MM FRANK, JA GELFAND, JP ATKINSON - Annals of Internal Medicine, 1976 - Am Coll Physicians Hereditary angioedema is manifested by attacks of swelling of the extremities,
face, trunk, airway, or abdominal viscera, occurring spontaneously or secondary
to trauma. It is inherited as an autosomal dominant trait and is due to ... Cited by 312 - Related articles - All 3 versions
JA Gelfand, RJ Sherins, DW Alling, MM Frank - New England Journal of Medicine, 1976 - content.nejm.org Danazol, an androgen derivative, was evaluated for its effectiveness in
preventing attacks of hereditary angioedema in a double-blind study with nine
patients. Of 47 placebo courses, 44 ended with attacks, but during 46 ... Cited by 289 - Related articles - All 2 versions
VH Donaldson, RR Evans - The American Journal of Medicine, 1963 - Elsevier Affected persons in three families with hereditary angioneurotic edema
completely lack naturally occurring serum inhibitor of C′1esterase. This
inhibitor is also absent from some younger relatives who have not yet had ... Cited by 525 - Related articles - All 2 versions
MM Frank, JS Sergent, MA Kane, DW Alling - The New England journal of medicine, 1972 - ncbi.nlm.nih.gov 1: N Engl J Med. 1972 Apr 13;286(15):808-12. Epsilon aminocaproic acid therapy
of hereditary angioneurotic edema. A double-blind study. ... Cited by 137 - Related articles
W Osler - The American Journal of the Medical Sciences, 1888 - journals.lww.com 362 OSLEB, HEBEDITABT Aλ GIO-NEUROTIC (EDEMA. HEREDITARY ANGIO-NEUROTIC
ŒDEMA.1 By William Oslek,MD, гхогеыок or cusical xtBiciKt «r rax
cnitsjuitt or гсхквптАкм, putii пак to тек ukitìmitt ... Cited by 209 - Related articles - All 2 versions
FS Rosen, J Pensky, V Donaldson, P … - Science (New York, NY), 1965 - ncbi.nlm.nih.gov 1: Science. 1965 May 14;148:957-8. HEREDITARY ANGIONEUROTIC EDEMA: TWO GENETIC
VARIANTS. ROSEN FS, PENSKY J, DONALDSON V, CHARACHE P. ... Cited by 219 - Related articles - All 3 versions
WB Spaulding - Annals of Internal Medicine, 1960 - Am Coll Physicians Iste morbo rar, que affice ambe sexos, se transmitte geneticamente con le
configuration mendelian de un anormalitate dominante. Le characteristica
essential del condition es es le apparition e propagation rapide de un ... Cited by 100 - Related articles
A AGOSTONI, M CICARDI - Medicine, 1992 - journals.lww.com HEREDITARY AND ACQUIRED CI INHIBITOR DEFICIENCY 207 Diagnostic criteria
Diagnosis of HAE was based on a personal and/or family history of recurrent
non-inflammatory subcutaneous edema, episodic abdominal pain, and laryngeal ... Cited by 232 - Related articles - All 3 versions
JE Gadek, SW Hosea, JA Gelfand, M … - New England Journal of Medicine, 1980 - content.nejm.org Although considerable progress has been made during the past two decades in the
use of androgens to prevent attacks of hereditary angioedema, replacement of the
deficient C1-inhibitor protein would provide a useful menas of treatment ... Cited by 119 - Related articles - All 2 versions
CJ Jaffe, JP Atkinson, JA Gelfand, MM Frank - The Journal of allergy and clinical immunology, 1975 - ncbi.nlm.nih.gov Six patients with hereditary anagioedema (HAE) undergoing 7 episodes of dental
surgery received transfusions with fresh frozen plasma one day before surgery.
Although the morbidity observed in these patients following similar ... Cited by 64 - Related articles
