Detalhe da pesquisa
1.
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis.
J Neurol Neurosurg Psychiatry
; 86(8): 873-8, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25430934
2.
Strategy for genetic testing in Charcot-Marie-disease.
Acta Myol
; 30(2): 109-16, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22106713
3.
Immunoaffinity chromatography combined on-line with high-performance liquid chromatography-mass spectrometry for the determination of corticosteroids.
J Chromatogr A
; 794(1-2): 37-43, 1998 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-9491555
4.
MFN2 mutations cause severe phenotypes in most patients with CMT2A.
Neurology
; 76(20): 1690-6, 2011 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-21508331
5.
Effects of cell-free perfusion and almitrine bismesylate on the ultrastructure of type-I cell mitochondria in the cat carotid body.
Adv Exp Med Biol
; 337: 51-9, 1993.
Artigo
em Inglês
| MEDLINE | ID: mdl-8109433
6.
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
Neurology
; 72(3): 246-52, 2009 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-19153371