proline and Eye Disorders

proline has been researched along with Eye Disorders in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's2 (33.33)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chang, MH; Demirci, FY; Gorin, MB; Mah, TS; Romero, MF1
Muthulakshmi, R; Nallathambi, J; Namperumalsamy, P; Rajendran, A; Shukla, D; Sundaresan, P1
Ferlini, A; Forabosco, A; Gobbi, P; Mencucci, R; Michelucci, R; Plasmati, R; Salvi, F; Salvi, G; Santangelo, M; Volpe, R1
Greco, GM; Magli, A1
Naess, O; Nicolaissen, B; Ringvold, A1
Duvall, J; Goldberg, MF; Puck, A; Sugar, J; Tso, MO; Yue, BY1

Reviews

1 review(s) available for proline and Eye Disorders

ArticleYear
[Eye manifestations of amino acid disorders].
    Minerva pediatrica, 1978, May-31, Volume: 30, Issue:10

    Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria; Eye Diseases; Eye Manifestations; Glycine; Hartnup Disease; Hepatolenticular Degeneration; Homocystinuria; Humans; Lysine; Oculocerebrorenal Syndrome; Oxidoreductases; Phenylketonurias; Proline; Pyruvates

1978

Other Studies

5 other study(ies) available for proline and Eye Disorders

ArticleYear
Proximal renal tubular acidosis and ocular pathology: a novel missense mutation in the gene (SLC4A4) for sodium bicarbonate cotransporter protein (NBCe1).
    Molecular vision, 2006, Apr-10, Volume: 12

    Topics: Acidosis, Renal Tubular; Adult; Amino Acid Sequence; Animals; Base Sequence; Biological Transport; Cell Membrane; Eye Diseases; Homozygote; Humans; Leucine; Male; Molecular Sequence Data; Mutation, Missense; Oocytes; Proline; Sodium-Bicarbonate Symporters; Xenopus

2006
Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.
    Molecular vision, 2006, Sep-21, Volume: 12

    Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Asian People; Cysteine; Exons; Exudates and Transudates; Eye Diseases; Fluorescein Angiography; Frizzled Receptors; Fundus Oculi; Humans; India; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Phenylalanine; Proline; Receptors, G-Protein-Coupled; Retinal Diseases; Serine; Vitreous Body

2006
Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families.
    Ophthalmic paediatrics and genetics, 1993, Volume: 14, Issue:1

    Topics: Adult; Aged; Alanine; Amyloidosis; Eye Diseases; Female; Humans; Lens Diseases; Male; Middle Aged; Mutation; Pedigree; Prealbumin; Proline; Ultrasonography; Vitreous Body

1993
Amino acid incorporation in cell cultures from eyes with pseudo-exfoliation material.
    Acta ophthalmologica, 1992, Volume: 70, Issue:3

    Topics: Anterior Eye Segment; Cells, Cultured; Conjunctival Diseases; Extracellular Matrix; Eye Diseases; Humans; Leucine; Proline

1992
Nanophthalmic sclera. Morphologic and tissue culture studies.
    Ophthalmology, 1986, Volume: 93, Issue:4

    Topics: Adult; Cells, Cultured; Eye Diseases; Eye Proteins; Fundus Oculi; Glycosaminoglycans; Humans; Hyaluronic Acid; Male; Microscopy, Electron; Proline; Sclera

1986