Haberlandt, E.
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1

Epileptic phenotypes, electroclinical features and clinical..:

Haberlandt, E. ; Ensslen, M. ; Gruber-Sedlmayr, U....
European Journal of Paediatric Neurology.  21 (2017)  3 - p. 457-464 , 2017
 
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2

ASPP2 deficiency causes features of 1q41q42 microdeletion s..:

Zak, J ; Vives, V ; Szumska, D...
Cell Death & Differentiation.  23 (2016)  12 - p. 1973-1984 , 2016
 
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3

Ketogenic diets in patients with inherited metabolic disord..:

Scholl‐Bürgi, S. ; Höller, A. ; Pichler, K....
Journal of Inherited Metabolic Disease.  38 (2015)  4 - p. 765-773 , 2015
 
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5

PP7.1 – 1956 Effectiveness and tolerability of perampanel i..:

Biro, A ; Stephani, U ; Tarallo, T...
European Journal of Paediatric Neurology.  17 (2013)  - p. S47-S48 , 2013
 
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7

Peripheral neuropathy as the sole initial finding in three ..:

Haberlandt, E. ; Scholl-Bürgi, S. ; Neuberger, J....
European Journal of Paediatric Neurology.  13 (2009)  3 - p. 257-260 , 2009
 
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Levetiractam in the treatment of two children with myocloni..:

Haberlandt, E. ; Sigl, S. Baumgartner ; Scholl-Buergi, S....
European Journal of Paediatric Neurology.  13 (2009)  6 - p. 546-549 , 2009
 
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The relation of cerebrospinal fluid and plasma glycine leve..:

Scholl-Bürgi, S. ; Korman, S. H. ; Applegarth, D. A....
Journal of Inherited Metabolic Disease.  31 (2008)  3 - p. 395-398 , 2008
 
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10

Amino acids in CSF and plasma in hyperammonaemic coma due t..:

Scholl‐Bürgi, S. ; Baumgartner Sigl, S. ; Häberle, J....
Journal of Inherited Metabolic Disease.  31 (2008)  S2 - p. 323-328 , 2008
 
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