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M P Manitto

Showing results (1-10 of 11) with videos related to

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Ophthalmic Genetics|September 1, 1994
Macular dysplasia and pigmented paravenous retino-choroidal atrophyP Nucci, M P Manitto, A Piantanida, et al.
Archivio Italiano Di Anatomia E Di Embriologia. Italian Journal of Anatomy and Embryology|January 1, 1991
[Neuron-specific enolase in ophthalmology]P Nucci, G Tredici, M P Manitto, et al.
European Journal of Ophthalmology|October 30, 1998
Ectopia lentis et pupillae with patchy depigmentation of the skin, hair and lashes: a new associationM P Manitto, R Brancato, N Lombardo, et al.
The International Journal of Biological Markers|October 1, 1992
Neuron-specific enolase and embryology of the trabecular meshwork of the rat eye: an immunohistochemical studyP Nucci, G Tredici, M P Manitto, et al.
Ophthalmic Genetics|September 1, 1994
Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defectP Nucci, M P Manitto, A Faiella, et al.
La Clinica Terapeutica|June 1, 1992
Ocular pharmacokinetics of rufloxacin a new fluoroquinolone antibioticP Nucci, N Lombardo, F Cremonesi, et al.
Ophthalmic Research|November 27, 2001
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian populationF Simonelli, M Margaglione, F Testa, et al.
The British Journal of Ophthalmology|June 16, 2006
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian populationF Simonelli, G Frisso, F Testa, et al.
Human Genetics|November 10, 2001
Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patientsA Fumagalli, M Ferrari, N Soriani, et al.
The British Journal of Ophthalmology|August 21, 2003
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian familiesF Simonelli, G Cennamo, C Ziviello, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Ophthalmic Genetics|September 1, 1994
Macular dysplasia and pigmented paravenous retino-choroidal atrophyP Nucci, M P Manitto, A Piantanida, et al.
Archivio Italiano Di Anatomia E Di Embriologia. Italian Journal of Anatomy and Embryology|January 1, 1991
[Neuron-specific enolase in ophthalmology]P Nucci, G Tredici, M P Manitto, et al.
European Journal of Ophthalmology|October 30, 1998
Ectopia lentis et pupillae with patchy depigmentation of the skin, hair and lashes: a new associationM P Manitto, R Brancato, N Lombardo, et al.
The International Journal of Biological Markers|October 1, 1992
Neuron-specific enolase and embryology of the trabecular meshwork of the rat eye: an immunohistochemical studyP Nucci, G Tredici, M P Manitto, et al.
Ophthalmic Genetics|September 1, 1994
Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defectP Nucci, M P Manitto, A Faiella, et al.
La Clinica Terapeutica|June 1, 1992
Ocular pharmacokinetics of rufloxacin a new fluoroquinolone antibioticP Nucci, N Lombardo, F Cremonesi, et al.
Ophthalmic Research|November 27, 2001
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian populationF Simonelli, M Margaglione, F Testa, et al.
The British Journal of Ophthalmology|June 16, 2006
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian populationF Simonelli, G Frisso, F Testa, et al.
Human Genetics|November 10, 2001
Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patientsA Fumagalli, M Ferrari, N Soriani, et al.
The British Journal of Ophthalmology|August 21, 2003
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian familiesF Simonelli, G Cennamo, C Ziviello, et al.
Pageof 2