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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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P C Giordano

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Archives of Disease in Childhood|June 26, 2010

One-third of the new paediatric patients with sickle cell disease in The Netherlands are immigrants and do not benefit from neonatal screeningM Peters, K Fijnvandraat, X W van den Tweel, et al.

British Journal of Haematology|December 1, 1996

An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch familiesC L Harteveld, J G Heister, P C Giordano, 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.

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.

Human Genetics|October 1, 1988

Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, IndiaR Fodde, M Losekoot, M H van den Broek, et al.

Journal of Medical Screening|December 21, 2011

Relationship between neonatal screening results by HPLC and the number of α-thalassaemia gene mutations; consequences for the cut-off valueM J Bouva, C Sollaino, L Perseu, 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.

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.

Bone Marrow Transplantation|June 11, 2003

Paediatric allogeneic bone marrow transplantation for homozygous beta-thalassaemia, the Dutch experienceL M Ball, A C Lankester, P C Giordano, et al.

Prenatal Diagnosis|June 6, 2006

Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot studyP C Giordano, A Plancke, C A Van Meir, et al.

Pageof 8

Search research articles

Showing results (61-70 of 72) with videos related to

Sort By:

Pageof 8

Archives of Disease in Childhood|June 26, 2010

One-third of the new paediatric patients with sickle cell disease in The Netherlands are immigrants and do not benefit from neonatal screeningM Peters, K Fijnvandraat, X W van den Tweel, et al.

British Journal of Haematology|December 1, 1996

An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch familiesC L Harteveld, J G Heister, P C Giordano, 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.

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.

Human Genetics|October 1, 1988

Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, IndiaR Fodde, M Losekoot, M H van den Broek, et al.

Journal of Medical Screening|December 21, 2011

Relationship between neonatal screening results by HPLC and the number of α-thalassaemia gene mutations; consequences for the cut-off valueM J Bouva, C Sollaino, L Perseu, 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.

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.

Bone Marrow Transplantation|June 11, 2003

Paediatric allogeneic bone marrow transplantation for homozygous beta-thalassaemia, the Dutch experienceL M Ball, A C Lankester, P C Giordano, et al.

Prenatal Diagnosis|June 6, 2006

Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot studyP C Giordano, A Plancke, C A Van Meir, et al.

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