'Iron overload' diaporamas de présentation

Gastroentrology & Hepatology day

Gastroentrology & Hepatology day. Today we are going to learn about : Jaundice ,Investigations and Management Chronic Liver diseases Cirrhosis Hepatic encephalopathy Esophageal diseases & Peptic Ulcer. Jaundice Approach, investigation & management. Yasir M Khayyat MBcHB,FRCPC,FACP

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Oxidative Stress in Congenital and Acquired Hemolytic Anemias

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Genetic Screening for Relatives of Hemochromatosis Patients

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Factors that affect Protein Activity and Protein Mechanism

Factors that affect Protein Activity and Protein Mechanism. Chapter 6 (Page 212-218, 225-231). 1. Factors that affect Enzyme Activity. Inhibitors Proteolytic activation Protein modifications Subunit cooperativity and modulators pH. 1I. Proteolytic Activation.

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Metal Ion Transport and Storage

Metal Ion Transport and Storage. Tim Hubin March 3, 1998. References. J. J. R. Frausto da Silva and R. J. P. Williams The Biological Chemistry of the Elements , Clarendon Press, Oxford, 1991. J. A. Cowan Inorganic Biochemistry : An Introduction VCH Publishers, 1994.

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THE THALASSAEMIAS

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A Courtroom Drama: Iron Overload and Chelation Therapy in Myelodysplastic Syndromes (MDS)

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GENETIC/METABOLIC EFFECT OF IRON METABOLISM & RARE ANEMIAS

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Clinical approach to increased serum ferritin

Clinical approach to increased serum ferritin. Yuly Paulin Mendoza DAS hepatology - University of Bern 14 th November 2018. Female B.B. Born 18.9.55. Referred Sep 2018 from obesity consultation for increased serum ferritin . Asymptomatic Medical and personal history

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Biochemistry

Biochemistry. Robert F. Waters PhD. Porphyrin Rings. Produced mainly in: Liver Erythrocyte producing cells of bone marrow Not mature erythrocytes (lack of mitochondria) Initial step and last three steps are in the mitochondria Glycine and Succinyl CoA are precursors

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Indications for Successful Iron Overload Treatment and Monitoring: Other Anaemias

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Mediterranean Anemia-Thalassemia

Mediterranean Anemia-Thalassemia. Kakavoulis Nikolaos Patras Ioannis. What is Thalassaemia ?. Thalassaemia is a group of inherited disorders of hemoglobin synthesis characterized by reduced or absen ce of one or more of the globin chains of adult hemoglobin .

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Ali T. Taher, MD

Ali T. Taher, MD Professor Department of Internal Medicine American University of Beirut Medical Center Beirut, Lebanon. Clinical Case: Managing Iron Overload in a Patient with Transfusion-Independent Thalassaemia Intermedia. Patient Presentation.

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NYU Medical Grand Rounds Clinical Vignette

NYU Medical Grand Rounds Clinical Vignette. Jeffrey Mayne, MD Third Year Resident Internal Medicine 1/17/2012. U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS. Chief Complaint. U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS.

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DRUG,TOXIC AND METABOLIC DISORDERS

DRUG,TOXIC AND METABOLIC DISORDERS. DRUGS AND THE LIVER. Summary of types of drug-induced liver disease. Necrosis - zonal (usually zone 3), diffuse, massive.

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MAGNETIC IRON DETECTOR (MID) WHOLE LIVER IRON OVERLOAD MEASUREMENT BY A NON CRYOGENIC

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Laura Mangiarini 1

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Cardiac Effects of Iron Overload

Cardiac Effects of Iron Overload. Dudley Pennell, MD, FRCP, FACC, FES Director, CMR Unit Royal Brompton Hospital Professor of Cardiology National Heart and Lung Institute Imperial College London, United Kingdom. Why Is the Heart Important in Thalassemia Major?.

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Iron Metabolism

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Controversies in Iron Chelation in Myelodysplastic Syndromes

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