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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 20.201 a 20.220 di 46.912

L'abitare informale: l'esperienza del Premio Ance-In/Arch

2011-01-01 Andriani, Carmela

Sulla nozione di Patrimonio

2011-01-01 Andriani, Carmela

Progettare … Libera! Workshop internazionale per il recupero sostenibile ed eticamente responsabile di due immobili sequestrati alle Mafie, Scurcola Marsicana

2013-01-01 Rovigatti, Pietro

Due edifici pubblici in Olanda. Istituto di ricerca a Wageningen Centro sportivo a Eindhoven

2013-01-01 Bilo', Federico

Progetto Corinto

2013-01-01 Zazzara, Lucio

No-Waste

2013-01-01 Pavia, Rosario

Zingiberene attenuates hydrogen peroxide-induced toxicity in neuronal cells

2015-01-01 Togar, B.; Turkez, Hasan; DI STEFANO, Antonio; Tatar, A; Cetin, D.

A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.

2013-01-01 Schanze, D; Harakalova, M; Stevens, Ca; Brancati, Francesco; Dallapiccola, B; Farndon, P; Ferraz, Ve; McDonald McGinn, Dm; Zackai, Eh; Wright, M; van Lieshout, S; Vogel, Mj; van Haelst, Mm; Zenker, M.

Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa.

2013-01-01 Dimopoulou, A; Fischer, B; Gardeitchik, T; Schröter, P; Kayserili, H; Schlack, C; Li, Y; Brum, Jm; Barisic, I; Castori, M; Spaich, C; Fletcher, E; Mahayri, Z; Bhat, M; Girisha, Km; Lachlan, K; Johnson, D; Phadke, S; Gupta, N; Simandlova, M; Kabra, M; David, A; Nijtmans, L; Chitayat, D; Tuysuz, B; Brancati, Francesco; Mundlos, S; Van Maldergem, L; Morava, E; Wollnik, B; Kornak, U.

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases.

2014-01-01 Fallerini, C; Dosa, L; Tita, R; Del Prete, D; Feriozzi, S; Gai, G; Clementi, M; La Manna, A; Miglietti, N; Mancini, R; Mandrile, G; Ghiggeri, Gm; Piaggio, G; Brancati, Francesco; Diano, L; Frate, E; Pinciaroli, Ar; Giani, M; Castorina, P; Bresin, E; Giachino, D; De Marchi, M; Mari, F; Bruttini, M; Renieri, A; Ariani, F.

The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP.

2013-01-01 Nikkel, Sm; Dauber, A; de Munnik, S; Connolly, M; Hood, Rl; Caluseriu, O; Hurst, J; Kini, U; Nowaczyk, Mj; Afenjar, A; Albrecht, B; Allanson, Je; Balestri, P; Ben Omran, T; Brancati, Francesco; Cordeiro, I; da Cunha, Bs; Delaney, La; Destrée, A; Fitzpatrick, D; Forzano, F; Ghali, N; Gillies, G; Harwood, K; Hendriks, Ym; Héron, D; Hoischen, A; Honey, Em; Hoefsloot, Lh; Ibrahim, J; Jacob, Cm; Kant, Sg; Kim, Ca; Kirk, Ep; Knoers, Nv; Lacombe, D; Lee, C; Lo, If; Lucas, Ls; Mari, F; Mericq, V; Moilanen, Js; Møller, St; Moortgat, S; Pilz, Dt; Pope, K; Price, S; Renieri, A; Sá, J; Schoots, J; Silveira, El; Simon, Me; Slavotinek, A; Temple, Ik; van der Burgt, I; de Vries, Bb; Weisfeld Adams, Jd; Whiteford, Ml; Wierczorek, D; Wit, Jm; Yee, Cf; Beaulieu, Cl; FORGE Canada, Consortium; White, Sm; Bulman, De; Bongers, E; Brunner, H; Feingold, M; Boycott, Km

The syndrome of deafness-dystonia: clinical and genetic heterogeneity.

2013-01-01 Kojovic, M; Pareés, I; Lampreia, T; Pienczk Reclawowicz, K; Xiromerisiou, G; Rubio Agusti, I; Kramberger, M; Carecchio, M; Alazami, Am; Brancati, Francesco; Slawek, J; Pirtosek, Z; Valente, Em; Alkuraya, Fs; Edwards, Mj; Bhatia, K. P.

Nectinopathies: an emerging group of ectodermal dysplasia syndromes.

2013-01-01 Brancati, Francesco; Agolini, E; Fortugno, P.

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders.

2013-01-01 Travaglini L, 1. 3.; Brancati, Francesco; Silhavy, J; Iannicelli, M; Nickerson, E; Elkhartoufi, N; Scott, E; Spencer, E; Gabriel, S; Thomas, S; Ben Zeev, B; Bertini, E; Boltshauser, E; Chaouch, M; Roberta Cilio, M; de Jong, Mm; Kayserili, H; Ogur, G; Poretti, A; Signorini, S; Uziel, G; Zaki, Ms; International JSRD Study, Group; Johnson, C; Attié Bitach, T; Gleeson, Jg; Valente, E. M.

Impact of IL-33 on PGD2 generation by activated human cord blood-derived mast cell: Lack of effect on tryptase release

2013-01-01 Nicoletti, Mauro; Maccauro, G; Tripodi, Domenico; Saggini, A; Potalivo, G; Castellani, Maria Luisa; Conti, Fiorella; Rosati, M; Toniato, Elena; Caraffa, A; Antinolfi, P; Conti, Pio; Theoharides, T. C.

Anti-hemorragic agents in oral and dental practice: an update

2013-01-01 Scarano, A; Murmura, G; di Cerbo, A; Palmieri, B; Pinchi, V; Mavriqi, L; Varvara, G.

Reciprocal cross-talk between Prostaglandin E2 and bone in prostate cancer: a current review.

2011-01-01 S. D., Francesco; P., Castellan; R., Manco; Tenaglia, Raffaele

[Trans-scrotal penile degloving, a new procedure for corporoplasties].

2012-01-01 E., Austoni; V. M., Altieri; Tenaglia, Raffaele

Recurrence and progression in non-muscle-invasive bladder cancer using EORTC risk tables.

2012-01-01 V. M., Altieri; R., Castellucci; P., Palumbo; Verratti, Vittore; M., Sut; R., Olivieri; R., Manco; S., Ricciardulli; M., Nicolai; P., Criniti; Tenaglia, Raffaele

[Bone metabolism, renal function and immune structure in prostate cancer. Our experience].

2013-01-01 S. D., Francesco; Tenaglia, Raffaele

Titolo	Data di pubblicazione	Autore(i)
L'abitare informale: l'esperienza del Premio Ance-In/Arch	2011	Andriani, Carmela
Sulla nozione di Patrimonio	2011	Andriani, Carmela
Progettare … Libera! Workshop internazionale per il recupero sostenibile ed eticamente responsabile di due immobili sequestrati alle Mafie, Scurcola Marsicana	2013	Rovigatti, Pietro
Due edifici pubblici in Olanda. Istituto di ricerca a Wageningen Centro sportivo a Eindhoven	2013	Bilo', Federico
Progetto Corinto	2013	Zazzara, Lucio
No-Waste	2013	Pavia, Rosario
Zingiberene attenuates hydrogen peroxide-induced toxicity in neuronal cells	2015	Togar, B.; Turkez, Hasan; DI STEFANO, Antonio; Tatar, A; Cetin, D.
A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.	2013	Schanze, D; Harakalova, M; Stevens, Ca; Brancati, Francesco; Dallapiccola, B; Farndon, P; Ferraz, Ve; McDonald McGinn, Dm; Zackai, Eh; Wright, M; van Lieshout, S; Vogel, Mj; van Haelst, Mm; Zenker, M.
Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa.	2013	Dimopoulou, A; Fischer, B; Gardeitchik, T; Schröter, P; Kayserili, H; Schlack, C; Li, Y; Brum, Jm; Barisic, I; Castori, M; Spaich, C; Fletcher, E; Mahayri, Z; Bhat, M; Girisha, Km; Lachlan, K; Johnson, D; Phadke, S; Gupta, N; Simandlova, M; Kabra, M; David, A; Nijtmans, L; Chitayat, D; Tuysuz, B; Brancati, Francesco; Mundlos, S; Van Maldergem, L; Morava, E; Wollnik, B; Kornak, U.
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases.	2014	Fallerini, C; Dosa, L; Tita, R; Del Prete, D; Feriozzi, S; Gai, G; Clementi, M; La Manna, A; Miglietti, N; Mancini, R; Mandrile, G; Ghiggeri, Gm; Piaggio, G; Brancati, Francesco; Diano, L; Frate, E; Pinciaroli, Ar; Giani, M; Castorina, P; Bresin, E; Giachino, D; De Marchi, M; Mari, F; Bruttini, M; Renieri, A; Ariani, F.
The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP.	2013	Nikkel, Sm; Dauber, A; de Munnik, S; Connolly, M; Hood, Rl; Caluseriu, O; Hurst, J; Kini, U; Nowaczyk, Mj; Afenjar, A; Albrecht, B; Allanson, Je; Balestri, P; Ben Omran, T; Brancati, Francesco; Cordeiro, I; da Cunha, Bs; Delaney, La; Destrée, A; Fitzpatrick, D; Forzano, F; Ghali, N; Gillies, G; Harwood, K; Hendriks, Ym; Héron, D; Hoischen, A; Honey, Em; Hoefsloot, Lh; Ibrahim, J; Jacob, Cm; Kant, Sg; Kim, Ca; Kirk, Ep; Knoers, Nv; Lacombe, D; Lee, C; Lo, If; Lucas, Ls; Mari, F; Mericq, V; Moilanen, Js; Møller, St; Moortgat, S; Pilz, Dt; Pope, K; Price, S; Renieri, A; Sá, J; Schoots, J; Silveira, El; Simon, Me; Slavotinek, A; Temple, Ik; van der Burgt, I; de Vries, Bb; Weisfeld Adams, Jd; Whiteford, Ml; Wierczorek, D; Wit, Jm; Yee, Cf; Beaulieu, Cl; FORGE Canada, Consortium; White, Sm; Bulman, De; Bongers, E; Brunner, H; Feingold, M; Boycott, Km
The syndrome of deafness-dystonia: clinical and genetic heterogeneity.	2013	Kojovic, M; Pareés, I; Lampreia, T; Pienczk Reclawowicz, K; Xiromerisiou, G; Rubio Agusti, I; Kramberger, M; Carecchio, M; Alazami, Am; Brancati, Francesco; Slawek, J; Pirtosek, Z; Valente, Em; Alkuraya, Fs; Edwards, Mj; Bhatia, K. P.
Nectinopathies: an emerging group of ectodermal dysplasia syndromes.	2013	Brancati, Francesco; Agolini, E; Fortugno, P.
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders.	2013	Travaglini L, 1. 3.; Brancati, Francesco; Silhavy, J; Iannicelli, M; Nickerson, E; Elkhartoufi, N; Scott, E; Spencer, E; Gabriel, S; Thomas, S; Ben Zeev, B; Bertini, E; Boltshauser, E; Chaouch, M; Roberta Cilio, M; de Jong, Mm; Kayserili, H; Ogur, G; Poretti, A; Signorini, S; Uziel, G; Zaki, Ms; International JSRD Study, Group; Johnson, C; Attié Bitach, T; Gleeson, Jg; Valente, E. M.
Impact of IL-33 on PGD2 generation by activated human cord blood-derived mast cell: Lack of effect on tryptase release	2013	Nicoletti, Mauro; Maccauro, G; Tripodi, Domenico; Saggini, A; Potalivo, G; Castellani, Maria Luisa; Conti, Fiorella; Rosati, M; Toniato, Elena; Caraffa, A; Antinolfi, P; Conti, Pio; Theoharides, T. C.
Anti-hemorragic agents in oral and dental practice: an update	2013	Scarano, A; Murmura, G; di Cerbo, A; Palmieri, B; Pinchi, V; Mavriqi, L; Varvara, G.
Reciprocal cross-talk between Prostaglandin E2 and bone in prostate cancer: a current review.	2011	S. D., Francesco; P., Castellan; R., Manco; Tenaglia, Raffaele
[Trans-scrotal penile degloving, a new procedure for corporoplasties].	2012	E., Austoni; V. M., Altieri; Tenaglia, Raffaele
Recurrence and progression in non-muscle-invasive bladder cancer using EORTC risk tables.	2012	V. M., Altieri; R., Castellucci; P., Palumbo; Verratti, Vittore; M., Sut; R., Olivieri; R., Manco; S., Ricciardulli; M., Nicolai; P., Criniti; Tenaglia, Raffaele
[Bone metabolism, renal function and immune structure in prostate cancer. Our experience].	2013	S. D., Francesco; Tenaglia, Raffaele

Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 20.201 a 20.220 di 46.912

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