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Title: Files for neuromuscular diseases (2011) - nr 18/11

Creator:

Fidziańska-Dolot, Anna (1930–2015)

Date issued/created:

2011

Resource type:

Text ; Image

More

Contributor:

Mossakowski Medical Research Center Polish Academy of Sciences. Department of Neuromuscular

Place of publishing:

Warsaw

Description:

Muscle segment examination in light and electron microscopy

Abstract:

A 34-year-old patient with suspected myopathy was examined. A biopsy of quadriceps dexter was performed. Electronmicroscopy analysis revealed that some muscle fibers were ultrastructurally unchanged and characterized by normal sarcomere and myofibrils structure (Fig. 1,2). Also muscle fibers of smaller diameter, characterized by the presence of multiply cell nuclei were seen (Fig. 3,4,5,6). At the same time mononuclear myotubes-like muscle fibers showing significant disrupture of the contractile apparatus were observed (Fig. 7,8,9,10,11).

Detailed Resource Type:

Photography ; Files

Format:

pdf

Resource Identifier:

oai:rcin.org.pl:123939

Language:

pol

Rights:

Creative Commons Attribution BY 4.0 license

Terms of use:

Copyright-protected material. [CC BY 4.0] May be used within the scope specified in Creative Commons Attribution BY 4.0 license, full text available at: ; -

Digitizing institution:

Mossakowski Medical Research Institute PAS

Original in:

Library of the Mossakowski Medical Research Institute PAS

Projects co-financed by:

Operational Program Digital Poland, 2014-2020, Measure 2.3: Digital accessibility and usefulness of public sector information; funds from the European Regional Development Fund and national co-financing from the state budget.

Access:

Open

Subject and keywords:

Myopathy

Object collections:

• Digital Repository of Scientific Institutes > Partners' collections > Mossakowski Medical Research Institute PAS > Research data > File of neuromuscular diseases of Prof. A. Fidziańska-Dolot
• Digital Repository of Scientific Institutes > Scientific data and objects > Medical science > File of medical cases

Last modified:

Feb 1, 2022

In our library since:

May 12, 2020

Number of object content downloads / hits:

55

All available object's versions:

https://rcin.org.pl./publication/112028

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OAI-PMH

• Fidziańska-Dolot, Anna (1930-2015), Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych Prof. dr hab. Anny Fidziańskiej-Dolot (1993-2014)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (1993)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (1994)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2002)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2003)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2004)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2005)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2006)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2007)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2008)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2009)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2010)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2011)
    • opis nr 1/11-1
    • opis nr 1/11-2
    • opis nr 2/11
    • opis nr 3/11
    • opis nr 4/11
    • opis nr 4/11-2
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    • opis nr 6/11
    • opis nr 7/11
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    • opis nr 8/11-2
    • opis nr 9/11
    • opis nr 10/11
    • opis nr 11/11
    • opis nr 12/11
    • opis nr 13/11
    • opis nr 14/11
    • opis nr 15/11
    • opis nr 16/11
    • opis nr 17/11
    • opis nr 18/11
    • opis nr 20/11
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    • opis nr 37/11
    • opis nr 38/11
    • opis nr 39/11
    • opis nr 40/11
    • opis nr 41/11
    • opis nr 123/11
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2012)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2013)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (2014)
  • Kartoteka przypadków klinicznych chorób nerwowo-mięśniowych (CZD)

Edition name	Date
opis nr 18/11	Feb 1, 2022

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