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Items: 1 to 20 of 75

1.

Autosomal dominant "spheroid body myopathy".

Goebel HH, Muller J, Gillen HW, Merritt AD.

Muscle Nerve. 1978 Jan-Feb;1(1):14-26.

PMID:
571956
2.

Desmin pathology in neuromuscular diseases.

Goebel HH, Bornemann A.

Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;64(3):127-35. Review.

PMID:
8242173
3.

Spheroid-cytoplasmic complexes in a congenital myopathy.

Halbig L, Goebel HH, Hopf HC, Moll R.

Rev Neurol (Paris). 1991;147(4):300-7.

PMID:
1648255
4.

Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases.

Nakano S, Engel AG, Waclawik AJ, Emslie-Smith AM, Busis NA.

J Neuropathol Exp Neurol. 1996 May;55(5):549-62.

PMID:
8627346
5.

Autosomal dominant neuromuscular disease with cylindrical spirals.

Taratuto AL, Matteucci M, Barreiro C, Saccolitti M, Sevlever G.

Neuromuscul Disord. 1991;1(6):433-41.

PMID:
1822355
6.

Autosomal dominant hyaline body myopathy presenting as scapuloperoneal syndrome: clinical features and muscle pathology.

Masuzugawa S, Kuzuhara S, Narita Y, Naito Y, Taniguchi A, Ibi T.

Neurology. 1997 Jan;48(1):253-7.

PMID:
9008527
7.

[Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency].

Chapon F, Viader F, Fardeau M, Tomé F, Daluzeau N, Berthelin C, Thénint JP, Lechevalier B.

Rev Neurol (Paris). 1989;145(6-7):460-5. Review. French.

PMID:
2552561
8.

Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees.

Bethlem J, Wijngaarden GK.

Brain. 1976 Mar;99(1):91-100.

PMID:
963533
9.

Autosomal dominant hyaline body myopathy: clinical variability and pathologic findings.

Bohlega S, Lach B, Meyer BF, Al Said Y, Kambouris M, Al Homsi M, Cupler EJ.

Neurology. 2003 Dec 9;61(11):1519-23.

PMID:
14663035
10.

[Inclusion body myositis and neuromuscular diseases with rimmed vacuoles].

Figarella-Branger D, Pellissier JF, Pouget J, Calore EE, Azulay JP, Desnuelle C, Serratrice G.

Rev Neurol (Paris). 1992;148(4):281-90. Review. French.

PMID:
1332175
11.
12.

Mallory body-like inclusions in a hereditary congenital neuromuscular disease.

Fidzianska A, Goebel HH, Osborn M, Lenard HG, Osse G, Langenbeck U.

Muscle Nerve. 1983 Mar-Apr;6(3):195-200.

PMID:
6343859
13.

[Cytoplasmic inclusion bodies: a study in several diseases and a review of the literature].

Scola RH, Werneck LC, Franco CR.

Arq Neuropsiquiatr. 1996 Jun;54(2):245-59. Review. Portuguese.

PMID:
8984983
14.

Spheroid body myopathy revisited.

Goebel HH, D'Agostino AN, Wilson J, Cole G, Foroud T, Koller D, Farlow M, Azzarelli B, Muller J.

Muscle Nerve. 1997 Sep;20(9):1127-36.

PMID:
9270668
15.

A new familial congenital myopathy in children with desmin and dystrophin reacting plaques.

Fidziańska A, Ryniewicz B, Barcikowska M, Goebel HH.

J Neurol Sci. 1995 Jul;131(1):88-95.

PMID:
7561954
16.

Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.

Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C.

Brain. 2005 Jul;128(Pt 7):1716-27. Epub 2005 Apr 27.

PMID:
15857933
17.

Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free diet.

Askanas V, Engel WK, Kwan HH, Reddy NB, Husainy T, Carlo J, Siddique T, Schwartzman RJ, Hanna CJ.

Neurology. 1985 Jan;35(1):66-72.

PMID:
3966003
18.

Granular nuclear inclusion body disease: fine structure of tibial muscle and sural nerve.

Schröder JM, Krämer KG, Hopf HC.

Muscle Nerve. 1985 Jan;8(1):52-9.

PMID:
2997602
19.

Dominantly inherited cytoplasmic body myopathy in a Japanese kindred.

Abe K, Kobayashi K, Chida K, Kimura N, Kogure K.

Tohoku J Exp Med. 1993 Aug;170(4):261-72.

20.

[Infantile form of nemaline (rod inclusion) myopathy].

Berger W, Grisold W, Jellinger K.

Wien Klin Wochenschr. 1988 Jun 10;100(12):407-12. German.

PMID:
2841810

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