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L Leclerc

Showing results (141-150 of 155) with videos related to

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Journal of Cardiovascular Pharmacology|August 1, 1993
Administration of nebivolol after coronary artery bypass in patients with altered left ventricular functionM Goldstein, J L Vincent, J M De Smet, et al.
Inhalation Toxicology|August 7, 2012
Size of submicrometric and nanometric particles affect cellular uptake and biological activity of macrophages in vitroL Leclerc, W Rima, D Boudard, et al.
Thyroid : Official Journal of the American Thyroid Association|December 14, 2004
Thyroid carcinomas involving follicular and parafollicular C cells: seventeen cases with characterization of RET oncogenic activationM-C Vantyghem, P Pigny, E Leteurtre, et al.
Hemoglobin|March 19, 1999
Southeast Asian ovalocytosis in White personsP O Schischmanoff, T Cynober, F Miélot, et al.
Clinical Endocrinology|March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Clinical Endocrinology|May 14, 1998
Prognostic factors for survival and for biochemical cure in medullary thyroid carcinoma: results in 899 patients. The GETC Study Group. Groupe d'étude des tumeurs à calcitonineE Modigliani, R Cohen, J M Campos, et al.
Annales De Chirurgie|September 30, 1998
[Early therapeutic management of patients genetically predisposed to medullary thyroid cancer]A Murat, E Modigliani, B Conte-Devolx, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1995
Developmental and regional expression pattern of a novel NMDA receptor-like subunit (NMDAR-L) in the rodent brainN J Sucher, S Akbarian, C L Chi, et al.
Neurology|September 11, 2009
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortN Ticozzi, V Silani, A L LeClerc, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosisN Ticozzi, C Vance, A L Leclerc, et al.
Pageof 16

Showing results (141-150 of 155) with videos related to

Sort By:
Pageof 16
Journal of Cardiovascular Pharmacology|August 1, 1993
Administration of nebivolol after coronary artery bypass in patients with altered left ventricular functionM Goldstein, J L Vincent, J M De Smet, et al.
Inhalation Toxicology|August 7, 2012
Size of submicrometric and nanometric particles affect cellular uptake and biological activity of macrophages in vitroL Leclerc, W Rima, D Boudard, et al.
Thyroid : Official Journal of the American Thyroid Association|December 14, 2004
Thyroid carcinomas involving follicular and parafollicular C cells: seventeen cases with characterization of RET oncogenic activationM-C Vantyghem, P Pigny, E Leteurtre, et al.
Hemoglobin|March 19, 1999
Southeast Asian ovalocytosis in White personsP O Schischmanoff, T Cynober, F Miélot, et al.
Clinical Endocrinology|March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Clinical Endocrinology|May 14, 1998
Prognostic factors for survival and for biochemical cure in medullary thyroid carcinoma: results in 899 patients. The GETC Study Group. Groupe d'étude des tumeurs à calcitonineE Modigliani, R Cohen, J M Campos, et al.
Annales De Chirurgie|September 30, 1998
[Early therapeutic management of patients genetically predisposed to medullary thyroid cancer]A Murat, E Modigliani, B Conte-Devolx, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1995
Developmental and regional expression pattern of a novel NMDA receptor-like subunit (NMDAR-L) in the rodent brainN J Sucher, S Akbarian, C L Chi, et al.
Neurology|September 11, 2009
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortN Ticozzi, V Silani, A L LeClerc, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosisN Ticozzi, C Vance, A L Leclerc, et al.
Pageof 16