MAGLI, ADRIANO
MAGLI, ADRIANO
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
2003 YAMADA K. ANDREWS C. CHAN WM MCKEOWN CA DE BERARDINIS T., Loewenstein; Magli, Adriano; Engle, Ec
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
2010 Tischfield, Ma; Baris, Hn; Wu, C; Rudolph, G; Van Maldergem, L; He, W; Chan, Wm; Andrews, C; Demer, Jl; Robertson, Rl; Mackey, Da; Ruddle, Jb; Bird, Td; Gottlob, I; Pieh, C; Traboulsi, Ei; Pomeroy, Sl; Hunter, Dg; Soul, Js; Newlin, A; Sabol, Lj; Doherty, Ej; de Uzcátegui, Ce; de Uzcátegui, N; Collins, Ml; Sener, Ec; Wabbels, B; Hellebrand, H; Meitinger, T; DE BERARDINIS, Teresa; Magli, Adriano; Schiavi, C; Pastore Trossello, M; Koc, F; Wong, Am; Levin, Av; Geraghty, Mt; Descartes, M; Flaherty, M; Jamieson, Rv; Møller, Hu; Meuthen, I; Callen, Df; Kerwin, J; Lindsay, S; Meindl, A; Gupta ML, Jr; Pellman, D; Engle, E. C.
Clinical and surgical data of affected members of a classic CFEOM 1 family.
2003 Magli, Adriano; DE BERARDINIS, Teresa; D'Esposito, F; Gagliardi, V.
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX.
2002 ENGLE EC MCINTOSH N. YAMADA K. LEE BA JOHNSON R. O'KEEFE M. LETSON R., LONDON A; Magli, Adriano; DE BERARDINIS, Teresa
Clinical and surgical data of affected members of a classic CFEOM 1 family.
2003 Magli, Adriano; DE BERARDINIS, Teresa; D'Esposito, F; Gagliardi, V.
Congenital fibrosis of the extraocular muscles type 1 (CFEOM1), additional CFEOM1 families, and a reduction of the critical region on chromosome 12.
2000 Engle, E. C.; Mcintosh, N.; Lee, B. A.; Jhonson, R; O'Keefe, M.; Letson, R.; Krawiecki, N.; Shoffner, J; Ruttum, M; Sabol, Lj; Magli, Adriano; DE BERARDINIS, Teresa
Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly.
2008 Ginocchio, V. M.; DE BRASI, D.; Genesio, R.; Ciccone, R.; Gimelli, S.; Fimiani, F.; DE BERARDINIS, Teresa; Nitsch, Lucio; Banfi, S.; Magli, Adriano; DELLA CASA, Roberto
Oftalmoplegie familiari ad insorgenza precoce e tardiva.
1999 Magli, Adriano; DE BERARDINIS, Teresa; Gagliardi, V.
Ophthalmic assessment of children at risk for congenital toxoplasmosis: follow-up and clinical experience.
2009 Magli, Adriano; Vassallo, P.; Rombetto, L.; Matarazzo, F.; Di Meglio, M.; R. C. A. R. E. L. L. I.,
SIOP
2009 Magli, Adriano
Hydrocephalus combined with congenital cataract and microphthalmia.
1979 Cennamo, Giovanni; Gangemi, Michelangelo; Magli, Adriano
LASIK and PRK in refractive accommodative esotropia: a retrospective study on 20 adolescent and adult patients.
2009 Magli, Adriano; Iovine, A.; Gagliardi, V.; Fimiani, F.; Nucci, P.
Simultaneous surgery in bilateral congenital cataract.
2009 Magli, Adriano; Fimiani, F.; Passaro, V.; Iovine, A.
Treatment of blepharospasm with botulinum neurotoxin type A: long term results
2003 P., Calace; G., Cortese; R., Piscopo; G., Della Volpe; V., Gagliardi; Magli, Adriano; De Berardinis, Teresa
Oftalmoplegia congenita esterna:conferma della presenza di un locus genetico sul cromosoma 12.
1992 D'Esposito, F.; Magli, Adriano; DE BERARDINIS, Teresa; Bhattacharya, S. S.
Clinical and genetic data of two (classic) CFEOM1 families and one atypical CFEOM family.
2003 DE BERARDINIS, Teresa; V., Gagliardi; C., Andrews; E. C., Engle; Magli, Adriano
VIII Congresso S.I.C.S.S.O. international scientific meeting
2009 Magli, Adriano
Pazienti affetti da cataratta bilaterale:valutazione e follow-up dopo estrazione primaria ed impianto.
2009 Magli, Adriano
VIII Congresso S.I.C.S.S.O. international scientific meeting
2009 Magli, Adriano
Le Varietà di strabismo sensibili al trattamento con tossina botulinica
1998 Calace, P.; Magli, Adriano; DE BERARDINIS, Teresa
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). | 1.1 Articolo in rivista | 2003 | YAMADA K. ANDREWS C. CHAN WM MCKEOWN CA DE BERARDINIS T., Loewenstein; Magli, Adriano; Engle, Ec | |
| Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. | 1.1 Articolo in rivista | 2010 | Tischfield, Ma; Baris, Hn; Wu, C; Rudolph, G; Van Maldergem, L; He, W; Chan, Wm; Andrews, C; Demer, Jl; Robertson, Rl; Mackey, Da; Ruddle, Jb; Bird, Td; Gottlob, I; Pieh, C; Traboulsi, Ei; Pomeroy, Sl; Hunter, Dg; Soul, Js; Newlin, A; Sabol, Lj; Doherty, Ej; de Uzcátegui, Ce; de Uzcátegui, N; Collins, Ml; Sener, Ec; Wabbels, B; Hellebrand, H; Meitinger, T; DE BERARDINIS, Teresa; Magli, Adriano; Schiavi, C; Pastore Trossello, M; Koc, F; Wong, Am; Levin, Av; Geraghty, Mt; Descartes, M; Flaherty, M; Jamieson, Rv; Møller, Hu; Meuthen, I; Callen, Df; Kerwin, J; Lindsay, S; Meindl, A; Gupta ML, Jr; Pellman, D; Engle, E. C. | |
| Clinical and surgical data of affected members of a classic CFEOM 1 family. | 1.1 Articolo in rivista | 2003 | Magli, Adriano; DE BERARDINIS, Teresa; D'Esposito, F; Gagliardi, V. | |
| CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX. | 1.1 Articolo in rivista | 2002 | ENGLE EC MCINTOSH N. YAMADA K. LEE BA JOHNSON R. O'KEEFE M. LETSON R., LONDON A; Magli, Adriano; DE BERARDINIS, Teresa | |
| Clinical and surgical data of affected members of a classic CFEOM 1 family. | 1.1 Articolo in rivista | 2003 | Magli, Adriano; DE BERARDINIS, Teresa; D'Esposito, F; Gagliardi, V. | |
| Congenital fibrosis of the extraocular muscles type 1 (CFEOM1), additional CFEOM1 families, and a reduction of the critical region on chromosome 12. | 5.14 Altro ministeriale | 2000 | Engle, E. C.; Mcintosh, N.; Lee, B. A.; Jhonson, R; O'Keefe, M.; Letson, R.; Krawiecki, N.; Shoffner, J; Ruttum, M; Sabol, Lj; Magli, Adriano; DE BERARDINIS, Teresa | |
| Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly. | 1.1 Articolo in rivista | 2008 | Ginocchio, V. M.; DE BRASI, D.; Genesio, R.; Ciccone, R.; Gimelli, S.; Fimiani, F.; DE BERARDINIS, Teresa; Nitsch, Lucio; Banfi, S.; Magli, Adriano; DELLA CASA, Roberto | |
| Oftalmoplegie familiari ad insorgenza precoce e tardiva. | 1.1 Articolo in rivista | 1999 | Magli, Adriano; DE BERARDINIS, Teresa; Gagliardi, V. | |
| Ophthalmic assessment of children at risk for congenital toxoplasmosis: follow-up and clinical experience. | 8.02 Comunicazioni a Convegni o Seminari | 2009 | Magli, Adriano; Vassallo, P.; Rombetto, L.; Matarazzo, F.; Di Meglio, M.; R. C. A. R. E. L. L. I., | |
| SIOP | 8.05 Partecip. Consigli Scientifici/Direttivi | 2009 | Magli, Adriano | |
| Hydrocephalus combined with congenital cataract and microphthalmia. | 1.1 Articolo in rivista | 1979 | Cennamo, Giovanni; Gangemi, Michelangelo; Magli, Adriano | |
| LASIK and PRK in refractive accommodative esotropia: a retrospective study on 20 adolescent and adult patients. | 1.1 Articolo in rivista | 2009 | Magli, Adriano; Iovine, A.; Gagliardi, V.; Fimiani, F.; Nucci, P. | |
| Simultaneous surgery in bilateral congenital cataract. | 1.1 Articolo in rivista | 2009 | Magli, Adriano; Fimiani, F.; Passaro, V.; Iovine, A. | |
| Treatment of blepharospasm with botulinum neurotoxin type A: long term results | 1.1 Articolo in rivista | 2003 | P., Calace; G., Cortese; R., Piscopo; G., Della Volpe; V., Gagliardi; Magli, Adriano; De Berardinis, Teresa | |
| Oftalmoplegia congenita esterna:conferma della presenza di un locus genetico sul cromosoma 12. | 4.1 Articoli in Atti di convegno | 1992 | D'Esposito, F.; Magli, Adriano; DE BERARDINIS, Teresa; Bhattacharya, S. S. | |
| Clinical and genetic data of two (classic) CFEOM1 families and one atypical CFEOM family. | 4.1 Articoli in Atti di convegno | 2003 | DE BERARDINIS, Teresa; V., Gagliardi; C., Andrews; E. C., Engle; Magli, Adriano | |
| VIII Congresso S.I.C.S.S.O. international scientific meeting | 8.02 Comunicazioni a Convegni o Seminari | 2009 | Magli, Adriano | |
| Pazienti affetti da cataratta bilaterale:valutazione e follow-up dopo estrazione primaria ed impianto. | 8.02 Comunicazioni a Convegni o Seminari | 2009 | Magli, Adriano | |
| VIII Congresso S.I.C.S.S.O. international scientific meeting | 8.01 Chairman di Sessioni di Convegni Internazionali | 2009 | Magli, Adriano | |
| Le Varietà di strabismo sensibili al trattamento con tossina botulinica | 1.1 Articolo in rivista | 1998 | Calace, P.; Magli, Adriano; DE BERARDINIS, Teresa |