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Neuropediatrics
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March 30, 2011
Absence of mutation in the SLC2A1 gene in a cohort of patients with alternating hemiplegia of childhood (AHC)
S Vuillaumier-Barrot, E Panagiotakaki, C Le Bizec, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
April 5, 2001
Evaluation of local abciximab delivery from the surface of a polymer-coated covered stent: in vivo canine studies
A B Fontaine, J J Borsa, S Dos Passos, et al.
Global Change Biology
|
February 10, 2019
Carbon consequences of drought differ in forests that resprout
Lewis L Walden, Joseph B Fontaine, Katinka X Ruthrof, et al.
American Journal of Human Genetics
|
November 1, 1990
Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting
B Fontaine, G A Rouleau, B Seizinger, et al.
Investigational New Drugs
|
August 1, 1990
Phase I study of idarubicin administered orally on a daily x 3 schedule
D J Stewart, S Verma, J A Maroun, et al.
Neurology
|
September 25, 1999
Localized proton magnetic resonance spectroscopy in relapsing remitting versus secondary progressive multiple sclerosis
A Tourbah, J L Stievenart, O Gout, et al.
Journal of Medical Genetics
|
August 2, 2005
Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases
C Depienne, C Tallaksen, J Y Lephay, et al.
Genomics
|
March 1, 1993
A set of STS assays targeting the chromosome 22 physical framework markers
M MacCollin, D Romano, M Budarf, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma)
B Fontaine, G A Rouleau, B R Seizinger, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
March 15, 2000
Primary placement of Palmaz long medium stents in transjugular intrahepatic portosystemic shunts
J J Borsa, A B Fontaine, E K Hoffer, et al.
Page
of 22
Search research articles
Search
Showing results (131-140 of 212) with videos related to
Sort By:
Page
of 22
Neuropediatrics
|
March 30, 2011
Absence of mutation in the SLC2A1 gene in a cohort of patients with alternating hemiplegia of childhood (AHC)
S Vuillaumier-Barrot, E Panagiotakaki, C Le Bizec, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
April 5, 2001
Evaluation of local abciximab delivery from the surface of a polymer-coated covered stent: in vivo canine studies
A B Fontaine, J J Borsa, S Dos Passos, et al.
Global Change Biology
|
February 10, 2019
Carbon consequences of drought differ in forests that resprout
Lewis L Walden, Joseph B Fontaine, Katinka X Ruthrof, et al.
American Journal of Human Genetics
|
November 1, 1990
Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting
B Fontaine, G A Rouleau, B Seizinger, et al.
Investigational New Drugs
|
August 1, 1990
Phase I study of idarubicin administered orally on a daily x 3 schedule
D J Stewart, S Verma, J A Maroun, et al.
Neurology
|
September 25, 1999
Localized proton magnetic resonance spectroscopy in relapsing remitting versus secondary progressive multiple sclerosis
A Tourbah, J L Stievenart, O Gout, et al.
Journal of Medical Genetics
|
August 2, 2005
Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases
C Depienne, C Tallaksen, J Y Lephay, et al.
Genomics
|
March 1, 1993
A set of STS assays targeting the chromosome 22 physical framework markers
M MacCollin, D Romano, M Budarf, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma)
B Fontaine, G A Rouleau, B R Seizinger, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
March 15, 2000
Primary placement of Palmaz long medium stents in transjugular intrahepatic portosystemic shunts
J J Borsa, A B Fontaine, E K Hoffer, et al.
Page
of 22