Pathology-Molecular Genetic Articles

Article Name

Abciximab
Abetalipoproteinemia
Acanthocytosis
Achondroplasia
Acrodermatitis Enteropathica
Acrokeratoelastoidosis
Acrokeratosis Verruciformis of Hopf
Acute Promyelocytic Leukemia (APL, APML)
Acute Retinal Necrosis
Afatinib
Agammaglobulinemia
Alagille Syndrome
Albright Hereditary Osteodystrophy
Alpha 1 Antitrypsin Mutation
Alpha Thalassemia (Hemoglobin H Disease)
Alport Syndrome
Amyloid Beta Peptide
Anatomy, Abdomen and Pelvis, Bowman Capsule
Anatomy, Back, Sacral Vertebrae
Androgen Insensitivity Syndrome
Anemia Screening
Anhidrosis
Aplasia Cutis Congenita
Aplastic Anemia
Apoptosis
Arginase Deficiency (Argininemia)
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atypical Breast Hyperplasia
Atypical Fibroxanthoma
Autoimmune Myopathies (Dermatomyositis And Polymyositis)
Axenfeld Anomaly
Bacterial DNA Mutations
Balint Syndrome
Bartter Syndrome
Basal Cell Carcinoma
Basophilia
BAX Gene
Becker Muscular Dystrophy
Beckwith Wiedemann Syndrome
Beevor Sign
Biochemistry, Bombesin
Biochemistry, Ceruloplasmin
Biochemistry, Chylomicron
Biochemistry, DNA Structure
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, Glycogenolysis
Biochemistry, Immunoglobulin M (IgM)
Biochemistry, Merosin
Biochemistry, Presenilin
Biochemistry, Protein Catabolism
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Biochemistry, Secondary Protein Structure
Biochemistry, Substance P
Biochemistry, Superoxides
Biochemistry, Ubiquitination
Biochemstry, Fatty Acid Oxidation
Birdshot Retinopathy
Birt Hogg Dube Syndrome
Bloom Syndrome (Congenital Telangiectatic Erythema)
Blue Nevus
Bone Marrow Failure
Botulinum Toxin
BRCA 1 and 2
Breast Cancer
Breast Milk Jaundice
Brugada Syndrome
Cancer Breast Screening
Cancer, Acral Lentiginous Melanoma
Cancer, Acute Myeloid Leukemia (AML, Erythroid Leukemia, Myelodysplasia-Related Leukemia, BCR-ABL Chronic Leukemia)
Cancer, Anaplastic Large Cell Lymphoma (ALCL Ki 1+)
Cancer, Anaplastic Thyroid
Cancer, Angiosarcoma
Cancer, Anorexia and Cachexia
Cancer, Basal Cell
Cancer, Benign Mesothelioma
Cancer, Bronchoalveolar
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Dermatofibrosarcoma Protuberans
Cancer, Germ Cell (Seminoma, Germinoma)
Cancer, Leukemia Cutis
Cancer, Lobular Breast Carcinoma
Cancer, Lung
Cancer, Lung Small Cell (Oat Cell)
Cancer, Lymphoblastic Lymphoma
Cancer, Male Breast Cancer
Cancer, Mantle Cell Lymphoma
Cancer, Microcystic Adnexal Carcinoma (Sclerosing Sweat Gland)
Cancer, Myeloproliferative Neoplasms
Cancer, Neuroblastoma
Cancer, Ocular Melanoma
Cancer, Parathyroid
Cancer, Plasmablastic Lymphoma
Cancer, Rectal (Rectum)
Cancer, Renal
Cancer, Retinoblastoma
Cancer, Soft Tissue Clear Cell Sarcoma
Cancer, T Cell Prolymphocytic Leukemia
Cancer, Tubular Breast Carcinoma
Cancer, Tumor-Suppressor Genes
Carbapenem Resistant Enterobacteriacea (CRE)
Cardiac Manifestations Of Coronavirus (COVID-19)
Carney Complex
Caroli Disease
Cerebral Amyloid Angiopathy
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Cerebral Palsy
CHARGE Syndrome
Chediak Higashi Syndrome
Chemotherapy Acral Erythema (Palmar-Plantar Erythrodysesthesia, Palmoplantar Erythrodysesthesia, Hand-Foot Syndrome)
Child Syndrome
Childhood Brain Tumors
Chordoma
Chorea
Chronic Granulomatous Disease
Chronic Transplantation Rejection
Cicatricial Pemphigoid
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Hand (Ectrodactyly, Split Hand)
Complement Deficiency
Congenital Hereditary Endothelial Dystrophy
Corneal Dystrophy
Cornelia de Lange Syndrome
Cowden Disease (Multiple Hamartoma Syndrome)
Cyclic Neutropenia
Cylindroma
Cystic Fibrosis
Cystic Fibrosis And Liver Disease
Cystic Fibrosis Related Diabetes (CFRD)
Dermal Melanocytosis (Mongolian Spot), Congenital
Dermatosis Papulosa Nigra
Diamond Blackfan Anemia
DiGeorge Syndrome
Digoxin Immune Fab
Dowling Degos Disease
Down Syndrome (Trisomy 21)
Drug Induced Pemphigus
Dyskeratosis Congenita
Dystonia
Dystrophinopathies
Ehlers Danlos Syndrome
Embryology, Branchial Arches
Embryology, Epidermis
Embryology, Gastrulation
Embryology, Hand
Embryology, Kidney, Bladder, and Ureter
Embryology, Optic Cup
Embryology, Optic Fissure
Embryology, Rectum and Anal Canal
Embryology, Sexual Development
Embryology, Wolffian Ducts
Enchondroma
Endocardial Fibroelastosis
Endometrial Cancer
Enterobacter Infections
Enzyme Linked Immunosorbent Assay (ELISA)
Epidermal Nevus Syndromes
Epidermodysplasia Verruciformis
Epidermolytic Hyperkeratosis (Bullous Ichthyosiform Erythroderma)
Eptifibatide
Erlotinib
Erythromelalgia
Extramammary Paget Disease
Eyelid Coloboma
Fabry Disease
Factor XIII Deficiency
Familial Adenomatous Polyposis
Familial Hypercholesterolemia
Fanconi Anemia
Fatal Familial Insomnia
Fetal Alcohol Syndrome
Fragile X Syndrome
Frontotemporal Lobe Dementia
Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance)
Fuchs Endothelial Dystrophy (FED)
Gaucher Disease
Genetics, Chromosome Abnormalities
Genetics, Chromosomes
Genetics, DNA Damage and Repair
Genetics, Human Major Histocompatibility Complex (MHC)
Genetics, Mosaicism
Genetics, Transposons
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Giant Cell Tumor
Gitelman Syndrome
Gliomas
Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type II (Pompe Disease)
Good Samaritan Laws
Gorlin Syndrome (Basal Cell Nevus)
Gyrate Atrophy Of The Choroid and Retina
Hemiplegic Migraine
Hemochromatosis
Henoch Schonlein Purpura (Anaphylactoid Purpura, HSP)
Hepatic Cirrhosis
Hepatoblastoma
Hereditary Fructose Intolerance
Hereditary Spherocytosis
Herpes Virus Type 8 (HHV 8)
High Grade Squamous Intraepithelial Lesion (HSIL)
Histology, Astrocytes
Histology, Cell
Histology, Meissner Corpuscle
Histology, Parathyroid Gland
Histolology, Platelets
Holt Oram Syndrome
Human Papillomavirus
Hydranencephaly
Hyperacusis
Hypercholesterolemia
Hyperhomocysteinemia
Hyperphosphatemia
Hypokalemic Periodic Paralysis
Hypophosphatemia
Ichthyosis X-Linked
Idiopathic Guttate Hypomelanosis
Idiopathic Interstitial Pneumonia With Autoimmune Features (IPAF)
Imatinib
Immunoglobulin E
Immunophenotyping
Immunotherapy
Inborn Errors Of Metabolism
Infantile Cortical Hyperostosis (Caffey Disease)
Insulin Resistance
Insulinoma
Iron Overload
Jacobs (XYY) Syndrome
Keratosis Follicularis (Darier Disease)
Klinefelter Syndrome
Lafora Disease
Lesch Nyhan Syndrome
Li-Fraumeni Syndrome
Linear IGA Dermatosis
Lipoid Pneumonia
Lisch Nodules
Littoral Cell Splenic Angioma
Lymphoproliferative Disorders
Lynch Syndrome
Mallory Bodies
Mastocytoma
May Hegglin Anomaly
Medulloblastoma
Melas Syndrome
Meningococcal Vaccine
Mercaptopurine
Methicillin Resistant Staphylococcus Aureus (MRSA)
Muir-Torre Syndrome
Myelodysplastic Syndrome
Myotonic Dystrophy
Neuroanatomy, Dentate Nucleus
Neuroanatomy, Neural Tube Development and Stages
Neuroanatomy, Nodes of Ranvier
Neuroanatomy, Nucleus Caudate
Neuroanatomy, Unmyelinated Nerve Fibers
Nevus Anemicus
Nevus Comedonicus
Nevus Sebaceous
Newborn Screening
Nonketotic Hyperglycinemia
Noonan Syndrome
Normocalcemic Hyperparathyroidism
Oligodendroglioma
Optic Atrophy
Ornithine Transcarbamylase Deficiency
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteochondroma
Osteogenesis Imperfecta
Osteopetrosis
Palmoplantar Psoriasis
Papillary Thyroid Carcinoma (PTC)
Paraneoplastic Syndromes
Pemphigoid Gestationis
Pemphigus Foliaceus
Pemphigus Vegetans
Pendred Syndrome
Pericholangitis
Pernio (Chilblains)
Pfeiffer Syndrome
PHACE Syndrome
Phenol Toxicity
Photopic Vision
Physiology, Cellular Receptor
Physiology, Chorionic Gonadotropin
Physiology, Factor V
Physiology, Gluconeogenesis
Physiology, Gonadotropin Inhibitor
Physiology, Male Reproductive System
Physiology, Membrane
Physiology, Synuclein
Piebaldism
Pigmented Villonodular Synovitis
Poikiloderma Congenitale
Polycystic Kidney Disease Of Childhood
Polycythemia
Polycythemia Vera
Polygenic Hypercholesterolemia
Prader-Willi Syndrome
Precocious Puberty
Prenatal Genetic Screening
Progressive Supranuclear Palsy
Protein S and C
Pseudomyxoma Peritonei
Radial Dysplasia (Clubhand)
Radiology, Image Production and Evaluation
Reed Sternberg Cells
Refractory Anemia With Ring Sideroblasts
Renal Oncocytoma
Retinal Detachment
Rett Syndrome
Rotor Syndrome
Scleroderma And Primary Myocardial Disease
Sertoli-Cell-Only Syndrome
Short Stature
Single Ventricle
Somatostatinoma
Spiradenoma
Splenic Sequestration Crisis
Sports Physicals
Steatorrhea
Stevens Johnson Syndrome (Toxic Epidermal Necrolysis)
Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome)
Sweat Testing
Syndactyly
Syndromic Sensorineural Hearing Loss (SSHL)
Thrombin
Thyroxine-Binding Globulin Deficiency
Tort
Trinucleotide Repeat Disorders
Trisomy 13
Tropical Pulmonary Eosinophilia
Tubular Adenoma
Turcot Syndrome
Vaginal Cancer
Vascular Ring Double Aortic Arch
Velocardiofacial Syndrome
Vemurafenib
Vernix Caseosa
Vismodegib
Vohwinkel Syndrome
Wellens Syndrome
Werdnig Hoffmann Disease
White Dot Syndromes
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wiskott-Aldrich Syndrome
Xeroderma Pigmentosum