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Nickel adsorption by variable charge soils: effect of pH and ionic strength

Brazilian archives of biology and technology, 2011-02, Vol.54 (1), p.207-220

2011

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Zinc adsorption in highly weathered soils

Pesquisa agropecuaria brasileira, 2008, Vol.43 (1), p.131-139

Casagrande, José Carlos(Universidade Federal de São Carlos Centro de Ciências Agrárias Departamento de Recursos Naturais e Proteção Ambiental)
Soares, Marcio Roberto(Universidade Federal de São Carlos Centro de Ciências Agrárias Departamento de Recursos Naturais e Proteção Ambiental)
Mouta, Ernesto Rinaldi(Universidade Federal de São Carlos Centro de Ciências Agrárias Departamento de Recursos Naturais e Proteção Ambiental)

2008

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Effect of Ionic Strength and pH on Cadmium Adsorption by Brazilian Variable-Charge Soils

Communications in soil science and plant analysis, 2009-01, Vol.40 (13-14), p.2132-2151

2009

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Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase

Human mutation, 2011-12, Vol.32 (12), p.1460-1469

2011

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Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains

Human mutation, 2001-08, Vol.18 (2), p.109-119

2001

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Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients

Investigative ophthalmology & visual science, 2007-09, Vol.48 (9), p.4284-4290

2007

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Genotype-Phenotype Correlation in Italian Families with Stargardt Disease

Ophthalmic research, 2005-05, Vol.37 (3), p.159-167

2005

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Zinc adsorption in highly weathered soils Adsorção de zinco em solos altamente intemperizados

Pesquisa agropecuaria brasileira, 2008-01, Vol.43 (1), p.131-139

2008

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New ABCR Mutations and Clinical Phenotype in Italian Patients with Stargardt Disease

Investigative ophthalmology & visual science, 2000-03, Vol.41 (3), p.892-897

2000

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Apolipoprotein E Polymorphisms in Age-Related Macular Degeneration in an Italian Population

Ophthalmic research, 2001-11, Vol.33 (6), p.325-328

2001

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Adsorção de selênio em latossolos Selenium adsorption in oxisols

Revista brasileira de ciência do solo, 2008-06, Vol.32 (3), p.1033-1041

2008

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Adsorção de selênio em latossolos

Revista brasileira de ciência do solo, 2008-06, Vol.32 (3), p.1033-1041

2008

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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Human mutation, 2001-08, Vol.18 (2), p.101-108

2001

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Association of a Homozygous Nonsense Mutation in the ABCA4 (ABCR) Gene with Cone-Rod Dystrophy Phenotype in an Italian Family

Ophthalmic research, 2004-03, Vol.36 (2), p.82-88

2004

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Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity

Clinical genetics, 1998-10, Vol.54 (4), p.315-320

1998

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Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

Biochemical and biophysical research communications, 2003-08, Vol.308 (3), p.414-421

2003

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Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

Gene, 2002-09, Vol.297 (1), p.33-38

2002

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Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa

European journal of human genetics : EJHG, 1999-09, Vol.7 (6), p.687-694

1999

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An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration

Journal of pediatric ophthalmology and strabismus, 2002-09, Vol.39 (5), p.288

2002

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Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa

British journal of ophthalmology, 1998-06, Vol.82 (6), p.709-709

1998

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ArF 193 nm Excimer Laser Corneal Surgery as a Possible Risk Factor in Cataractogenesis

Experimental eye research, 1994-04, Vol.58 (4), p.453-457

1994

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Evaluation of fatty acids in membrane phospholipids of erythrocytes in retinitis pigmentosa patients

Ophthalmic research, 1996-01, Vol.28 (2), p.93

1996

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Fatty acid composition of membrane phospholipids of cataractous human lenses

Ophthalmic research, 1996, Vol.28 Suppl 1, p.101

1996

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Effect of vitamin E on glutathione content in red blood cells, aqueous humor and lens of humans and other species

Experimental eye research, 1986-12, Vol.43 (6), p.905-914

1986

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Nickel adsorption by variable charge soils: effect of pH and ionic strength

Zinc adsorption in highly weathered soils

Effect of Ionic Strength and pH on Cadmium Adsorption by Brazilian Variable-Charge Soils

Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase

Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains

Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients

Genotype-Phenotype Correlation in Italian Families with Stargardt Disease

Zinc adsorption in highly weathered soils Adsorção de zinco em solos altamente intemperizados

New ABCR Mutations and Clinical Phenotype in Italian Patients with Stargardt Disease

Apolipoprotein E Polymorphisms in Age-Related Macular Degeneration in an Italian Population

Adsorção de selênio em latossolos Selenium adsorption in oxisols

Adsorção de selênio em latossolos

Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Association of a Homozygous Nonsense Mutation in the ABCA4 (ABCR) Gene with Cone-Rod Dystrophy Phenotype in an Italian Family

Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity

Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa

An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration

Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains: RP2 Mutations and Functional Domains

Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa

ArF 193 nm Excimer Laser Corneal Surgery as a Possible Risk Factor in Cataractogenesis

Evaluation of fatty acids in membrane phospholipids of erythrocytes in retinitis pigmentosa patients

Fatty acid composition of membrane phospholipids of cataractous human lenses

Effect of vitamin E on glutathione content in red blood cells, aqueous humor and lens of humans and other species

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