Literature DB >> 14295660

CONGENITAL HEREDITARY LYMPHOEDEMA.

J R ESTERLY.   

Abstract

Entities:  

Keywords:  BLOOD GROUPS; CHILD; GENETICS, HUMAN; MILROY'S DISEASE

Mesh:

Substances:

Year:  1965        PMID: 14295660      PMCID: PMC1012841          DOI: 10.1136/jmg.2.2.93

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  7 in total

1.  A clinical appraisal of the plasma concentration and endogenous clearance of creatinine.

Authors:  P D DOOLAN; E L ALPEN; G B THEIL
Journal:  Am J Med       Date:  1962-01       Impact factor: 4.965

2.  Genetic control of isoniazid metabolism in man.

Authors:  D A EVANS; K A MANLEY; V A McKUSICK
Journal:  Br Med J       Date:  1960-08-13

3.  Primary lymphoedema; clinical and lymphangiographic studies of a series of 107 patients in which the lower limbs were affected.

Authors:  J B KINMONTH; G W TAYLOR; G D TRACY; J D MARSH
Journal:  Br J Surg       Date:  1957-07       Impact factor: 6.939

4.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

5.  STUDIES IN CONGESTIVE HEART FAILURE: I. The Effect of Edema on Oxygen Utilization.

Authors:  T R Harrison; C Pilcher
Journal:  J Clin Invest       Date:  1930-02       Impact factor: 14.808

6.  MILROY'S DISEASE: REPORT OF TWO CASES.

Authors:  C W Page
Journal:  Cal West Med       Date:  1928-08

7.  Chronic hereditary lymphedema (Nonne-Milroy-Meige's Disease).

Authors:  E SCHROEDER; H F HELWEG-LARSEN
Journal:  Acta Med Scand       Date:  1950
  7 in total
  7 in total

1.  Primary Upper Limb Lymphedema: Case Report of a Rare Pathology.

Authors:  Michael Ec Mcfarlane
Journal:  Perm J       Date:  2016-11-09

2.  Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Authors:  A Irrthum; M J Karkkainen; K Devriendt; K Alitalo; M Vikkula
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

3.  Lymphoedema in hereditary recurrent cholestasis from birth.

Authors:  O Aagenaes; H Sigstad; R Bjorn-Hansen
Journal:  Arch Dis Child       Date:  1970-10       Impact factor: 3.791

4.  Acute jejunal ileus in intestinal lymphangiectasia.

Authors:  R Lenzhofer; M Lindner; A Moser; J Berger; C Schuschnigg; J Thurner
Journal:  Clin Investig       Date:  1993-07

5.  Early onset lymphoedema, recessive form--a new form of genetic lymphoedema syndrome.

Authors:  J Mücke; W Hoepffner; G Scheerschmidt; H Gornig; K Beyreiss
Journal:  Eur J Pediatr       Date:  1986-08       Impact factor: 3.183

6.  Syndrome of lymphoedema and distichiasis.

Authors:  Z Pap; T Biró; L Szabó; Z Papp
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A.

Authors:  Yu Sui; Yongping Lu; Meina Lin; Xiang Ni; Xinren Chen; Huan Li; Miao Jiang
Journal:  BMC Med Genomics       Date:  2021-06-08       Impact factor: 3.063

  7 in total

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