Course Information Year 2 Courses: Gastro-Intestinal/Nutrition
See Blackboard (Content>Lecture Materials or Content> Lab Materials) for Weekly Objective and PowerPoint slides.
List of Boards and Beyond Videos along with length
Note: If you are logged into Board and Beyond, these links should go directly to the video.
This Week: 196 minutes total
Gastroenterology
Liver Tumors - Boards and Beyond
10 minutes
Assigned in Weeks 5 & 6
Wilson’s Disease and Hemochromatosis - Boards and Beyond
15 minutes
Assigned in Weeks 5 & 6
Acute Pancreatitis - Boards and Beyond
22 minutes
Assigned in Weeks 5 & 6
Biochemistry
21 minutes
B Vitamins - Boards and Beyond
23 minutes
Assigned in Weeks 5 & 6
20 minutes
Assigned in Weeks 5 & 6
Other Vitamins - Boards and Beyond
33 minutes
Assigned in Weeks 5 & 6
Biostats/Epi
Study Designs - Boards and Beyond
17 minutes
Assigned in Weeks 5 & 6
Sensitivity and Specificity - Boards and Beyond
22 minutes
Assigned in Weeks 2 & 5
Also assigned in CVP
Positive and Negative Predictive Value - Boards and Beyond
13 minutes
Assigned in Weeks 2 & 5
Also assigned in CVP
Ch 325 Nutrient Requirements and Dietary Assessment IN: Harrison’s Principles of Internal Medicine
Ch 328 Enteral and Parenteral Nutrition IN: Harrison’s Principles of Internal Medicine
Ch 45 Jaundice IN: Harrison’s Principles of Internal Medicine
Ch 78 Tumors of the Liver and Biliary Tree IN: Harrison’s Principles of Internal Medicine
Ch 330 Evaluation of Liver Function IN: Harrison’s Principles of Internal Medicine
Ch 331 The Hyperbilirubinemias IN: Harrison’s Principles of Internal Medicine
Ch 333 Toxic and Drug-Induced Hepatitis IN: Harrison’s Principles of Internal Medicine
Ch 332 Viral Hepatitis IN: Harrison’s Principles of Internal Medicine
Ch 334 Chronic Hepatitis IN: Harrison’s Principles of Internal Medicine
Also assigned for Lecture 16
Ch 337 Cirrhosis and Its Complications IN: Harrison’s Principles of Internal Medicine
Also assigned for Lecture 15 & 16
Scroll to Liver Failure Section - read through the Clinical Features - stop at Portal Hypertension
Stop after Key Concepts box
Scroll to Hemachromatosis section the stop after the Clinical Features in the Wilson’s Disease section (before alpha-1 anti-trypsin deficiency)
pages 858-859
Stop after Clinical Features (before Primary Sclerosing Cholangitis)
Stop after Table 5-7 (before Disorders Associated with Defects in Proteins That Regulate Cell Growth)
Stop after Galactosemia (exclude Cystic Fibrosis)
For the following, read Synonyms, General Discussion, Signs & Symptoms, and Causes.
Disregard sections on Affected Populations, Related Disorders, and Therapies
Rare Disease Database, National Organization of Rare Disorders
Homocystinuria due to Cystathionine Beta-Synthase Deficiency
Rare Disease Database, National Organization of Rare Disorders
Rare Disease Database, National Organization of Rare Disorders
Lysosomal Storage Diseases
Lysosomal Storage Disorders in the Newborn
Staretz-Chacham O, Lang TC, LaMarca ME, Krasnewich D, Sidransky E. Lysosomal storage disorders in the newborn. Pediatrics. 2009 Apr;123(4):1191-207. doi: 10.1542/peds.2008-0635.
Lysosomal Storage Disease (in emedicine)
Kruer MC, Steiner RD. Lysosomal storage disease. In: Kao, A, ed. emedicine. New York, NY: Medscape from WebMD; 2015. Available at: https://emedicine.medscape.com/article/1182830-overview
Ch. 411 Lysosomal Storage Diseases IN: Harrison’s Principles of Internal Medicine
Glycogen Storage Disease Type I
Glycogen Storage Disease Type I IN: GeneReviews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Glycogen Storage Disease Type II (Pompe Disease)
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Glycogen Storage Diseases Types I-VII (in emedicine)
Anastasopoulou C, Avichal D, de Lima Corvino DF. Gylcogen storage diseases types I-VII. In: Griffing GT, ed. emedicine. New York, NY: Medscape from WebMD; 2017. Available at: https://emedicine.medscape.com/article/1116574-overview
Glycogen Storage Disease Type III
Glycogen Storage Disease Type III IN: GeneReviews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Glycogen Storage Disease Type V
Glycogen Storage Disease Type V IN: GeneReviews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Mucopolysaccharidoses
Mucopolysaccharidosis Type I IN: GeneReviews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Mucopolysaccharidoses Types I-VII (emedicine)
Baloghova J. Mucopolysaccharidoses Types I-VII In: Elston DM, ed. emedicine. New York, NY: Medscape from WebMD; 2017. Available at: https://emedicine.medscape.com/article/1115193-overview
Mucopolysaccharide and Glycolipid Disorders
from the Medical Biochemistry Page.org
Fabry Disease
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Genetics of Fabry Disease (emedicine)
Desnick RJ. Genetics of Fabry disease. In: Descartes M, ed. emedicine. New York, NY: Medscape from WebMD; 2018. Available at: https://emedicine.medscape.com/article/951451-overview
Fabry Disease:Perspectives from 5 Years of FOS
[Optional reading for those interested in the subject]
Mehta A, Beck M, Linhart A, et al. History of lysosomal storage diseases: an overview. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry Disease: Perspectives from 5 Years of FOS. Oxford: Oxford PharmaGenesis; 2006. Available from: https://www.ncbi.nlm.nih.gov/books/NBK11615/
Gaucher Disease
Gaucher Disease IN: GeneReviews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Sidransky E. Gaucher disease. In: Descartes M, ed. emedicine. New York, NY: Medscape from WebMD; 2018. Available at: https://emedicine.medscape.com/article/944157-overview
Niemann-Pick (Acid Sphingomyelinase Deficiency)
Acid Sphingomyelinase Deficiency IN: GeneReiews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Tay-Sachs Disease (Hexosaminidase A Deficiency)
Hexosaminidase A Deficiency IN: GeneReviews
at least read summary, can read diagnosis and clinical characteristics section if interested (very short reads, with high yield)
Other Metabolic Storage Disease Readings
Defects in Amino and Organic Acid Metabolism
from the Medical Biochemistry Page.org
from the Medical Biochemistry Page.org
Errors in Fatty Acid Metabolism
from the Medical Biochemistry Page.org
from the Medical Biochemistry Page.org
Porphyrias
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Captured on May 5, 2021