Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marie O. Russell"'
Autor:
Joanne Halus, Haewon C. Kim, Herbert I. Goldberg, Andrew Hodson, Marie O. Russell, Elias Schwartz, Martin Reivich
Publikováno v:
Blood. 63:162-169
Stroke is a relatively frequent and severe complication of sickle cell disease. We performed cerebral arteriograms in 30 patients with sickle cell disease to evaluate the cause of acute neurologic deficits and to assess the effects of transfusion the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a89c98dca547774dc5b342ea1cf62206
https://doi.org/10.1182/blood.v63.1.162.bloodjournal631162
https://doi.org/10.1182/blood.v63.1.162.bloodjournal631162
Autor:
Marie O. Russell, Amelia C. Finan, Frances M. Gill, Melanie A. Elmer, Shortie McKinney, Sharon R. Sasanow
Publikováno v:
American journal of diseases of children (1960). 142(2)
• A study of growth and nutrition was conducted with 20 growth-retarded (GR) and 20 growth-normal (GN) preadolescent children with sickle cell disease (SCD). All children were matched for age, sex, hemoglobin disorder, and hematologic values. Ten n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae47ee5971c349d6773ad28c21f587dd
https://pubmed.ncbi.nlm.nih.gov/3341331
https://pubmed.ncbi.nlm.nih.gov/3341331
Publikováno v:
American journal of diseases of children (1960). 135(4)
Chronic granulomatous disease (CGD) is usually a sex-linked recessive disorder characterized by recurrent purulent infections of the skin and lymph nodes. Affected granulocytes form diminished quantities of superoxide 1 and can ingest but not kill ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf05a48f98e5ce712ffebcf311164b2
https://pubmed.ncbi.nlm.nih.gov/7211803
https://pubmed.ncbi.nlm.nih.gov/7211803
Publikováno v:
The Journal of pediatrics. 86(2)
n e u r o b l a s t o m a . Paren t s are i n s t ruc t ed to b r ing the first m o r n i n g u r ina ry s p e c i m e n if possible, and the spot t e s t is d o n e at every clinic visit. A n y changes f rom prev ious resul ts , e i t he r f rom pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13820470c40a533e761db2dec07df415
https://pubmed.ncbi.nlm.nih.gov/1111689
https://pubmed.ncbi.nlm.nih.gov/1111689
Autor:
M.D. Shlomo Friedman, R.N. Linda Reis, Marie O. Russell, M.D. Robert Slater, Martin Reivich, M.D. Elias Schwartz, M.D. Herbert I. Goldberg
Publikováno v:
The Journal of pediatrics. 88(3)
Cerebral angiograms were performed in patients with sickle cell disease and symptoms of stroke to evaluate transfusion therapy for cerebrovascular accidents. Three patients who were transfused repeatedly for one year to maintain less than 30% hemoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da9a03b5ff5ff300b33df526bbf1ea21
https://pubmed.ncbi.nlm.nih.gov/1245948
https://pubmed.ncbi.nlm.nih.gov/1245948
Publikováno v:
Clinical nuclear medicine. 14(4)
To determine whether imaging techniques can differentiate osteomyelitis from bone infarction in sickle cell disorders, 39 sets of bone scans (BS) and bone marrow scans (BMS) were performed on 31 patients with sickling disorders and bone pain. In addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5a0fc07bbd0f065b6dcd37b7275ef2
https://pubmed.ncbi.nlm.nih.gov/2706866
https://pubmed.ncbi.nlm.nih.gov/2706866
Publikováno v:
Pediatric Research. 8:408-408
Cerebrovascular accidents (CVA) are a major clinical problem in sickle cell disease. We have studied four affected children soon after CVA and one year later to evaluate the effect of chronic transfusion therapy on arterial abnormalities. Percutaneou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbab2393323c3ff254c49ce7259d95cd
https://doi.org/10.1203/00006450-197404000-00409
https://doi.org/10.1203/00006450-197404000-00409
Publikováno v:
Clinical Orthopaedics and Related Research. :158
Osteonecrosis secondary to sickling disorders differs from most other forms of osteonecrosis, because vaso-occlusive episodes generally involve many other organs. For this reason optimum management and care of these patients requires a team approach.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::041e0a4fae53a158bc2a57b809d4407f
https://doi.org/10.1097/00003086-197801000-00016
https://doi.org/10.1097/00003086-197801000-00016
Publikováno v:
Pediatric Research. 11:473-473
Differentiation of osteomyelitis (OSTEO) from bone infarction (BI) in patients with sickling disorders is a difficult clinical problem. In patients with OSTEO there is increased uptake of isotope on bone scan (BS) soon after onset of symptoms. We hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b35cedd9dae32aaea29a95f245a3dab2
https://doi.org/10.1203/00006450-197704000-00620
https://doi.org/10.1203/00006450-197704000-00620
Autor:
Ellas Schwartz, Marie O. Russell, Melanle A Elmer, Amelia Finan, Frances M. Gill, Sharon R. Moskowitz
Publikováno v:
Pediatric Research. 15:586-586
Of 170 sickle cell patients 2-12 years old, 22% had height and/or weight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9698d7f95ec193e24dd0cbe8d5d99f70
https://doi.org/10.1203/00006450-198104001-00890
https://doi.org/10.1203/00006450-198104001-00890