Pathology-Molecular Genetic Articles

Article Name

21 Hydroxylase Deficiency
A Review Of Hereditary Colorectal Cancers
Acrokeratosis Verruciformis of Hopf
Acute Retinal Necrosis
Alagille Syndrome
Alpha 1 Antitrypsin Mutation
Alport Syndrome
Alzheimer Disease
Amyloid Beta Peptide
Androgen Insensitivity Syndrome
Apert Syndrome
Aplasia Cutis Congenita
Aplastic Anemia
Arginase Deficiency (Argininemia)
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atypical Breast Hyperplasia
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, Protein Synthesis
Biochemistry, Pseudogenes
Bloom Syndrome (Congenital Telangiectatic Erythema)
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, Burkitt Lymphoma
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, Papillary Thyroid Carcinoma (PTC)
Cancer, Parathyroid
Cancer, Plasma Cell
Cancer, Plasmablastic Lymphoma
Cancer, Pleuropulmonary Blastoma
Cancer, Rectal (Rectum)
Cancer, Soft Tissue Clear Cell Sarcoma
Cancer, Tubular Breast Carcinoma
Cancer, Tumor-Suppressor Genes
Caplan Syndrome
Cardiac Fibroma
Case Study: 24-Year-Old Male Presenting With Polyarthralgias
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Chediak Higashi Syndrome
Child Syndrome
Choanal Atresia
Chronic Granulomatous Disease
Cicatricial Pemphigoid
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cockayne Syndrome
Colitis, Ulcerative
Cowden Disease (Multiple Hamartoma Syndrome)
Creatine Phosphokinase
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crouzon Syndrome
Cystic Fibrosis Related Diabetes (CFRD)
Danon Disease
Dermatomyositis And Polymyositis
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, Optic Cup
Epidermodysplasia Verruciformis
Extramammary Paget Disease
Familial Adenomatous Polyposis
Fatal Familial Insomnia
Fetal Alcohol Syndrome
Forensic Odontology
Fragile X Syndrome
Fuchs Endothelial Dystrophy (FED)
Gardner Syndrome
Genetics, Autosomal Recessive
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
Hepatic Cirrhosis
Hepatitis C
Hereditary Spherocytosis
High Grade Squamous Intraepithelial Lesion (HSIL)
Histology, Astrocytes
Histology, Parathyroid Gland
Holt Oram Syndrome
Human Papillomavirus
Hurler Syndrome
Ichthyosis X-Linked
Idiopathic Guttate Hypomelanosis
IgA Pemphigus
Impaired Bilirubin Conjugation
Inborn Errors Of Metabolism
Infantile Cortical Hyperostosis (Caffey Disease)
Infantile Spasm (West Syndrome)
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
Lynch Syndrome
Mallory Bodies
McCune Albright Syndrome
Medical Error Prevention
Medical Ethics
Melas Syndrome
Membranous Glomerulonephritis
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
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
Pemphigus Foliaceus
Pemphigus Vegetans
Pemphigus, Herpetiformis
Perimortem Cesarean Delivery
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Phenol Toxicity
Physiology, Factor V
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)
Precocious Puberty
Progeria (Werner Syndrome)
Progressive Supranuclear Palsy
Prune Belly Syndrome
Pseudocholinesterase Deficiency
Pseudomyxoma Peritonei
Reactive Perforating Collagenosis
Recognizing Alcohol and Drug Impairment in the Workplace in Florida
Reed Sternberg Cells
Refractory Anemia With Ring Sideroblasts
Renal Oncocytoma
Rett Syndrome
Reye Syndrome
Rhythm, QT Prolongation
Rotor Syndrome
Sertoli-Cell-Only Syndrome
Severe Combined Immunodeficiency
Stages of Labor
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
Turcot Syndrome
Velocardiofacial Syndrome
Vohwinkel Syndrome
Von Hippel Lindau Syndrome
Wellens Syndrome
Western Blot (Protein Immunoblot)
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wiskott-Aldrich Syndrome
X-linked Agammaglobulinemia
Young Syndrome