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International Journal of Legal Medicine
|
February 5, 1999
Basement membrane thickness of the vocal cord in cases of sudden infant death
F K van Landeghem, B Brinkmann, T Bajanowski
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 15, 2000
Multiple lesions originating from the ventricular wall
W Meissner, T Lempert, F K Van Landeghem, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndrome
A von Moers, F K van Landeghem, R D Cohn, et al.
Glia
|
August 9, 2001
Early expression of glutamate transporter proteins in ramified microglia after controlled cortical impact injury in the rat
F K van Landeghem, J F Stover, I Bechmann, et al.
Clinical Neuropathology
|
April 25, 2000
Aqueductal stenosis and hydrocephalus in an infant due to aspergillus infection
F K van Landeghem, B Stiller, T N Lehmann, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy
B Kerst, D Mennerich, M Schuelke, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
International Journal of Legal Medicine
|
February 5, 1999
Basement membrane thickness of the vocal cord in cases of sudden infant death
F K van Landeghem, B Brinkmann, T Bajanowski
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 15, 2000
Multiple lesions originating from the ventricular wall
W Meissner, T Lempert, F K Van Landeghem, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndrome
A von Moers, F K van Landeghem, R D Cohn, et al.
Glia
|
August 9, 2001
Early expression of glutamate transporter proteins in ramified microglia after controlled cortical impact injury in the rat
F K van Landeghem, J F Stover, I Bechmann, et al.
Clinical Neuropathology
|
April 25, 2000
Aqueductal stenosis and hydrocephalus in an infant due to aspergillus infection
F K van Landeghem, B Stiller, T N Lehmann, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy
B Kerst, D Mennerich, M Schuelke, et al.
Page
of 1