Cargando…

Effect of standard phlebotomy on myocardial and hepatic iron levels in newly diagnosed cardiac asymptomatic hereditary hemochromatosis subjects with C282Y homozygosity

Detalles Bibliográficos
Autores principales:	Shizukuda, Yukitaka, Patricia Bandettini, W., Rosing, Douglas R.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2023
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188495/ https://www.ncbi.nlm.nih.gov/pubmed/37206277 http://dx.doi.org/10.1002/jha2.662

Ejemplares similares

Clinical Penetrance of Hereditary Hemochromatosis-Related End-Organ Damage of C282Y Homozygosity, A Newfoundland Experience
por: Lim, Dennis R., et al.
Publicado: (2020)

Effect of Native American ancestry on iron-related phenotypes of Alabama hemochromatosis probands with HFE C282Y homozygosity
por: Barton, James C, et al.
Publicado: (2006)

HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity
por: Barton, James C., et al.
Publicado: (2022)

Iron overload and arrhythmias: Influence of confounding factors
por: Shizukuda, Yukitaka, et al.
Publicado: (2019)

Autoimmune Conditions in 235 Hemochromatosis Probands with HFE C282Y Homozygosity and Their First-Degree Relatives
por: Barton, James C., et al.
Publicado: (2015)

Phlebotomy increases cadmium uptake in hemochromatosis.
por: Akesson, A, et al.
Publicado: (2000)

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama
por: Barton, James C, et al.
Publicado: (2002)

A farewell to phlebotomy—use of placenta-derived drugs Laennec and Porcine for improving hereditary hemochromatosis without phlebotomy: a case report
por: Hamada, Yuki, et al.
Publicado: (2022)

Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox
por: Lescano, Manuel A, et al.
Publicado: (2017)

Effect of C282Y Genotype on Self-Reported Musculoskeletal Complications in Hereditary Hemochromatosis
por: Camacho, António, et al.
Publicado: (2015)

A predictive model for estimating the number of erythrocytapheresis or phlebotomy treatments for patients with naïve hereditary hemochromatosis
por: Rombout‐Sestrienkova, Eva, et al.
Publicado: (2020)

Patients with hereditary hemochromatosis reach safe range of transferrin saturation sooner with erythrocytaphereses than with phlebotomies
por: Rombout‐Sestrienkova, Eva, et al.
Publicado: (2021)

Total blood lymphocyte counts in hemochromatosis probands with HFE C282Y homozygosity: relationship to severity of iron overload and HLA-A and -B alleles and haplotypes
por: Barton, James C, et al.
Publicado: (2005)

Hereditary Hemochromatosis and Iron Metabolism
por: Carlson, Joyce, et al.
Publicado: (2001)

Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients
por: Terzi, Yunus Kasım, et al.
Publicado: (2016)

NTBI levels in C282Y homozygotes after therapeutic phlebotomy
por: Ryan, Eleanor, et al.
Publicado: (2022)

Abdominal pain and cirrhosis at diagnosis of hemochromatosis: Analysis of 219 referred probands with HFE p.C282Y homozygosity and a literature review
por: Barton, James C., et al.
Publicado: (2021)

Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype
por: Adams, Paul, et al.
Publicado: (2018)

HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasian is extremely rare in Korean population.
por: Lee, J. Y., et al.
Publicado: (2000)

Non-alcoholic fatty liver disease in hemochromatosis probands with iron overload and HFE p.C282Y/p.C282Y
por: Barton, James C., et al.
Publicado: (2023)

Histologic Lesions of Porto-Sinusoidal Vascular Disease Following Phlebotomy in Hemochromatosis
por: El Jabbour, Tony, et al.
Publicado: (2020)

In vivo adenine base editing reverts C282Y and improves iron metabolism in hemochromatosis mice
por: Rovai, Alice, et al.
Publicado: (2022)

Hereditary hemochromatosis
por: Geller, Stephen A., et al.
Publicado: (2015)

Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y
por: Barton, James C., et al.
Publicado: (2022)

Hereditary hemochromatosis beyond hyperferritinemia: Clinical and laboratory investigation of the patient’s profile submitted to phlebotomy in two reference centers in southern Brazil
por: Kersting, Nathalia, et al.
Publicado: (2023)

Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan
por: Sharif, Yasir, et al.
Publicado: (2019)

Expression of hereditary hemochromatosis C282Y HFE protein in HEK293 cells activates specific endoplasmic reticulum stress responses
por: Lawless, Matthew W, et al.
Publicado: (2007)

Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
por: Dostalikova-Cimburova, Marketa, et al.
Publicado: (2012)

Comment on: Hemochromatosis (HFE) gene mutations (H63D and C282Y) and iron overload in beta-thalassemia major
por: Yasri, Sora
Publicado: (2019)

Porphyria cutanea tarda associated with HFE C282Y homozygosity, iron overload, and use of a contraceptive vaginal ring
por: Barton, James C., et al.
Publicado: (2016)

Polycythemia and Anemia in Hereditary Hemochromatosis
por: Khan, Adnan Aman, et al.
Publicado: (2020)

Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network
por: Gallego, Carlos J., et al.
Publicado: (2015)

Leukocyte telomere length is associated with iron overload in male adults with hereditary hemochromatosis
por: Martín, Maximilino, et al.
Publicado: (2020)

The effect of a natural polyphenol supplement on iron absorption in adults with hereditary hemochromatosis
por: Buerkli, Simone, et al.
Publicado: (2022)

Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay
por: Cukjati, Marko, et al.
Publicado: (2007)

Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis
por: Santos, Paulo C. J. L., et al.
Publicado: (2012)

Hypogonadotropic hypogonadism in men with hereditary hemochromatosis
por: El Osta, Rabih, et al.
Publicado: (2017)

Hereditary Hemochromatosis: A Cardiac Perspective
por: Joshi, Pranay K, et al.
Publicado: (2021)

Overview of Ankle Arthropathy in Hereditary Hemochromatosis
por: Calori, Sara, et al.
Publicado: (2023)

A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload
por: Cruz, Eugénia, et al.
Publicado: (2006)

Cannot write session to /tmp/vufind_sessions/sess_5buo2q2qhbp45om2jabanjqug1