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Annals of Neurology
|
March 1, 1997
Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles
E C Engle, B C Goumnerov, C A McKeown, et al.
The New England Journal of Medicine
|
May 17, 1990
Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy
J L Patten, D R Johns, D Valle, et al.
Annals of Neurology
|
June 1, 1990
Phosphorus magnetic resonance spectroscopy of patients with mitochondrial cytopathies demonstrates decreased levels of brain phosphocreatine
S M Eleff, P B Barker, S J Blackband, et al.
G3 (Bethesda, Md.)
|
January 25, 2018
Genome-Wide Screen for New Components of the <i>Drosophila melanogaster</i> Torso Receptor Tyrosine Kinase Pathway
Alex R Johns, Michelle A Henstridge, Melissa J Saligari, et al.
Genomics
|
May 16, 2001
Low mutational burden of individual acquired mitochondrial DNA mutations in brain
D K Simon, M T Lin, C H Ahn, et al.
American Journal of Ophthalmology
|
September 15, 1992
Ophthalmic involvement in myo-neuro-gastrointestinal encephalopathy syndrome
A B Threlkeld, N R Miller, K C Golnik, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]
|
January 12, 2007
Interferon Alfa-2b or not 2b? Significant differences exist in the decision-making process between melanoma patients who accept or decline high-dose adjuvant interferon Alfa-2b treatment
Tracy B Bramlette, David H Lawson, Carl V Washington, et al.
Muscle & Nerve
|
July 1, 1996
Myotonia in colchicine myoneuropathy
S B Rutkove, U De Girolami, D C Preston, et al.
Muscle & Nerve
|
March 31, 2004
Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation
Mark A Tarnopolsky, David K Simon, Brian D Roy, et al.
The American Journal of Surgical Pathology
|
September 16, 1998
Mitochondrial neurogastrointestinal encephalomyopathy: diagnosis by rectal biopsy
A R Perez-Atayde, V Fox, J E Teitelbaum, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 207) with videos related to
Sort By:
Page
of 21
Annals of Neurology
|
March 1, 1997
Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles
E C Engle, B C Goumnerov, C A McKeown, et al.
The New England Journal of Medicine
|
May 17, 1990
Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy
J L Patten, D R Johns, D Valle, et al.
Annals of Neurology
|
June 1, 1990
Phosphorus magnetic resonance spectroscopy of patients with mitochondrial cytopathies demonstrates decreased levels of brain phosphocreatine
S M Eleff, P B Barker, S J Blackband, et al.
G3 (Bethesda, Md.)
|
January 25, 2018
Genome-Wide Screen for New Components of the <i>Drosophila melanogaster</i> Torso Receptor Tyrosine Kinase Pathway
Alex R Johns, Michelle A Henstridge, Melissa J Saligari, et al.
Genomics
|
May 16, 2001
Low mutational burden of individual acquired mitochondrial DNA mutations in brain
D K Simon, M T Lin, C H Ahn, et al.
American Journal of Ophthalmology
|
September 15, 1992
Ophthalmic involvement in myo-neuro-gastrointestinal encephalopathy syndrome
A B Threlkeld, N R Miller, K C Golnik, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]
|
January 12, 2007
Interferon Alfa-2b or not 2b? Significant differences exist in the decision-making process between melanoma patients who accept or decline high-dose adjuvant interferon Alfa-2b treatment
Tracy B Bramlette, David H Lawson, Carl V Washington, et al.
Muscle & Nerve
|
July 1, 1996
Myotonia in colchicine myoneuropathy
S B Rutkove, U De Girolami, D C Preston, et al.
Muscle & Nerve
|
March 31, 2004
Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation
Mark A Tarnopolsky, David K Simon, Brian D Roy, et al.
The American Journal of Surgical Pathology
|
September 16, 1998
Mitochondrial neurogastrointestinal encephalomyopathy: diagnosis by rectal biopsy
A R Perez-Atayde, V Fox, J E Teitelbaum, et al.
Page
of 21