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Klinische Padiatrie
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November 23, 2011
[Treating Neonates with Levetiracetam: a survey among German University Hospitals]
A Koppelstäetter, C Bührer, A M Kaindl
Endocrine Research
|
January 18, 2003
New insights into the molecular basis of the triple A syndrome
A Huebner, A M Kaindl, R Braun, et al.
Klinische Padiatrie
|
November 3, 2006
Acute ascending motoric paraplegia following intrathecal chemotherapy for treatment of acute lymphoblastic leukemia in children: case reports and review of the literature
N Rolf, H Boehm, A M Kaindl, et al.
Clinical Neuropathology
|
November 16, 2010
In utero development of symmetric thalamic and brainstem necrosis in a preterm hydropic stillborn
D P Szekessy, C Bamberg, C Blechschmidt, et al.
Endocrine Research
|
January 26, 2005
The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex
Angela Huebner, A M Kaindl, K P Knobeloch, et al.
Cellular and Molecular Life Sciences : CMLS
|
January 4, 2006
Antiepileptic drugs and the developing brain
A M Kaindl, S Asimiadou, D Manthey, et al.
Brain, Behavior, and Immunity
|
November 12, 2009
Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro
J M Dean, X Wang, A M Kaindl, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 23, 2008
[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]
A M Kaindl, U-P Guenther, S Rudnik-Schöneborn, et al.
Cell Death and Differentiation
|
October 29, 2005
Acute and long-term proteome changes induced by oxidative stress in the developing brain
A M Kaindl, M Sifringer, C Zabel, et al.
Neuromuscular Disorders : NMD
|
December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis
M von der Hagen, J Schallner, A M Kaindl, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Klinische Padiatrie
|
November 23, 2011
[Treating Neonates with Levetiracetam: a survey among German University Hospitals]
A Koppelstäetter, C Bührer, A M Kaindl
Endocrine Research
|
January 18, 2003
New insights into the molecular basis of the triple A syndrome
A Huebner, A M Kaindl, R Braun, et al.
Klinische Padiatrie
|
November 3, 2006
Acute ascending motoric paraplegia following intrathecal chemotherapy for treatment of acute lymphoblastic leukemia in children: case reports and review of the literature
N Rolf, H Boehm, A M Kaindl, et al.
Clinical Neuropathology
|
November 16, 2010
In utero development of symmetric thalamic and brainstem necrosis in a preterm hydropic stillborn
D P Szekessy, C Bamberg, C Blechschmidt, et al.
Endocrine Research
|
January 26, 2005
The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex
Angela Huebner, A M Kaindl, K P Knobeloch, et al.
Cellular and Molecular Life Sciences : CMLS
|
January 4, 2006
Antiepileptic drugs and the developing brain
A M Kaindl, S Asimiadou, D Manthey, et al.
Brain, Behavior, and Immunity
|
November 12, 2009
Microglial MyD88 signaling regulates acute neuronal toxicity of LPS-stimulated microglia in vitro
J M Dean, X Wang, A M Kaindl, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 23, 2008
[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]
A M Kaindl, U-P Guenther, S Rudnik-Schöneborn, et al.
Cell Death and Differentiation
|
October 29, 2005
Acute and long-term proteome changes induced by oxidative stress in the developing brain
A M Kaindl, M Sifringer, C Zabel, et al.
Neuromuscular Disorders : NMD
|
December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis
M von der Hagen, J Schallner, A M Kaindl, et al.
Page
of 1