipomatous hamartomas of the median nerve in infancy and childhood - hallmarks, symptomatology, treatment
No full textVideobasierte, markerlose 2D-Ganganalyse basierend auf Transferlernen mit tiefen neuronalen Netzen - erste Daten
No full text"Asymptomatic ventriculomegaly" or "Arrested hydrocephalus" in children - a treatment concept based on ICP analysis and CSF dynamics
No full textAsymptomatic treatment failure in pediatric hydrocephalus - features of an under diagnosed (?) entity
No full textVergleich von Ultraschall (US) und MRT ONSD - klinisch ergänzende Anwendung beider Verfahren in der Pädiatrischen Neurochirurgie
No full textChirurgische Therapie und Langzeit-Outcome von ELBW-Frühgeborenen mit intestinaler Perforation
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