Zobrazeno 1 - 10
of 50
pro vyhledávání: '"R. D. Jolly"'
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0190030 (2017)
Familial episodic ataxia of lambs is a congenital transient autosomal dominant disorder of newborn lambs, with varying expressivity. Affected lambs show episodes of an asymmetric ataxic gait, base-wide extensor hypertonia of the thoracic limbs and fl
Externí odkaz:
https://doaj.org/article/54245de6b13248cebea8f3a6918fdfbb
Publikováno v:
New Zealand Veterinary Journal. 50:199-202
To describe the gross and histological lesions of a neurological disease in Borderdale sheep characterised clinically by blindness and circling, as a basis to its classification.Formalin-fixed tissues were processed into paraffin wax and epoxy resin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42fcc081ceff65e1c08888178da6875c
https://doi.org/10.1080/00480169.2002.36311
https://doi.org/10.1080/00480169.2002.36311
Publikováno v:
Veterinary Record. 148:564-567
A four-year-old wire-haired dachshund developed progressive neurological signs of ataxia, intention tremor and finally dysuria. Two years later, histopathology showed that neurons throughout the brain and spinal cord were distended with lipopigment w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16897de4e5be1edd0966d950571bce6c
https://doi.org/10.1136/vr.148.18.564
https://doi.org/10.1136/vr.148.18.564
Autor:
D. N. Palmer, R. D. Jolly
Publikováno v:
Neuropathology and Applied Neurobiology. 21:50-60
The ceroid-lipofuscinoses are a group of inherited neurodegenerative diseases of human beings characterized by the accumulation of a fluorescent lipopigment in neurons and other cells within the body. There is usually atrophy of both brain and retina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d5cacf24b4634aef908c8b108e3cf80
https://doi.org/10.1111/j.1365-2990.1995.tb01028.x
https://doi.org/10.1111/j.1365-2990.1995.tb01028.x
Publikováno v:
Neuropathology and applied neurobiology. 39(6)
To investigate routes of dispersal of enzyme, its regional uptake and the effect of posture when replacement enzyme is administered directly into the cerebrospinal fluid (CSF).Dispersal pathways of particles and solutes were investigated using intrac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a2d2b84115730e2d3cb1ec74a6e0197
https://pubmed.ncbi.nlm.nih.gov/23252616
https://pubmed.ncbi.nlm.nih.gov/23252616
Publikováno v:
Neuropathology and applied neurobiology. 37(4)
The research concerns enzyme replacement therapy in lysosomal storage diseases with central nervous system involvement. The principle aim was to understand the routes of entry of enzyme into the brain when delivered directly into the cerebrospinal fl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a083aab26b3d2036148eb2077b31f10
https://pubmed.ncbi.nlm.nih.gov/21175738
https://pubmed.ncbi.nlm.nih.gov/21175738
Publikováno v:
New Zealand veterinary journal. 47(3)
Aim. To determine the cause and nature of a disease in newborn New Zealand Romney lambs characterised by progressive weakness and premature death. Methods. Affected lambs were examined clinically, humanely killed and submitted to necropsy. Selected f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb60fdbcebfb2840a1913b9beb53c11
https://pubmed.ncbi.nlm.nih.gov/16032085
https://pubmed.ncbi.nlm.nih.gov/16032085
Publikováno v:
Australian veterinary journal. 80(5)
Objective To characterise neuronal ceroid lipofuscinosis (NCL) in Merino sheep. Design A prospective clinical, pathological, biochemical and genetic study. Procedure NCL cases were studied from a medium-wool Merino flock, the stud of origin of its re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846de15c87b9830a008c9032b758e46f
https://pubmed.ncbi.nlm.nih.gov/12418508
https://pubmed.ncbi.nlm.nih.gov/12418508
Autor:
R D Jolly
Publikováno v:
Australian veterinary journal. 80(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbf8a3dc2ae86e6d854fbdbf90aef68b
https://pubmed.ncbi.nlm.nih.gov/12074310
https://pubmed.ncbi.nlm.nih.gov/12074310
Publikováno v:
Electrophoresis. 22(9)
The neuronal ceroid-lipofuscinose (NCL) are recessively inherited lysosomal storage diseases in children and animals. The major stored protein in many of these diseases is subunit c of the mitochondrial inner membrane H+-transporting ATP-synthase. Pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd47c5ee537996d510ef5198dc6268b2
https://pubmed.ncbi.nlm.nih.gov/11425233
https://pubmed.ncbi.nlm.nih.gov/11425233