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Interceptive use of pendulum for advance resolution of class II patient: a guided eruption plan to reduce stress on permanent teeth root
Interceptive use of pendulum for advance resolution of class II patient: a guided eruption plan to reduce stress on permanent teeth root
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Interceptive use of pendulum for advance resolution of class II patient: a guided eruption plan to reduce stress on permanent teeth root

Favero, V ; Zanotti, G ; Franchi, L ; Zago, G ; Zarantonello, M ; Winkler, A ; Sivolella, S ; De Santis, D ; Favero, L

Journal of biological regulators and homeostatic agents, 2020-11, Vol.34 (6 Suppl. 2), p.21-36 [Periódico revisado por pares]

Italy

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2
Communication through telemedicine: home teleassistance in orthodontics
Communication through telemedicine: home teleassistance in orthodontics
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Communication through telemedicine: home teleassistance in orthodontics

Favero, L ; Pavan, L ; Arreghini, A

European journal of paediatric dentistry, 2009-12, Vol.10 (4), p.163-167 [Periódico revisado por pares]

Italy

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3
Resurgence of pertussis at the age of vaccination: clinical, epidemiological, and molecular aspects
Resurgence of pertussis at the age of vaccination: clinical, epidemiological, and molecular aspects
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Resurgence of pertussis at the age of vaccination: clinical, epidemiological, and molecular aspects

Torres, Rosângela S.L.A. ; Santos, Talita Z. ; Torres, Robson A.A. ; Pereira, Valéria V.G. ; Fávero, Lucas A.F. ; Filho, Otavio R.M. ; Penkal, Margareth L. ; Araujo, Leni S.

Jornal de pediatria, 2015-07, Vol.91 (4), p.333-338 [Periódico revisado por pares]

Brazil: Elsevier Editora Ltda

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4
Reduced blood pressure in sickle cell disease is associated with decreased angiotensin converting enzyme (ACE) activity and is not modulated by ACE inhibition
Reduced blood pressure in sickle cell disease is associated with decreased angiotensin converting enzyme (ACE) activity and is not modulated by ACE inhibition
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Reduced blood pressure in sickle cell disease is associated with decreased angiotensin converting enzyme (ACE) activity and is not modulated by ACE inhibition

Brito, Pamela L ; Dos Santos, Alisson F ; Chweih, Hanan ; Favero, Maria E ; Gotardo, Erica M F ; Silva, Juliete A F ; Leonardo, Flavia C ; Franco-Penteado, Carla F ; de Oliveira, Mariana G ; Ferreira, Jr, Wilson A ; Zaidan, Bruna C ; Billis, Athanase ; Baldanzi, Giorgio ; Mashima, Denise A ; Antunes, Edson ; Saad, Sara T Olalla ; Costa, Fernando F ; Conran, Nicola Connes, Philippe

PloS one, 2022-02, Vol.17 (2), p.e0263424-e0263424 [Periódico revisado por pares]

United States: Public Library of Science

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5
Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
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Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome

Delvaeye, Mieke ; Noris, Marina ; De Vriese, Astrid ; Esmon, Charles T ; Esmon, Naomi L ; Ferrell, Gary ; Del-Favero, Jurgen ; Plaisance, Stephane ; Claes, Bart ; Lambrechts, Diether ; Zoja, Carla ; Remuzzi, Giuseppe ; Conway, Edward M

The New England journal of medicine, 2009-07, Vol.361 (4), p.345-357 [Periódico revisado por pares]

Waltham, MA: Massachusetts Medical Society

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6
Levofloxacin to Prevent Bacterial Infection in Patients with Cancer and Neutropenia
Levofloxacin to Prevent Bacterial Infection in Patients with Cancer and Neutropenia
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Levofloxacin to Prevent Bacterial Infection in Patients with Cancer and Neutropenia

Bucaneve, Giampaolo ; Micozzi, Alessandra ; Menichetti, Francesco ; Martino, Pietro ; Dionisi, M. Stella ; Martinelli, Giovanni ; Allione, Bernardino ; D'Antonio, Domenico ; Buelli, Maurizio ; Nosari, A. Maria ; Cilloni, Daniela ; Zuffa, Eliana ; Cantaffa, Renato ; Specchia, Giorgina ; Amadori, Sergio ; Fabbiano, Francesco ; Deliliers, Giorgio Lambertenghi ; Lauria, Francesco ; Foà, Robin ; Del Favero, Albano

The New England journal of medicine, 2005-09, Vol.353 (10), p.977-987 [Periódico revisado por pares]

Boston, MA: Massachusetts Medical Society

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7
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
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Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1

Suls, Arvid ; Dedeken, Peter ; Goffin, Karolien ; Van Esch, Hilde ; Dupont, Patrick ; Cassiman, David ; Kempfle, Judith ; Wuttke, Thomas V. ; Weber, Yvonne ; Lerche, Holger ; Afawi, Zaid ; Vandenberghe, Wim ; Korczyn, Amos D. ; Berkovic, Samuel F. ; Ekstein, Dana ; Kivity, Sara ; Ryvlin, Philippe ; Claes, Lieve R. F. ; Deprez, Liesbet ; Maljevic, Snezana ; Vargas, Alberto ; Van Dyck, Tine ; Goossens, Dirk ; Del-Favero, Jurgen ; Van Laere, Koen ; De Jonghe, Peter ; Van Paesschen, Wim

Brain (London, England : 1878), 2008-07, Vol.131 (7), p.1831-1844 [Periódico revisado por pares]

England: Oxford University Press

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8
Mutations in SACS cause atypical and late-onset forms of ARSACS
Mutations in SACS cause atypical and late-onset forms of ARSACS
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Mutations in SACS cause atypical and late-onset forms of ARSACS

BAETS, J ; DECONINCK, T ; ROBBERECHT, W ; DE MEIRLEIR, L ; MICHIELSENS, B ; DEL-FAVERO, J ; JORDANOVA, A ; DE JONGHE, P ; SMETS, K ; GOOSSENS, D ; VAN DEN BERGH, P ; DAHAN, K ; SCHMEDDING, E ; SANTENS, P ; MILIC RASIC, V ; VAN DAMME, P

Neurology, 2010-09, Vol.75 (13), p.1181-1188 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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9
Mucormycosis in hematologic patients
Mucormycosis in hematologic patients
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Mucormycosis in hematologic patients

Pagano, L ; Offidani, M ; Fianchi, L ; Nosari, A ; Candoni, A ; Piccardi, M ; Corvatta, L ; D'Antonio, D ; Girmenia, C ; Martino, P ; Del Favero, A ; GIMEMA (Gruppo Italiano Malattie EMatologiche dell'Adulto) Infection Program

Haematologica (Roma), 2004-02, Vol.89 (2), p.207-214 [Periódico revisado por pares]

Pavia: Haematologica

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10
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy
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De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

Claes, Lieve ; Ceulemans, Berten ; Audenaert, Dominique ; Smets, Katrien ; Löfgren, Ann ; Del-Favero, Jurgen ; Ala-Mello, Sirpa ; Basel-Vanagaite, Lina ; Plecko, Barbara ; Raskin, Salmo ; Thiry, Paul ; Wolf, Nicole I. ; Van Broeckhoven, Christine ; De Jonghe, Peter

Human mutation, 2003-06, Vol.21 (6), p.615-621 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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