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Journal of the Neurological Sciences
|
March 1, 1980
Beriberi neuropathy. Morphometric study of sural nerve
A Ohnishi, S Tsuji, H Igisu, et al.
Journal of Biochemistry
|
October 1, 1993
Phosphatidylserine specific binding protein in rat brain: purification and characterization
T Nakaoka, N Kojima, T Hamamoto, et al.
Genomics
|
June 1, 1997
Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene
S N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1988
Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals
S Tsuji, B M Martin, J A Barranger, et al.
Journal of Cardiovascular Pharmacology
|
January 29, 2002
Effects of angiotensin converting enzyme inhibitor and angiotensin II type 1 receptor blocker on cardiac dysfunction induced by isoproterenol in dogs
T Ohta, N Hasebe, S Tsuji, et al.
Clinical Nuclear Medicine
|
September 1, 1993
Comparative SPECT study of stroke using Tc-99m ECD, I-123 IMP, and Tc-99m HMPAO
H Matsuda, Y M Li, S Higashi, et al.
Human Genetics
|
April 1, 1997
Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy
E Kondo-Iida, K Saito, H Tanaka, et al.
The Science of the Total Environment
|
September 9, 2006
Abandoned Mid-Canada Radar Line sites in the Western James region of Northern Ontario, Canada: a source of organochlorines for First Nations people?
Leonard J S Tsuji, Bruce C Wainman, Ian D Martin, et al.
Environmental Monitoring and Assessment
|
August 10, 2006
Identifying potential receptors and routes of contaminant exposure in the traditional territory of the Ouje-Bougoumou Cree: land use and a geographical information system
Leonard J S Tsuji, Harry Manson, Bruce C Wainman, et al.
The Journal of Clinical Investigation
|
August 1, 1992
An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgrounds
B McInnes, M Potier, N Wakamatsu, et al.
Page
of 99
Search research articles
Search
Showing results (691-700 of 990) with videos related to
Sort By:
Page
of 99
Journal of the Neurological Sciences
|
March 1, 1980
Beriberi neuropathy. Morphometric study of sural nerve
A Ohnishi, S Tsuji, H Igisu, et al.
Journal of Biochemistry
|
October 1, 1993
Phosphatidylserine specific binding protein in rat brain: purification and characterization
T Nakaoka, N Kojima, T Hamamoto, et al.
Genomics
|
June 1, 1997
Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene
S N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1988
Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals
S Tsuji, B M Martin, J A Barranger, et al.
Journal of Cardiovascular Pharmacology
|
January 29, 2002
Effects of angiotensin converting enzyme inhibitor and angiotensin II type 1 receptor blocker on cardiac dysfunction induced by isoproterenol in dogs
T Ohta, N Hasebe, S Tsuji, et al.
Clinical Nuclear Medicine
|
September 1, 1993
Comparative SPECT study of stroke using Tc-99m ECD, I-123 IMP, and Tc-99m HMPAO
H Matsuda, Y M Li, S Higashi, et al.
Human Genetics
|
April 1, 1997
Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy
E Kondo-Iida, K Saito, H Tanaka, et al.
The Science of the Total Environment
|
September 9, 2006
Abandoned Mid-Canada Radar Line sites in the Western James region of Northern Ontario, Canada: a source of organochlorines for First Nations people?
Leonard J S Tsuji, Bruce C Wainman, Ian D Martin, et al.
Environmental Monitoring and Assessment
|
August 10, 2006
Identifying potential receptors and routes of contaminant exposure in the traditional territory of the Ouje-Bougoumou Cree: land use and a geographical information system
Leonard J S Tsuji, Harry Manson, Bruce C Wainman, et al.
The Journal of Clinical Investigation
|
August 1, 1992
An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgrounds
B McInnes, M Potier, N Wakamatsu, et al.
Page
of 99