Cargando…

Hæmochromatosis

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Thacker 1936
Materias:	Reviews
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5170576/

Ejemplares similares

A CASE OF HÆMOCHROMATOSIS.—THE RELATION OF HÆMOCHROMATOSIS TO BRONZED DIABETES
por: Opie, Eugene L.
Publicado: (1899)

Haemochromatosis revisited
por: Alvarenga, Aline Morgan, et al.
Publicado: (2022)

The unfolded protein response in hereditary haemochromatosis
por: De Almeida, SF, et al.
Publicado: (2008)

Two Cases of Hæmochromatosis
por: Harrington, Archibald W., et al.
Publicado: (1939)

REPORT ON CASE OF HÆMOCHROMATOSIS OR BRONZED DIABETES
por: Coates, Foster
Publicado: (1936)

Pseudogout, chondrocalcinosis and the early recognition of haemochromatosis.
por: Elborn, J. S., et al.
Publicado: (1992)

Hepatocellular Carcinoma Arising in Non-Cirrhotic Haemochromatosis
por: Thompson, N. P., et al.
Publicado: (1995)

Secondary Haemochromatosis in a Patient with Thalassemia Intermedia
por: ROTARU, IONELA, et al.
Publicado: (2014)

Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
por: Riley, Matthew J., et al.
Publicado: (2020)

A Late and Complex Presentation of Hereditary Haemochromatosis
por: Kurian, Roshini, et al.
Publicado: (2022)

Quality of life utility values for hereditary haemochromatosis in Australia
por: de Graaff, Barbara, et al.
Publicado: (2016)

Difficult diagnosis of cardiac haemochromatosis: a case report
por: Sudmantaitė, Vaida, et al.
Publicado: (2020)

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
por: Smyk, Daniel S., et al.
Publicado: (2013)

Haemochromatosis in a kidney transplant recipient: a case report
por: Zakrocka, Izabela, et al.
Publicado: (2021)

The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
por: van Bommel, Erik JM, et al.
Publicado: (2021)

Pulmonary Haemosiderosis Secondary to Hereditary Haemochromatosis; a Case Report
por: Jehangir, Waqas, et al.
Publicado: (2020)

Haemochromatosis patients' research priorities: Towards an improved quality of life
por: Romero‐Cortadellas, Lídia, et al.
Publicado: (2023)

22. Hereditary Haemochromatosis presented as a case of early Rheumatoid Arthritis
por: Hum, Ryan, et al.
Publicado: (2017)

Systemic iron reduction by venesection alters the gut microbiome in patients with haemochromatosis
por: Parmanand, Bhavika, et al.
Publicado: (2020)

A pathological study of idiopathic haemochromatosis and its relationship to siderosis in liver cirrhosis.
por: Sinniah, R.
Publicado: (1973)

Acute Free-Iron Exposure Does Not Explain the Impaired Haemorheology Associated with Haemochromatosis
por: McNamee, Antony P., et al.
Publicado: (2016)

Haemochromatosis in end-stage renal disease: when waste is a treatment option
por: Oettl, Tobias, et al.
Publicado: (2009)

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
por: Dejaco, Christian, et al.
Publicado: (2017)

An efficient machine learning-based approach for screening individuals at risk of hereditary haemochromatosis
por: Martins Conde, Patricia, et al.
Publicado: (2020)

Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
por: Pilling, Luke C, et al.
Publicado: (2019)

Increased transferrin saturation is associated with subgingival microbiota dysbiosis and severe periodontitis in genetic haemochromatosis
por: Boyer, Emile, et al.
Publicado: (2018)

Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
Publicado: (2019)

Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
por: King, Caitriona, et al.
Publicado: (2006)

Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
por: de Graaff, Barbara, et al.
Publicado: (2016)

A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population
por: Hubacek, J.A., et al.
Publicado: (2023)

Ferroportin-related haemochromatosis associated with novel Y64H mutation of the SCL40A1 gene
por: Raszeja-Wyszomirska, Joanna, et al.
Publicado: (2014)

Key-interventions derived from three evidence based guidelines for management and follow-up of patients with HFE haemochromatosis
por: Vanclooster, Annick, et al.
Publicado: (2016)

Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
por: Krasin, Elisha, et al.
Publicado: (2021)

SLN124, a GalNAc-siRNA Conjugate Targeting TMPRSS6, Efficiently Prevents Iron Overload in Hereditary Haemochromatosis Type 1
por: Altamura, Sandro, et al.
Publicado: (2019)

A Review of Nutrients and Compounds, Which Promote or Inhibit Intestinal Iron Absorption: Making a Platform for Dietary Measures That Can Reduce Iron Uptake in Patients with Genetic Haemochromatosis
por: Milman, Nils Thorm
Publicado: (2020)

Letter to the editor regarding: “A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population” clinica chimica acta 538 (2023) 211–215
por: Atkins, Janice L., et al.
Publicado: (2023)

Medical Research Council: The Nutritive Value of Fruits, Vegetables and Nuts
Publicado: (1936)

Clinical Heart Disease
Publicado: (1936)

Diseases of the Respiratory Tract: Eighth Annual Graduate Fortnight of the New York Academy of Medicine. 1936
Publicado: (1936)

Medical Research Council: Investigations on Respiratory Dust Disease in Operatives in the Cotton Industry
Publicado: (1936)

Cannot write session to /tmp/vufind_sessions/sess_t6e1b3a06163s6a0qc421i2sh8