The turkish hereditary angioedema pilot study (TURHAPS): The first turkish series of hereditary angioedema

International Archives of Allergy and Immunology

Volumn 156, Issue 4, 2011, Pages 443-450

  Kesim, Belgin ^a   Uyguner, Zehra Oya ^b   Gelincik, Asli ^c   Gökmen, Nihal Mete ^e   Sin, Aytül Z ^e   Karakaya, Gül ^f   Erdenen, Füsun ^d   Ardeniz, Ömür ^e   Özşeker, Ferhan ^c   Gülbahar, Okan ^e   Çolakoǧlu, Bahattin ^c   Dal, Murat ^c   Büyüköztürk, Suna ^c  

^a Sisli Etfal Training and Education Hospital   (Turkey)

^b Department of Medical Genetics ^*  (Turkey)

^c ISTANBUL UNIVERSITY   (Turkey)

^d ISTANBUL TRAINING AND RESEARCH HOSPITAL   (Turkey)

^e EGE UNIVERSITY   (Turkey)

^f HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Clinical trial; Genetics; Hereditary angioedema

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR;

ABDOMINAL PAIN; ADULT; ALLELE; ANGIONEUROTIC EDEMA; ARTICLE; BLOOD CLOTTING FACTOR DEFICIENCY; DISEASE DURATION; ERYTHEMA; EXON; FACE EDEMA; FEMALE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HEREDITY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LARYNX EDEMA; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD REVIEW; MUTATIONAL ANALYSIS; NONSENSE MUTATION; PERIPHERAL EDEMA; PRIORITY JOURNAL; RELATIVE; SKIN EDEMA; SPLICING DEFECT; TONGUE EDEMA; TURKEY (REPUBLIC);

ADOLESCENT; ADULT; ANGIOEDEMAS, HEREDITARY; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; COMPLEMENT C1 INACTIVATOR PROTEINS; EXONS; FEMALE; GENOTYPE; HUMANS; INFANT; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; PILOT PROJECTS; TURKEY; YOUNG ADULT;

EID: 81155158691     PISSN: 10182438     EISSN: 14230097     Source Type: Journal    
DOI: 10.1159/000323915     Document Type: Article

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