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Bernard-soulier Syndrome
Bernard-Soulier syndrome
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Blood disorders
(127)
Acquired hemolytic anemia
Agranulocytosis
Alpha Thalassemia
Antiphospholipid syndrome
Drug-induced autoimmune hemolytic anemia
Drug-induced autoimmune hemolytic anemia
Drug-induced nonautoimmune hemolytic anemia
Glanzmann's thrombasthenia
Haemophilia A
May Hegglin Anomaly
Thrombocytopenia
Triosephosphate isomerase deficiency
Von willebrand disease
Acute eosinophilic leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid dendritic cell leukemia
Acute myeloid leukemia
Acute promyelocytic leukemia
Adult T-cell leukemia/lymphoma
Aggressive NK-cell leukemia
Amyloid purpura
Analbuminaemia
Anaplastic large cell lymphoma
Anemia
Anemia of chronic disease
Anemia of prematurity
Angioimmunoblastic T-cell lymphoma
Aplastic anemia
Atransferrinemia
Autoimmune hemolytic anemia
Autoimmune neutropenia
B symptoms
Beta-thalassemia
Bisalbuminemia
Blood hammer
Cavernous sinus thrombosis
Chemothera- py-induced neutropenia
Chromosome 5q deletion syndrome
Chronic myelogenous leukemia
Chronic neutrophilic leukemia
Congenital amegakaryocytic thrombocytopenia
Congenital dyserythropoietic anemia
Congenital hemolytic anemia
Contaminated haemophilia blood products
Cyclic neutropenia
Deaths from blood disease
Delta-thalassemia
Diamond-Blackfan anemia
Enteropath- y-associated T-cell lymphoma
Eosinopenia
Essential thrombocytosis
Evans syndrome
Familial dysfibrinogenemia
Haemophilia
Haemophilia B
Haemophilia C
Haemorrhagic and haematological disorders of fetus and newborn
Hairy cell leukemia
Harris platelet syndrome
Hematological malignancy
Hematology
Hemoglobin variants
Hemoglobinemia
Hemolytic anemia
Hemolytic disease of the newborn
Hemolytic disease of the newborn (ABO)
Hemolytic disease of the newborn (anti-Kell)
Hemolytic disease of the newborn (anti-RhE)
Hemolytic disease of the newborn (anti-Rhc)
Hemophagocytic lymphohistiocytosis
Hepatosplenic T-cell lymphoma
Hereditary elliptocytosis
Hereditary pyropoikilocytosis
Hereditary spherocytosis
Hodgkin's lymphoma
Hypersegmented neutrophil
Hypochromic anemia
Hypoprothrombinemia
Idiopathic thrombocytopenic purpura
Laminopathy
Large granular lymphocytic leukemia
Leukemia
Leukopenia
Lindsay Tribunal
List of hemophilia organizations
Loxoscelism
Lymphocytopenia
Lymphoma
Macrocytic anemia
Mantle cell lymphoma
Mast cell leukemia
Megaloblastic anemia
Methemoglobinemia
Minimally differentiated acute myeloblastic leukemia
Monoclonal B-cell lymphocytosis
Monoclonal gammopathy of undetermined significance
Myeloid sarcoma
Myelophthisic anemia
Neonatal alloimmune thrombocytopenia
Neutropenia
Nodular lymphocyte predominant Hodgkin's lymphoma
Non-Hodgkin lymphoma
Paroxysmal cold hemoglobinuria
Pel-Ebstein fever
Plummer-Vinson syndrome
Polycythemia vera
Primary effusion lymphoma
Protein S deficiency
Pseudo gray platelet syndrome
Quebec Platelet Disorder
Refractory anemia
Rh disease
Richter's transformation
Scott syndrome
Sickle cell trait
Sickle-cell disease
Spherocytosis
Splenic marginal zone lymphoma
T-cell prolymphocytic leukemia
Thalassemia
Thrombocytosis
Vaso-occlusive crisis
Waldenström's macroglobulinemia
Warm autoimmune hemolytic anemia
Wiskott-Aldrich syndrome
Working Formulation
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Genetic disorders
(19)
Benign paroxysmal peritonitis
Activated protein c resistance
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fukuyama type muscular dystrophy
Biedl-Bardet syndrome
Gray platelet syndrome
Galactosemias
Bilateral Acoustic Neurofibromatosis
Pelger-Huet anomaly
Multiple sulfatase deficiency
Alpha Thalassemia
Von willebrand disease
Glanzmann's thrombasthenia
May Hegglin Anomaly
Haemophilia A
Triosephosphate isomerase deficiency
more...
Autosomal recessive disorders
Benign paroxysmal peritonitis
Glanzmann's thrombasthenia
Leukodystrophy, globoid cell
Triosephosphate isomerase deficiency
Multiple sulfatase deficiency
Diseases and disorders
(56)
Blount disease
Giant platelet syndrome
Hyperproth- rombinemia
Hematologic disease
Basopenia
Basopenia
Enzymopathy
Platelet
Sulfhemoglobinemia
Antithrombin iii deficiency
Glossopharyngeal nerve diseases
Bowen syndrome
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Morvan disease
Intervertebral disk displacement
Idiopathic cold hemagglutinin syndrome
Platelet storage pool deficiency
Rosenthal syndrome
Myelodysplastic syndromes
Brachial plexus neuropathies
Metatropic dwarfism
Optic neuropathy, ischemic
Thrombosis
Bile duct cancer extrahepatic
Marinesco sjogren syndrome
Benign paroxysmal peritonitis
Agranulocytosis
Antiphospholipid syndrome
Activated protein c resistance
Alpha Thalassemia
Von willebrand disease
Glanzmann's thrombasthenia
Hyperostosis, cortical, congenital
May Hegglin Anomaly
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Thrombocytopenia
Fukuyama type muscular dystrophy
Biedl-Bardet syndrome
Gray platelet syndrome
Galactosemias
Haemophilia A
Triosephosphate isomerase deficiency
Bilateral Acoustic Neurofibromatosis
Pelger-Huet anomaly
Multiple sulfatase deficiency
more...
Chemical pathology
Beta HCG
Lupus anticoagulant
Ristocetin
Rheumatology
Benign paroxysmal peritonitis
Antiphospholipid syndrome
Purpura, schoenlein-henoch
Lupus erythematosus, cutaneous
Lupus anticoagulant
Hematology
(15)
Von willebrand factor
Monocytopenia
Haemostasis
Bleeding disorder
Thrombophilia
Thrombophilia
Mycosis fungoides
Drug-induced nonautoimmune hemolytic anemia
Acquired hemolytic anemia
Drug-induced autoimmune hemolytic anemia
Antiphospholipid syndrome
Hematologic disease
Activated protein c resistance
Myelodysplastic syndromes
Lupus anticoagulant
Thrombosis
more...
Coagulation system
(35)
Coagulation factors
Factor viii
Factor xiii deficiency
Fibrinogen
Thrombin
Thrombin
Tissue factor
Antithrombin iii deficiency
Bone hemostasis
Clot retraction
Cofact
Des-gamma carboxyprothrombin
Factor IX
Factor V
Factor VII
Factor X
Factor XI
Factor XII
Fibrinogenolysis
Haemostasis
High-molec- ular-weight kininogen
Human Activated Protein C
Medical Laboratory Scientist
Platelet
Platelet activation
Prekallikrein
Protein C
Protein S
Protein Z
Protein Z-related protease inhibitor
Prothrombin complex concentrate
Prothrombinase
Tenase
Thrombomodulin
Tissue factor pathway inhibitor
Von willebrand factor
more...
Clusters of differentiation
Glycoprotein IX
GP1BB
GP1BA
Tissue factor
Platelet
Platelet aggregation
Platelet count
Platelet (Cytokine signalling)
Platelet (Histology)
See also
(20)
Bioaccumulants
Biological magnification
Cytosis
Immune disorders
Penia
Penia
Myeloid
Glycoprotein Ib
Pro Wrestling (Nintendo Entertainment System)
Malignancy
Jean Pierre Soulier
Bandemia
MYH9
Br. J. Haematol.
Hereditary
EMD GP9
Chromosome 17
Platelet alpha-granule
Glycoprotein VI
Abnormal bleeding
Visual pathway glioma
more...
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