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	1.	[Treating Neonates with Levetiracetam: a survey among German University Hospitals]. [electronic resource] by Koppelstäetter, A Bührer, C Kaindl, A M Producer: 20120705 In: Klinische Padiatrie vol. 223 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	New insights into the molecular basis of the triple A syndrome. [electronic resource] by Huebner, A Kaindl, A M Braun, R Handschug, K Producer: 20030716 In: Endocrine research vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Acute ascending motoric paraplegia following intrathecal chemotherapy for treatment of acute lymphoblastic leukemia in children: case reports and review of the literature. [electronic resource] by Rolf, N Boehm, H Kaindl, A M Lauterbach, I Suttorp, M Producer: 20070126 In: Klinische Padiatrie vol. 218 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	In utero development of symmetric thalamic and brainstem necrosis in a preterm hydropic stillborn. [electronic resource] by Szekessy, D P Bamberg, C Blechschmidt, C Kaindl, A M Stoltenburg-Didinger, G Producer: 20110106 In: Clinical neuropathology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex. [electronic resource] by Huebner, Angela Kaindl, A M Knobeloch, K P Petzold, H Mann, P Koehler, K Producer: 20050610 In: Endocrine research vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Antiepileptic drugs and the developing brain. [electronic resource] by Kaindl, A M Asimiadou, S Manthey, D Hagen, M V D Turski, L Ikonomidou, C Producer: 20060421 In: Cellular and molecular life sciences : CMLS vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro. [electronic resource] by Dean, J M Wang, X Kaindl, A M Gressens, P Fleiss, B Hagberg, H Mallard, C Producer: 20100913 In: Brain, behavior, and immunity vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]. [electronic resource] by Kaindl, A M Guenther, U-P Rudnik-Schöneborn, S Varon, R Zerres, K Gressens, P Schuelke, M Hubner, C von Au, K Producer: 20081216 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Novel RYR1 missense mutation causes core rod myopathy. [electronic resource] by von der Hagen, M Kress, W Hahn, G Brocke, K S Mitzscherling, P Huebner, A Müller-Reible, C Stoltenburg-Didinger, G Kaindl, A M Producer: 20080507 In: European journal of neurology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Acute and long-term proteome changes induced by oxidative stress in the developing brain. [electronic resource] by Kaindl, A M Sifringer, M Zabel, C Nebrich, G Wacker, M A Felderhoff-Mueser, U Endesfelder, S von der Hagen, M Stefovska, V Klose, J Ikonomidou, C Producer: 20061107 In: Cell death and differentiation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Missense mutations of ACTA1 cause dominant congenital myopathy with cores. [electronic resource] by Kaindl, A M Rüschendorf, F Krause, S Goebel, H-H Koehler, K Becker, C Pongratz, D Müller-Höcker, J Nürnberg, P Stoltenburg-Didinger, G Lochmüller, H Huebner, A Producer: 20050414 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis. [electronic resource] by von der Hagen, M Schallner, J Kaindl, A M Koehler, K Mitzscherling, P Abicht, A Grieben, U Korinthenberg, R Kress, W von Moers, A Müller, J S Schara, U Vorgerd, M Walter, M C Müller-Reible, C Hübner, C Lochmüller, H Huebner, A Producer: 20060412 In: Neuromuscular disorders : NMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)