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Diagnosis and current management of retinoblastoma

Oncogene, 2006-08, Vol.25 (38), p.5341-5349

2006

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Effect of Fermented Cocoa Pod Husk Level in Concentrate on Etawah Grade Semen Quality

IOP conference series. Earth and environmental science, 2018-02, Vol.119 (1), p.12035

Munier, F.F.

2018

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Greenhouse Gas Emission (GHG) from ruminant on 2016 at Central Sulawesi Province

IOP conference series. Earth and environmental science, 2020-04, Vol.492 (1), p.12092

2020

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Retinoblastoma: From genes to patient care

European journal of medical genetics, 2023-01, Vol.66 (1), p.104674-104674, Article 104674

2023

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Retinocytoma Undergoing Retinoblastoma Transformation in an Adult Patient

Case reports in ophthalmological medicine, 2023-07, Vol.2023, p.8127245-4

2023

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Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

Nature genetics, 1997-03, Vol.15 (3), p.247-251

1997

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Potential blindness in children of patients with hereditary bone disease

Osteoporosis international, 2016-02, Vol.27 (2), p.841-844

2016

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The Identification of Rice Varieties Used in Central Sulawesi

E3S Web of Conferences, 2021, Vol.232, p.3013

2021

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A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

Nature genetics, 1999-06, Vol.22 (2), p.199-202

1999

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An ICI reduction scheme for OFDM system with phase noise over fading channels

IEEE transactions on communications, 2008-07, Vol.56 (7), p.1119-1126

2008

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Retinal toxicity following intra‐vitreal injections of melphalan

Acta ophthalmologica (Oxford, England), 2016-10, Vol.94 (S256), p.n/a

2016

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The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer

American journal of human genetics, 1999-11, Vol.65 (5), p.1261-1267

1999

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Genotype–phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphism

British journal of ophthalmology, 2008-04, Vol.92 (4), p.513-517

2008

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Genetic Heterogeneity of the Coppock-like Cataract: A Mutation in CRYBB2 on Chromosome 22q11.2

Investigative ophthalmology & visual science, 2000-01, Vol.41 (1), p.159-165

2000

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Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa

Acta ophthalmologica (Oxford, England), 2015-10, Vol.93 (S255), p.n/a

2015

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Late intraocular relapses in retinoblastoma

Acta ophthalmologica (Oxford, England), 2016-10, Vol.94 (S256), p.n/a

2016

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A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

Journal of medical genetics, 2003-11, Vol.40 (11), p.e124-124

2003

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Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina

Gene therapy, 2003-05, Vol.10 (9), p.818-821

2003

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Aberrant Accumulation of EFEMP1 Underlies Drusen Formation in Malattia Leventinese and Age-Related Macular Degeneration

Proceedings of the National Academy of Sciences - PNAS, 2002-10, Vol.99 (20), p.13067-13072

2002

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Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration

Investigative ophthalmology & visual science, 2000-05, Vol.41 (6), p.1291-1296

2000

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Clinical aspects of Autosomic Recessive Retinitis Pigmentosa Caused by USH2A Mutations in Consanguineous Tunisian Families

Acta ophthalmologica (Oxford, England), 2015-10, Vol.93 (S255), p.n/a

2015

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Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrier

Gene therapy, 2005-06, Vol.12 (11), p.942-947

2005

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Molecular Analysis of NOTCH2 in Patients with Primary Open-Angle Glaucoma

Klinische Monatsblatter fur Augenheilkunde, 2015-04, Vol.232 (4), p.427

2015

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Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy

American journal of human genetics, 2005-07, Vol.77 (1), p.54-63

2005

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

European journal of human genetics : EJHG, 2005-03, Vol.13 (3), p.302-308

2005

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Diagnosis and current management of retinoblastoma

Effect of Fermented Cocoa Pod Husk Level in Concentrate on Etawah Grade Semen Quality

Greenhouse Gas Emission (GHG) from ruminant on 2016 at Central Sulawesi Province

Retinoblastoma: From genes to patient care

Retinocytoma Undergoing Retinoblastoma Transformation in an Adult Patient

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

Potential blindness in children of patients with hereditary bone disease

The Identification of Rice Varieties Used in Central Sulawesi

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

An ICI reduction scheme for OFDM system with phase noise over fading channels

Retinal toxicity following intra‐vitreal injections of melphalan

The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer

Genotype–phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphism

Genetic Heterogeneity of the Coppock-like Cataract: A Mutation in CRYBB2 on Chromosome 22q11.2

Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa

Late intraocular relapses in retinoblastoma

A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina

Aberrant Accumulation of EFEMP1 Underlies Drusen Formation in Malattia Leventinese and Age-Related Macular Degeneration

Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration

Clinical aspects of Autosomic Recessive Retinitis Pigmentosa Caused by USH2A Mutations in Consanguineous Tunisian Families

Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrier

Molecular Analysis of NOTCH2 in Patients with Primary Open-Angle Glaucoma

Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

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