DISEASES OF THE BLOOD
5q- syndrome, Aagenaes syndrome, Abdominal aortic aneurysm, Abetalipoproteinemia, Acatalasemia, Aceruloplasminemia, Acquired agranulocytosis, Acquired hemophilia […]
[…] Acquired hemophilia A, Acquired pure red cell aplasia, Acquired Von Willebrand syndrome, Acute erythroid leukemia, Acute graft versus host disease, Acute monoblastic leukemia, Acute myeloblastic leukemia with maturation, Acute myeloblastic leukemia without maturation, Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22), Acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2), Acute myelomonocytic leukemia, Acute panmyelosis with myelofibrosis, Acute promyelocytic leukemia, Adenosine Deaminase 2 deficiency, Adrenocortical carcinoma, Adult T-cell leukemia/lymphoma, Afibrinogenemia, ALK+ histiocytosis, Alpha-thalassemia x-linked intellectual disability syndrome, AML with myelodysplasia-related features, Anemia due to Adenosine triphosphatase deficiency, Anemia sideroblastic & spinocerebellar ataxia, Aneurysm of sinus of Valsalva, Angioimmunoblastic T-cell lymphoma, Angioma hereditary neurocutaneous, Angioma serpiginosum, autosomal dominant, Angioma serpiginosum, X-linked, Antiphospholipid syndrome, Aplasia cutis congenita intestinal lymphangiectasia, Aplastic anemia, Arterial calcification of infancy, Arterial tortuosity syndrome, Atransferrinemia, Atypical hemolytic uremic syndrome, Autoimmune lymphoproliferative syndrome, Autosomal recessive protein C deficiency, Bannayan-Riley-Ruvalcaba syndrome, Behçet disease, Beta-thalassemia, Blastic plasmacytoid dendritic cell, Bleeding disorder due to P2RY12 defect, Bloom syndrome, Blue rubber bleb nevus syndrome, Buerger disease, Burkitt lymphoma, Campomelia Cumming type, Castleman disease, Cerebral cavernous malformation, Chediak-Higashi syndrome, Chromosome 17q11.2 deletion syndrome, Chronic myeloid leukemia, Chylous ascites, CLOVES syndrome, Cobb syndrome, Cold agglutinin disease, Congenital amegakaryocytic thrombocytopenia, Congenital analbuminemia, Congenital dyserythropoietic anemia type 1, Congenital dyserythropoietic anemia type 2, Congenital dyserythropoietic anemia type 3, Congenital erythropoietic porphyria, Congenital myasthenic syndrome with episodic apnea, Congenital pulmonary lymphangiectasia, Congenital thrombotic thrombocytopenic purpura, Cutaneous mastocytoma, Cutis laxa, autosomal recessive type 1, Cutis marmorata telangiectatica congenita, Cyclic neutropenia, Cyclic thrombocytopenia, Cystic medial necrosis of aorta, Dahlberg Borer Newcomer syndrome, Deafness-lymphedema-leukemia syndrome, Dehydrated hereditary stomatocytosis, Dehydrated hereditary stomatocytosis pseudohyperkalemia & perinatal edema, Diamond-Blackfan anemia, Diamond-Blackfan anemia 2, Diamond-Blackfan anemia 3, Dysfibrinogenemia, Dyskeratosis congenita, Dyskeratosis congenita autosomal dominant, Dyskeratosis congenita autosomal recessive, Dyskeratosis congenita X-linked, Ehlers-Danlos syndrome, dysfibronectinemic type, Eosinophilic granulomatosis with polyangiitis, Erythema elevatum diutinum, Essential thrombocythemia, Evans syndrome, Extranodal nasal NK/T cell lymphoma, Fabry disease, Factor V deficiency, Factor V Leiden thrombophilia, Factor VII deficiency, Factor X deficiency, Factor XI deficiency, Factor XII deficiency, Factor XIII deficiency, Familial hyperthyroidism due to mutations in TSH receptor, Familial LCAT deficiency, Familial platelet disorder with associated myeloid malignancy, Familial thoracic aortic aneurysm & dissection, Fanconi anemia, Fetal & neonatal alloimmune thrombocytopenia, Fibromuscular dysplasia, Follicular lymphoma, Genuine diffuse phlebectasia, Giant cell arteritis, Giant platelet syndrome, Glanzmann thrombasthenia, Glucocorticoid-remediable aldosteronism, Glutamate formiminotransferase deficiency, Glycogen storage disease type 12, Glycogen storage disease type 7, Glycoprotein VI deficiency, Goodpasture syndrome, Gorham’s disease, Granulomatosis with polyangiitis, Granulomatous slack skin disease, Gray platelet syndrome, Hairy cell leukemia, Hashimoto-Pritzker syndrome, Heinz body anemias, Hemangioma thrombocytopenia syndrome, Hemochromatosis, Hemochromatosis type 2, Hemochromatosis type 3, Hemochromatosis type 4, Hemoglobin C disease, Hemoglobin E disease, Hemoglobin SC disease, Hemoglobin SE disease, Hemolytic anemia lethal congenital nonspherocytic with genital & other abnormalities, Hemolytic uremic syndrome, Hemophilia A, Hemophilia B, Hemorrhagic shock & encephalopathy syndrome, Hennekam syndrome, Henoch-Schonlein purpura, Heparin-induced thrombocytopenia, Hereditary antithrombin deficiency, Hereditary elliptocytosis, Hereditary folate malabsorption, Hereditary hemorrhagic telangiectasia, Hereditary hemorrhagic telangiectasia type 2, Hereditary hemorrhagic telangiectasia type 3, Hereditary hemorrhagic telangiectasia type 4, Hereditary lymphedema type II, Hereditary methemoglobinemia, Hereditary paraganglioma-pheochromocytoma, Hereditary spherocytosis, Hermansky Pudlak syndrome 2, High molecular weight kininogen deficiency, Histiocytosis-lymphadenopathy plus syndrome, Hoyeraal Hreidarsson syndrome, Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency, Hypereosinophilic syndrome, Hypersensitivity vasculitis, Hypocomplementemic urticarial vasculitis, Hypofibrinogenemia, familial, Hypotrichosis-lymphedema-telangiectasia syndrome, Idiopathic neutropenia, Idiopathic thrombocytopenic purpura, Imerslund-Grasbeck syndrome, Inclusion body myopathy 2, Inherited bone marrow failure syndrome, Internal carotid agenesis, Intrinsic factor deficiency, Iron-refractory iron deficiency anemia, Jacobsen syndrome, Juvenile myelomonocytic leukemia, Juvenile temporal arteritis, Kanzaki disease, Kaposi sarcoma, Kaposiform Hemangioendothelioma, Kawasaki disease, Klippel-Trenaunay syndrome, Langerhans cell sarcoma, Large granular lymphocyte leukemia, Lesch Nyhan syndrome, Liddle syndrome, Lipedema, Lissencephaly 2, Loeys-Dietz syndrome, Loeys-Dietz syndrome type 1, Loeys-Dietz syndrome type 2, Loeys-Dietz syndrome type 3, Loeys-Dietz syndrome type 4, Lymphedema & cerebral arteriovenous anomaly, Lymphedema-distichiasis syndrome, Lymphomatoid papulosis, Maffucci syndrome, Majeed syndrome, Mantle cell lymphoma, McLeod neuroacanthocytosis syndrome, Megalencephaly-capillary malformation syndrome, Megaloblastic anemia due to dihydrofolate reductase deficiency, Methemoglobinemia, beta-globin type, Methylcobalamin deficiency cbl G type, Methylmalonic acidemia & homocysteinemia type cblX, Methylmalonic acidemia with homocystinuria type cblC, Methylmalonic acidemia with homocystinuria type cblD, Methylmalonic acidemia with homocystinuria type cblF, Methylmalonic acidemia with homocystinuria type cblJ, Microcystic lymphatic malformation, Microscopic polyangiitis, Milroy disease, MPI-CDG (CDG-Ib), Multicentric Castleman Disease, Multifocal lymphangioendotheliomatosis with thrombocytopenia, Multiple myeloma, Multisystemic smooth muscle dysfunction syndrome, Myelodysplastic syndromes, Myelofibrosis, Myeloid sarcoma, MYH9 related thrombocytopenia, Neonatal hemochromatosis, Neutropenia chronic familial, Neutropenia lethal congenital with eosinophilia, Non-involuting congenital hemangioma, Nonspherocytic hemolytic anemia due to hexokinase deficiency, Noonan syndrome, Orotic aciduria type 1, Paris-Trousseau thrombocytopenia, Parkes Weber syndrome, Paroxysmal cold hemoglobinuria, Paroxysmal nocturnal hemoglobinuria, Pearson syndrome, PEHO syndrome, PHACE syndrome, Pheochromocytoma, Phosphoglycerate kinase deficiency, Plasmablastic lymphoma, Plasminogen activator inhibitor type 1 deficiency, Platelet storage pool deficiency, Plummer Vinson syndrome, POEMS syndrome, Poikiloderma with neutropenia, Polycythemia vera, Prekallikrein deficiency, congenital, Primary angiitis of the central nervous system, Primary central nervous system lymphoma, Primary familial & congenital polycythemia, Primary intestinal lymphangiectasia, Primary release disorder of platelets, Prolidase deficiency, Protein C deficiency, Protein S deficiency, Proteus syndrome, Prothrombin deficiency, Pseudo-Von Willebrand disease, Pseudohyperkalemia Cardiff, Pseudoxanthoma elasticum, Pulmonary arterio-veinous fistula, Pulmonary atresia with intact ventricular septum, Pulmonary vein stenosis, Purpura simplex, Pyropoikilocytosis hereditary, Pyruvate kinase deficiency, Quebec platelet disorder, Red cell phospholipid defect with hemolysis, Refractory cytopenia with unilineage dysplasia, Revesz syndrome, Reynolds syndrome, Rh deficiency syndrome, Rosai-Dorfman disease, Rotor syndrome, Scott syndrome, Severe congenital neutropenia autosomal dominant, Severe congenital neutropenia autosomal recessive 3, Sezary syndrome, Shwachman-Diamond syndrome, Sickle beta thalassemia, Sickle cell – hemoglobin D disease, Sickle cell anemia, Sideroblastic anemia, Sideroblastic anemia & mitochondrial myopathy, Sideroblastic anemia pyridoxine-refractory autosomal recessive, Sideroblastic anemia pyridoxine-responsive autosomal recessive, Slow-channel congenital myasthenic syndrome, Sneddon syndrome, Stomatocytosis I, Stomatocytosis II, Sturge-Weber syndrome, Supraumbilical midabdominal raphe & facial cavernous hemangiomas, Supravalvular aortic stenosis, Susac syndrome, Swyer syndrome, Systemic mastocytosis, T-cell/histiocyte rich large B cell lymphoma, Takayasu arteritis, TAR syndrome, Thalassemia, Thiamine responsive megaloblastic anemia syndrome, Thoracolaryngopelvic dysplasia, Thrombocytopathy asplenia miosis, Thrombocytopenia 2, Thrombocytopenia with elevated serum IgA & renal disease, Thrombomodulin anomalies, Thrombotic thrombocytopenic purpura, Transient erythroblastopenia, Transient myeloproliferative syndrome, Triosephosphate isomerase deficiency, Tuberous sclerosis, Tufted angioma, Twin to twin transfusion syndrome, Type 1 plasminogen deficiency, Unicentric Castleman disease, Vascular Ehlers-Danlos syndrome, Vein of Galen aneurysm, Von Hippel-Lindau disease, Von Willebrand disease, Warm antibody hemolytic anemia, White platelet syndrome, Williams syndrome, Wiskott Aldrich syndrome, WT limb blood syndrome, Wyburn-Mason syndrome, X-linked sideroblastic anemia, X-linked thrombocytopenia, Yellow nail syndrome, Vampyrismus.
Louis Armand is the author of the novels Glasshouse (2018), The Combinations (2016) & Cairo (2014; longlisted for the Dublin IMPAC Award). In addition, he has published collections of poetry, including East Broadway Rundown (2015) & The Rube Goldberg Variations (2015). He lives in Prague.