Literature DB >> 4910660

Type I muscle fibre atrophy and central nuclei. A rare familial neuromuscular disease.

G Karpati, S Carpenter, R F Nelson.   

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Year:  1970        PMID： 4910660     DOI： 10.1016/0022-510x(70)90027-4

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


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  13 in total

1.  A case of type 1 muscle fibre hypotrophy and internal nuclei.

Authors:  T Inokuchi; H Umezaki; T Santa
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-05       Impact factor: 10.154

2.  Centronuclear myopathy.

Authors:  P L Bill; G Cole; N S Proctor
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-06       Impact factor: 10.154

3.  A case of centronuclear myopathy.

Authors:  I Lolova; T Bojinova; N Kilimov; A Gerchev
Journal:  Z Neurol       Date:  1973-08-29

4.  Hypotrophy of type I fibres with central nuclei: recovery 4 years after diagnosis.

Authors:  J R Ricoy; A Cabello
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-02       Impact factor: 10.154

5.  Teaching monograph: pathology of skeletal muscle diseases.

Authors:  U U DeGirolami; T W Smith
Journal:  Am J Pathol       Date:  1982-05       Impact factor: 4.307

6.  [Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

Authors:  W Mortier; E Michaelis; J Becker; L Gerhard
Journal:  Humangenetik       Date:  1975

7.  Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.

Authors:  H Sugie; R Hanson; G Rasmussen; M A Verity
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-06       Impact factor: 10.154

8.  Myotonia in centronuclear myopathy.

Authors:  A Gil-Peralta; E Rafel; J Bautista; R Alberca
Journal:  J Neurol Neurosurg Psychiatry       Date:  1978-12       Impact factor: 10.154

Review 9.  The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies.

Authors:  C Wallgren-Pettersson; A Clarke; F Samson; M Fardeau; V Dubowitz; H Moser; T Grimm; R J Barohn; P G Barth
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

10.  [Diagnostic value of muscle biopsy findings in myotonic dystrophy (Curschmann-Steinert) (author's transl)].

Authors:  D Pongratz; D Schultz; C Koppenwallner; G Hübner
Journal:  Klin Wochenschr       Date:  1979-03-01
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