Pathology-Molecular Genetic Articles

Article Name

21 Hydroxylase Deficiency
A Review Of Hereditary Colorectal Cancers
Acrodermatitis Enteropathica
Acrokeratosis Verruciformis of Hopf
Acute Retinal Necrosis
Alagille Syndrome
Alpha 1 Antitrypsin Mutation
Alpha Thalassemia (Hemoglobin H Disease)
Alport Syndrome
Alzheimer Disease
Amyloid Beta Peptide
Anatomy, Back, Sacral Vertebrae
Androgen Insensitivity Syndrome
Anemia Screening
Apert Syndrome
Aplasia Cutis Congenita
Aplastic Anemia
Arginase Deficiency (Argininemia)
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atypical Breast Hyperplasia
Autoimmune Myopathies (Dermatomyositis And Polymyositis)
Axenfeld Anomaly
Balint Syndrome
Bartter Syndrome
Basal Cell Carcinoma
Beevor Sign
Best Disease
Biochemistry, Bombesin
Biochemistry, Chylomicron
Biochemistry, Dopamine Receptors
Biochemistry, Epidermal Growth Factor Receptor
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Birt Hogg Dube Syndrome
Bloom Syndrome (Congenital Telangiectatic Erythema)
Blue Nevus
Blue Rubber Bleb Nevus Syndrome
Bone Marrow Failure
Bouveret Syndrome
BRCA 1 and 2
Brugada Syndrome
Calcifying Epithelioma of Malherbe
Cancer, Acute Myeloid Leukemia (AML, Erythroid Leukemia, Myelodysplasia-Related Leukemia, BCR-ABL Chronic Leukemia)
Cancer, Acute Promyelocytic Leukemia (APL, APML)
Cancer, Anaplastic Large Cell Lymphoma (ALCL Ki 1+)
Cancer, Angiosarcoma
Cancer, Basal Cell
Cancer, Breast
Cancer, Bronchoalveolar
Cancer, Burkitt Lymphoma
Cancer, Chemotherapy Acral Erythema (Palmar-Plantar Erythrodysesthesia, Palmoplantar Erythrodysesthesia, Hand-Foot Syndrome)
Cancer, Chondroblastoma
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Colon
Cancer, Dermatofibrosarcoma Protuberans
Cancer, Endometrial
Cancer, Esophageal
Cancer, Gastric
Cancer, Hairy Cell Leukemia
Cancer, Kaposi Sarcoma
Cancer, Leukemia Cutis
Cancer, Lung
Cancer, Lymphoblastic Lymphoma
Cancer, Lymphoplasmacytic Lymphoma (Waldenstrom Macroglobulinemia)
Cancer, Male Breast Cancer
Cancer, Mantle Cell Lymphoma
Cancer, Medulloblastoma
Cancer, Melanoma Pathology
Cancer, Mesothelioma, Benign
Cancer, Metastatic Melanoma
Cancer, Myeloproliferative Neoplasms
Cancer, Neuroblastoma
Cancer, Ocular Melanoma
Cancer, Papillary Thyroid Carcinoma (PTC)
Cancer, Parathyroid
Cancer, Plasma Cell
Cancer, Plasmablastic Lymphoma
Cancer, Pleuropulmonary Blastoma
Cancer, Rectal (Rectum)
Cancer, Retinoblastoma
Cancer, Soft Tissue Clear Cell Sarcoma
Cancer, T Cell Prolymphocytic Leukemia
Cancer, Tubular Breast Carcinoma
Cancer, Tumor-Suppressor Genes
Caplan Syndrome
Carbapenem Resistant Enterobacteriacea (CRE)
Cardiac Fibroma
Caroli Disease
Case Study: 24-Year-Old Male Presenting With Polyarthralgias
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Chediak Higashi Syndrome
Child Syndrome
Choanal Atresia
Chronic Granulomatous Disease
Chronic Transplantation Rejection
Cicatricial Pemphigoid
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cockayne Syndrome
Cowden Disease (Multiple Hamartoma Syndrome)
Creatine Phosphokinase
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crouzon Syndrome
Cystic Fibrosis
Cystic Fibrosis Related Diabetes (CFRD)
Danon Disease
Dermatosis Papulosa Nigra
Diabetes, Maturity Onset in the Young (MODY)
Diamond Blackfan Anemia
DiGeorge Syndrome
Dowling Degos Disease
Down Syndrome (Trisomy 21)
Drug Induced Pemphigus
Dyskeratosis Congenita
Eagle Syndrome
Ehlers Danlos Syndrome
Embryology, Branchial Arches
Embryology, Hand
Embryology, Kidney, Bladder, and Ureter
Embryology, Optic Cup
Embryology, Rectum and Anal Canal
Epidermodysplasia Verruciformis
Epidermolytic Hyperkeratosis (Bullous Ichthyosiform Erythroderma)
Extramammary Paget Disease
Fabry Disease
Familial Adenomatous Polyposis
Familial Hyperlipidemia Type 1
Fatal Familial Insomnia
Fetal Alcohol Syndrome
Forensic Odontology
Fragile X Syndrome
Fuchs Endothelial Dystrophy (FED)
Gardner Syndrome
Genetics, Autosomal Recessive
Genetics, Human Major Histocompatibility Complex (MHC)
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Gitelman Syndrome
Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type II (Pompe Disease)
Good Samaritan Laws
Gorlin Syndrome (Basal Cell Nevus)
Health Insurance Portability and Accountability Act (HIPAA)
Helicobacter Pylori
Henoch Schonlein Purpura (Anaphylactoid Purpura, HSP)
Hepatic Cirrhosis
Hepatitis C
Hereditary Spherocytosis
High Grade Squamous Intraepithelial Lesion (HSIL)
Histology, Astrocytes
Histology, Meissner Corpuscle
Histology, Parathyroid Gland
Histology, Spermatogenesis
Holt Oram Syndrome
Human Papillomavirus
Hurler Syndrome
Ichthyosis X-Linked
Idiopathic Guttate Hypomelanosis
IgA Pemphigus
Immunoglobulin E
Impaired Bilirubin Conjugation
Inborn Errors Of Metabolism
Infantile Cortical Hyperostosis (Caffey Disease)
Infantile Spasm (West Syndrome)
Insulin Resistance
Iron Overload
Job Syndrome (Hyperimmunoglobulin E)
Kasabach Merritt Syndrome
Kearns Sayre Syndrome
Keratosis Follicularis (Darier Disease)
Klinefelter Syndrome
Lafora Disease
Lennox Gastaut Syndrome
Li Fraumeni Syndrome
Linear IGA Dermatosis
Littoral Cell Splenic Angioma
Lymphoproliferative Disorders
Lynch Syndrome
Mallory Bodies
McCune Albright Syndrome
Medical Error Prevention
Medical Ethics
Melas Syndrome
Membranous Glomerulonephritis
Meningococcal Vaccine
Methods Of Estimation Of Time Since Death
Millard Gubler Syndrome
Muir-Torre Syndrome
Multiple Endocrine Neoplasia Type 1 (MEN I, Wermer Syndrome)
Multiple Endocrine Neoplasias, Type 2 (MEN II, Pheochromocytoma and Amyloid Producing Medullary Thyroid Carcinoma, Sipple Syndrome)
Munchausen Syndrome
Myelodysplastic Syndrome
Neonatal Abstinence Syndrome
Neuroanatomy, Nodes of Ranvier
Neuroanatomy, Posterior Cerebral Arteries
Nevus Anemicus
Nevus Comedonicus
Nevus Sebaceous
Noonan Syndrome
Ornithine Transcarbamylase Deficiency
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteogenesis Imperfecta
Palmoplantar Psoriasis
Paraneoplastic Syndromes
Pemphigoid Gestationis
Pemphigus Foliaceus
Pemphigus Vegetans
Pemphigus, Herpetiformis
Pendred Syndrome
Perimortem Cesarean Delivery
Pernio (Chilblains)
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Phenol Toxicity
Physiology, Complement Cascade
Physiology, Factor V
Physiology, Gonadotropin Inhibitor
Physiology, Synuclein
Pigmented Villonodular Synovitis
Poikiloderma Congenitale
Polycystic Kidney Disease Of Childhood
Polycystic Ovarian Disease (Stein-Leventhal Syndrome)
Polyglandular Autoimmune Syndrome Type I
Polyglandular Autoimmune Syndrome, Type II (Carpenters, Schmidt)
Prader-Willi Syndrome
Precocious Puberty
Progeria (Werner Syndrome)
Progressive Supranuclear Palsy
Prune Belly Syndrome
Pseudocholinesterase Deficiency
Pseudomyxoma Peritonei
Radiology, Image Production and Evaluation
Reactive Perforating Collagenosis
Recognizing Alcohol and Drug Impairment in the Workplace in Florida
Reed Sternberg Cells
Refractory Anemia With Ring Sideroblasts
Renal Oncocytoma
Retinal Detachment
Rett Syndrome
Reye Syndrome
Rhythm, QT Prolongation
Rotor Syndrome
Sertoli-Cell-Only Syndrome
Severe Combined Immunodeficiency
Splenic Sequestration Crisis
Stages of Labor
Stevens Johnson Syndrome (Toxic Epidermal Necrolysis)
Sturge-Weber Syndrome
Supravalvar Aortic Stenosis (SVAS)
Sweat Testing
Syndromic Sensorineural Hearing Loss (SSHL)
Thrombotic Thrombocytopenic Purpura Evaluation and Management
Thyroxine-Binding Globulin Deficiency
Tourette Syndrome And Other Tic Disorders
Tubular Adenoma
Turcot Syndrome
Ulcerative Colitis
Velocardiofacial Syndrome
Vohwinkel Syndrome
Von Hippel Lindau Syndrome
Wellens Syndrome
Western Blot (Protein Immunoblot)
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wiskott-Aldrich Syndrome
Xeroderma Pigmentosum
X-linked Agammaglobulinemia
Young Syndrome