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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
Hemophilia -- Treatment -- Complications.   2
Hemophilia -- United States -- History   2
  Hemophilia, Vascular -- 2 Related Subjects   2
Hemophiliacs   2
Hemophiliacs -- Australia -- Biography. : April Fool's Day : a modern tragedy / Bryce Courtenay  1993 1
Hemophiliacs -- Biography. : April Fool's Day : a modern tragedy / Bryce Courtenay  1993 1
Hemophiliacs -- Infections -- United States : Blood on their hands : how greedy companies, inept bureaucracy, and bad science killed thousands of hemophiliacs / Eric Weinberg, Donna Shaw  2017 1
Hemophiliacs -- Legal status, laws, etc. -- United States : Blood on their hands : how greedy companies, inept bureaucracy, and bad science killed thousands of hemophiliacs / Eric Weinberg, Donna Shaw  2017 1
Hemophiliacs -- New Zealand : Haemophilia in Aotearoa New Zealand : more than a bleeding nuisance / Julie Park, Kathryn M. Scott, Deon York, and Michael Carnahan  2019 1
Hemophiliacs -- Russia -- Biography. : Nicholas and Alexandra / Robert K. Massie  1969 1
Hemophiliacs -- Services for -- Australia. : X factors : a history of haemophilia in Australia / Cheryl Crockett  2003 1
Hemophiliacs -- Surgery   2
Hemophiliacs -- Virginia -- Biography : Bleeder : a Memoir / Shelby Smoak  2013 1
 

Hemophilias, 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
 

Hemophilic factor A -- See Blood coagulation factor VIII


  1
 

Hemophilic factor B -- See Blood coagulation factor IX


  1
 

Hemophilics -- See Hemophiliacs


  1
 

Hemophilus -- See Haemophilus


A genus of PASTEURELLACEAE that consists of several species occurring in animals and humans. Its organisms are described as gram-negative, facultatively anaerobic, coccobacillus or rod-shaped, and nonmotile 		  1
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