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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
 

Hemophagocytic Syndrome -- See Lymphohistiocytosis, Hemophagocytic


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

Hemophagocytic Syndrome, Infection-Associated -- See Lymphohistiocytosis, Hemophagocytic


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

Hemophagocytic Syndrome, Reactive -- See Lymphohistiocytosis, Hemophagocytic


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

Hemophagocytic Syndromes -- See Lymphohistiocytosis, Hemophagocytic


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

Hemophilia -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
Hemophilia.   24
  Hemophilia A -- 3 Related Subjects   3
Hemophilia A   13
 

Hemophilia A, Autosomal -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
Hemophilia A -- complications   4
 

Hemophilia A, Congenital -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
Hemophilia A -- history   3
Hemophilia A -- immunology. : Inhibitors in patients with haemophilia / edited by E.C. Rodriguez-Merchan, C.A. Lee  2002 1
Hemophilia A -- physiopathology.   2
Hemophilia A -- prevention & control : Current and future issues in hemophilia care / edited by Emérito-Carlos Rodríguez-Merchán, Leonard A. Valentino  2011 1
Hemophilia A -- rehabilitation. : Physiotherapy management of haemophilia / edited by Brenda Buzzard and Karen Beeton  2000 1
Hemophilia A -- surgery : Orthopedic surgery in patients with hemophilia / edited by Horacio Caviglia, Luigi Piero Solimeno  2008 1
Hemophilia A -- therapy   2
 

Hemophilia As -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
 

Hemophilia As, Autosomal -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
 

Hemophilia As, Congenital -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
Hemophilia -- Australia -- History. : X factors : a history of haemophilia in Australia / Cheryl Crockett  2003 1
 

Hemophilia B -- See Also Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage 		  1
Hemophilia B   4
Hemophilia B -- complications : Orthopedic surgery in patients with hemophilia / edited by Horacio Caviglia, Luigi Piero Solimeno  2008 1
Hemophilia B -- immunology. : Inhibitors in patients with haemophilia / edited by E.C. Rodriguez-Merchan, C.A. Lee  2002 1
 

Hemophilia B Leyden -- See Hemophilia B


A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) 		  1
 

Hemophilia B(M) -- See Hemophilia B


A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) 		  1
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