Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
2010 1
2011 1
2012 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

3 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal muscle fiber merosin expression"
Page 1
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins.
van der Ven PF, Jap PH, ter Laak HJ, Nonaka I, Barth PG, Sengers RC, Stadhouders AM, Ramaekers FC. van der Ven PF, et al. J Neurol Sci. 1995 Apr;129(2):199-213. doi: 10.1016/0022-510x(94)00282-s. J Neurol Sci. 1995. PMID: 7608737 Free article.
We have studied the expression and distribution patterns of the intermediate filament proteins desmin and vimentin, the sarcomere components titin, nebulin and myosin, the basement membrane constituents collagen type IV and laminin, and the reticular layer component …
We have studied the expression and distribution patterns of the intermediate filament proteins desmin and vimentin, the sarcomere com …
Sequential neuroradiological and neurophysiological studies in a Japanese girl with merosin-deficient congenital muscular dystrophy.
Fujii Y, Sugiura C, Fukuda C, Maegaki Y, Ohno K. Fujii Y, et al. Brain Dev. 2011 Feb;33(2):140-4. doi: 10.1016/j.braindev.2010.02.003. Epub 2010 Mar 19. Brain Dev. 2011. PMID: 20303224
We describe the early manifestation and sequential assessment of the central and peripheral nervous system in a Japanese girl with merosin-deficient congenital muscular dystrophy. She showed severe hypotonia (''floppy infant") and suffered mild respiratory failure p …
We describe the early manifestation and sequential assessment of the central and peripheral nervous system in a Japanese girl with merosi …
Cytoskeletal and extracellular matrix alterations in limb girdle muscular dystrophy 2I muscle fibers.
Sabatelli P, Pellegrini C, Faldini C, Merlini L. Sabatelli P, et al. Neurol India. 2012 Sep-Oct;60(5):510-1. doi: 10.4103/0028-3886.103200. Neurol India. 2012. PMID: 23135029 Free article.
In this detailed muscle biopsy study of a patient with molecularly confirmed diagnosis of limb-girdle muscular dystrophy 2I (LGMD2I) we show some new data, that is the presence of altered expression pattern of costamere components as integrin alpha7B and integrin be …
In this detailed muscle biopsy study of a patient with molecularly confirmed diagnosis of limb-girdle muscular dystrophy 2I (LGMD2I) …