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Results: 1 to 20 of 119

Similar articles for PubMed (Select 23514382)

1.

Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis.

Sáez A, Rivas E, Montero-Sánchez A, Paradas C, Acha B, Pascual A, Serrano C, Escudero LM.

BMC Med. 2013 Mar 20;11:77. doi: 10.1186/1741-7015-11-77.

2.

Skeletal muscle CK-B activity in neurogenic muscular atrophies.

Vretou-Jockers E, Vassilopoulos D.

J Neurol. 1989 Jul;236(5):284-7.

PMID:
2760646
3.
4.

[Neurogenic muscular atrophy and selective fibre type atrophies : Groundbreaking findings in the biopsy diagnosis of neuromuscular disease].

Weis J, Nikolin S, Nolte K.

Pathologe. 2009 Sep;30(5):379-83. doi: 10.1007/s00292-009-1171-y. Review. German.

PMID:
19633853
5.

Neuromuscular disease classification system.

Sáez A, Acha B, Montero-Sánchez A, Rivas E, Escudero LM, Serrano C.

J Biomed Opt. 2013 Jun;18(6):066017. doi: 10.1117/1.JBO.18.6.066017.

PMID:
23804164
6.

Neurogenic muscle involvement in myasthenia gravis. A clinical and histopathological study.

Oosterhuis H, Bethlem J.

J Neurol Neurosurg Psychiatry. 1973 Apr;36(2):244-54.

7.

Possible neurogenic factor in muscular dystrophy: its similarity to denervation atrophy.

Dastur DK, Razzak ZA.

J Neurol Neurosurg Psychiatry. 1973 Jun;36(3):399-410.

8.

Congenital muscular dystrophy: correlation of muscle biopsy and clinical features.

Parano E, Fiumara A, Falsperla R, Vita G, Trifiletti RR.

Pediatr Neurol. 1994 May;10(3):233-6.

PMID:
8060426
9.

Ultrasound imaging in the diagnosis of muscle disease.

Heckmatt JZ, Leeman S, Dubowitz V.

J Pediatr. 1982 Nov;101(5):656-60.

PMID:
7131136
10.

Muscle imaging in neuromuscular disease using computerized real-time sonography.

Fischer AQ, Carpenter DW, Hartlage PL, Carroll JE, Stephens S.

Muscle Nerve. 1988 Mar;11(3):270-5.

PMID:
3280997
11.

Objective quantification of muscle and fat in human dystrophic muscle by magnetic resonance image analysis.

Phoenix J, Betal D, Roberts N, Helliwell TR, Edwards RH.

Muscle Nerve. 1996 Mar;19(3):302-10.

PMID:
8606693
12.

Neurogenic muscular atrophy simulating facioscapulohumeral muscular dystrophy with particular reference to the heterogeneity of Kugelberg-Welander disease.

Furukawa T, Tsukagoshi H, Sugita H, Toyokura Y.

J Neurol Sci. 1969 Sep-Oct;9(2):389-97. No abstract available.

PMID:
5345117
13.

Real-time ultrasonography in neuromuscular problems in children.

Kamala D, Suresh S, Githa K.

J Clin Ultrasound. 1985 Sep;13(7):465-8.

PMID:
3932477
14.

[The value of imaging procedures in myology].

Nägele M, Reimers CD, Fenzl G, Witt TN, Götz AE, Reimers K, Pongratz DE, Hahn D.

Bildgebung. 1987-1989;56(5):172-8. German.

PMID:
3078433
15.

Morphometric approaches to perifascicular atrophy in muscle biopsy: do they help to diagnose polymyositis?

Paljärvi L, Snäll EV.

Neuropathol Appl Neurobiol. 1984 Sep-Oct;10(5):333-41.

PMID:
6521843
16.
17.

[Facioscapulohumeral neuromuscular syndromes--problems of differential and early diagnosis and genetic counseling].

Bachmann H, Ziegan J, Steinbicker V, von Rohden L, Wagner A.

Psychiatr Neurol Med Psychol (Leipz). 1989 Oct;41(10):586-95. German.

PMID:
2608758
18.

Infantile progressive muscular atrophy; value of muscle biopsy in the diagnosis of and its differentiation from muscular dystrophy.

ROSENBERG HS, McADAMS AJ.

AMA Arch Pathol. 1954 Dec;58(6):604-12. No abstract available.

PMID:
13217576
19.

Immunohistochemical analysis of the distribution of MyoD1 in muscle biopsies of primary myopathies and neurogenic atrophy.

Parham DM, Dias P, Bertorini T, von Wronski MA, Horner L, Houghton P.

Acta Neuropathol. 1994;87(6):605-11.

PMID:
7522388
20.

Diagnostic protein expression in human muscle biopsies.

Bornemann A, Anderson LV.

Brain Pathol. 2000 Apr;10(2):193-214. Review.

PMID:
10764040
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