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/vufind/Search/Results?lookfor=%22Bellone%2C+Emilia%22&type=Person&page=13
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PubPharm (127)
121
Three Novel Mutations in the Von Hippel-Lindau Tumour Suppressor Gene in Italian Parents
enthalten in:
Human mutation
| 1998
von
Mandich, P.
|
Montera, M.
|
Bellone, E.
| +3
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122
Correlation Between PMP-22 Messenger RNA Expression and Phenotype in Hereditary Neuropathy with Liability to Pressure Palsies
enthalten in:
Annals of neurology
| 1997
von
Schenone, A.
|
Nobbio, L.
|
Caponnetto, C.
| +7
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123
De Novo Duplication in Charcot-Marie-Tooth Type 1A
enthalten in:
American journal of human genetics
| 1996
von
Mandich, P.
|
Bellone, E.
|
Schenone, A.
| +3
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124
Identification of a 4 bp Deletion (1560del4) in Po Gene in a Family With Severe Charcot-Marie-Tooth Disease
enthalten in:
Human mutation
| 1996
von
Bellone, E.
|
Mandich, P.
|
James, R.
| +4
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125
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients
in:
Journal of neurology
| 1995
von
Mandich, P.
|
James, R.
|
Nassani, S.
| +8
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126
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients
enthalten in:
Journal of neurology
| 1995
von
Mandich, P.
|
James, R.
|
Nassani, S.
| +8
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127
Parental Origin of Chromosome 4p Deletion in Wolf-Hirschhorn Syndrome
enthalten in:
American journal of medical genetics
| 1993
von
Dallapiccola, B.
|
Mandich, P.
|
Bellone, E.
| +4
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Human mutation
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Journal of the peripheral nervous system : JPNS
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Amyotrophic lateral sclerosis : official public...
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European journal of medical genetics
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neuropathy
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DNA-Binding Proteins
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Proteins
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Transcription Factors
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CMT1A
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Charcot-Marie-Tooth disease
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Genetic counseling
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HSP27 Heat-Shock Proteins
4
HSPB1 protein, human
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Heat-Shock Proteins
4
Molecular Chaperones
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Myelin P0 Protein
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Myelin Proteins
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Nerve Tissue Proteins
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