Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal levels of cystine in the cells of all organs. It is treated by regular administration of the aminothiol, cysteamine. Corneal crystal deposition is one of the most troublesome complications affecting patients and requires the hourly administration of cysteamine eye drops. In an attempt to reduce this frequency and improve the treatment, the preformulation and evaluation of cysteamine containing gels is reported. Suitability for ophthalmic delivery was determined by analysis of rheology, bioadhesion, dissolution and stability. The results demonstrated that three polymers were suitable for ophthalmic delivery of cysteamine; namely sodium hyaluronate...
Ocular cystinosis is a rare metabolic disorder characterized by the presence of insoluble cystine cr...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is a hereditary genetic disease that results in the accumulation of cystine crystals in t...
Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal leve...
Cystinosis is a rare, metabolic, genetic disease with less than 2,000 patients in the U.S. Intralyso...
Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal leve...
Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal leve...
Background: Cystinosis is a rare genetic disorder characterized by the accumulation of cystine cryst...
Cystinosis is a rare genetic disorder characterized by the accumulation of cystine crystals in diffe...
Full copyright for enhanced digital features is owned by the authors. Article full text The fu...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Summary: Cysteamine bitartrate capsules (Cystagon) have been approved by the US Food and Drug Admini...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Ocular cystinosis is a rare metabolic disorder characterized by the presence of insoluble cystine cr...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is a hereditary genetic disease that results in the accumulation of cystine crystals in t...
Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal leve...
Cystinosis is a rare, metabolic, genetic disease with less than 2,000 patients in the U.S. Intralyso...
Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal leve...
Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal leve...
Background: Cystinosis is a rare genetic disorder characterized by the accumulation of cystine cryst...
Cystinosis is a rare genetic disorder characterized by the accumulation of cystine crystals in diffe...
Full copyright for enhanced digital features is owned by the authors. Article full text The fu...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Summary: Cysteamine bitartrate capsules (Cystagon) have been approved by the US Food and Drug Admini...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Ocular cystinosis is a rare metabolic disorder characterized by the presence of insoluble cystine cr...
Cystinosis is an autosomal recessive inherited lysosomal storage disease. It is characterized by gen...
Cystinosis is a hereditary genetic disease that results in the accumulation of cystine crystals in t...