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Heart (British Cardiac Society)
|
August 19, 2003
Body surface mapping improves early diagnosis of acute myocardial infarction in patients with chest pain and left bundle branch block
S J Maynard, I B A Menown, G Manoharan, et al.
Transfusion
|
November 13, 2012
Retrograde patient blood flow and rouleaux preventing red blood cell transfusion
Nancy M Dunbar, Cynthia R Marx-Wood, Kimberly J Maynard, et al.
Journal of Inorganic Biochemistry
|
April 1, 2006
Gender and genetic background effects on brain metal levels in APP transgenic and normal mice: implications for Alzheimer beta-amyloid pathology
Christa J Maynard, Roberto Cappai, Irene Volitakis, et al.
Cellular and Molecular Neurobiology
|
April 22, 2009
Chronic exposure to high levels of zinc or copper has little effect on brain metal homeostasis or Abeta accumulation in transgenic APP-C100 mice
Christa J Maynard, Roberto Cappai, Irene Volitakis, et al.
Archives of Disease in Childhood
|
September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)
P E Jardine, M C Koch, P W Lunt, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy
P W Lunt, P E Jardine, M Koch, et al.
Animals : an Open Access Journal From MDPI
|
June 28, 2023
Impact of Phytase Supplementation on Meat Quality of Heat-Stressed Broilers
Clay J Maynard, Craig W Maynard, Garrett J Mullenix, et al.
Muscle & Nerve. Supplement
|
April 12, 2013
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy
P W Lunt, P E Jardine, M Koch, et al.
Vaccine
|
April 1, 1997
Integration of hepatitis B vaccination into the expanded programme on immunization in Chonburi and Chiangmai provinces, Thailand
S Chunsuttiwat, B A Biggs, J Maynard, et al.
Human Molecular Genetics
|
December 14, 2001
Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberin
A K Hodges, S Li, J Maynard, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 213) with videos related to
Sort By:
Page
of 22
Heart (British Cardiac Society)
|
August 19, 2003
Body surface mapping improves early diagnosis of acute myocardial infarction in patients with chest pain and left bundle branch block
S J Maynard, I B A Menown, G Manoharan, et al.
Transfusion
|
November 13, 2012
Retrograde patient blood flow and rouleaux preventing red blood cell transfusion
Nancy M Dunbar, Cynthia R Marx-Wood, Kimberly J Maynard, et al.
Journal of Inorganic Biochemistry
|
April 1, 2006
Gender and genetic background effects on brain metal levels in APP transgenic and normal mice: implications for Alzheimer beta-amyloid pathology
Christa J Maynard, Roberto Cappai, Irene Volitakis, et al.
Cellular and Molecular Neurobiology
|
April 22, 2009
Chronic exposure to high levels of zinc or copper has little effect on brain metal homeostasis or Abeta accumulation in transgenic APP-C100 mice
Christa J Maynard, Roberto Cappai, Irene Volitakis, et al.
Archives of Disease in Childhood
|
September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)
P E Jardine, M C Koch, P W Lunt, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy
P W Lunt, P E Jardine, M Koch, et al.
Animals : an Open Access Journal From MDPI
|
June 28, 2023
Impact of Phytase Supplementation on Meat Quality of Heat-Stressed Broilers
Clay J Maynard, Craig W Maynard, Garrett J Mullenix, et al.
Muscle & Nerve. Supplement
|
April 12, 2013
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy
P W Lunt, P E Jardine, M Koch, et al.
Vaccine
|
April 1, 1997
Integration of hepatitis B vaccination into the expanded programme on immunization in Chonburi and Chiangmai provinces, Thailand
S Chunsuttiwat, B A Biggs, J Maynard, et al.
Human Molecular Genetics
|
December 14, 2001
Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberin
A K Hodges, S Li, J Maynard, et al.
Page
of 22