Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Paul Carango"'
Autor:
Paul Carango, Nicolas Saporito, Samuel Geathers, Mark Martin, Jacquelyn Gerhart, Christopher S. Little, Brian Balin, Denah Appelt
Publikováno v:
The FASEB Journal. 36
Autor:
Priscilla A. Moses, Vicky L. Funanage, Kenneth R. Singleton, Iris L. Gonzalez, Harold G. Marks, Paul Carango, Richard Frisch
Publikováno v:
Molecular Genetics and Metabolism. 74:281-291
Myotonic dystrophy (DM), an autosomal dominant neuromuscular disease, is associated with expansion of a polymorphic (CTG) n repeat in the 3′-untranslated region of the DM protein kinase ( DMPK ) gene. The repeat expansion results in decreased level
Publikováno v:
Annals of Neurology. 38:610-617
Pelizaeus-Merzbacher disease is a rare, sex-linked recessive, dysmyelinating disease of the central nervous system that has been associated with mutations in the myelin proteolipid protein (PLP) gene. Only 25% of patients studied with Pelizaeus-Merzb
Autor:
Elizabeth Roeder, Claudia Abbruzzese, Tetsuo Ashizawa, Paul Carango, M. Giacanelli, Ralf Krahe, Vicky L. Funanage, Michael J. Siciliano
Publikováno v:
Genomics. 28:1-14
The myotonic dystrophy (DM) mutation has been identified as an unstable, expanded (CTG) n repeat in the 3′ untranslated region of a gene designated DM protein kinase ( DMPK ). Both decreased and increased levels of mutant DMPK mRNA as well as decre
Publikováno v:
Genomics. 18:340-348
Myotonic dystrophy is an autosomally dominant inherited disease in which system-wide abnormalities are caused by a triplet repeat expansion within the 3[prime] untranslated region of the myotonic dystrophy protein kinase (DMPK) gene. To determine the
Publikováno v:
Spine. 15(10)
Several cases of occipito-atlantal instability have been reported in patients with Down's syndrome. However, standards for radiographic measurement and normal values for translational motion at the occiput-C1 level have not been established for the D
Autor:
Dan E. Mason, Paul Carango
Publikováno v:
Spine. 16:S404
Forty-one patients with idiopathic scoliosis having a primary right thoracic and a compensatory left lumbar curve underwent posterior spinal fusion of the primary curve only. Twenty-four patients had instrumentation with a Harrington rod or variant,