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Hemoglobinuria, Paroxysmal   2
 

Hemoglobinuria, Paroxysmal Cold -- See Hemoglobinuria, Paroxysmal


A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins 		  1
Hemoglobinuria, Paroxysmal -- drug therapy : Paroxysmal nocturnal hemoglobinuria : from bench to bedside / Yuzuru Kanakura, Taroh Kinashita, Jun-ichi Nishimura, editors  2017 1
 

Hemoglobinuria, Paroxysmal Nocturnal -- See Hemoglobinuria, Paroxysmal


A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins 		  1
Hemoglobinuria, Paroxysmal -- physiopathology : Paroxysmal nocturnal hemoglobinuria : from bench to bedside / Yuzuru Kanakura, Taroh Kinashita, Jun-ichi Nishimura, editors  2017 1
 

Hemoglobulin -- See Hemoglobin


  1
 

Hemogram -- See Blood cell count


  1
Hemolymph.   2
 

Hemolyses, Extravascular -- See Hemolysis


The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity 		  1
 

Hemolyses, Intravascular -- See Hemolysis


The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity 		  1
 

Hemolysis -- See Also Anemia, Hemolytic


A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES) 		  1
Hemolysis : Hemolysis : an unresolved dispute in laboratory medicine / [edited by] Giuseppe Lippi [and others]  2012 1
 

Hemolysis and hemolysins -- See Also the narrower term Hemolytic anemia


  1
Hemolysis and hemolysins. : Hemolysis : an unresolved dispute in laboratory medicine / [edited by] Giuseppe Lippi [and others]  2012 1
 

Hemolysis, Extravascular -- See Hemolysis


The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity 		  1
 

Hemolysis, Intravascular -- See Hemolysis


The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity 		  1
  Hemolytic Anemia -- 6 Related Subjects   6
Hemolytic anemia. : Renaissance Of Sickle Cell Disease Research In The Genome Era  2007 1
 

Hemolytic Anemia, Acquired -- See Anemia, Hemolytic


A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES) 		  1
Hemolytic anemia, Autoimmune   2
Hemolytic anemia, Autoimmune -- Case studies : Case studies in immunology : a clinical companion : autoimmune hemolytic anemia / Raif Geha, Fred Rosen  2010 1
Hemolytic anemia, Autoimmune -- Diagnosis : Autoimmune hemolytic anemia (AIHA) : symptoms, diagnosis and treatment / Jean Harmon, editor  2016 1
Hemolytic anemia, Autoimmune -- Patients : Case studies in immunology : a clinical companion : autoimmune hemolytic anemia / Raif Geha, Fred Rosen  2010 1
Hemolytic anemia, Autoimmune -- Treatment : Autoimmune hemolytic anemia (AIHA) : symptoms, diagnosis and treatment / Jean Harmon, editor  2016 1
Hemolytic anemia -- Complications : Parvovirus B19 and hematological disorders in children / Maysaa El Sayed Zaki  2010 1
 

Hemolytic Complement -- See Complement System Proteins


Serum glycoproteins participating in the host defense mechanism of COMPLEMENT ACTIVATION that creates the COMPLEMENT MEMBRANE ATTACK COMPLEX. Included are glycoproteins in the various pathways of complement activation (CLASSICAL COMPLEMENT PATHWAY; ALTERNATIVE COMPLEMENT PATHWAY; and LECTIN COMPLEMENT PATHWAY) 		  1
 

Hemolytic disorder, Autoimmune -- See Hemolytic anemia, Autoimmune


  1
 

Hemolytic Transfusion Reaction -- See Transfusion Reaction


Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility 		  1
 

Hemolytic Transfusion Reactions -- See Transfusion Reaction


Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility 		  1
Hemolytic-uremic syndrome.   3
Hemon, Aleksandar, 1964- Islands : Short stories for students. Volume 22 : presenting analysis, context, and criticism on commonly studied short stories / Ira Mark Milne, project editor ; foreword by Thomas E. Barden  2006 1
Hemoperfusion. : Dialysis, dialyzers, and sorbents : where are we going? / volume editors, C. Ronco, J.F. Winchester  2001 1
Hemoperfusion -- methods   2
 

Hemoperfusions -- See Hemoperfusion


Removal of toxins or metabolites from the circulation by the passing of blood, within a suitable extracorporeal circuit, over semipermeable microcapsules containing adsorbents (e.g., activated charcoal) or enzymes, other enzyme preparations (e.g., gel-entrapped microsomes, membrane-free enzymes bound to artificial carriers), or other adsorbents (e.g., various resins, albumin-conjugated agarose) 		  1
  Hemopericardium -- 2 Related Subjects   2
 

Hemophagocytic Histiocytoses, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Histiocytosis, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Hymphohistiocytoses, Primary -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Hymphohistiocytosis, Primary -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphocytoses, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphocytosis, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytoses -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytoses, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytoses, Primary -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytosis -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytosis, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytosis Familial -1 -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Lymphohistiocytosis, Primary -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Reticuloses, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
 

Hemophagocytic Reticulosis, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive 		  1
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