Vanitha A Jagannath
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Explore the profile of Vanitha A Jagannath including associated specialties, affiliations and a list of published articles.
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205
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Recent Articles
1.
Sharma A, Jagannath V, Puri L
Cochrane Database Syst Rev
. 2021 Apr;
4:CD008708.
PMID: 33880750
Background: Thalassaemia is an autosomal recessive blood disorder, caused by mutations in globin genes or their regulatory regions, resulting in a reduced rate of synthesis of one of the globin...
2.
Jagannath V, Thaker V, Chang A, Price A
Cochrane Database Syst Rev
. 2020 Jun;
6:CD008482.
PMID: 32497260
Background: Malabsorption and deficiency of fat-soluble vitamins K may occur in cystic fibrosis, a genetic disorder affecting multiple organs. Vitamin K is known to play an important role in both...
3.
Jagannath V, Pucci E, Asokan G, Robak E
Cochrane Database Syst Rev
. 2019 Jun;
5:CD009903.
PMID: 31150100
Background: Multiple sclerosis (MS) is a leading cause of neurological disability in young adults. The most widely accepted hypothesis regarding its pathogenesis is that it is an immune-mediated disease. It...
4.
Jagannath V, Filippini G, Di Pietrantonj C, Asokan G, Robak E, Whamond L, et al.
Cochrane Database Syst Rev
. 2018 Sep;
9:CD008422.
PMID: 30246874
Background: This review is an update of a previously published review, "Vitamin D for the management of multiple sclerosis" (published in the Cochrane Library; 2010, Issue 12). Multiple sclerosis (MS)...
5.
Jagannath V, Thaker V, Chang A, Price A
Cochrane Database Syst Rev
. 2017 Aug;
8:CD008482.
PMID: 28829533
Background: Cystic fibrosis is a genetic disorder which can lead to multiorgan dysfunction. Malabsorption of fat and fat-soluble vitamins (A, D, E, K) may occur and can cause subclinical deficiencies...
6.
Jagannath V, Fedorowicz Z, Al Hajeri A, Sharma A
Cochrane Database Syst Rev
. 2016 Dec;
11:CD008708.
PMID: 27900772
Background: Thalassemia is an inherited autosomal recessive blood disorder, caused by mutations in globin genes or their regulatory regions. This results in a reduced rate of synthesis of one of...
7.
Jagannath V, Asokan G, Fedorowicz Z, Lee T
Cochrane Database Syst Rev
. 2016 Feb;
2:CD008139.
PMID: 26905631
Background: Cystic fibrosis is the most common, life-threatening, recessively inherited disease of Caucasian populations. It is a multisystem disorder caused by a mutation in the gene encoding the cystic fibrosis...
8.
Jagannath V, Fedorowicz Z, Thaker V, Chang A
Cochrane Database Syst Rev
. 2015 Apr;
1:CD008482.
PMID: 25879106
Background: Cystic fibrosis is a genetic disorder which can lead to multiorgan dysfunction. Malabsorption of fat and fat-soluble vitamins (A, D, E, K) may occur and can cause subclinical deficiencies...
9.
Jagannath V, Fedorowicz Z, Al Hajeri A, Sharma A
Cochrane Database Syst Rev
. 2014 Oct;
(10):CD008708.
PMID: 25316103
Background: Thalassemia is an inherited blood disorder, caused by mutations in regulatory genes and transmitted as an autosomal recessive disorder, which results in a reduced rate of synthesis of one...
10.
Jagannath V, Asokan G, Fedorowicz Z, Lee T
Cochrane Database Syst Rev
. 2014 Feb;
(2):CD008139.
PMID: 24515341
Background: Cystic fibrosis is the most common, life-threatening, recessively inherited disease of Caucasian populations. It is a multisystem disorder caused by a mutation in the gene encoding the cystic fibrosis...