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European Journal of Pediatrics
|
September 19, 2009
A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum
Udo Koehler, Elke Holinski-Feder, Birgit Ertl-Wagner, et al.
European Journal of Pain (London, England)
|
August 4, 2018
Static magnetic field exposure in 1.5 and 3 Tesla MR scanners does not influence pain and touch perception in healthy volunteers
Katharina Kamm, Andreas Pomschar, Ruth Ruscheweyh, et al.
Brain Stimulation
|
May 16, 2018
Testing assumptions on prefrontal transcranial direct current stimulation: Comparison of electrode montages using multimodal fMRI
Jana Wörsching, Frank Padberg, Stephan Goerigk, et al.
Neuroradiology
|
March 22, 2017
MR imaging differentiation of Fe<sup>2+</sup> and Fe<sup>3+</sup> based on relaxation and magnetic susceptibility properties
Olaf Dietrich, Johannes Levin, Seyed-Ahmad Ahmadi, et al.
Investigative Radiology
|
August 23, 2016
Dynamic Contrast-Enhanced Magnetic Resonance Imaging Suggests Normal Perfusion in Normal-Appearing White Matter in Multiple Sclerosis
Michael Ingrisch, Steven Sourbron, Sina Herberich, et al.
Neuroimage. Clinical
|
September 15, 2024
Corrigendum to "Impact of adult-onset multiple sclerosis on MRI-based intracranial volume: A study in clinically discordant monozygotic twins" [NeuroImage Clin. 42 (2024) 103597]
Matin Mortazavi, Lisa Ann Gerdes, Öznur Hizarci, et al.
Onkologie
|
October 28, 2006
Feasibility of photofrin II as a radiosensitizing agent in solid tumors--preliminary results
Moshe Schaffer, Birgit Ertl-Wagner, Pamela Manuela Schaffer, et al.
Neuromuscular Disorders : NMD
|
July 2, 2017
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient
Elena Ikenberg, Ivan Karin, Birgit Ertl-Wagner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 26, 2017
Pediatric idiopathic intracranial hypertension - Is the fixed threshold value of elevated LP opening pressure set too high?
Lucia Gerstl, Nikola Schoppe, Lucia Albers, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2009
Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum
Chayim Can Schell-Apacik, Birgit Ertl-Wagner, Axel Panzel, et al.
Page
of 23
Search research articles
Search
Showing results (71-80 of 230) with videos related to
Sort By:
Page
of 23
European Journal of Pediatrics
|
September 19, 2009
A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum
Udo Koehler, Elke Holinski-Feder, Birgit Ertl-Wagner, et al.
European Journal of Pain (London, England)
|
August 4, 2018
Static magnetic field exposure in 1.5 and 3 Tesla MR scanners does not influence pain and touch perception in healthy volunteers
Katharina Kamm, Andreas Pomschar, Ruth Ruscheweyh, et al.
Brain Stimulation
|
May 16, 2018
Testing assumptions on prefrontal transcranial direct current stimulation: Comparison of electrode montages using multimodal fMRI
Jana Wörsching, Frank Padberg, Stephan Goerigk, et al.
Neuroradiology
|
March 22, 2017
MR imaging differentiation of Fe<sup>2+</sup> and Fe<sup>3+</sup> based on relaxation and magnetic susceptibility properties
Olaf Dietrich, Johannes Levin, Seyed-Ahmad Ahmadi, et al.
Investigative Radiology
|
August 23, 2016
Dynamic Contrast-Enhanced Magnetic Resonance Imaging Suggests Normal Perfusion in Normal-Appearing White Matter in Multiple Sclerosis
Michael Ingrisch, Steven Sourbron, Sina Herberich, et al.
Neuroimage. Clinical
|
September 15, 2024
Corrigendum to "Impact of adult-onset multiple sclerosis on MRI-based intracranial volume: A study in clinically discordant monozygotic twins" [NeuroImage Clin. 42 (2024) 103597]
Matin Mortazavi, Lisa Ann Gerdes, Öznur Hizarci, et al.
Onkologie
|
October 28, 2006
Feasibility of photofrin II as a radiosensitizing agent in solid tumors--preliminary results
Moshe Schaffer, Birgit Ertl-Wagner, Pamela Manuela Schaffer, et al.
Neuromuscular Disorders : NMD
|
July 2, 2017
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient
Elena Ikenberg, Ivan Karin, Birgit Ertl-Wagner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 26, 2017
Pediatric idiopathic intracranial hypertension - Is the fixed threshold value of elevated LP opening pressure set too high?
Lucia Gerstl, Nikola Schoppe, Lucia Albers, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2009
Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum
Chayim Can Schell-Apacik, Birgit Ertl-Wagner, Axel Panzel, et al.
Page
of 23