Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Michael G Pike"'
Autor:
Michael, Absoud, Ming J, Lim, Richard, Appleton, Anu, Jacob, Joanna, Kitley, M Isabel, Leite, Michael G, Pike, Angela, Vincent, Evangeline, Wassmer, Patrick, Waters, Mark, Woodhall, Cheryl, Hemingway, Jacqueline, Palace
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 86(4)
Neuromyelitis Optica (NMO) is a severe and rare inflammatory condition, where relapses are predictive of disability.We describe a national paediatric NMO cohort's clinical, MRI, outcome, and prognostic features in relation to Aquaporin-4 antibody (AQ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d8bc26ae4f85621808671b95bb11d57
https://pubmed.ncbi.nlm.nih.gov/25091363
https://pubmed.ncbi.nlm.nih.gov/25091363
Autor:
James E. Dimmick, Henry G. Dunn, Michael G. Pike, Aubrey J. Tingle, Heather Harris, Derek A. Applegarth, J. K. Chantler, Stephen Bamforth, Judith G. Hall, Betty J. Wood
Publikováno v:
The Journal of pediatrics. 116(1)
An infant girl had the clinical and immunologic findings of congenital rubella syndrome but also had arthrogryposis multiplex and calcific epiphyseal stippling. Spastic quadriparesis developed, and both physical and behavioral development were slow.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44d55ad15290af751cc59549a4492878
https://pubmed.ncbi.nlm.nih.gov/2295968
https://pubmed.ncbi.nlm.nih.gov/2295968
Autor:
Michael G. Pike, Michael Baraitser
Publikováno v:
Journal of Medical Genetics. 27:341-341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b0dcd51c3fb3afeca3821a13d911631
https://doi.org/10.1136/jmg.27.5.341
https://doi.org/10.1136/jmg.27.5.341
Publikováno v:
Pediatric Dermatology. 6:10-12
Severe allergic protein-losing enteropathy has been described in childhood atopic dermatitis (AD). Minor morphologic and functional abnormalities of the gastrointestinal mucosa, including altered permeability to oligosaccharides, are not uncommon in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be9168e6052d74aa37ead00da7cfa0b0
https://doi.org/10.1111/j.1525-1470.1989.tb00258.x
https://doi.org/10.1111/j.1525-1470.1989.tb00258.x
Publikováno v:
American journal of diseases of children (1960). 143(6)
• Ninety-seven children who were born between 1954 and 1986 and presented to the Visually Impaired Program of British Columbia's Children's Hospital, Vancouver, Canada, with a primary ophthalmologic diagnosis of cataracts, were assessed neurologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c25b68bdc088bb80097d688da168fe56
https://pubmed.ncbi.nlm.nih.gov/2729215
https://pubmed.ncbi.nlm.nih.gov/2729215
Publikováno v:
The Journal of pediatrics. 108(1)
Un cas est decrit chez une fille suivie jusqu'a l'âge actuel de 9 ans. La transmission serait donc autosomique recessive plutot que liee a l'X. Le taux de sodium dans la sueur peut etre eleve et faire croire, comme ici, dans la petite enfance a un f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b63e55584600e2605c2ccb5347c08617
https://pubmed.ncbi.nlm.nih.gov/3944674
https://pubmed.ncbi.nlm.nih.gov/3944674
Autor:
Nuno JV Cordeiro, Kate R Gardner, Susan M Huson, Helen Stewart, John S Elston, Emma L Howard, Kjell O Tullus, Michael G Pike
Publikováno v:
Developmental Medicine & Child Neurology; Jan2006, Vol. 48 Issue 1, p58-59, 2p