Citations - Naso Maurizio

Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused by a heterozygous loss of function variant in the NF1 gene, which encodes a protein called neurofibromin. The absence of neurofibromin causes increased activity in the Rat sarcoma protein (RAS) signalling pathway, which results in an increased... Read more
Published on: 2020-07-02
Source: Naso Maurizio
By: Thomas Foiadelli
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused by a heterozygous loss of function variant in the NF1 gene, which encodes a protein called neurofibromin. The absence of neurofibromin causes increased activity in the Rat sarcoma protein (RAS) signalling pathway, which results in an increased... Read more
Published on: 2020-07-02
Source: Naso Maurizio
By: Thomas Foiadelli
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused by a heterozygous loss of function variant in the NF1 gene, which encodes a protein called neurofibromin. The absence of neurofibromin causes increased activity in the Rat sarcoma protein (RAS) signalling pathway, which results in an increased... Read more
Published on: 2020-07-02
Source: Naso Maurizio
By: Thomas Foiadelli
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused by a heterozygous loss of function variant in the NF1 gene, which encodes a protein called neurofibromin. The absence of neurofibromin causes increased activity in the Rat sarcoma protein (RAS) signalling pathway, which results in an increased... Read more
Published on: 2020-07-02
Source: Naso Maurizio
By: Thomas Foiadelli
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused by a heterozygous loss of function variant in the NF1 gene, which encodes a protein called neurofibromin. The absence of neurofibromin causes increased activity in the Rat sarcoma protein (RAS) signalling pathway, which results in an increased... Read more
Published on: 2020-07-02
Source: Naso Maurizio
By: Thomas Foiadelli
Neurofibromatosis Type 1 (NF1) is an autosomal dominant tumor-predisposition disorder that is caused by a heterozygous loss of function variant in the NF1 gene, which encodes a protein called neurofibromin. The absence of neurofibromin causes increased activity in the Rat sarcoma protein (RAS) signalling pathway, which results in an increased... Read more
Published on: 2020-07-02
Source: Naso Maurizio
By: Thomas Foiadelli
CONCLUSION: The tested formulation seems to be effective and also free of side effects.... Read more
Published on: 2020-05-06
Source: Naso Maurizio
By: Mariangela Rondanelli
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