Primary pulmonary hypertension, cerebrovascular malformation, and lymphoedema feet in a family.

Author:

Avasthey P,Roy S B

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference22 articles.

1. Pathological findings in nine children with "primary" pulmonary hypertension;Berthrong, M.; Cochran, T.H.;Bull. Johns Hopk. Hosp,1955

2. Primary pulmonary hypertension: familial incidence;Boiteau, G.M.; Libanoff, A.J.;Aniology,1963

3. Cahen, P., Gonin, A., Froment, R., and Dalloz, C. (1961).

4. On certain abnormalities, congenital and acquired, of the pulmonary artery;Clarke, R.C.; Coombs, C.F.; Hadfield, G.; Todd, A.T.;Quart. J7. Med,1927

5. Primary pulmonary hypertension in three sibs;Coleman, P.N.; Edmunds, A.W.B.; Tregillus, J.;Brit. Heart_J,1959

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1. Special Issues in Pediatric Primary Lymphedema;Lymphedema;2011

2. Lymphœdèmes primaires des membres;La Presse Médicale;2010-12

3. Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome?;American Journal of Medical Genetics Part A;2010-06-25

4. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

5. A family with IgA nephropathy and hereditary lymphoedema praecox;Journal of Internal Medicine;2002-05

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