Topics: Wernicke–Korsakoff’s syndrome, Othello syndrome, Munchausen’s syndrome, Landau–Kleffner syndrome, Kanner’s syndrome, Gilles de la Tourette’s syndrome, Gerstmann’s syndrome, Ge´ lineau’s syndrome, Ganser’s syndrome, Fre´ goli’s syndrome, Folie a` deux, Ekbom’s syndrome, Down’s syndrome, De Cle´ rambault’s syndrome, Down’s syndrome, Da Costa’s syndrome, Couvade’s syndrome, Capgras’s syndrome, Briquet’s syndrome, Asperger’s syndrome, Word salad, Transference, Torticollis, Tics, Thought withdrawal, Thought insertion, Thought broadcast, Thought blocking, Tardive dyskinesia, Stereotypy, Somatic passivity, Somatic symptoms, Repression, Psychosis, Puerperal, Regression, Repression, Psychomotor retardation, Psychomotor agitation, Psychomotor, Psychoactive substance, Pseudohallucination, Pseudodementia, Prosopagnosia, Prodrome, Post-ictal, Phaeochromocytoma, Parasuicide, Palilalia, Organic disorder, Neurosis, psychopathology, Neologism, Mutism, Monomania, Logoclonia, Lanugo hair, Labile affect, Knight’s move t

Topics: Congenital immunodeficiencies, primary immunodeficiencies, Chronic infection, Opportunistic infection, Recurrent infection, Phagocytic disorders, Complement immunodeficiencies, Phagocytic Disorders, Chronic Granulomatous Disease, Leucocyte Adhesion Deficiency, Chediak Higashi Syndrome, Lazy Leucocyte Syndrome, C1-inactivator deficiency, C3b-inactivator deficiency, C3 deficiency, B cell Deficiency, X-linked Agammaglobulinaemia, Bruton’s Agammaglobulinaemia, Transient hypogammaglobulinaemia, Common variable immunodeficiency, T cell Deficiency, Cellular immunodeficiency, Di George syndrome, T cell lymphopaenia, Chronic mucocutaneous candidiasis, T Lymphocyte Deficiencies, B Lymphocyte Deficiencies, severe combined immunodeficiency, X-linked SCID, Adenine deaminase deficiency SCID, Reticular dysgenesis, Secondary Immunodeficiency, Haemoglobinopathies, Immunosuppressive drugs, Tumour growth

Topics: Immune Hemolytic disorder, Auto-immune Hemolytic anemia, Cold AIHA, Paroxysmal Cold hemoglobinuria, Allo-immune Hemolytic anemia, immune Thrombocytopenic purpura, Evan's syndrome, IMMUNE HEMOLYTIC ANEMIA, Antibody-mediated hemolysis, AUTOIMMUNE HEMOLYTIC ANEMIA, Red cell destruction, cold AIHA syndrome, warm AIHA, ALLOIMMUNE HEMOLYTIC ANEMIA, DRUG-INDUCED HEMOLYTIC ANEMIA, ACQUIRED NON-IMMUNE HEMOLYTIC ANEMIA, INTRAVASCULAR HEMOLYSIS, BLACK WATER FEVER, HEMOPHAGOCYTIC SYNDROME, FRAGMENTATION HEMOLYSIS, MECHANICAL HEMOLYTIC ANEMIA, RED CELL FRAGMENTATION SYNDROME, MICROANGIOPATHIC HEMOLYTIC ANEMIA, HEMOLYTIC UREMIC SYNDROME, THROMBOTIC THROMBOCYTOPENIC PURPURA

Topics: Gene Transcription, Messenger RNA, DNA Mutation, gene expression, Lineage Commitment, Micro-RNAs, Regulatory Noncoding RNAs, DNA Replication, Telomeres, Cell Cycle, Apoptosis, Cellular Debris, Lysosomes, Protein Ubiquitination,  Clonal Hematologic Disorders, Erythropoiesis, Bone Marrow, Peripheral Blood, Hypochromic Microcytic Anemias, Iron Metabolism, Iron Absorption, Hepcidin, Iron Homeostasis, Iron‐Deficiency Anemia, Hypochromic Anemias, Sideroblastic Anemia, Lead Poisoning, alchohol, Lead Poisoning, Hematopoiesis, Hematopoietic Niche, growth factor signaling, Congenital Erythropoietic Porphyria, Congenital Erythropoietic Protoporphyria, iron overload, porphyrias, megoblastic anemia, Bone Marrow Appearances, Phagocytic Function, Leukocytosis, Leukoerythroblastic Reaction, Neutropenia, Myelokathexis, Lysosomal Storage Diseases, Hereditary Hemolytic Anemia, Hemolytic Anemia, Acquired Hemolytic Anemia, genetic disorders, Thalassemia, α‐Thalassemia, T Cells, B cells, Natural Killer Cells, Lymphocyte Proliferation, Somatic Hypermutation, Lymphocyte Circulation, Lymphocytosis, Lymphadenopathy, Primary Immunodeficiency Disorders, Granulopoiesis, Monocyte Production, Neutrophils, Polymorphs, Mononuclear Phagocytic System, Reticuloendothelial System, Autoimmune Lymphoproliferative Syndrome, Acquired Immunodeficiency Syndrome, Aplastic Anemia, Red Cell Aplasia, Congenital Dyserythropoietic Anemias, MYELODYSPLASTIC SYNDROMES, molecular genetics, Mirage Syndrome, Clonal Hematopoiesis, HEMATOLOGIC NEOPLASMS, MYELOID LEUKEMIA, Acute Myeloid Leukemia, MYELOPROLIFERATIVE NEOPLASMS, Chronic Myeloid Leukemia, Chronic Neutrophilic Leukemia, Nonleukemic Myeloproliferative Diseases, Polycythemia Vera, Myelofibrosis, Chronic Eosinophilic Leukemia, Myeloproliferative Disorder, ACUTE LYMPHOBLASTIC LEUKEMIA, Mastocytosis, Paraneoplastic Pemphigus, Myeloid Neoplasm, Lymphoid Neoplasm, Myelodysplastic Neoplasm, Myeloproliferative Neoplasm, Ring Sideroblast, Thrombocytosis, Juvenile Myelomonocytic Leukemia, CHRONIC LYMPHOCYTIC LEUKEMIA, Mature B‐Cell Leukemia, Mature T‐C

Topics: Immunodeficiency states, phagocytic disorders, complement abnormalities, T Cell deficiency, Stem cell deficiency, secondary Immunodeficiency, graft rejection

Topics: Radiographic Pathology, specialized imaging technique, Respiratory System, Congenital Diseases, Hereditary Diseases, Diffuse Lung Disease, neoplasms, vascular diseases, lung disorders, pluera disorder, diaphragm, skeletal system, inflammatory disorders, infectious disorders, Metabolic Bone Disease, Fibrous Dysplasia, Benign Bone Tumors, Malignant Bone Tumors, Bone Metastases, fractures, Scoliosis, Spondylolysis, Spondylolisthesis, Gastrointestinal System, stomach, Urinary System, Urinary Calculi, Urinary Tract Obstruction, Renal Vein Thrombosis, Chronic Renal Failure, Acute Renal Failure, Cardiovascular System, Acquired Vascular Disease, Valvular Disease, Pericardial Effusion, Venous Disease, tumors Central Nervous System, Multiple Sclerosis, Epilepsy, Convulsive Disorders, Hematopoietic System, Pituitary Gland, Thyroid Gland, parathyroid Gland, Diabetes Mellitus, Undescended Testis, Cryptorchidism, Testicular Torsion, Epididymitis, Testicular Tumors, Pelvic Inflammatory Disease, cysts, tumors, breast lesions, Nutritional Diseases, Systemic Lupus Erythematosus, Melanoma, Muscular Dystrophy, Ischemia, Infarction, edema, Hemorrhage, neoplasia, immunity disorder, Acquired Immunodeficiency Syndrome, Mammography, ultrasound, Computed Tomography, Magnetic Resonance Imaging, Single-Photon Emission Computed Tomography, Positron Emission Tomography, fusion imaging, Pneumonia, anthrax, Lung Abscess, Tuberculosis, Pulmonary Mycosis, Respiratory Syncytial Virus, Chronic Obstructive Pulmonary Disease, Sarcoidosis, Pneumoconiosis, Solitary Pulmonary Nodule, Bronchial Adenoma, Bronchogenic Carcinoma, Pulmonary Metastases, pulmonary Embolism, Septic Embolism, Pulmonary Arteriovenous Fistula, Atelectasis, Adult Respiratory Distress Syndrome, Intrabronchial Foreign Bodies, Mediastinal Emphysema, Pneumomediastinum, Subcutaneous Emphysema, Pneumothorax, Pleural Effusion, Empyema, Mediastinal Masses, Diaphragmatic Paralysis, Vertebral Anomalies, Spina Bifida, Osteopetrosis, Osteogenesis Imperfecta, Achondroplasia, Congenital Hip Dysplasia, Rheumatoid Arthritis, Ankylosing Spondylitis, Reiter’s Syndrome, Psoriatic Arthritis, Osteoarthritis, Infectious Arthritis, Bursitis, Bacterial Osteomyelitis, Tuberculous Osteomyelitis, Osteoporosis, osteomalacia, rickets, gout, Paget's disease, lead poisoning, fracture healing, Battered-Child Syndrome, Tracheoesophageal Fistula, Esophagitis, Esophageal Cancer, Esophageal Diverticula, Hiatal Hernia, Achalasia, Gastritis, Pyloric Stenosis, Peptic Ulcer Disease, stomach cancer, Crohn’s Disease, Regional Enteritis, Small Bowel Obstruction, Adynamic Ileus, Intussusception, Diverticulosis, Diverticulitis, Appendicitis, Ulcerative Colitis, Ischemic Colitis, Irritable Bowel Syndrome, colon cancer, Large Bowel Obstruction, Gallstones, Cholelithiasis, Acute Cholecystitis, Emphysematous Cholecystitis, Porcelain Gallbladder, Hepatitis, liver Cirrhosis, Hepatocellular Carcinoma, Hepatic Metastases

Topics: Adenomatous polyps, adenomas, Tubular Adenomas, Villous Adenomas, Tubulovillous Adenoma, adenoma formation, POLYPOSIS SYNDROMES, ADENOMATOUS POLYPOSIS SYNDROMES, Gardner’s syndrome, Turcot’s Syndrome, HARMATOMATOUS POLYPOSIS SYNDROME, Peutz-Jeghers syndrome, Familial Juvenile Polyposis, Cronkhite-Canada Syndrome, Cowden’s Disease, NON-NEOPLASTIC POLYPS, Lymphoid polyps, Inflammatory polyps, Juvenil e polyps

Topics: Immune haemolytic anaemia, Non-immune acquired haemolytic anaemia, INTRAVASCULAR HAEMOLYSIS, BLACK WATER FEVER, Malaria, haemophagocytic syndrome, Acute intravascular haemolysis, FRAGMENTATION HAEMOLYSIS, MICROANGIOPATHIC HAEMOLYTIC ANAEMIAS, Haemolytic uraemic syndrome, Thrombotic thrombocytopenic purpura, DRUG-INDUCED IMMUNE HAEMOLYTIC ANAEMIA, Drug adsorption mechanism, Membrane modification mechanism, Immune complex innocent bystander mechanism

Topics: Respiratory System, Cardiovascular System, Gastrointestinal, Urinary system, Nervous System, Nervous System, Tuberculosis, Pneumonia, Asthma, Measles, Congestive cardiac failure, neurology, Body Swelling, Haematuria, Dark Coloured Urine, Periorbital swelling, facial swelling, NEONATOLOGY, jaundice, Neck stiffness, Neonatal tetanus, ONCOLOGY, Jaw Swelling, Bowing of Legs, genetics, Beckwith’s syndrome, Potter’s syndrome, Pierre-Robin syndrome, Mandibules hypoplasia, Unilateral Cleft lip, Seborrhoeic dermatitis, Ritter’s disease, Fetal alcohol syndrome, Down’s syndrome, Trisomy 18, Edward’s syndrome, Turner’s syndrome, Hemihypertrophy, Clindactyly, Arachnodactyly, funnel chest, Pectus carinatum, Pigeon chest, Epicanthic folds, Macroglossia, Lesch-Nyan syndrome, Enhlers-Danlos syndrome, Erythema multiformes, Rectal prolapse, Umbilical herniaMyelomeningocoele, Encephalocoele, Duchenne Muscular Dystrophy, ptosis, Myopathic facies, Tuberous sclerosis, Neurofibomatosis, Sturge Weber syndrome, Diabetic Lipoatrophy, Mongoless blue spot, progeria, eczema, Vitiligo, Chronic renal failure

Topics: DNA split, human karyogram, mutation, Genetic disorder, CYTOGENETIC DISORDER, AUTOSOMAL CYTOGENETIC DISORDER, down syndrome, EDWARD SYNDROME, PATAU SYNDROME, Lyonization, X-chromosome, Y-chromosome, Klinefelter's Syndrome, Testicular Dysgenesis, Male hypogonadism, Klinefelter Syndrome, Turner Syndrome, MENDELIAN DISORDER, Autosomal Dominant Disorder, Marfan Syndrome, Achondroplasia, Osteogenesis imperfecta, brittle bone disease, Ehlers-Danlos Syndrome, Autosomal recessive disorder, X-LINKED DISORDER, Multifactorial disorder, Hereditary Cancer Syndrome, DEFECTIVE DNA REPAIR, Single-Gene Disorder, TRIPLET-REPEAT MUTATION, FRAGILE-X SYNDROME, LEBER HEREDITARY OPTIC NEUROPATHY, GENOMIC IMPRINTING