Phlegmasia Cerulea Dolens Complicated by Methylenetetrahydrofolate Reductase Genetic Mutation

International Journal of Case Reports and Images
doi 10.5348/ijcri-201655-cr-10643
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Edorium Journals Pvt. Ltd.

Related search

A Case of Phlegmasia Cerulea Dolens

SAJ Case Reports
2017English

Spontaneous Psoas Abscess: Presenting With Phlegmasia Cerulea Dolens

Annals of the Royal College of Surgeons of England
MedicineSurgery
2011English

Phlegmasia Cerulea Dolens Report of a Case With Unusual Presentation

Angiology and Vascular Surgery
2019English

Phlegmasia Cerulea Dolens and May–Thurner Syndrome in the First Trimester of Pregnancy

AJP Reports
GynecologyChild HealthPediatricsPerinatologyObstetrics
2015English

Management of Bilateral Phlegmasia Cerulea Dolens in a Patient With Subacute Splenic Laceration

Annals of Vascular Diseases
2008English

Further Researches on the Pathology of Phlegmasia Dolens

Journal of the Royal Society of Medicine
Medicine
1853English

Effect of Common Methylenetetrahydrofolate Reductase Gene Mutation on Coronary Artery Disease in Familial Hypercholesterolemia

American Journal of Cardiology
Cardiovascular MedicineCardiology
2000English

Methylenetetrahydrofolate Reductase Deficiency: Rare but Considerable

Turkish Journal of Anesthesia and Reanimation
2018English

Betaine for Treatment of Homocystinuria Caused by Methylenetetrahydrofolate Reductase Deficiency.

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1989English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy