Zobrazeno 1 - 10
of 22
pro vyhledávání: '"W. M. Lawton"'
Autor:
W. M. Lawton
Publikováno v:
Известия Иркутского государственного университета: Серия "Математика", Vol 46, Iss 1, Pp 98-109 (2023)
In 1921 Mellin published a Comptes Rendu paper computing the principal solution of a polynomial using generalized hypergeometric functions of its coefficients. He used an integral transform nowadays bearing his name. Slightly over three pages, the pa
Externí odkaz:
https://doaj.org/article/a4b23095ca484194b83ccea68bed6887
Publikováno v:
Scandinavian Journal of Haematology. 13:276-280
In congenital erythroid hypoplasia (Diamond-Blackfan syndrome) a genetic transmission has been described in only a few cases. We report a family where the evidence points to an autosomal dominant mode of inheritance, the first report of this kind whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df831be805d21c6323ef543b30d8893f
https://doi.org/10.1111/j.1600-0609.1974.tb00270.x
https://doi.org/10.1111/j.1600-0609.1974.tb00270.x
Autor:
I. D. Gardner, J. W. M. Lawton
Publikováno v:
Scandinavian Journal of Haematology. 27:79-86
Human blood monocytes were separated by centrifugation over modified Ficoll-Hypaque and by this one-step procedure relatively high proportions (mean 54%) and yields of monocytes were obtained. Yields ranged from 0.22 times 109 to 0.98 times 109/1 of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e5a41147976a3d0ac0b818a3ac1e715
https://doi.org/10.1111/j.1600-0609.1981.tb00456.x
https://doi.org/10.1111/j.1600-0609.1981.tb00456.x
Publikováno v:
Clinical and Experimental Immunology. 85:202-208
SUMMARY We report a Chinese girl with the moderate phenotype of leucocyte adhesion deficiency (LAD), presenting with persistent omphalitis and recurrent soft tissue infections. She had subnormal adhesion-dependent neutrophil functions, such as chemot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3871bad54e3a1e7f2f0494d4b134523b
https://doi.org/10.1111/j.1365-2249.1991.tb05705.x
https://doi.org/10.1111/j.1365-2249.1991.tb05705.x
Autor:
J. W. M. Lawton, Sai Siong Wong
Publikováno v:
Journal of Gastroenterology and Hepatology. 11:1161-1163
Primary sclerosing cholangitis is rare among Chinese. We report on a 71 year old male patient who presented with clinical features consistent with the disorder. Subsequent investigations confirmed the diagnosis. The patient was found to have anti-neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23c4c626b20986dc78af741c6652fd51
https://doi.org/10.1111/j.1440-1746.1996.tb01845.x
https://doi.org/10.1111/j.1440-1746.1996.tb01845.x
Autor:
John W M Lawton, Shui Shan Lee
Thirty seven patients tested positive for antibody against proteinase 3 (anti-PR3) using either one of the two in-house ELISA methods at the Immunology Laboratory, University of Hong Kong. All except three were Chinese. Systemic vasculitis was diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63eda8eb313731dc957f9ad38a0d6f74
https://europepmc.org/articles/PMC1741572/
https://europepmc.org/articles/PMC1741572/
Publikováno v:
Annals of the Rheumatic Diseases. 60:725-726
α1 Antitrypsin (α1AT) is a 52 kDa proteinase encoded by a gene locus Pi on chromosomal segment 14q32.1. It is a natural inhibitor of proteinase 3 (PR3), a neutrophil granular protein and a major autoantigen of antineutrophil cytoplasmic antibody (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aa35cb11a911d3d1373acfba0d9d908
https://doi.org/10.1136/ard.60.7.725
https://doi.org/10.1136/ard.60.7.725
Publikováno v:
Journal of paediatrics and child health. 28(5)
A unique case of a Chinese boy with Wiskott-Aldrich syndrome (WAS) associated with Takayasu's arteritis is reported. He had eczema, epistaxis and recurrent infections since early infancy and was found to have thrombocytopenia, negative delayed-type s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aa7b1ace73cf657770b74706b72dbda
https://pubmed.ncbi.nlm.nih.gov/1356386
https://pubmed.ncbi.nlm.nih.gov/1356386
Publikováno v:
Journal of paediatrics and child health. 28(3)
A 2 year old Chinese boy was reported in whom there was an association between usual interstitial pneumonitis (UIP) and serum antineutrophil cytoplasmic antibody of the classical cytoplasmic type (cANCA). The concentration of cANCA reflected disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7e03bee6c89c1cb2b8dc26520ee9505
https://pubmed.ncbi.nlm.nih.gov/1605983
https://pubmed.ncbi.nlm.nih.gov/1605983
Publikováno v:
Journal of paediatrics and child health. 27(4)
From July 1988 to December 1989, six boys with chronic granulomatous disease were diagnosed in our institutions. Their clinical features were reviewed in order to delineate the pattern of infections which seems to have both similarities and differenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7573f1d946d9f8212d80cc20d359990d
https://pubmed.ncbi.nlm.nih.gov/1958423
https://pubmed.ncbi.nlm.nih.gov/1958423