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F Bernini

Showing results (161-170 of 172) with videos related to

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Human Genetics|January 1, 1984
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch familyF H Menko, O L Bijvoet, P Meera Khan, et al.
Annals of Hematology|January 6, 1999
Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G-->T) mutationP C Giordano, C L Harteveld, J J Michiels, et al.
Contemporary Clinical Dentistry|June 26, 2014
Unusual bilateral dentigerous cysts in a nonsyndromic patient assessed by cone beam computed tomographyThaís Sumie Nozu Imada, V Tieghi Neto, G F Bernini, et al.
British Journal of Haematology|March 1, 1997
Atypical HbH disease in a Surinamese patient resulting from a combination of the -SEA and -alpha 3.7 deletions with HbC heterozygosityP C Giordano, C L Harteveld, J J Michiels, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Annals of Human Genetics|January 1, 1983
Absence of close linkage between Hereditary spherocytosis (SPH) and 24 genetic marker systems including HLA and GMB M de Jongh, H A Blacklock, P Reekers, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 30, 2018
Vitamin D replacement ameliorates serum lipoprotein functions, adipokine profile and subclinical atherosclerosis in pre-menopausal womenD Greco, D Kocyigit, M P Adorni, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|November 2, 2023
Neural Stimulation Hardware for the Selective Intrafascicular Modulation of the Vagus NerveI Strauss, F Agnesi, C Zinno, et al.
Atherosclerosis|May 28, 2016
Lomitapide affects HDL composition and functionR Yahya, E Favari, L Calabresi, et al.
APL Bioengineering|October 9, 2023
Decoding bladder state from pudendal intraneural signals in pigsA Giannotti, S Lo Vecchio, S Musco, et al.
Pageof 18

Showing results (161-170 of 172) with videos related to

Sort By:
Pageof 18
Human Genetics|January 1, 1984
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch familyF H Menko, O L Bijvoet, P Meera Khan, et al.
Annals of Hematology|January 6, 1999
Phenotype variability of the dominant beta-thalassemia induced in four Dutch families by the rare cd121 (G-->T) mutationP C Giordano, C L Harteveld, J J Michiels, et al.
Contemporary Clinical Dentistry|June 26, 2014
Unusual bilateral dentigerous cysts in a nonsyndromic patient assessed by cone beam computed tomographyThaís Sumie Nozu Imada, V Tieghi Neto, G F Bernini, et al.
British Journal of Haematology|March 1, 1997
Atypical HbH disease in a Surinamese patient resulting from a combination of the -SEA and -alpha 3.7 deletions with HbC heterozygosityP C Giordano, C L Harteveld, J J Michiels, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Annals of Human Genetics|January 1, 1983
Absence of close linkage between Hereditary spherocytosis (SPH) and 24 genetic marker systems including HLA and GMB M de Jongh, H A Blacklock, P Reekers, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|June 30, 2018
Vitamin D replacement ameliorates serum lipoprotein functions, adipokine profile and subclinical atherosclerosis in pre-menopausal womenD Greco, D Kocyigit, M P Adorni, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|November 2, 2023
Neural Stimulation Hardware for the Selective Intrafascicular Modulation of the Vagus NerveI Strauss, F Agnesi, C Zinno, et al.
Atherosclerosis|May 28, 2016
Lomitapide affects HDL composition and functionR Yahya, E Favari, L Calabresi, et al.
APL Bioengineering|October 9, 2023
Decoding bladder state from pudendal intraneural signals in pigsA Giannotti, S Lo Vecchio, S Musco, et al.
Pageof 18