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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.   25
  Hemophilia A -- 3 Related Subjects   3
Hemophilia A   14
 

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 -- diagnosis : Contemporary approaches to hemophilia / editor, Erik Berntorp  2014 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   3
 

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
Hemophilia B -- physiopathology.   2
Hemophilia B -- surgery : Orthopedic surgery in patients with hemophilia / edited by Horacio Caviglia, Luigi Piero Solimeno  2008 1
 

Hemophilia Bs -- 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 Bs (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
 

Hemophilia C -- See Factor XI Deficiency


A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia 		  1
Hemophilia -- Chemotherapy : Prothrombin complex concentrates : advances in research and clinical applications / Michael S. Firstenberg, editor  2017 1
 

Hemophilia, Classic -- 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 -- Complications.   5
 

Hemophilia Complications and sequelae -- See Hemophilia Complications


  1
Hemophilia -- Complications -- Physical therapy. : Physiotherapy management of haemophilia / edited by Brenda Buzzard and Karen Beeton  2000 1
Hemophilia -- Congresses   4
Hemophilia -- Diagnosis : Contemporary approaches to hemophilia / editor, Erik Berntorp  2014 1
Hemophilia -- Genetic aspects : Advances in hemophilia treatment from genetics to joint health / E. Carlos Rodríguez-Merchán, editor  2022 1
Hemophilia -- Immunological aspects.   2
Hemophilia -- Law and legislation -- United States -- Criminal provisions : Blood on their hands : how greedy companies, inept bureaucracy, and bad science killed thousands of hemophiliacs / Eric Weinberg, Donna Shaw  2017 1
Hemophilia -- New Zealand : Haemophilia in Aotearoa New Zealand : more than a bleeding nuisance / Julie Park, Kathryn M. Scott, Deon York, and Michael Carnahan  2019 1
Hemophilia -- Pathophysiology.   2
 

Hemophilia Patients -- See Hemophiliacs


  1
Hemophilia -- Periodicals   2
Hemophilia -- Russia. : Nicholas and Alexandra / Robert K. Massie  1969 1
Hemophilia -- Treatment   5
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