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P L Hartlage

Showing results (11-20 of 17) with videos related to

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AJNR. American Journal of Neuroradiology|January 1, 1987
MR imaging of moyamoya in neurofibromatosisB S Brooks, T el Gammal, R J Adams, et al.
Pediatric Research|March 1, 1980
Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading testH Kihara, C K Ho, A L Fluharty, et al.
Neuropediatrics|February 1, 1986
Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)F A Hommes, R A Roesel, K Metoki, et al.
Muscle & Nerve|March 1, 1988
Muscle imaging in neuromuscular disease using computerized real-time sonographyA Q Fischer, D W Carpenter, P L Hartlage, et al.
Journal of Mental Deficiency Research|December 1, 1985
Serum carnosinase deficiency: a non-disabling phenotype?M Cohen, P L Hartlage, N Krawiecki, et al.
Pediatric Neurology|March 1, 1986
Urinary sialic acid screening in neurologic disordersJ E Carroll, R A Roesel, R H DuRant, et al.
Journal of Child Neurology|May 1, 1995
Giant axonal neuropathy in a child with insulin-dependent diabetes mellitusW H Hoffman, J E Carroll, G Y Perry, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
AJNR. American Journal of Neuroradiology|January 1, 1987
MR imaging of moyamoya in neurofibromatosisB S Brooks, T el Gammal, R J Adams, et al.
Pediatric Research|March 1, 1980
Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading testH Kihara, C K Ho, A L Fluharty, et al.
Neuropediatrics|February 1, 1986
Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)F A Hommes, R A Roesel, K Metoki, et al.
Muscle & Nerve|March 1, 1988
Muscle imaging in neuromuscular disease using computerized real-time sonographyA Q Fischer, D W Carpenter, P L Hartlage, et al.
Journal of Mental Deficiency Research|December 1, 1985
Serum carnosinase deficiency: a non-disabling phenotype?M Cohen, P L Hartlage, N Krawiecki, et al.
Pediatric Neurology|March 1, 1986
Urinary sialic acid screening in neurologic disordersJ E Carroll, R A Roesel, R H DuRant, et al.
Journal of Child Neurology|May 1, 1995
Giant axonal neuropathy in a child with insulin-dependent diabetes mellitusW H Hoffman, J E Carroll, G Y Perry, et al.
Pageof 2