Suchergebnisse - "Bellone, Emilia"

PubPharm (4)

1

A CMT2 family carrying the P7R mutation in the N- terminal region of the HSPB1 gene

enthalten in: Clinical neurology and neurosurgery | 2017

von Fortunato, F. | Neri, M. | Geroldi, A. | +4

2

Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis : The Role of HSPB1

enthalten in: Human mutation | 2016

von Capponi, S. | Geuens, T. | Geroldi, A. | +12

3

HSPB1 and HSPB8 in inherited neuropathies : study of an Italian cohort of dHMN and CMT2 patients

enthalten in: Journal of the peripheral nervous system : JPNS | 2011

von Capponi, S. | Geroldi, A. | Fossa, P. | +6

4

Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 gene

enthalten in: Journal of child neurology | 2010

von Mandich, P. | Grandis, M. | Varese, A. | +10

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