Search research articles
Contact Us
Filters
Showing results (801-810 of 1,314) with videos related to
Page
of 132
Sort By:
Diabetologia
|
March 1, 1984
In vivo imaging and quantitative analysis of insulin-receptor interaction in lean and obese Zucker rats
J C Sodoyez, F Sodoyez-Goffaux, S Treves, et al.
Therapie
|
March 1, 1997
[Methotrexate and non-steroidal anti-inflammatory agent combination in rheumatoid arthritis]
P Bertin, N Carpentier, P Vergne, et al.
The Journal of Biological Chemistry
|
October 24, 2001
B-lymphocytes from malignant hyperthermia-susceptible patients have an increased sensitivity to skeletal muscle ryanodine receptor activators
T Girard, D Cavagna, E Padovan, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
October 9, 2002
Acute hematogenous osteomyelitis of children: assessment of skeletal scintigraphy-based diagnosis in the era of MRI
Leonard P Connolly, Susan A Connolly, Laura A Drubach, et al.
Biochemistry
|
April 18, 1995
Calmodulin binding sites of the skeletal, cardiac, and brain ryanodine receptor Ca2+ channels: modulation by the catalytic subunit of cAMP-dependent protein kinase?
R Guerrini, P Menegazzi, R Anacardio, et al.
Neurology
|
March 1, 1995
Low-dose clozapine in the treatment of levodopa-induced mental disturbances in Parkinson's disease
J M Rabey, T A Treves, M Y Neufeld, et al.
Joint Bone Spine
|
January 26, 2010
Ultrasonography in chondrocalcinosis
Carine Dufauret-Lombard, Pascale Vergne-Salle, Anne Simon, et al.
Journal of Biomedical Materials Research. Part A
|
May 14, 2009
In vitro biocompatibility evaluation of surface-modified titanium alloys
Cristina Treves, Maria Martinesi, Maria Stio, et al.
Clinical Nuclear Medicine
|
August 1, 1996
Localization of Tc-99m MDP in neuroblastoma metastases to the liver and lung
L P Connolly, D A Bloom, H Kozakewich, et al.
Human Molecular Genetics
|
April 4, 2020
Molecular basis of impaired extraocular muscle function in a mouse model of congenital myopathy due to compound heterozygous Ryr1 mutations
Jan Eckhardt, Christoph Bachmann, Sofia Benucci, et al.
Page
of 132
Search research articles
Search
Showing results (801-810 of 1,314) with videos related to
Sort By:
Page
of 132
Diabetologia
|
March 1, 1984
In vivo imaging and quantitative analysis of insulin-receptor interaction in lean and obese Zucker rats
J C Sodoyez, F Sodoyez-Goffaux, S Treves, et al.
Therapie
|
March 1, 1997
[Methotrexate and non-steroidal anti-inflammatory agent combination in rheumatoid arthritis]
P Bertin, N Carpentier, P Vergne, et al.
The Journal of Biological Chemistry
|
October 24, 2001
B-lymphocytes from malignant hyperthermia-susceptible patients have an increased sensitivity to skeletal muscle ryanodine receptor activators
T Girard, D Cavagna, E Padovan, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
October 9, 2002
Acute hematogenous osteomyelitis of children: assessment of skeletal scintigraphy-based diagnosis in the era of MRI
Leonard P Connolly, Susan A Connolly, Laura A Drubach, et al.
Biochemistry
|
April 18, 1995
Calmodulin binding sites of the skeletal, cardiac, and brain ryanodine receptor Ca2+ channels: modulation by the catalytic subunit of cAMP-dependent protein kinase?
R Guerrini, P Menegazzi, R Anacardio, et al.
Neurology
|
March 1, 1995
Low-dose clozapine in the treatment of levodopa-induced mental disturbances in Parkinson's disease
J M Rabey, T A Treves, M Y Neufeld, et al.
Joint Bone Spine
|
January 26, 2010
Ultrasonography in chondrocalcinosis
Carine Dufauret-Lombard, Pascale Vergne-Salle, Anne Simon, et al.
Journal of Biomedical Materials Research. Part A
|
May 14, 2009
In vitro biocompatibility evaluation of surface-modified titanium alloys
Cristina Treves, Maria Martinesi, Maria Stio, et al.
Clinical Nuclear Medicine
|
August 1, 1996
Localization of Tc-99m MDP in neuroblastoma metastases to the liver and lung
L P Connolly, D A Bloom, H Kozakewich, et al.
Human Molecular Genetics
|
April 4, 2020
Molecular basis of impaired extraocular muscle function in a mouse model of congenital myopathy due to compound heterozygous Ryr1 mutations
Jan Eckhardt, Christoph Bachmann, Sofia Benucci, et al.
Page
of 132