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Magnetic Resonance Imaging
|
January 1, 1990
Magnetic resonance imaging and computed tomography in Pelizaeus-Merzbacher disease
P A Caro, H G Marks
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress
|
February 5, 1999
[Primary liver and bile duct tumors: approach to conservative therapy]
D Henne-Bruns, H G Marks
Pediatrics
|
November 1, 1977
Fisher's syndrome in children
H G Marks, P Augustyn, R J Allen
Foot & Ankle
|
November 1, 1984
Foot deformity in myotonic dystrophy
S Ray, J R Bowen, H G Marks
Nature Genetics
|
July 1, 1994
The rumpshaker mutation in spastic paraplegia
H Kobayashi, E P Hoffman, H G Marks
American Journal of Medical Genetics
|
April 1, 1991
Maternal muscle biopsy in X-linked recessive centronuclear (myotubular) myopathy
G N Breningstall, W D Grover, H G Marks
Genomics
|
November 1, 1993
Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy
P Carango, J E Noble, H G Marks, et al.
Neurology
|
August 1, 1988
Neonatal rhabdomyolysis as a presentation of muscular dystrophy
G N Breningstall, W D Grover, S Barbera, et al.
Journal of Pediatric Orthopedics
|
March 1, 1988
Scoliosis in Rett syndrome
D Keret, G S Bassett, W P Bunnell, et al.
Neurofibromatosis
|
January 1, 1988
Aqueductal stenosis in neurofibromatosis
J J Riviello, H G Marks, M S Lee, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Magnetic Resonance Imaging
|
January 1, 1990
Magnetic resonance imaging and computed tomography in Pelizaeus-Merzbacher disease
P A Caro, H G Marks
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress
|
February 5, 1999
[Primary liver and bile duct tumors: approach to conservative therapy]
D Henne-Bruns, H G Marks
Pediatrics
|
November 1, 1977
Fisher's syndrome in children
H G Marks, P Augustyn, R J Allen
Foot & Ankle
|
November 1, 1984
Foot deformity in myotonic dystrophy
S Ray, J R Bowen, H G Marks
Nature Genetics
|
July 1, 1994
The rumpshaker mutation in spastic paraplegia
H Kobayashi, E P Hoffman, H G Marks
American Journal of Medical Genetics
|
April 1, 1991
Maternal muscle biopsy in X-linked recessive centronuclear (myotubular) myopathy
G N Breningstall, W D Grover, H G Marks
Genomics
|
November 1, 1993
Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy
P Carango, J E Noble, H G Marks, et al.
Neurology
|
August 1, 1988
Neonatal rhabdomyolysis as a presentation of muscular dystrophy
G N Breningstall, W D Grover, S Barbera, et al.
Journal of Pediatric Orthopedics
|
March 1, 1988
Scoliosis in Rett syndrome
D Keret, G S Bassett, W P Bunnell, et al.
Neurofibromatosis
|
January 1, 1988
Aqueductal stenosis in neurofibromatosis
J J Riviello, H G Marks, M S Lee, et al.
Page
of 3