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H G Marks

Showing results (11-20 of 29) with videos related to

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AJNR. American Journal of Neuroradiology|March 27, 1999
MR imaging findings in children with merosin-deficient congenital muscular dystrophyP A Caro, M Scavina, E Hoffman, et al.
Pediatric Emergency Care|June 1, 1990
Delayed cervical central cord syndrome after trivial traumaJ J Riviello, H G Marks, E N Faerber, et al.
Journal of Pediatric Orthopedics|September 1, 1985
Hip dysplasia associated with Charcot-Marie-Tooth disease in the older child and adolescentS J Kumar, H G Marks, J R Bowen, et al.
Journal of the Neurological Sciences|May 1, 1996
Molecular genetics of familial spastic paraplegia: a multitude of responsible genesH Kobayashi, C A Garcia, G Alfonso, et al.
Muscle & Nerve|August 1, 1997
Krabbe's disease presenting as a peripheral neuropathyH G Marks, M T Scavina, E H Kolodny, et al.
Zentralblatt Fur Chirurgie|January 1, 1989
[Locoregional chemotherapy of liver tumors]D Henne-Bruns, H G Marks, V Marks, et al.
Neurology|February 1, 1995
A novel mutation in exon 3 of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseV M Pratt, S Naidu, S R Dlouhy, et al.
Journal of Pediatric Orthopedics|September 1, 1988
Intraspinal tumors in children presenting primarily with hip symptoms: a report of three casesS J Kumar, H G Marks, J D Ghiragossian, et al.
Annals of Neurology|October 1, 1995
Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher diseaseP Carango, V L Funanage, R E Quirós, et al.
Human Genetics|May 1, 1995
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methodsH Kobayashi, T C Matise, M W Perlin, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
AJNR. American Journal of Neuroradiology|March 27, 1999
MR imaging findings in children with merosin-deficient congenital muscular dystrophyP A Caro, M Scavina, E Hoffman, et al.
Pediatric Emergency Care|June 1, 1990
Delayed cervical central cord syndrome after trivial traumaJ J Riviello, H G Marks, E N Faerber, et al.
Journal of Pediatric Orthopedics|September 1, 1985
Hip dysplasia associated with Charcot-Marie-Tooth disease in the older child and adolescentS J Kumar, H G Marks, J R Bowen, et al.
Journal of the Neurological Sciences|May 1, 1996
Molecular genetics of familial spastic paraplegia: a multitude of responsible genesH Kobayashi, C A Garcia, G Alfonso, et al.
Muscle & Nerve|August 1, 1997
Krabbe's disease presenting as a peripheral neuropathyH G Marks, M T Scavina, E H Kolodny, et al.
Zentralblatt Fur Chirurgie|January 1, 1989
[Locoregional chemotherapy of liver tumors]D Henne-Bruns, H G Marks, V Marks, et al.
Neurology|February 1, 1995
A novel mutation in exon 3 of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseV M Pratt, S Naidu, S R Dlouhy, et al.
Journal of Pediatric Orthopedics|September 1, 1988
Intraspinal tumors in children presenting primarily with hip symptoms: a report of three casesS J Kumar, H G Marks, J D Ghiragossian, et al.
Annals of Neurology|October 1, 1995
Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher diseaseP Carango, V L Funanage, R E Quirós, et al.
Human Genetics|May 1, 1995
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methodsH Kobayashi, T C Matise, M W Perlin, et al.
Pageof 3