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La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
March 29, 1984
[Early coronary atherosclerosis in a malignant pheochromocytoma. Apropos of a case]
J E Touze, A Monnier, T Mardelle, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
December 17, 2009
ALS with respiratory onset: clinical features and effects of non-invasive ventilation on the prognosis
Guillaume Gautier, Annie Verschueren, Armelle Monnier, et al.
The European Respiratory Journal
|
November 1, 1993
Tracheobronchial amyloidosis with hilar lymphadenopathy associated with a serum monoclonal immunoglobulin
B Crestani, A Monnier, M Kambouchner, et al.
Gene Therapy
|
October 12, 1999
A photosensitising adenovirus for photodynamic therapy
J Gagnebin, M Brunori, M Otter, et al.
The Journal of Biological Chemistry
|
March 5, 1989
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo
F Hayase, R H Nagaraj, S Miyata, et al.
Human Molecular Genetics
|
April 30, 2003
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia
Nicole Monnier, Ana Ferreiro, Isabelle Marty, et al.
Zygote (Cambridge, England)
|
August 18, 2001
Protein translation during early cell divisions of sea urchin embryos regulated at the level of polypeptide chain elongation and highly sensitive to natural polyamines
A Monnier, J Morales, P Cormier, et al.
La Nouvelle Presse Medicale
|
October 23, 1982
[Chronic insulin urticaria. Therapeutic efficacy and good tolerability of human insulins]
J Mirouze, L Monnier, M Rodier, et al.
Trends in Cell Biology
|
December 24, 2016
RGMs: Structural Insights, Molecular Regulation, and Downstream Signaling
Christian Siebold, Toshihide Yamashita, Philippe P Monnier, et al.
Human Genetics
|
August 1, 1989
Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian family
M C Vinet, C Dodé, O Pascal, et al.
Page
of 239
Search research articles
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Showing results (831-840 of 2,384) with videos related to
Sort By:
Page
of 239
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
March 29, 1984
[Early coronary atherosclerosis in a malignant pheochromocytoma. Apropos of a case]
J E Touze, A Monnier, T Mardelle, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
December 17, 2009
ALS with respiratory onset: clinical features and effects of non-invasive ventilation on the prognosis
Guillaume Gautier, Annie Verschueren, Armelle Monnier, et al.
The European Respiratory Journal
|
November 1, 1993
Tracheobronchial amyloidosis with hilar lymphadenopathy associated with a serum monoclonal immunoglobulin
B Crestani, A Monnier, M Kambouchner, et al.
Gene Therapy
|
October 12, 1999
A photosensitising adenovirus for photodynamic therapy
J Gagnebin, M Brunori, M Otter, et al.
The Journal of Biological Chemistry
|
March 5, 1989
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo
F Hayase, R H Nagaraj, S Miyata, et al.
Human Molecular Genetics
|
April 30, 2003
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia
Nicole Monnier, Ana Ferreiro, Isabelle Marty, et al.
Zygote (Cambridge, England)
|
August 18, 2001
Protein translation during early cell divisions of sea urchin embryos regulated at the level of polypeptide chain elongation and highly sensitive to natural polyamines
A Monnier, J Morales, P Cormier, et al.
La Nouvelle Presse Medicale
|
October 23, 1982
[Chronic insulin urticaria. Therapeutic efficacy and good tolerability of human insulins]
J Mirouze, L Monnier, M Rodier, et al.
Trends in Cell Biology
|
December 24, 2016
RGMs: Structural Insights, Molecular Regulation, and Downstream Signaling
Christian Siebold, Toshihide Yamashita, Philippe P Monnier, et al.
Human Genetics
|
August 1, 1989
Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian family
M C Vinet, C Dodé, O Pascal, et al.
Page
of 239