Relation between the location of elements in the periodic table and various organ-uptake rates
A Ando, I Ando, T Hiraki, K Hisada - … . Part B. Nuclear Medicine and Biology, 1989 - Elsevier
Fifty four elements and 65 radioactive compounds were examined to determine the organ
uptake rates for rats 3, 24 and 48 h after iv injection of these compounds. They were …
uptake rates for rats 3, 24 and 48 h after iv injection of these compounds. They were …
Measurement of whole-body nitrogen by neutron-activation analysis
TC Harvey, PW Dykes, NS Chen, KV Ettinger, S Jain… - The Lancet, 1973 - Elsevier
Whole-body nitrogen was measured in man using a new technique of neutron-activation
analysis. Patients were irradiated with a small dose of fast neutrons and the capture γ rays …
analysis. Patients were irradiated with a small dose of fast neutrons and the capture γ rays …
Research in muscular dystrophy
JN Walton - nature, 1970 - nature.com
Research in Muscular Dystrophy Page 1 © 1970 Nature Publishing Group NATURE VOL.
228 OCTOBER 31 1970 417 Research in Muscular Dystrophy by JN WALTON Department …
228 OCTOBER 31 1970 417 Research in Muscular Dystrophy by JN WALTON Department …
Whole-body counting
GA Andrews, WD Gibbs, AC Morris Jr… - Seminars in Nuclear …, 1973 - Elsevier
Whole-body counting has been directed toward two uses, one having to do with the
detection and measurement of minute amounts of natural or accidentally acquired …
detection and measurement of minute amounts of natural or accidentally acquired …
Muscular dystrophy and other myopathies: Troponin activity of natural actomyosin from skeletal muscle
T Furukawa, JB Peter - Archives of Neurology, 1972 - jamanetwork.com
Troponin activity of natural actomyosin in various muscle diseases was determined. The
activities were expressed as the trypsin-sensitive calciumbinding of natural actomyosin …
activities were expressed as the trypsin-sensitive calciumbinding of natural actomyosin …
Studies on the carrier state in X-linked recessive (Duchenne) muscular dystrophy
WHS Thomson, JC Sweetin, TE Hilditch - Clinica Chimica Acta, 1975 - Elsevier
Observations in 12 normal women and 12 female carriers of X-linked recessive Duchenne
muscular dystrophy (DMD), of whom 4 had symptoms and 8 had none, were compared …
muscular dystrophy (DMD), of whom 4 had symptoms and 8 had none, were compared …
Duchenne Muscular Dystrophy: Use of Rubidium Chloride Rb 86 in the Detection of Carriers of the Gene
WG Bradley, D Gardner-Medwin, J Haggith… - Archives of …, 1971 - jamanetwork.com
Female carriers of the gene for Duchenne muscular dystrophy have been reported to have a
decreased total body potassium concentration and a reduced biological half-life of rubidium …
decreased total body potassium concentration and a reduced biological half-life of rubidium …
Radiation Dose to Patients from Radiopharmaceuticals
Task Group of Committee 2 - Annals of the ICRP, 1987 - journals.sagepub.com
(1) The administration of radioactive substances to humans for diagnosis, therapy or
research purposes is a well-established and developing branch of medical practice, and is …
research purposes is a well-established and developing branch of medical practice, and is …
[HTML][HTML] Hypokalemia-induced cardiac arrest in a Duchenne muscular dystrophy patient
X Zikou, G Papathanakos, E Dounousi, G Nakos… - Hippokratia, 2016 - ncbi.nlm.nih.gov
Background: Duchenne muscular dystrophy (DMD) is a progressive myopathic disorder,
inherited as X-linked recessive traits, in which muscle weakness is the primary symptom …
inherited as X-linked recessive traits, in which muscle weakness is the primary symptom …
[CITATION][C] Carrier detection and genetic counselling in Duchenne dystrophy
V Dubowitz - Developmental Medicine & Child Neurology, 1975 - Wiley Online Library
MUSCULAR dystrophy of the Duchenne type is usually inherited through an x-linked
recessive mechanism and female carriers do not as a rule show any clinical manifestations …
recessive mechanism and female carriers do not as a rule show any clinical manifestations …