Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L Cartier

Showing results (71-80 of 105) with videos related to

Pageof 11
Sort By:
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.
American Journal of Public Health|December 1, 1982
Prevention of mental retardation in offspring of hyperphenylalaninemic mothersL Cartier, C L Clow, A Lippman-Hand, et al.
Acta Neurologica Scandinavica|March 1, 1991
Evoked potential abnormalities in progressive spastic paraparesis associated to HTLV-1J L Castillo, L Cartier, F Araya, et al.
Neuroscience Letters|August 16, 1996
Segmental demyelination induced by cerebrospinal fluid of progressive spastic paraparesis: correlation with altered proteolytic parametersJ Schmidt, J K Nien, A Scherson, et al.
Journal of Pharmaceutical Sciences|September 23, 2003
Simultaneous intravenous and intramiddle-ear dosing to determine cefditoren influx and efflux clearances in middle ear fluid in freely moving chinchillasTong Zhu, Belinda W Y Cheung, Linda L Cartier, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 29, 2000
T lymphocytes activated by persistent viral infection differentially modify the expression of metalloproteinases and their endogenous inhibitors, TIMPs, in human astrocytes: relevance to HTLV-I-induced neurological diseaseP Giraudon, R Szymocha, S Buart, et al.
American Journal of Human Genetics|September 1, 1984
Beta-thalassemia disease prevention: genetic medicine appliedC R Scriver, M Bardanis, L Cartier, et al.
Fetal Diagnosis and Therapy|February 5, 2005
Large hepatic mesenchymal hamartoma leading to mid-trimester fetal demiseJ-M Laberge, Y Patenaude, V Desilets, et al.
Journal of the Neurological Sciences|October 11, 1992
Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20P Brown, S Gálvez, L G Goldfarb, et al.
Revista Medica De Chile|June 1, 1990
[HTLV-I retrovirus in Chile: study on 140 neurological patients]L Cartier, F Araya, J L Castillo, et al.
Pageof 11

Showing results (71-80 of 105) with videos related to

Sort By:
Pageof 11
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.
American Journal of Public Health|December 1, 1982
Prevention of mental retardation in offspring of hyperphenylalaninemic mothersL Cartier, C L Clow, A Lippman-Hand, et al.
Acta Neurologica Scandinavica|March 1, 1991
Evoked potential abnormalities in progressive spastic paraparesis associated to HTLV-1J L Castillo, L Cartier, F Araya, et al.
Neuroscience Letters|August 16, 1996
Segmental demyelination induced by cerebrospinal fluid of progressive spastic paraparesis: correlation with altered proteolytic parametersJ Schmidt, J K Nien, A Scherson, et al.
Journal of Pharmaceutical Sciences|September 23, 2003
Simultaneous intravenous and intramiddle-ear dosing to determine cefditoren influx and efflux clearances in middle ear fluid in freely moving chinchillasTong Zhu, Belinda W Y Cheung, Linda L Cartier, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 29, 2000
T lymphocytes activated by persistent viral infection differentially modify the expression of metalloproteinases and their endogenous inhibitors, TIMPs, in human astrocytes: relevance to HTLV-I-induced neurological diseaseP Giraudon, R Szymocha, S Buart, et al.
American Journal of Human Genetics|September 1, 1984
Beta-thalassemia disease prevention: genetic medicine appliedC R Scriver, M Bardanis, L Cartier, et al.
Fetal Diagnosis and Therapy|February 5, 2005
Large hepatic mesenchymal hamartoma leading to mid-trimester fetal demiseJ-M Laberge, Y Patenaude, V Desilets, et al.
Journal of the Neurological Sciences|October 11, 1992
Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20P Brown, S Gálvez, L G Goldfarb, et al.
Revista Medica De Chile|June 1, 1990
[HTLV-I retrovirus in Chile: study on 140 neurological patients]L Cartier, F Araya, J L Castillo, et al.
Pageof 11