Zobrazeno 1 - 8
of 8
pro vyhledávání: '"R. K. H. Petty"'
Publikováno v:
Neurochemical research. 18(11)
5- and 6-Hydroxydopamine, which we had earlier identified as naturally occurring amines in human urine, were quantified in Parkinson's patients treated with L-DOPA, Parkinson's patients whose treatment did not include L-DOPA and in age matched contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc4fea40830a2173f9328157cc4d53a4
https://pubmed.ncbi.nlm.nih.gov/8255370
https://pubmed.ncbi.nlm.nih.gov/8255370
Publikováno v:
Neuropathology and Applied Neurobiology. 28:155-155
Introduction: Marfan's syndrome (MFS) is the commonest inherited disorder of connective tissue. It is defined by major features in the cardiovascular, skeletal and ocular systems, and minor features in the integument and lungs. Patients who fulfil th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39b0558cd125cdf139d9360c31f962b7
https://doi.org/10.1046/j.1365-2990.2002.39286_20.x
https://doi.org/10.1046/j.1365-2990.2002.39286_20.x
Publikováno v:
Neuropathology and Applied Neurobiology. 15:175-183
We report the association of paraneoplastic cerebellar cortical degeneration with small-cell oesophageal carcinoma in a 60-year-old woman and describe the histopathological findings. We believe this to be the first report of such an occurrence. The c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6b50a9662a1fc32eff31e6b49cc1795
https://doi.org/10.1111/j.1365-2990.1989.tb01219.x
https://doi.org/10.1111/j.1365-2990.1989.tb01219.x
Publikováno v:
Journal of Neurology. 233:108-114
A young adult male is described with muscular dystrophy of probable X-linked recessive inheritance. An onset of muscle weakness in late adolescence was preceded by contractures of the neck and elbows dating back to childhood. The distribution of musc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe467dacf77b0b11141d30cbdd8e6429
https://doi.org/10.1007/bf00313856
https://doi.org/10.1007/bf00313856
Publikováno v:
Journal of medical genetics. 25(8)
Of 71 index cases with histologically defined mitochondrial myopathy, 13 (18%) had relatives who were definitely affected with a similar disorder. Eight familial cases from four families were confined to a single generation. In five families maternal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d16e9389ee16a570e16967495e591f4e
https://pubmed.ncbi.nlm.nih.gov/3050098
https://pubmed.ncbi.nlm.nih.gov/3050098
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 103(12)
In a series of 61 patients with the morphologic and histochemical features of mitochondrial myopathy, 22 (36%) had pigmentary retinopathy. Three patterns of retinopathy were identified. Eighteen patients had a "salt and pepper" type of retinal appear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f88a788deaeca5aa0adf86172117e8ff
https://pubmed.ncbi.nlm.nih.gov/4074172
https://pubmed.ncbi.nlm.nih.gov/4074172
Autor:
John B. Clark, R. K. H. Petty, M.J. Brosnan, D. J. Hayes, George K. Radda, J. A. Morgan-Hughes, E.A. Shoubridge, J. M. Cooper, R. A. J. Challiss
Publikováno v:
Journal of the neurological sciences. 83(2-3)
Chronic administration of the NADH-CoQ reductase inhibitor, diphenyleneiodonium to rats at two dose levels, 1.0 and 1.5 mg/kg per day, caused a 40% and 60% reduction, respectively, in the in vitro rate of NAD-linked respiration by skeletal muscle mit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7141905f65b35f25a1ea820fc37c7917
https://pubmed.ncbi.nlm.nih.gov/3128647
https://pubmed.ncbi.nlm.nih.gov/3128647