Zobrazeno 1 - 10 of 50 pro vyhledávání: '"H G, Dunn"'
2
Interstitial Lung Disease Developing during Treatment with Cyclosporine in a patient with Diffuse Scleroderma, Aplastic Anemia and Crohn's Disease: Implications for Pathogenesis and Treatment
Autor: J M, Davies, H G, Dunn
Publikováno v: Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 1(5)
Systemic sclerosis (scleroderma) is an uncommon disease of as-yet-unknown etiology. The hallmark of scleroderma is proliferation of collagen, particularly types I and III, with associated vascular changes. Visceral involvement, particularly pulmonary
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0501ec431646aaf065a865652abaf20d
https://pubmed.ncbi.nlm.nih.gov/19077999
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4
Acute encephalopathy and status epilepticus associated with human herpes virus 6 infection
Autor: C M, Jones, H G, Dunn, E E, Thomas, R W, Cone, J M, Weber
Publikováno v: Developmental medicine and child neurology. 36(7)
A previously healthy 22-month-old boy presented in status epilepticus with high fever. He was comatose, with upper respiratory-tract infection. The seizures responded to anticonvulsant therapy. The boy's temperature returned to normal within 24 hours
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f95543ac87444a24f033837e9f33703e
https://pubmed.ncbi.nlm.nih.gov/8034128
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5
Distribution of the CPS
Autor: H G, Dunn
Publikováno v: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne. 144(3)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::76c8936e6e712f1fc9a3eae16743becf
https://pubmed.ncbi.nlm.nih.gov/1989703
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7
Further delineation of X-linked mental retardation
Autor: F. J. Dill, H. G. Dunn, Dagmar K. Kalousek, L. W. Krywaniuk, Diana S. Herbst
Publikováno v: Human Genetics. 58:366-372
Chromosomal, clinical, and psychological data are presented on members of six families with X-linked mental retardation. Affected males in three of these families express the fra(X)(q28) marker, while the retarded males in the other three do not. Sim
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2075300e73d3f06d03047b49b6ba1344
https://doi.org/10.1007/bf00282817
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