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G Neri

Showing results (171-180 of 628) with videos related to

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Clinical Pharmacology and Therapeutics|March 1, 1987
Effects of indenolol on blood pressure, lower limb blood flow, adrenergic reflexes, and plasma renin activityL Poggesi, G Masotti, M Boddi, et al.
Nanotechnology|March 6, 2019
α-MoO<sub>3</sub> nanostructure on carbon cloth substrate for dopamine detectionD Murugesan, K Moulaee, G Neri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 9, 2016
Italian neurologists' perception on cognitive symptoms in major depressive disorderG Neri, C Serrati, P Zolo, et al.
Journal of Chemotherapy (Florence, Italy)|July 1, 1989
Effect of quinolones on the production of colony stimulating factors by macrophagesA Pessina, M G Neri, E Mineo, et al.
Peptides|April 15, 2000
Secretin, glucagon, gastric inhibitory polypeptide, parathyroid hormone, and related peptides in the regulation of the hypothalamus- pituitary-adrenal axisG G Nussdorfer, M Bahçelioglu, G Neri, et al.
American Journal of Medical Genetics|October 1, 1984
Sensorineural deafness in the FG syndrome: report on four new casesG Neri, B Blumberg, P V Miles, et al.
American Journal of Hematology|January 1, 1995
Constitutional trisomy 8 mosaicism evolving to primary myelodysplastic syndrome: a new subset of biologically related patients?R Mastrangelo, A Tornesello, S Mastrangelo, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|October 8, 2004
Rhinopharynx endoscopy in the diagnosis of chronic otitis media with effusion in infancyG Neri, E Mennucci, R Ortore, et al.
Clinical Genetics|November 1, 1990
Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivityM Genuardi, M Zollino, A Bellussi, et al.
American Journal of Medical Genetics|May 8, 1999
Cardiac anomalies in the Simpson-Golabi-Behmel syndromeA E Lin, G Neri, R Hughes-Benzie, et al.
Pageof 63

Showing results (171-180 of 628) with videos related to

Sort By:
Pageof 63
Clinical Pharmacology and Therapeutics|March 1, 1987
Effects of indenolol on blood pressure, lower limb blood flow, adrenergic reflexes, and plasma renin activityL Poggesi, G Masotti, M Boddi, et al.
Nanotechnology|March 6, 2019
α-MoO<sub>3</sub> nanostructure on carbon cloth substrate for dopamine detectionD Murugesan, K Moulaee, G Neri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 9, 2016
Italian neurologists' perception on cognitive symptoms in major depressive disorderG Neri, C Serrati, P Zolo, et al.
Journal of Chemotherapy (Florence, Italy)|July 1, 1989
Effect of quinolones on the production of colony stimulating factors by macrophagesA Pessina, M G Neri, E Mineo, et al.
Peptides|April 15, 2000
Secretin, glucagon, gastric inhibitory polypeptide, parathyroid hormone, and related peptides in the regulation of the hypothalamus- pituitary-adrenal axisG G Nussdorfer, M Bahçelioglu, G Neri, et al.
American Journal of Medical Genetics|October 1, 1984
Sensorineural deafness in the FG syndrome: report on four new casesG Neri, B Blumberg, P V Miles, et al.
American Journal of Hematology|January 1, 1995
Constitutional trisomy 8 mosaicism evolving to primary myelodysplastic syndrome: a new subset of biologically related patients?R Mastrangelo, A Tornesello, S Mastrangelo, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|October 8, 2004
Rhinopharynx endoscopy in the diagnosis of chronic otitis media with effusion in infancyG Neri, E Mennucci, R Ortore, et al.
Clinical Genetics|November 1, 1990
Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivityM Genuardi, M Zollino, A Bellussi, et al.
American Journal of Medical Genetics|May 8, 1999
Cardiac anomalies in the Simpson-Golabi-Behmel syndromeA E Lin, G Neri, R Hughes-Benzie, et al.
Pageof 63