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A J Spiro

Showing results (11-20 of 27) with videos related to

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Archives of Neurology|March 1, 1970
A new mitochondrial myopathy in a patient with salt cravingA J Spiro, J W Prineas, C L Moore
Neuropediatrics|February 1, 1987
The coexistence of myasthenia gravis and myotonic dystrophy in one familyJ Maytal, A J Spiro, S Sinnar, et al.
Archives of Neurology|October 1, 1970
Cretinism with muscular hypertrophy (Kocher-Debré-Sémélaigne syndrome). Histochemical and ultrastructural study of skeletal muscleA J Spiro, A Hirano, R L Beilin, et al.
Pediatrics|January 1, 1988
Gastroesophageal reflux associated with nemaline myopathy of infancyS Berezin, L J Newman, S M Schwarz, et al.
Neurology|January 1, 1982
Ipecac-induced myopathy simulating dermatomyositisH S Bennett, A J Spiro, M A Pollack, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)|February 1, 1971
Autosomal recessive deafnessassociated with short stature, vitiligo, muscle wasting and achalasiaD L Rozycki, R J Ruben, I Rapin, et al.
Muscle & Nerve|November 1, 1986
Duchenne dystrophic muscle develops lesions in long-term coculture with mouse spinal cordE R Peterson, E B Masurovsky, A J Spiro, et al.
Archives of Neurology|August 1, 1970
A cytochrome-related inherited disorder of the nervous system and muscleA J Spiro, C L Moore, J W Prineas, et al.
Muscle & Nerve|May 1, 1981
Acute hypokalemic, hypophosphatemic myopathy in chronic alcoholismM Daras, B M Singh, A E Fass, et al.
American Journal of Human Genetics|November 1, 1988
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Archives of Neurology|March 1, 1970
A new mitochondrial myopathy in a patient with salt cravingA J Spiro, J W Prineas, C L Moore
Neuropediatrics|February 1, 1987
The coexistence of myasthenia gravis and myotonic dystrophy in one familyJ Maytal, A J Spiro, S Sinnar, et al.
Archives of Neurology|October 1, 1970
Cretinism with muscular hypertrophy (Kocher-Debré-Sémélaigne syndrome). Histochemical and ultrastructural study of skeletal muscleA J Spiro, A Hirano, R L Beilin, et al.
Pediatrics|January 1, 1988
Gastroesophageal reflux associated with nemaline myopathy of infancyS Berezin, L J Newman, S M Schwarz, et al.
Neurology|January 1, 1982
Ipecac-induced myopathy simulating dermatomyositisH S Bennett, A J Spiro, M A Pollack, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)|February 1, 1971
Autosomal recessive deafnessassociated with short stature, vitiligo, muscle wasting and achalasiaD L Rozycki, R J Ruben, I Rapin, et al.
Muscle & Nerve|November 1, 1986
Duchenne dystrophic muscle develops lesions in long-term coculture with mouse spinal cordE R Peterson, E B Masurovsky, A J Spiro, et al.
Archives of Neurology|August 1, 1970
A cytochrome-related inherited disorder of the nervous system and muscleA J Spiro, C L Moore, J W Prineas, et al.
Muscle & Nerve|May 1, 1981
Acute hypokalemic, hypophosphatemic myopathy in chronic alcoholismM Daras, B M Singh, A E Fass, et al.
American Journal of Human Genetics|November 1, 1988
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.
Pageof 3