hemophilia A

Herein, we reported a case of the spontaneous intracholecystic hemorrhage in a 35-year-old male with hemophilia A .

Individuals with mild hemophilia A are often not diagnosed until later in life.

Perhaps the most important cause of congenital disease is heredity. Hemophilia, a disease in which the blood does not clot, is hereditary.

We report on a male infant with hemophilia A who was referred to our hospital on day 18 because of pallor and jaundice.

Gene therapy is the best method to approach the complete cure of hemophilia A .

In any individual with hemophilia A, bleeding episodes may be more frequent in childhood and adolescence than in adulthood.

Here, we review the advance in the research of retroviral vector in the hemophilia A gene therapy.

Living -related- donor spleen transplantation to treat 5 patients with hemophilia A .

People with hemophilia A, the most common form of the disease, are deficient in Factor VIII and suffer episodes of uncontrolled bleeding

Acquired hemophilia A in patients with systemic lupus erythematosus: report of a case and review of literature

Individuals with severe hemophilia A are usually diagnosed during the first year of life;

Surveillance: For individuals with severe or moderately severe hemophilia A, annual assessments at an HTC are recommended;

Clinical observation of the cadaveric spleen transplantation in the treatment of Hemophilia A

Diagnostic Analysis of Hemophilia A with High Titer Antibody in A Patient's Below-knee Computation

Genetic counseling in two particular hemophilia A families

Individuals with moderately severe hemophilia A seldom have spontaneous bleeding;

Study of Prenatal Diagnosis in Hemophilia A by Fetal Umbilical Blood

Symptomatic form of hemophilia A in female carriers

Individuals with mild hemophilia A do not have spontaneous bleeding;

Perioperative management of orthopaedic patients with hemophilia A

Application of long distance-PCR to hemophilia A carrier detection and prenatal diagnosis

Direct Sequencing in Hemophilia A Carrier Diagnosis and Prenatal Diagnosis

Preliminary experimental research on gene therapy for hemophilia A

Possibility of the transfected adipose tissue-derived stromal cells in the gene therapy of hemophilia A

Carrier detection and prenatal diagnosis for hemophilia A

Progress of Gene Diagnosis and Prenatal Diagnosis of Hemophilia A

Progress on DNA diagnosis of hemophilia A by microsatellite

The progress of retroviral vector in hemophilia A gene therapy

Progress in gene advances of gene therapy for hemophilia A

Prenatal diagnosis of hemophilia A

Using four kinds of molecular biological technologies to take genetic diagnosis for hemophilia A family ancestry

The research current of hemophilia A

An intervention model for improving the life quality of patients with hemophilia A