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European Heart Journal
|
June 1, 1988
The use of endomyocardial biopsy in heart failure
B Maisch, E Bauer, G Hufnagel, et al.
Neurology
|
March 1, 1983
A dominantly inherited myopathy with excessive tubular aggregates
R Rohkamm, K Boxler, K Ricker, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
August 1, 1986
[Nuclear magnetic resonance tomography in the diagnosis of muscular diseases]
W A Kaiser, B C Schalke, R Rohkamm
Der Nervenarzt
|
April 1, 1983
[Plasma exchange treatment in neurologic diseases]
P Reuther, D Wiebecke, R Rohkamm, et al.
Clinical Neurology and Neurosurgery
|
February 1, 1997
Solitary Langerhans cell histiocytosis lesion of the parieto-occipital lobe: a case report and review of the literature
M Bergmann, Y Yuan, W Brück, et al.
Archives of Neurology
|
September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
H Reichmann, R Rohkamm, M Zeviani, et al.
European Journal of Pediatrics
|
November 1, 1987
Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases
A Kohlschütter, H P Willig, D Schlamp, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
European Heart Journal
|
June 1, 1988
The use of endomyocardial biopsy in heart failure
B Maisch, E Bauer, G Hufnagel, et al.
Neurology
|
March 1, 1983
A dominantly inherited myopathy with excessive tubular aggregates
R Rohkamm, K Boxler, K Ricker, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
August 1, 1986
[Nuclear magnetic resonance tomography in the diagnosis of muscular diseases]
W A Kaiser, B C Schalke, R Rohkamm
Der Nervenarzt
|
April 1, 1983
[Plasma exchange treatment in neurologic diseases]
P Reuther, D Wiebecke, R Rohkamm, et al.
Clinical Neurology and Neurosurgery
|
February 1, 1997
Solitary Langerhans cell histiocytosis lesion of the parieto-occipital lobe: a case report and review of the literature
M Bergmann, Y Yuan, W Brück, et al.
Archives of Neurology
|
September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
H Reichmann, R Rohkamm, M Zeviani, et al.
European Journal of Pediatrics
|
November 1, 1987
Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases
A Kohlschütter, H P Willig, D Schlamp, et al.
Page
of 2