Double trouble: Duchenne muscular dystrophy and hemophilia

Pediatric Blood and Cancer

Volumn 60, Issue 3, 2013, Pages 525-

  Gokce, Muge ^a   Haliloǧlu, Göknur ^a   Serdaroǧlu, Esra ^a   Caǧlayan, Hande ^b   Gümrük, Fatma ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

^b BOGAZICI UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 9;

BLOOD CHEMISTRY; CASE REPORT; CHILD; CHROMOSOME XQ; CHROMOSOME XQ27.1; CIRCUMCISION; DISEASE ASSOCIATION; DISEASE SEVERITY; DUCHENNE MUSCULAR DYSTROPHY; ECHOCARDIOGRAPHY; ELECTROMYOGRAPHY; FAMILY HISTORY; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; HEMOPHILIA B; HUMAN; IMMUNOHISTOCHEMISTRY; JOINT LAXITY; LABORATORY TEST; LETTER; LUNG FUNCTION TEST; MALE; MOLECULAR GENETICS; MUSCLE BIOPSY; MUSCLE HYPERTROPHY; MUSCLE STRENGTH; MUSCLE WEAKNESS; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; POSTOPERATIVE HEMORRHAGE; PRIORITY JOURNAL; RISK FACTOR; SCHOOL CHILD; STAINING; WALKING DIFFICULTY;

CHILD; DYSTROPHIN; FACTOR IX; HEMOPHILIA B; HUMANS; MALE; MUSCULAR DYSTROPHY, DUCHENNE;

EID: 84872434413     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.24376     Document Type: Letter

References (3)

1. Manucci PM, Tuddenham EG. The hemophilias-From royal genes to gene therapy. N Engl J Med 2001; 344: 1773-1779.
2. Bushby K, Finkel R, Birnkrant DJ, et al. Diagnosis and management of Duchenne muscular dystrophy, Part 1: Diagnosis, and pharmacological and psychosocial management. Lancet Neurol 2010; 9: 77-93.
3. Konagaya M, Takayanagi T, Kamiya T, et al. Genetic linkage study of Duchenne muscular dystrophy and Hemophilia A. Neurol 1982; 32: 1046.