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Treatment of corneal cystine crystal accumulation in patients with cystinosis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archopht.118.10.1329openalex-snapshot
Ultrasound Biomicroscopy of the Eye in Cystinosis
inferredcites →https://doi.org/10.1001/archopht.120.12.1742openalex-snapshot
In Vivo Confocal Microscopy of the Cornea in Nephropathic Cystinosis
inferredcites →https://doi.org/10.1001/archopht.1967.00980020363014openalex-snapshot
Alterations of Pigment Epithelium in Cystinosis
inferredcites →https://doi.org/10.1001/archopht.1986.01050170096030openalex-snapshot
Long-term Ocular Manifestations in Nephropathic Cystinosis
inferredcites →https://doi.org/10.1001/archopht.1990.01070070075038openalex-snapshot
A Randomized Placebo-Controlled Trial of Cysteamine Eye Drops in Nephropathic Cystinosis
inferredcites →https://doi.org/10.1001/jama.1957.02980040034009openalex-snapshot
CYSTINOSIS IN AN ADULT
inferredcites →https://doi.org/10.1001/jama.1993.03510180070036openalex-snapshot
Classic Nephropathic Cystinosis as an Adult Disease
inferredcites →https://doi.org/10.1002/humu.10141openalex-snapshot
Identification of 14 novelCTNS mutations and characterization of seven splice site mutations associated with cystinosis
inferredcites →https://doi.org/10.1006/mgme.1998.2725openalex-snapshot
A Randomized Clinical Trial of Topical Cysteamine Disulfide (Cystamine) versus Free Thiol (Cysteamine) in the Treatment of Corneal Cystine Crystals in Cystinosis
inferredcites →https://doi.org/10.1006/mgme.2000.3062openalex-snapshot
Corneal Crystals in Nephropathic Cystinosis: Natural History and Treatment with Cysteamine Eyedrops
inferredcites →https://doi.org/10.1006/mgme.2001.3218openalex-snapshot
CTNS Mutations in African American Patients with Cystinosis
inferredcites →https://doi.org/10.1007/bf00856532openalex-snapshot
Progression of chronic renal failure in a historical group of patients with nephropathic cystinosis
inferredcites →https://doi.org/10.1007/bf00858644openalex-snapshot
Update on nephropathic cystinosis
inferredcites →https://doi.org/10.1007/s001090050220openalex-snapshot
Clinical and molecular aspects of nephropathic cystinosis
inferredcites →https://doi.org/10.1007/s00467-007-0650-8openalex-snapshot
Nephropathic cystinosis: late complications of a multisystemic disease
inferredcites →https://doi.org/10.1016/0002-9343(62)90221-8openalex-snapshot
The Fanconi syndrome with cystinosis
inferredcites →https://doi.org/10.1016/0002-9394(86)90773-7openalex-snapshot
Pupillary-Block Glaucoma Associated with Childhood Cystinosis
inferredcites →https://doi.org/10.1016/0002-9394(87)90018-3openalex-snapshot
Recurrent Crystal Deposition After Keratoplasty in Nephropathic Cystinosis
inferredcites →https://doi.org/10.1016/0039-6257(82)90124-2openalex-snapshot
Metabolic tapetoretinal degenerations
inferredcites →https://doi.org/10.1016/j.ejpb.2013.04.017openalex-snapshot
Feasibility of corneal drug delivery of cysteamine using vitamin E modified silicone hydrogel contact lenses
inferredcites →https://doi.org/10.1016/j.ophtha.2005.12.026openalex-snapshot
Nephropathic Cystinosis
inferredcites →https://doi.org/10.1016/j.survophthal.2006.10.006openalex-snapshot
Ophthalmic Manifestations and Histopathology of Infantile Nephropathic Cystinosis: Report of a Case and Review of the Literature
inferredcites →https://doi.org/10.1016/j.ymgme.2013.12.298openalex-snapshot
A new gel formulation of topical cysteamine for the treatment of corneal cystine crystals in cystinosis: The Cystadrops OCT-1 study
inferredcites →https://doi.org/10.1016/s0021-9258(18)89141-4openalex-snapshot
Detection and characterization of carrier-mediated cationic amino acid transport in lysosomes of normal and cystinotic human fibroblasts. Role in therapeutic cystine removal?
inferredcites →https://doi.org/10.1016/s0022-3476(86)80221-9openalex-snapshot
Course of nephropathic cystinosis after age 10 years
inferredcites →https://doi.org/10.1038/eye.1991.139openalex-snapshot
A randomised placebo-controlled trial of topical cysteamine therapy in patients with nephropathic cystinosis
inferredcites →https://doi.org/10.1038/ki.1995.324openalex-snapshot
Renal proximal tubular epithelium from patients with nephropathic cystinosis: Immortalized cell lines as in vitro model systems
inferredcites →https://doi.org/10.1038/ki.2011.277openalex-snapshot
Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults
inferredcites →https://doi.org/10.1038/ki.2011.301openalex-snapshot
Cysteamine therapy: a treatment for cystinosis, not a cure
inferredcites →https://doi.org/10.1038/ng0498-319openalex-snapshot
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
inferredcites →https://doi.org/10.1056/nejmra020552openalex-snapshot
Cystinosis
inferredcites →https://doi.org/10.1073/pnas.1211198109openalex-snapshot
Heptahelical protein PQLC2 is a lysosomal cationic amino acid exporter underlying the action of cysteamine in cystinosis therapy
inferredcites →https://doi.org/10.1086/302118openalex-snapshot
CTNS Mutations in an American-Based Population of Cystinosis Patients
inferredcites →https://doi.org/10.1093/emboj/20.21.5940openalex-snapshot
Cystinosin, the protein defective in cystinosis, is a H+‐driven lysosomal cystine transporter
inferredcites →https://doi.org/10.1093/hmg/8.13.2507openalex-snapshot
Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin
inferredcites →https://doi.org/10.1093/ndt/gfp553openalex-snapshot
Renal phenotype of the cystinosis mouse model is dependent upon genetic background
inferredcites →https://doi.org/10.1097/00003226-200203000-00009openalex-snapshot
Age-Related Prevalence of Anterior Segment Complications in Patients With Infantile Nephropathic Cystinosis
inferredcites →https://doi.org/10.1097/00006982-198200230-00018openalex-snapshot
Metabolic Tapetoretinal Degenerations
inferredcites →https://doi.org/10.1097/01.asn.0000036867.49866.59openalex-snapshot
Lysosomal Cystine Storage Augments Apoptosis in Cultured Human Fibroblasts and Renal Tubular Epithelial Cells
inferredcites →https://doi.org/10.1111/j.1442-9071.2007.01467.xopenalex-snapshot
In vivo confocal microscopy and polarizing microscopy of the cornea in a patient with nephropathic cystinosis
inferredcites →https://doi.org/10.1128/mcb.22.21.7622-7632.2002openalex-snapshot
Intralysosomal Cystine Accumulation in Mice Lacking Cystinosin, the Protein Defective in Cystinosis
inferredcites →https://doi.org/10.1136/bjo.2005.074468openalex-snapshot
Confocal microscopy of the cornea in nephropathic cystinosis
inferredcites →https://doi.org/10.1136/bjo.73.8.665openalex-snapshot
Corneal thickness in nephropathic cystinosis.
inferredcites →https://doi.org/10.1136/bjo.75.5.311openalex-snapshot
Clearance of corneal crystals in nephropathic cystinosis by topical cysteamine 0.5%.
inferredcites →https://doi.org/10.1136/bjo.87.1.28openalex-snapshot
A multicentre randomised double masked clinical trial of a new formulation of topical cysteamine for the treatment of corneal cystine crystals in cystinosis
inferredcites →https://doi.org/10.1146/annurev.genom.2.1.69openalex-snapshot
Human Genetics: Lessons from Quebec Populations
inferredcites →https://doi.org/10.1159/000299940openalex-snapshot
Ueber die Cystinkrankheit im Kleinkindesalter unter besonderer Berücksichtigung des Augenbefundes
inferredcites →https://doi.org/10.1159/000305884openalex-snapshot
Ocular Manifestations of Cystinosis
inferredcites →https://doi.org/10.1159/000309288openalex-snapshot
Netzhautveränderungen bei Zystinose
inferredcites →https://doi.org/10.1172/jci108448openalex-snapshot
Cystinosis. Intracellular cystine depletion by aminothiols in vitro and in vivo.
inferredcites →https://doi.org/10.1172/jci115103openalex-snapshot
Role of adenosine triphosphate (ATP) and NaK ATPase in the inhibition of proximal tubule transport with intracellular cystine loading.
inferredcites →https://doi.org/10.1182/blood-2009-03-213934openalex-snapshot
Successful treatment of the murine model of cystinosis using bone marrow cell transplantation
inferredcites →https://doi.org/10.1203/00006450-200001000-00007openalex-snapshot
Ocular Nonnephropathic Cystinosis: Clinical, Biochemical, and Molecular Correlations
inferredcites →https://doi.org/10.1203/01.pdr.0000196334.46940.54openalex-snapshot
Decreased Intracellular ATP Content and Intact Mitochondrial Energy Generating Capacity in Human Cystinotic Fibroblasts
inferredcites →https://doi.org/10.1210/jc.80.11.3257openalex-snapshot
Effects of early cysteamine therapy on thyroid function and growth in nephropathic cystinosis
inferredcites →https://doi.org/10.1371/journal.pone.0042840openalex-snapshot
Stem Cell Microvesicles Transfer Cystinosin to Human Cystinotic Cells and Reduce Cystine Accumulation In Vitro
inferredcites →https://doi.org/10.1515/bchm2.1903.38.5-6.557openalex-snapshot
Familiäre Cystindiathese.
inferredcites →https://doi.org/10.3109/13816818709028529openalex-snapshot
Ocular changes in long-term evolution of infantile cystinosis
inferredcites →https://doi.org/10.3928/0191-3913-19790101-06openalex-snapshot
Long-Term Ocular Changes in Cystinosis: Observations in Renal Transplant Recipients
inferredcites →https://doi.org/10.3928/0191-3913-19900901-14openalex-snapshot
The Effect of Topical Cysteamine Drops on Reducing Crystal Formation Within the Cornea of Patients Affected by Nephropathic Cystinosis
inferredcites →https://doi.org/10.3928/0191-3913-19940701-18openalex-snapshot
Recurrent Corneal Erosion in Cystinosis
inferredcites →https://doi.org/10.7326/0003-4819-109-7-557openalex-snapshot
Cystinosis: Progress in a Prototypic Disease

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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An Innovative Hydrogen Peroxide‐Sensing Scaffold and Insight Towards its Potential as an ROS‐Activated Persulfide Donor
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An Innovative Hydrogen Peroxide‐Sensing Scaffold and Insight Towards its Potential as an ROS‐Activated Persulfide Donor
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Selenosulfides Tethered to gem ‐Dimethyl Esters: A Robust and Highly Versatile Framework for H 2 S Probe Development
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Bilaterale kristalline Einlagerungen im Hornhautstroma
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Clinical Practice: A Proposed Standardized Ophthalmological Assessment for Patients with Cystinosis
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The Ocular Status of Cystinosis Patients Receiving a Hospital Pharmacy-Made Preparation of Cysteamine Eye Drops: A Case Series
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The Use of a Viscous Cysteamine Eyedrop in a Belgian Cohort: Early 3-Year Results
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An Update on Nephropathic Cystinosis for the General Pediatrician
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Intermediate type cystinosis with a novel CTNS variant in a child: a case report
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Corneal Deposits
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Corneal abnormalities in childhood
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“My child seems to hate the bright light”
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Comprehensive Ocular Characteristics in Cystinosis after Hematopoietic Stem-Cell Gene Therapy Over 24 Months
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2018.11.031openalex-snapshot
In vitro and ex vivo implantation of cystine crystals and treatment by contact lens
inferred← citeshttps://doi.org/10.1016/j.ejpb.2016.07.009openalex-snapshot
Effect of pH and penetration enhancers on cysteamine stability and trans-corneal transport
inferred← citeshttps://doi.org/10.1016/j.exer.2021.108455openalex-snapshot
Systemic diseases and the cornea
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The TGM2 Inhibitor Cysteamine Hydrochloride Does Not Impact Corneal Epithelial and Stromal Wound Healing in Vitro and in Vivo
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Cysteamine polysaccharide hydrogels: Study of extended ocular delivery and biopermanence time by PET imaging
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Potential role of stromal collagen in cystine crystallization in cystinosis patients
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The gene therapy for corneal pathology with novel nonsense cystinosis mouse lines created by CRISPR Gene Editing
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Two dimensional solvothermal synthesis via ultrasound (2D-STSUS) of fluorescent tungsten-doped hBN nanosheets for the selective detection of cancer markers
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CTNS molecular genetics profile in a Persian nephropathic cystinosis population
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CTNS molecular genetics profile in a Persian nephropathic cystinosis population
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.6b00488openalex-snapshot
Synergistic Cysteamine Delivery Nanowafer as an Efficacious Treatment Modality for Corneal Cystinosis
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Corneal Manifestation in Patients with Infantile Nephropathic Cystinosis
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Ocular manifestations of the genetic renal tubulopathies
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Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosis
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Systemic associations of corneal deposits: a review and photographic guide
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Efficacy of topical cysteamine in nephropathic cystinosis
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Long-term follow-up of cystinosis patients treated with 0.55% cysteamine hydrochloride
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A New Viscous Cysteamine Eye Drops Treatment for Ophthalmic Cystinosis: An Open-Label Randomized Comparative Phase III Pivotal Study
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Value of Renal Biopsy in Diagnosing Infantile Nephropathic Cystinosis Associated With Secondary Nephrogenic Diabetes Insipidus
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Ocular manifestations of intermediate cystinosis: To treat or not to treat?
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Examination of corneal deposits in nephropathic cystinosis using in vivo confocal microscopy and anterior segment optical coherence tomography: an age-dependent cross sectional study
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Asymmetrical Ocular Manifestations of Nephropathic Cystinosis; A Case Report
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Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
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An Open-Label, Phase III Study to Assess the Efficacy and Safety of Cysteamine Ophthalmic Solution 0.55% in Japanese Cystinosis Patients
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Nephropathic Cystinosis: Symptoms, Treatment, and Perspectives of a Systemic Disease
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Synthetic and semi-synthetic antioxidants in medicine and food industry: a review
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The Pitfall of White Blood Cell Cystine Measurement to Diagnose Juvenile Cystinosis
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Development and Evaluation of Different Electrospun Cysteamine-Loaded Nanofibrous Webs: A Promising Option for Treating a Rare Lysosomal Storage Disorder
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Cystinuria and cystinosis are usually related to L-cystine: is this really the case for cystinosis? A physicochemical investigation at micrometre and nanometre scale
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Glycovecteurs pour le ciblage thérapeutique d'une maladie rare lysosomale : la maladie de Pompe
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