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USMLE – What's It
Purpose of this handout Congratulations on making it to Year 2 of medical school! You are that much closer to having your Doctor of Medicine degree. If you want to PRACTICE medicine, however, you have to be licensed, and in order to be licensed you must first pass all four United States Medical Licensing Exams. This book is intended as a starting point in your preparation for getting past the first hurdle, Step 1. It contains study tips, suggestions, resources, and advice. Please remember, however, that no single approach to studying is right for everyone. USMLE – What is it for? In order to become a licensed physician in the United States, individuals must pass a series of examinations conducted by the National Board of Medical Examiners (NBME). These examinations are the United States Medical Licensing Examinations, or USMLE. Currently there are four separate exams which must be passed in order to be eligible for medical licensure: Step 1, usually taken after the completion of the second year of medical school; Step 2 Clinical Knowledge (CK), this is usually taken by December 31st of Year 4 Step 2 Clinical Skills (CS), this is usually be taken by December 31st of Year 4 Step 3, typically taken during the first (intern) year of post graduate training. Requirements other than passing all of the above mentioned steps for licensure in each state are set by each state’s medical licensing board. For example, each state board determines the maximum number of times that a person may take each Step exam and still remain eligible for licensure. -
Eponyms in Digestive System Pathology
Panacea Journal of Medical Sciences 2020;10(2):58–67 Content available at: https://www.ipinnovative.com/open-access-journals Panacea Journal of Medical Sciences Journal homepage: www.ipinnovative.com Review Article Eponyms in digestive system pathology Ahmad Al Malki1, Hassan Al Solami2, Khalid Al Aboud3,*, Wafa Al Joaid3, Saleha Al Asmary4 1Dept. of Surgery, King Faisal Hospital, Makkah, Saudi Arabia 2Dept. of Gastroenterology, King Faisal Hospital, Makkah, Saudi Arabia 3Dept. of Public Health, King Faisal Hospital, Makkah, Saudi Arabia 4Nursing College, King Saud University, Riyadh, Saudi Arabia ARTICLEINFO ABSTRACT Article history: Eponyms are known type of medical terminology. This mini-review provide highlights on some of the Received 04-05-2020 eponyms of the digestive system pathology. Accepted 06-05-2020 Available online 26-08-2020 © 2020 Published by Innovative Publication. This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/) Keywords: Diseases Eponyms Gastroenterology 1. Introduction An eponym is a person, place, or thing after whom or which someone or something is named. There are several anatomical and pathological eponyms in the digestive systems. 1–4 We have reviewed selected eponyms of the digestive system pathology, and present it in a tabulation form in table.1. 5–41 The remarks surrounding the terms and eponyms in the digestive system are no different from those encountered in medicine in general. We are not interested to mention these are remarks, as these have been discussed extentensively in the medical literature. However, we list few examples. Some of the eponyms are no longer in use. -
Special Activities
59th Annual International Conference of the Wildlife Disease Association Abstracts & Program May 30 - June 4, 2010 Puerto Iguazú Misiones, Argentina Iguazú, Argentina. 59th Annual International Conference of the Wildlife Disease Association WDA 2010 OFFICERS AND COUNCIL MEMBERS OFFICERS President…………………………….…………………...………..………..Lynn Creekmore Vice-President………………………………...…………………..….Dolores Gavier-Widén Treasurer………………………………………..……..……….….……..…….Laurie Baeten Secretary……………………………………………..………..……………….…Pauline Nol Past President…………………………………………………..………Charles van Riper III COUNCIL MEMBERS AT LARGE Thierry Work Samantha Gibbs Wayne Boardman Christine Kreuder Johnson Kristin Mansfield Colin Gillin STUDENT COUNCIL MEMBER Terra Kelly SECTION CHAIRS Australasian Section…………………………..……………………….......Jenny McLelland European Section……………………..………………………………..……….….Paul Duff Nordic Section………………………..………………………………..………….Erik Ågren Wildlife Veterinarian Section……..…………………………………..…………Colin Gillin JOURNAL EDITOR Jim Mills NEWSLETTER EDITOR Jenny Powers WEBSITE EDITOR Bridget Schuler BUSINESS MANAGER Kay Rose EXECUTIVE MANAGER Ed Addison ii Iguazú, Argentina. 59th Annual International Conference of the Wildlife Disease Association ORGANIZING COMMITTEE Executive President and Press, media and On-site Volunteers Conference Chair publicity Judy Uhart Marcela Uhart Miguel Saggese Marcela Orozco Carlos Sanchez Maria Palamar General Secretary and Flavia Miranda Program Chair Registrations Elizabeth Chang Reissig Pablo Beldomenico Management Patricia Mendoza Hebe Ferreyra -
A Novel Splice Site Indel Alteration in the EIF2AK3 Gene Is Responsible For
Sümegi et al. BMC Medical Genetics (2020) 21:61 https://doi.org/10.1186/s12881-020-0985-6 RESEARCH ARTICLE Open Access A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary Andrea Sümegi1, Zoltán Hendrik2, Tamás Gáll1, Enikő Felszeghy3, Katalin Szakszon3, Péter Antal-Szalmás4, Lívia Beke2, Ágnes Papp3, Gábor Méhes2, József Balla1,5 and György Balla1,3* Abstract Background: Wolcott-Rallison Syndrome (WRS) is a rare autosomal recessive disease that is the most common cause of neonatal diabetes in consanguineous families. WRS is caused by various genetic alterations of the Eukaryotic Translation Initiation Factor 2-Alpha Kinase 3 (EIF2AK3) gene. Methods: Genetic analysis of a consanguineous family where two children were diagnosed with WRS was performed by Sanger sequencing. The altered protein was investigated by in vitro cloning, expression and immunohistochemistry. Results: The first cases in Hungary, − two patients in one family, where the parents were fourth-degree cousins - showed the typical clinical features of WRS: early onset diabetes mellitus with hyperglycemia, growth retardation, infection-induced multiple organ failure. The genetic background of the disease was a novel alteration in the EIF2AK3 gene involving the splice site of exon 11– intron 11–12 boundary: g.53051_53062delinsTG. According to cDNA sequencing this created a new splice site and resulted in a frameshift and the development of an early termination codon at amino acid position 633 (p.Pro627AspfsTer7). Based on in vitro cloning and expression studies, the truncated protein was functionally inactive. Immunohistochemistry revealed that the intact protein was absent in the islets of pancreas, furthermore insulin expressing cells were also dramatically diminished. -
Methodical Instruction for Lectures
Ministry of Public Health of Ukraine Ukrainian Medical Stomatological Academy Approved at the meeting of the department Infection diseases and epidemiology «28» August 2019 protocol № 1 from «28» August 2019 the Head of the Department _________ Koval T.I. Methodical Instruction for lectures Study discipline Infectious diseases and epidemiology Module № Infectious diseases and epidemiology Topic Acute respiratory viral infections. Clinical characteristics and prevention of influenza. Course 4 Faculty Stomatological Number of teaching hours: 2 Poltava -2019 1. Scientific and methodological substantiation of the topic. Infectious diseases today remain extremely relevant. In the past decades, previously unknown infections — HIV infection, Lyme disease, campylobacteriosis, SARS, and others — have spread, and the achieved reduction in the incidence of diphtheria and measles has not been maintained. There is an increase in the incidence of viral hepatitis, acute intestinal infectious diseases, tuberculosis among the population of Ukraine and other countries. The clinical manifestations of infectious diseases can be different, often atypical, can lead to hospitalization of the patient in a medical institution of any profile. The ability to recognize infectious pathology, correctly conduct differential diagnosis, prescribe appropriate treatment, ensure that the necessary preventive measures are taken that are necessary for a doctor of any specialty. In our country, the classification of infectious diseases, academician L.V. Gromashevsky, has become most widespread. The classification is based on the principle of the predominant localization of the pathogen in the body, which is due to a certain transmission mechanism. One of the most important components in the treatment of patients for infectious diseases is inpatient treatment. Infectious Diseases Hospital is a special medical institution, which has a number of structural and functional units in order to ensure effective treatment, examination and isolation of patients. -
Occupational Diseases
OCCUPATIONAL DISEASES OCCUPATIONAL DISEASES ОДЕСЬКИЙ ДЕРЖАВНИЙ МЕДИЧНИЙ УНІВЕРСИТЕТ THE ODESSA STATE MEDICAL UNIVERSITY Áiáëiîòåêà ñòóäåíòà-ìåäèêà Medical Student’s Library Започатковано 1999 р. на честь 100-річчя Одеського державного медичного університету (1900–2000 рр.) Initiated in 1999 to mark the Centenary of the Odessa State Medical University (1900–2000) 1 OCCUPATIONAL DISEASES Recommended by the Central Methodical Committee for Higher Medical Education of the Ministry of Health of Ukraine as a manual for students of higher medical educational establishments of the IV level of accreditation using English Odessa The Odessa State Medical University 2009 BBC 54.1,7я73 UDC 616-057(075.8) Authors: O. M. Ignatyev, N. A. Matsegora, T. O. Yermolenko, T. P. Oparina, K. A. Yarmula, Yu. M. Vorokhta Reviewers: Professor G. A. Bondarenko, the head of the Department of Occupational Diseases and Radiation Medicine of the Donetzk Medical University named after M. Gorky, MD Professor I. F. Kostyuk, the head of the Department of Internal and Occupational Diseases of the Kharkiv State Medical University, MD This manual contains information about etiology, epidemiology, patho- genesis of occupational diseases, classifications, new methods of exami- nation, clinical forms and presentation, differential diagnosis, complica- tions and treatment. It includes the questions of prophylaxis, modern trends in treatment according to WHO adopted instructions, working capacity expert exam. The represented material is composed according to occupational dis- eases study programme and it is recommended for the students of higher medical educational establishments of the IV accreditation standard and doctors of various specialities. Рекомендовано Центральним методичним кабінетом з вищої медичної освіти МОЗ України як навчальний посібник для студентів вищих медичних навчальних закладів IV рівня акредитації, які опановують навчальну дисципліну англiйською мовою (Протокол № 4 від 24.12.2007 р. -
Table I. Genodermatoses with Known Gene Defects 92 Pulkkinen
92 Pulkkinen, Ringpfeil, and Uitto JAM ACAD DERMATOL JULY 2002 Table I. Genodermatoses with known gene defects Reference Disease Mutated gene* Affected protein/function No.† Epidermal fragility disorders DEB COL7A1 Type VII collagen 6 Junctional EB LAMA3, LAMB3, ␣3, 3, and ␥2 chains of laminin 5, 6 LAMC2, COL17A1 type XVII collagen EB with pyloric atresia ITGA6, ITGB4 ␣64 Integrin 6 EB with muscular dystrophy PLEC1 Plectin 6 EB simplex KRT5, KRT14 Keratins 5 and 14 46 Ectodermal dysplasia with skin fragility PKP1 Plakophilin 1 47 Hailey-Hailey disease ATP2C1 ATP-dependent calcium transporter 13 Keratinization disorders Epidermolytic hyperkeratosis KRT1, KRT10 Keratins 1 and 10 46 Ichthyosis hystrix KRT1 Keratin 1 48 Epidermolytic PPK KRT9 Keratin 9 46 Nonepidermolytic PPK KRT1, KRT16 Keratins 1 and 16 46 Ichthyosis bullosa of Siemens KRT2e Keratin 2e 46 Pachyonychia congenita, types 1 and 2 KRT6a, KRT6b, KRT16, Keratins 6a, 6b, 16, and 17 46 KRT17 White sponge naevus KRT4, KRT13 Keratins 4 and 13 46 X-linked recessive ichthyosis STS Steroid sulfatase 49 Lamellar ichthyosis TGM1 Transglutaminase 1 50 Mutilating keratoderma with ichthyosis LOR Loricrin 10 Vohwinkel’s syndrome GJB2 Connexin 26 12 PPK with deafness GJB2 Connexin 26 12 Erythrokeratodermia variabilis GJB3, GJB4 Connexins 31 and 30.3 12 Darier disease ATP2A2 ATP-dependent calcium 14 transporter Striate PPK DSP, DSG1 Desmoplakin, desmoglein 1 51, 52 Conradi-Hu¨nermann-Happle syndrome EBP Delta 8-delta 7 sterol isomerase 53 (emopamil binding protein) Mal de Meleda ARS SLURP-1 -
Path Pulmonary Outline
Pathology Pulmonary ATELECTASIS Neonatal Atelectasis ‐ The lungs of the neonate never inflate, a consequence of congenital defect, premature birth (insufficient surfactant), or other consequence, also called Patchy Atelectasis Adult or Acquired Atelectasis ‐ Collapse of Previously Inflated lung, creating areas of “airless parenchyma” ‐ Produces a well‐perfused but poorly‐ventilated region, predisposing for infection Decreased Volume ‐ Is a reversible disorder (except in the case of contraction) outside pleural space ‐ Resorption Atelectasis o Consequence of complete obstruction without impairment to blood flow Blockage o A decreased lung volume results in a mediastinal shift towards affected lung o Caused by a mucous plug associated with Asthma, Bronchitis, or Aspiration Pneumonia ‐ Compression Atelectasis o Consequence of partially or totally filled pleura with exudate (CHF), tumor, air (pneumothorax), blood (hemothorax), when air pressure threatens the function of lungs and great vessels (tension pneumothorax), or with an extra‐pulmonary mass compressing Something within lung parenchyma. pleural space compressing o Compressed lung tissue cannot expand and is therefore poorly ventilated. parenchyma o Compression pushes lung resulting in a mediastinal shift away from affected lung ‐ Contraction Atelectasis o Fibrotic changes prevent expansion, resulting in reduced lung volume and ventilation Fibrotic o This form is irreversible Changes are Irreversible PULMONARY EDEMA Pulmonary Edema is simply the accumulation of fluid in the alveolar -
数字 Accessory Bronchus 副気管支 Accessory Fissure 副葉間裂
数字 accentuation 亢進 accessory 副の 数字 accessory bronchus 副気管支 accessory fissure 副葉間裂 10-year survival 10年生存 accessory lobe 副肺葉 18F-fluorodeoxy glucose (FDG) 18F-フルオロデオキシグルコース accessory lung 副肺 2,3-diphosphoglycerate (2,3-DPG) 2,3ジフォスフォグリセレート accessory nasal sinus 副鼻腔 201TI (thallium-201) タリウム accessory trachea 副気管 5-fluorouracil(FU) 5-フルオロウラシル acclimation 順化 5-HT3 receptor antagonist 5-HT3レセプター拮抗薬 acclimation 馴化 5-hydroxytryptamine 5-ヒドロオキシトリプタミン acclimatization 気候順応 5-year survival 5年生存 acclimatization 順化 99mTc-macroaggregated albumin (99mTc-MAA) 99mTc標識大 acclimatization 馴化 凝集アルブミン accommodation 順応 accommodation 調節 accommodation to high altitude 高所順(適)応 A ACE polymorphism ACE遺伝子多型 acetone body アセトン体 abdomen 腹部 acetonuria アセトン尿[症] abdominal 腹部[側]の acetylcholine(ACh) アセチルコリン abdominal breathing 腹式呼吸 acetylcholine receptor (AchR, AChR) アセチルコリン受容体(レセプ abdominal cavity 腹腔 ター) abdominal pressure 腹腔内圧 acetylcholinesterase (AchE, AChE) アセチルコリンエステラーゼ abdominal respiration 腹式呼吸 achalasia アカラシア abdominal wall reflex 腹壁反射 achalasia 弛緩不能症 abduction 外転 achalasia [噴門]無弛緩[症] aberrant 走性 achromatocyte (achromocyte) 無血色素[赤]血球 aberrant 迷入性 achromatocyte (achromocyte) 無へモグロビン[赤]血球 aberrant artery 迷入動脈 acid 酸 aberration 迷入 acid 酸性 ablation 剥離 acid base equilibrium 酸塩基平衡 abnormal breath sound(s) 異常呼吸音 acid fast 抗酸性の abortive 早産の acid fast bacillus 抗酸菌 abortive 頓挫性(型) acid-base 酸―塩基 abortive 不全型 acid-base balance 酸塩基平衡 abortive pneumonia 頓挫[性]肺炎 acid-base disturbance 酸塩基平衡異常 abrasion 剥離 acid-base equilibrium 酸塩基平衡 abscess 膿瘍 acid-base regulation 酸塩基調節 absolute -
1 Medical Student's Amnesia a Transient Selective Loss of Memory During an Exam That Prevents One from Remem
Medical Student’s Amnesia A transient selective loss of memory during an exam that prevents one from remembering the eponymically-named diseases discovered by old, dead doctors. Addison’s Disease 1. Primary adrenocortical deficiency Addisonian Anemia 2. Pernicious anemia (antibodies to intrinsic factor or parietal cells → ↓IF → ↓Vit B12 → megaloblastic anemia) Albright’s Syndrome 3. Polyostotic fibrous dysplasia, precocious puberty, café au lait spots, short stature, young girls Alport’s Syndrome 4. Hereditary nephritis with nerve deafness Alzheimer’s 5. Progressive dementia Argyll-Robertson Pupil 6. Loss of light reflex constriction (contralateral or bilateral) 7. “Prostitute’s Eye” – accommodates but does not react 8. Pathognomonic for 3°Syphilis 9. Lesion pretectal region of superior colliculus Arnold-Chiari Malformation 10. Cerebellar tonsil herniation through foramen magnum = see thoracolumbar meningomyelocele Barrett’s 11. Columnar metaplasia of lower esophagus (↑ risk of adenocarcinoma)- constant gastroesophageal reflux Bartter’s Syndrome 12. Hyperreninemia Becker’s Muscular Dystrophy 13. Similar to Duchenne, but less severe (mutation, not a deficiency, in dystrophin protein) Bell’s Palsy 14. CNVII palsy (entire face; recall that UMN lesion only affects lower face) Berger’s Disease 15. IgA nephropathy causing hematuria in kids, usually following infection Bernard-Soulier Disease 16. Defect in platelet adhesion (abnormally large platelets & lack of platelet-surface glycoprotein) Berry Aneurysm 17. Circle of Willis (subarachnoid bleed) Anterior Communicating artery 18. Often associated with ADPKD Bowen’s Disease 19. Carcinoma in situ on shaft of penis (↑ risk of visceral ca) [compare w/ Queyrat] Brill-Zinsser Disease 20. Recurrences of rickettsia prowazaki up to 50 yrs later Briquet’s Syndrome 21. -
In the Supreme Court of the United States ______
No. 01-963 In the Supreme Court of the United States __________ NORFOLK & WESTERN RAILWAY COMPANY, Petitioner, v. FREEMAN AYERS, et al., Respondents. __________ On Writ of Certiorari to the Circuit Court of Kanawha County, West Virginia __________ BRIEF OF RESPONDENTS __________ SEAN DONAHUE RICHARD J. LAZARUS* WASHINGTON & LEE UNIV. GEORGETOWN UNIVERSITY SCHOOL OF LAW LAW CENTER LEXINGTON, VA 24450 600 NEW JERSEY AVE., N.W. WASHINGTON, D.C. 20001 JAMES H. RION, JR. (202) 662-9129 NESS MOTLEY 28 BRIDGESIDE BLVD JAMES A. MCKOWEN MT. PLEASANT, SC 29465 JAMES F. HUMPHREYS & ASSOCIATES, L.C. LAWRENCE M. MANN 500 VIRGINIA STREET, EAST ALPER & MANN, P.C. CHARLESTON, WV 25301 1667 K STREET, N.W. (304) 347-5050 WASHINGTON, D.C. 20006 * Counsel of Record Counsel for Respondents QUESTIONS PRESENTED The Federal Employer’s Liability Act (FELA), 45 U.S.C. § 51, provides that a railroad is liable in damages for injuries to railroad employees “resulting in whole or in part” from the railroad’s negligence. Respondents prevailed in a jury trial brought pursuant to FELA against petitioner based on injuries resulting from petitioner’s negligence in exposing respondents to asbestos at the workplace. The questions presented are: 1. Whether the trial judge properly instructed the jury that a plaintiff railroad employee who has a reasonable fear of cancer because he is suffering from a physical disease caused by the defendant railroad employer’s negligently exposing the plaintiff to asbestos is entitled to be compensated for that mental injury under FELA. 2. Whether the trial judge properly declined to instruct the jury in a FELA lawsuit to apportion damages between the defendant railroad employer and absent third parties where the plaintiff railroad employees were suffering from indivisible injuries caused by the railroad’s negligence. -
1015 5 Jan 11 Coleman V2.Pages
The Armed Forces Institute of Pathology Department of Veterinary Pathology Wednesday Slide Conference 2010-2011 Conference 15 5 January 2011 Conference Moderator: Gary D. Coleman, DVM, PhD, Diplomate ACVP, Diplomate ACVPM CASE I: 09A731 (AFIP 3165087). Signalment: 5.65-year-old, female, Indian macaque (Macaca mulatta). History: Found dead in an outside breeding corral without history of previous illness. Gross Pathology: The animal was dehydrated with evidence of fecal soiling around the anus. Small intestine and colon were distended with fluid and gas. Contents were blood-tinged and foul smelling. Mesenteric lymph nodes were severely enlarged. Laboratory Results: Colonic swab cultures contained Yersinia pseudotuberculosis and Campylobacter coli. Histopathologic Description: Small intestine: Small intestinal mucosa contains multiple to confluent areas of necrosis and hemorrhage that in some areas extend to the muscularis mucosa. Necrotic foci are filled with neutrophils forming microabscesses with dense microcolonies of extracellular bacteria. Scattered hyalinized eosinophilic deposits around crypts and vessels in the lamina propria demonstrate apple green birefringence when stained with Congo red and observed with polarized light. Contributor’s Morphologic Diagnosis: 1. Enteritis, necrohemorrhagic, suppurative, multifocal, severe, with intra- lesion bacterial colonies. Etiology: Yersinia pseudotuberculosis 2. Amyloidosis, secondary, small intestine and mesenteric lymph node (not submitted) Contributor’s Comment: Yersinia pseudotuberculosis is a disease of rodents and birds but has been reported in rabbits, deer, dogs, cats, swine, sheep, goats, chinchillas, horses, non-human primates, man and exotic mammals. In cases where multiple pathogens are isolated, it may be difficult to associate lesions with a specific pathogen. However, necrotizing lesions in the small intestine, obvious bacterial colonization, and severe neutrophilic response are hallmarks of Yersiniosis.1 Three species of Yersinia are pathogenic for humans and non-human primates: Y.