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Hepatosplenomegaly
Phase 4 Medicine Intended Learning Outcomes (Ilos)
Alpha Thalassemia
Guideline for the Evaluation of Cholestatic Jaundice
Redalyc.Hepatobiliary Abnormalities in Pediatric Patients with Sickle Cell
Acute Gastrointestinal Infections Syndromic Approach
Portal Hypertension As Portrayed by Marked Hepatosplenomegaly: Case Report
Alpha-Thalassemia
Abdominal Mass/Hepatosplenomegaly 1 D a V I D T a T E
A 7 Year Old Girl with Anemia and Massive Hepatosplenomegaly Mohammad Mizanur Rahman, Md
Patients and Methods
A Study of Hepatobiliary Involvement in Adult Patients with Sickle Cell Disease
Does Streptococcus-A Cause Hepatosplenomegaly and Atypical Lymphocytosis ?: a Case Report
Assessment of Hepatosplenomegaly
A Rare Case of Wiskott-Aldrich Syndrome with Normal Platelet Size: a Case Report Mohd Farid Baharin1*, Jasbir Singh Dhaliwal2, Smrdhi V
Angioedema Associated with Urticaria Can Be a Silent Killer
H&P 360 Template
HBA1/HBA2 Genes and Alpha Thalassemia
Preventive Healthcare and Management for Acute Lymphoblastic Leukaemia in Adults: Case Report and Literature Review
Top View
Sickle Cell Pain Crisis Is a Diagnosis of Exclusion
A Case of Brucellosis Presenting with Multiple Hypodense Splenic Lesions and Bilateral Pleural Effusions
Subject Examinations
Peripheral Neuropathy Associated with Erythrophagocytic Lymphohistiocytosis
Nonmetastatic Nephrogenic Hepatosplenomegaly and Epilepsy S
WHO Recommended Strategies for the Prevention and Control of Communicable Diseases
Guideline for Infection Control in Health Care Personnel, 1998
Extramedullary Haemopoiesis in Hemoglobinopathies
CONTENT OUTLINE Pediatric Emergency Medicine
A 17-Month-Old Girl Presented with Jaundice, Hepatosplenomegaly, Ascites and Scaly Erythematous Skin Lesion
Boards' Fodder
Medical Parasitology
Alpha-Thalassemia Syndromes: from Clinical and Molecular Diagnosis to Bedside Management
Preventive Health Care
The Practice of Medicine II Academic Year 2011-2012
Approach to Jaundice Approach to Hepatosplenomegaly
Alpha Thalassemia
Table of Contents 2
Alpha Thalassemia
Approach to a Child with Hepatosplenomegaly
Review of Several Phenotypes of Omenn Syndrome and RAG1/RAG2
Alpha-Thalassemia Renzo Galanello, MD1, and Antonio Cao, MD2
Acute Hepatic Crisis in Sickle Cell Anemia: Favorable Outcome After Exchange Transfusion
Allergy and Immunology Supplemental Guide
An Official ATS Statement: Hepatotoxicity of Antituberculosis Therapy (2006)
Original Article Aetiology of Pyrexia with Hepatosplenomegaly
Two Leptospirosis Cases Presented with Fever, Anemia, and Hepatosplenomegaly
Dengue Fever As a Potential Cause of Sickle Cell Intrahepatic Cholestasis: a Report of Two Cases
CURRENT ESSENTIALS of MEDICINE
Study of Aetiological Profile, Clinical Presentation and Outcome of Hepatosplenomegaly in Children Between 1 Month and 14 Years of Age
Anaphylaxis-A Practice Parameter Update 2015
Lecture Notes on Internal Medicine
Fatal Splenic Sequestration Crisis in Adult Sickle Cell-Beta Thalassaemia
Subacute Liver Failure Secondary to Amyloid Light-Chain Amyloidosis
Antibiotic Induced Cutaneous Rash in Infectious Mononucleosis
Hepatosplenic Schistosomiasis: a Clinical Review
Prevention in Childhood of Health Problems in Adult Life