Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Carol West

Showing results (11-20 of 27) with videos related to

Pageof 3
Sort By:
Acta Haematologica|December 28, 2007
SLC40A1 c.1402G-->a results in aberrant splicing, ferroportin truncation after glycine 330, and an autosomal dominant hemochromatosis phenotypePauline L Lee, Terri Gelbart, Carol West, et al.
Blood Cells, Molecules & Diseases|May 11, 2007
SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descentJames C Barton, Ronald T Acton, Pauline L Lee, et al.
American Journal of Hematology|July 14, 2006
Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four casesJames C Barton, Pauline L Lee, Carol West, et al.
The Journal of Bone and Joint Surgery. American Volume|January 17, 2002
Erythrocyte viability in blood salvaged during total joint arthroplasty with cementClifford W Colwell, Ernest Beutler, Carol West, et al.
Blood Cells, Molecules & Diseases|February 25, 2005
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical featuresRonald L Sham, Pradyumna D Phatak, Carol West, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's diseasePauline L Lee, Terri Gelbart, Carol West, et al.
American Journal of Hematology|April 1, 2004
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiencyJames D Hoyer, Steven L Allen, Ernest Beutler, et al.
Blood|March 22, 2003
Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemiaJoan-Lluis Vives Corrons, Estefania Garcia, Joan J Tusell, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Genotypic and phenotypic heterogeneity of African Americans with primary iron overloadJames C Barton, Ronald T Acton, Charles A Rivers, et al.
Blood|October 7, 2004
Glucose-6-phosphate dehydrogenase (G6PD) deficiency-type Zurich: a splice site mutation as an uncommon mechanism producing enzyme deficiencyThomas Efferth, Esther B Bachli, Sonja M Schwarzl, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Acta Haematologica|December 28, 2007
SLC40A1 c.1402G-->a results in aberrant splicing, ferroportin truncation after glycine 330, and an autosomal dominant hemochromatosis phenotypePauline L Lee, Terri Gelbart, Carol West, et al.
Blood Cells, Molecules & Diseases|May 11, 2007
SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descentJames C Barton, Ronald T Acton, Pauline L Lee, et al.
American Journal of Hematology|July 14, 2006
Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four casesJames C Barton, Pauline L Lee, Carol West, et al.
The Journal of Bone and Joint Surgery. American Volume|January 17, 2002
Erythrocyte viability in blood salvaged during total joint arthroplasty with cementClifford W Colwell, Ernest Beutler, Carol West, et al.
Blood Cells, Molecules & Diseases|February 25, 2005
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical featuresRonald L Sham, Pradyumna D Phatak, Carol West, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's diseasePauline L Lee, Terri Gelbart, Carol West, et al.
American Journal of Hematology|April 1, 2004
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiencyJames D Hoyer, Steven L Allen, Ernest Beutler, et al.
Blood|March 22, 2003
Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemiaJoan-Lluis Vives Corrons, Estefania Garcia, Joan J Tusell, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Genotypic and phenotypic heterogeneity of African Americans with primary iron overloadJames C Barton, Ronald T Acton, Charles A Rivers, et al.
Blood|October 7, 2004
Glucose-6-phosphate dehydrogenase (G6PD) deficiency-type Zurich: a splice site mutation as an uncommon mechanism producing enzyme deficiencyThomas Efferth, Esther B Bachli, Sonja M Schwarzl, et al.
Pageof 3