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PubPharm (127)
31
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
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32
1993-2014 : two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa
enthalten in:
Molecular genetics & genomic medicine
| 2017
von
Mandich, P.
|
Lamp, M.
|
Gotta, F.
| +6
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33
Two novel cases of compound heterozygous mutations in mitofusin2 : Finding out the inheritance
enthalten in:
Neuromuscular disorders : NMD
| 2017
von
Geroldi, A.
|
Lastella, P.
|
Patruno, M.
| +9
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34
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance
enthalten in:
Neuromuscular disorders
| 2017
von
Geroldi, A.
|
Lastella, P.
|
Patruno, M.
| +9
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35
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
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36
Alternative Splicing in the Human PMP22 Gene : Implications in CMT1A Neuropathy
enthalten in:
Human mutation
| 2016
von
Visigalli, D.
|
Castagnola, P.
|
Capodivento, G.
| +6
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37
Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy
enthalten in:
Human mutation
| 2016
von
Visigalli, D.
|
Castagnola, P.
|
Capodivento, G.
| +6
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38
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
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39
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
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40
Innovative quantitative testing of hand function in Charcot-Marie-Tooth neuropathy
enthalten in:
Journal of the peripheral nervous system : JPNS
| 2015
von
Alberti, M.
|
Mori, L.
|
Francini, L.
| +12
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neuropathy
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DNA-Binding Proteins
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HSP27 Heat-Shock Proteins
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Myelin P0 Protein
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