F Bernini|R Paoletti - JoVE Visualize

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Hemoglobin|May 21, 1999

Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.

Laboratory Investigation; a Journal of Technical Methods and Pathology|August 1, 1996

Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene productD J Peters, L Spruit, R Klingel, et al.

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.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 23, 1998

Peripheral markers in testing pathophysiological hypotheses and diagnosing Alzheimer's diseaseL Gasparini, M Racchi, G Binetti, 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.

Cancer Research|February 1, 1995

In vivo enhanced antitumor activity of carmustine [N,N'-bis(2-chloroethyl)-N-nitrosourea] by simvastatinM R Soma, R Baetta, M R De Renzis, 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.

Advances in Experimental Medicine and Biology|January 1, 1978

Pilot epidemiological studies in thrombosisJ M Iacono, R M Dougherty, R Paoletti, et al.

Pageof 36

Showing results (251-260 of 357) with videos related to

Sort By:

Pageof 36

Hemoglobin|May 21, 1999

Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.

Laboratory Investigation; a Journal of Technical Methods and Pathology|August 1, 1996

Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene productD J Peters, L Spruit, R Klingel, et al.

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.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 23, 1998

Peripheral markers in testing pathophysiological hypotheses and diagnosing Alzheimer's diseaseL Gasparini, M Racchi, G Binetti, 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.

Cancer Research|February 1, 1995

In vivo enhanced antitumor activity of carmustine [N,N'-bis(2-chloroethyl)-N-nitrosourea] by simvastatinM R Soma, R Baetta, M R De Renzis, 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.

Advances in Experimental Medicine and Biology|January 1, 1978

Pilot epidemiological studies in thrombosisJ M Iacono, R M Dougherty, R Paoletti, et al.

Pageof 36