Sentences with word «mucopolysaccharidosis»

Today we have two programs in our pipeline for mucopolysaccharidosis Type IIIA (MPS IIIA) and GM1 gangliosidosis (GM1).

Researchers at the Biophysics Department of the Federal University of São Paulo (UNIFESP) in Brazil are developing a gene therapy for mucopolysaccharidosis type I...

Kyra Marsigliano - «Oronasal Fistula in a Stray Cat Presenting with Upper Respiratory Infection» Shari Perez - «Idiopathic Renal Hematuria in a 2 - year - old Cane Corso» Courtney O'Connell - «Managing Dysphagia Secondary to Gutteral Pouch Mycosis» Rebecca McBride - «A Case of Mucopolysaccharidosis in a Fifteen - week - old Boston Terrier»

(ref) You can read some key articles that describe mucopolysaccharidosis in puppies and kittens here: (ref1, ref2, ref3, ref4)

Jack Baird, who is four years old and from Sunderland, has the condition Sanfilippo Disease, also known as Mucopolysaccharidosis (MPS) III, which affects around one in 85,000 people in the UK.

Expression of clusterin, a protein implicated in other etiologies of cardiovascular disease, was assessed in canine and murine mucopolysaccharidosis type I aortas via Western blot and in situ immunohistochemistry.

Because this dog can be susceptible to a neurological disorder called Mucopolysaccharidosis Type IIIB, ask your breeder to provide a DNA test to verify the Schipperke parent was clear.

If mucopolysaccharidosis is the underlying problem, some neutrophil and lymphocyte cells in the blood film generally contain large numbers of small purplish granules (azurophilic granules).

Enzyme replacement therapy for mucopolysaccharidosis VI: growth and pubertal development in patients treated with recombinant human N - acetylgalactosamine 4 - sulfatase

In addition, a trial for Mucopolysaccharidosis type I (MPS - I) is planned to start in 2018.

Chris Hendrickson, a North Dakota native, who has Morquio Syndrome, or mucopolysaccharidosis type 4A, a degenerative disease that affects his bones,...

Chris Hendrickson, a North Dakota native, who has Morquio Syndrome, or mucopolysaccharidosis type 4A, a degenerative disease that affects his bones, recently had his wish of meeting T.J. Oshie come true.

Mucopolysaccharidosis type 7 (MPS 7) is an inherited metabolic disorder.

Lysogene's most advanced product is rAAV vector serotype rh.10 carrying the human N - sulfoglucosamine sulfohydrolase (hSGSH) for the treatment of the mucopolysaccharidosis type IIIA (MPS IIIA) or Sanfilippo syndrome type A. Lysogene's gene therapy is delivered directly to the CNS in one neurosurgical procedure.

Mucopolysaccharidosis type IIIA (MPS IIIA), or Sanfilippo syndrome type A, is a rare inherited neurodegenerative lysosomal storage disorder characterized by intractable behavioural problems and developmental regression resulting in early death.

Mucopolysaccharidosis is a rare inherited autosomal recessive metabolic disorder found in the German Shepherd dog and a few other breeds and is characterized by clouding of the corneas and skeletal deformities.

Lysosomal storage diseases such as Niemann - Pick disease, mucopolysaccharidosis and gangliosidosis (GM1) have been described in Siamese cats, as has systemic amyloidosis.