Zobrazeno 1 - 10
of 136
pro vyhledávání: '"K. Hugh-Jones"'
Publikováno v:
Clinical and Experimental Immunology. 88:512-519
SUMMARYImmunoglobulin class- and subclass-specific antibodies to a polyvalent pneumococcal capsular polysaccharide vaccine (Pneumovax II) were measured before and after immunization in children, 1 year or more after bone marrow transplantation for a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f059d7801ca333d766cc78c466b005
https://doi.org/10.1111/j.1365-2249.1992.tb06480.x
https://doi.org/10.1111/j.1365-2249.1992.tb06480.x
Publikováno v:
Journal of Inherited Metabolic Disease. 15:911-918
Allogeneic bone marrow transplantation was performed on twins with Sanfilippo B disease. They were the first two patients with this disorder to undergo the procedure. There was definite evidence of engraftment as shown by conversion to donor blood gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54e87a50b9b09bf751b30cce74bc9cb5
https://doi.org/10.1007/bf01800232
https://doi.org/10.1007/bf01800232
Publikováno v:
Archives of Disease in Childhood. 52:937-942
The clinical, radiological, and biochemical features of 2 male children with mannosidosis are described. Superficially they appeared to suffer from Hurler's syndrome, but the facies, eye signs, radiological and cytological features were atypical. Exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::570d42ef63ebf3e2f24e3ecca81fdcb2
https://doi.org/10.1136/adc.52.12.937
https://doi.org/10.1136/adc.52.12.937
Publikováno v:
Bioscience Reports. 1:933-944
1. Deoxyadenosine metabolism was compared in intact erythrocytes from two children with severe combined immunodeficiency: one had normal adenosine deaminase (ADA; EC 3.5.Lt.4) levels and the other, a homozygote for ADA deficiency, had (following a bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a460011159852a1ec8bd9db46abc67f8
https://doi.org/10.1007/bf01114963
https://doi.org/10.1007/bf01114963
Autor:
S. Williamson, D. Chambers, K. Hugh-Jones, D. V. Joss, D. C. O. James, S. Selwyn, J R Kendra, A J Barrett, K. Henry, N. Byrom, John R. Hobbs, T.R. Rogers, N. Foroozanfar, C. F. Lucas, H. Horsler, R. Phillips
Publikováno v:
Clinical & Laboratory Haematology. 5:131-143
Summary Twenty-four patients have received bone marrow transplantation for severe aplastic anaemia at the Westminster Hospitals since 1974. Twelve patients are long term survivors. Infectious complications in association with graft rejection, graft v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::712021ea070f7d0a33f4a76259fe1aa6
https://doi.org/10.1111/j.1365-2257.1983.tb01345.x
https://doi.org/10.1111/j.1365-2257.1983.tb01345.x
Publikováno v:
BMJ. 2:226-229
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f49078ab0535ec625da540f76f258d47
https://doi.org/10.1136/bmj.2.5403.226
https://doi.org/10.1136/bmj.2.5403.226
Publikováno v:
Archives of Disease in Childhood. 35:146-152
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71669e5257b5ba6973ce15c7ab70a1dc
https://doi.org/10.1136/adc.35.180.146
https://doi.org/10.1136/adc.35.180.146
Autor:
K. Hugh-Jones, G. I. M. Ross
Publikováno v:
Archives of Disease in Childhood. 33:543-551
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae1115797227491d0d51cf24bf34f23f
https://doi.org/10.1136/adc.33.172.543
https://doi.org/10.1136/adc.33.172.543
Publikováno v:
Archives of Disease in Childhood. 45:122-129
The characteristic clinical features of 2 cases of Pompe's disease are presented, namely, signs of a cardiomyopathy with skeletal hypotonia and a characteristic ECG with a short PR interval and high voltage QRS complexes. Glycogen storage disease is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1086e88a7ff10a88e7213c05a019a85c
https://doi.org/10.1136/adc.45.239.122
https://doi.org/10.1136/adc.45.239.122
Autor:
K. Hugh-Jones, J. G. Watson
Publikováno v:
Proceedings of the Royal Society of Medicine. 68:578-580
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27bf703882f62ec6c5cf988a88d950b0
https://doi.org/10.1177/003591577506800919
https://doi.org/10.1177/003591577506800919