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BJOG : an International Journal of Obstetrics and Gynaecology
|
September 29, 2020
Ondansetron should never be used in pregnancy: Against: Ondansetron in pregnancy revisited
P Damkier, Y C Kaplan, S Shechtman, et al.
International Journal of Epidemiology
|
August 24, 2018
Relationship of genetic determinants of height with cardiometabolic and pulmonary traits in the Hispanic Community Health Study/Study of Latinos
Tamar Sofer, Jee-Young Moon, Carmen R Isasi, et al.
Paediatrics and International Child Health
|
October 14, 2014
Malnutrition and disability: unexplored opportunities for collaboration
N Groce, E Challenger, R Berman-Bieler, et al.
The Milbank Quarterly
|
December 21, 2010
The influence of context on quality improvement success in health care: a systematic review of the literature
Heather C Kaplan, Patrick W Brady, Michele C Dritz, et al.
Thrombosis Research
|
June 15, 1990
Aequorin-detected calcium changes in stimulated thrombasthenic platelets. Aggregation-dependent calcium movement in response to ADP
T Lecompte, F Potevin, P Champeix, et al.
The European Respiratory Journal
|
August 13, 1999
Increased frequency of cystic fibrosis deltaF508 mutation in bronchiectasis associated with rheumatoid arthritis
X Puéchal, I Fajac, T Bienvenu, et al.
The American Journal of Cardiology
|
August 29, 2001
Body mass index and the risk of recurrent coronary events following acute myocardial infarction
T D Rea, S R Heckbert, R C Kaplan, et al.
British Journal of Haematology
|
April 1, 1990
Ras activation in myelodysplastic syndromes: clinical and molecular study of the chronic phase of the disease
C Melani, A Haliassos, J C Chomel, et al.
Croatian Medical Journal
|
November 7, 2000
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
N Canki-Klain, D Récan, D Milicić, et al.
Human Genetics
|
November 1, 1994
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria
K Nafa, A Reghis, N Osmani, et al.
Page
of 119
Search research articles
Search
Showing results (631-640 of 1,185) with videos related to
Sort By:
Page
of 119
BJOG : an International Journal of Obstetrics and Gynaecology
|
September 29, 2020
Ondansetron should never be used in pregnancy: Against: Ondansetron in pregnancy revisited
P Damkier, Y C Kaplan, S Shechtman, et al.
International Journal of Epidemiology
|
August 24, 2018
Relationship of genetic determinants of height with cardiometabolic and pulmonary traits in the Hispanic Community Health Study/Study of Latinos
Tamar Sofer, Jee-Young Moon, Carmen R Isasi, et al.
Paediatrics and International Child Health
|
October 14, 2014
Malnutrition and disability: unexplored opportunities for collaboration
N Groce, E Challenger, R Berman-Bieler, et al.
The Milbank Quarterly
|
December 21, 2010
The influence of context on quality improvement success in health care: a systematic review of the literature
Heather C Kaplan, Patrick W Brady, Michele C Dritz, et al.
Thrombosis Research
|
June 15, 1990
Aequorin-detected calcium changes in stimulated thrombasthenic platelets. Aggregation-dependent calcium movement in response to ADP
T Lecompte, F Potevin, P Champeix, et al.
The European Respiratory Journal
|
August 13, 1999
Increased frequency of cystic fibrosis deltaF508 mutation in bronchiectasis associated with rheumatoid arthritis
X Puéchal, I Fajac, T Bienvenu, et al.
The American Journal of Cardiology
|
August 29, 2001
Body mass index and the risk of recurrent coronary events following acute myocardial infarction
T D Rea, S R Heckbert, R C Kaplan, et al.
British Journal of Haematology
|
April 1, 1990
Ras activation in myelodysplastic syndromes: clinical and molecular study of the chronic phase of the disease
C Melani, A Haliassos, J C Chomel, et al.
Croatian Medical Journal
|
November 7, 2000
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
N Canki-Klain, D Récan, D Milicić, et al.
Human Genetics
|
November 1, 1994
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria
K Nafa, A Reghis, N Osmani, et al.
Page
of 119