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Showing results (121-130 of 133) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismL Monari, S G Chen, P Brown, et al.
Acta Neuropathologica|January 1, 1994
Creutzfeldt-Jakob disease and cerebral amyloid angiopathyF Gray, F Chrétien, P Cesaro, et al.
Cancer|January 15, 1990
Primary lymphoma of the central nervous system. An unresolved therapeutic problemG Socié, C Piprot-Chauffat, M Schlienger, et al.
The American Journal of Cardiovascular Pathology|January 1, 1990
Primary liposarcoma of the heartF Paraf, P Bruneval, A Balaton, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|January 1, 1990
MRI pattern of progressive multifocal leukoencephalopathy (PML) in AIDS. Pathological correlationsP M Trotot, R Vazeux, H K Yamashita, et al.
Gastroenterology|April 1, 1986
Digestive tract and renal small vessel hyalinosis, idiopathic nonarteriosclerotic intracerebral calcifications, retinal ischemic syndrome, and phenotypic abnormalities. A new familial syndromeJ C Rambaud, A Galian, G Touchard, et al.
Diabetes & Metabolism|June 1, 2006
Kearns Sayre syndrome: an unusual form of mitochondrial diabetesM Laloi-Michelin, M Virally, C Jardel, et al.
Neuropathology and Applied Neurobiology|November 26, 2002
High frequency of a 30-bp deletion of Epstein-Barr virus latent membrane protein 1 gene in primary HIV non-Hodgkin's brain lymphomasA-V Vallat-Decouvelaere, M-A Bretel, I Vassias, et al.
Clinical Endocrinology|November 3, 1998
The GnRH receptor gene is preferentially expressed in functioning gonadotroph adenomas and displays a Mae III polymorphism siteM L Kottler, D Seret-Bégué, N Lahlou, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismL Monari, S G Chen, P Brown, et al.
Acta Neuropathologica|January 1, 1994
Creutzfeldt-Jakob disease and cerebral amyloid angiopathyF Gray, F Chrétien, P Cesaro, et al.
Cancer|January 15, 1990
Primary lymphoma of the central nervous system. An unresolved therapeutic problemG Socié, C Piprot-Chauffat, M Schlienger, et al.
The American Journal of Cardiovascular Pathology|January 1, 1990
Primary liposarcoma of the heartF Paraf, P Bruneval, A Balaton, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|January 1, 1990
MRI pattern of progressive multifocal leukoencephalopathy (PML) in AIDS. Pathological correlationsP M Trotot, R Vazeux, H K Yamashita, et al.
Gastroenterology|April 1, 1986
Digestive tract and renal small vessel hyalinosis, idiopathic nonarteriosclerotic intracerebral calcifications, retinal ischemic syndrome, and phenotypic abnormalities. A new familial syndromeJ C Rambaud, A Galian, G Touchard, et al.
Diabetes & Metabolism|June 1, 2006
Kearns Sayre syndrome: an unusual form of mitochondrial diabetesM Laloi-Michelin, M Virally, C Jardel, et al.
Neuropathology and Applied Neurobiology|November 26, 2002
High frequency of a 30-bp deletion of Epstein-Barr virus latent membrane protein 1 gene in primary HIV non-Hodgkin's brain lymphomasA-V Vallat-Decouvelaere, M-A Bretel, I Vassias, et al.
Clinical Endocrinology|November 3, 1998
The GnRH receptor gene is preferentially expressed in functioning gonadotroph adenomas and displays a Mae III polymorphism siteM L Kottler, D Seret-Bégué, N Lahlou, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Pageof 14