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1118PD - Multiple Primary Melanomas from Same Patients Present Discrepant Somatic Alterations in Main Candidate Genes
1118PD - Multiple Primary Melanomas from Same Patients Present Discrepant Somatic Alterations in Main Candidate Genes
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1118PD - Multiple Primary Melanomas from Same Patients Present Discrepant Somatic Alterations in Main Candidate Genes

Colombino, M. ; Sini, M. ; De Giorgi, V. ; Lissia, A. ; Massi, D. ; Rubino, C. ; Cossu, A. ; Ayala, F. ; Ascierto, P.A. ; Palmieri, G.

Annals of oncology, 2012-09, Vol.23, p.ix364-ix364 [Periódico revisado por pares]

Elsevier Ltd

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2
1787–2005: Les débats constitutionnels, américain et européen, à la lumière de la pensée de Montesquieu. Convergences et divergences
1787–2005: Les débats constitutionnels, américain et européen, à la lumière de la pensée de Montesquieu. Convergences et divergences
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1787–2005: Les débats constitutionnels, américain et européen, à la lumière de la pensée de Montesquieu. Convergences et divergences

Guillaume Barrera Edgar Mass

Montesquieu zwischen den Disziplinen, 2010, p.247

Duncker & Humblot

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18 - Plasma-assisted techniques for growing hard nanostructured coatings: An overview
18 - Plasma-assisted techniques for growing hard nanostructured coatings: An overview
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18 - Plasma-assisted techniques for growing hard nanostructured coatings: An overview

Pessoa, R.S. ; Fraga, M.A. ; Santos, L.V. ; Galvão, N.K.A.M. ; Maciel, H.S. ; Massi, M.

Anti-Abrasive Nanocoatings, 2015, p.455-479

Elsevier Ltd

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4
[18F]Ethenesulfonyl Fluoride as a Practical Radiofluoride Relay Reagent
[18F]Ethenesulfonyl Fluoride as a Practical Radiofluoride Relay Reagent
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[18F]Ethenesulfonyl Fluoride as a Practical Radiofluoride Relay Reagent

Zhang, Bo ; Fraser, Benjamin H. ; Klenner, Mitchell A. ; Chen, Zhen ; Liang, Steven H. ; Massi, Massimiliano ; Robinson, Andrea J. ; Pascali, Giancarlo

Chemistry : a European journal, 2019-06, Vol.25 (32), p.7613-7617 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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5
2,7- and 4,9-Dialkynyldihydropyrene Molecular Switches: Syntheses, Properties, and Charge Transport in Single-Molecule Junctions
2,7- and 4,9-Dialkynyldihydropyrene Molecular Switches: Syntheses, Properties, and Charge Transport in Single-Molecule Junctions
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2,7- and 4,9-Dialkynyldihydropyrene Molecular Switches: Syntheses, Properties, and Charge Transport in Single-Molecule Junctions

Roemer, Max ; Gillespie, Angus ; Jago, David ; Costa-Milan, David ; Alqahtani, Jehan ; Hurtado-Gallego, Juan ; Sadeghi, Hatef ; Lambert, Colin J. ; Spackman, Peter R. ; Sobolev, Alexandre N. ; Skelton, Brian W. ; Grosjean, Arnaud ; Walkey, Mark ; Kampmann, Sven ; Vezzoli, Andrea ; Simpson, Peter V. ; Massi, Massimiliano ; Planje, Inco ; Rubio-Bollinger, Gabino ; Agraït, Nicolás ; Higgins, Simon J. ; Sangtarash, Sara ; Piggott, Matthew J. ; Nichols, Richard J. ; Koutsantonis, George A.

Journal of the American Chemical Society, 2022-07, Vol.144 (28), p.12698-12714 [Periódico revisado por pares]

United States: American Chemical Society

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6
A 10-Year-Old In Situ Melanoma?
A 10-Year-Old In Situ Melanoma?
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A 10-Year-Old In Situ Melanoma?

Carli, Paolo ; Massi, Daniela ; De Giorgi, Vincenzo ; Mannone, Francesca ; Giannotti, Benvenuto

Archives of dermatology (1960), 2002-07, Vol.138 (7), p.980-981

United States: American Medical Association

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7
A 10-Year-Old In Situ Melanoma?
A 10-Year-Old In Situ Melanoma?
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A 10-Year-Old In Situ Melanoma?

Carli, P.

Archives of dermatology (1960), 2002-07, Vol.138 (7), p.980-981

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8
A 10 year survey of acaricide residues in beeswax analysed in Italy
A 10 year survey of acaricide residues in beeswax analysed in Italy
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A 10 year survey of acaricide residues in beeswax analysed in Italy

Boi, Michela ; Serra, Giorgia ; Colombo, Roberto ; Lodesani, Marco ; Massi, Sergio ; Costa, Cecilia

Pest management science, 2016-07, Vol.72 (7), p.1366-1372 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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9
A (2-(naphthalen-2-yl)phenyl)rhodium() complex formed by a proposed intramolecular 1,4--to-′ Rh metal-atom migration and its efficacy as an initiator in the controlled stereospecific polymerisation of phenylacetylene
A (2-(naphthalen-2-yl)phenyl)rhodium() complex formed by a proposed intramolecular 1,4--to-′ Rh metal-atom migration and its efficacy as an initiator in the controlled stereospecific polymerisation of phenylacetylene
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A (2-(naphthalen-2-yl)phenyl)rhodium() complex formed by a proposed intramolecular 1,4--to-′ Rh metal-atom migration and its efficacy as an initiator in the controlled stereospecific polymerisation of phenylacetylene

Tan, Nicholas Sheng Loong ; Nealon, Gareth L ; Lynam, Jason M ; Sobolev, Alexandre N ; Rowles, Matthew R ; Ogden, Mark I ; Massi, Massimiliano ; Lowe, Andrew B

Dalton transactions : an international journal of inorganic chemistry, 2019-11, Vol.48 (43), p.16437-16447

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A (2-(naphthalen-2-yl)phenyl)rhodium( i ) complex formed by a proposed intramolecular 1,4- ortho -to- ortho ′ Rh metal-atom migration and its efficacy as an initiator in the controlled stereospecific polymerisation of phenylacetylene
A (2-(naphthalen-2-yl)phenyl)rhodium( i ) complex formed by a proposed intramolecular 1,4- ortho -to- ortho ′ Rh metal-atom migration and its efficacy as an initiator in the controlled stereospecific polymerisation of phenylacetylene
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A (2-(naphthalen-2-yl)phenyl)rhodium( i ) complex formed by a proposed intramolecular 1,4- ortho -to- ortho ′ Rh metal-atom migration and its efficacy as an initiator in the controlled stereospecific polymerisation of phenylacetylene

Tan, Nicholas Sheng Loong ; Nealon, Gareth L. ; Lynam, Jason M. ; Sobolev, Alexandre N. ; Rowles, Matthew R. ; Ogden, Mark I. ; Massi, Massimiliano ; Lowe, Andrew B.

Dalton transactions : an international journal of inorganic chemistry, 2019, Vol.48 (43), p.16437-16447 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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Deste Autor:

  1. Massi, A
  2. Massi, M
  3. Massi, L
  4. Maciel, H
  5. Mansano, R

Neste Assunto:

  1. Science & Technology
  2. Life Sciences & Biomedicine
  3. Humans
  4. Physical Sciences
  5. Male

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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