Neeraj Tomar
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Explore the profile of Neeraj Tomar including associated specialties, affiliations and a list of published articles.
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14
Citations
209
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Recent Articles
1.
Garg B, Tomar N, Biswas A, Mehta N, Malhotra R
JBJS Rev
. 2022 Apr;
10(4).
PMID: 35383688
»: An insight into musculoskeletal disorders through advancements in next-generation sequencing (NGS) promises to maximize benefits and improve outcomes through improved genetic diagnosis. »: The primary use of whole exome...
2.
Goswami R, Millo T, Mishra S, Das M, Kapoor M, Tomar N, et al.
J Clin Endocrinol Metab
. 2014 Feb;
99(5):1741-8.
PMID: 24552219
Background: Basal ganglia calcification (BGC) is an interesting example of ectopic calcification in patients with hypoparathyroidism. Its pathogenesis and reasons for predilection of calcification at basal ganglia are not clear....
3.
Tomar N, Gupta N, Goswami R
J Clin Endocrinol Metab
. 2013 Jul;
98(9):3884-91.
PMID: 23873991
Context: Data on calcium-sensing receptor autoantibodies (CaSRAbs) in hypoparathyroidism are variable. Objective: We assessed the prevalence and significance of CaSRAbs in idiopathic hypoparathyroidism. Design: This was a case-control study. Subjects:...
4.
Tomar N, Kaushal E, Das M, Gupta N, Betterle C, Goswami R
J Clin Endocrinol Metab
. 2012 Jan;
97(4):1219-26.
PMID: 22278434
Context: Role of parathyroid autoimmunity in idiopathic hypoparathyroidism (IH) is not clear. Recently, parathyroid-specific NACHT leucine-rich-repeat protein 5 (NALP5) autoantibodies (Ab) have been reported in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. Objective:...
5.
Tomar N, Bora H, Singh R, Gupta N, Kaur P, Chauhan S, et al.
Eur J Endocrinol
. 2009 Nov;
162(2):407-21.
PMID: 19940031
Objective: Glial cells missing 2 (GCM2) gene encodes a parathyroid-specific transcription factor. We assessed GCM2 gene sequence in patients with isolated hypoparathyroidism (IH). Design: Case-control study. Methods: Complete DNA sequencing...
6.
Kanakamani J, Tomar N, Kaushal E, Tandon N, Goswami R
Calcif Tissue Int
. 2009 Nov;
86(1):33-41.
PMID: 19921089
Vitamin D-dependent rickets type II (VDDR-type II) is a rare disorder caused by mutations in the vitamin D receptor (VDR) gene. Here, we describe a patient with VDDR-type II with...
7.
Goswami R, Goel S, Tomar N, Gupta N, Lumb V, Sharma Y
Clin Endocrinol (Oxf)
. 2009 Jun;
72(3):328-33.
PMID: 19549251
Background: Remission of disease activity is a characteristic feature of autoimmune endocrine disorders such as Graves' disease, Addison's disease and occasionally in patients with premature ovarian failure. Autoimmunity is also...
8.
Goswami R, Marwaha R, Gupta N, Tandon N, Sreenivas V, Tomar N, et al.
Br J Nutr
. 2009 Feb;
102(3):382-6.
PMID: 19203420
25-Hydroxy vitamin D (25(OH)D) deficiency is linked with predisposition to autoimmune type 1 diabetes and multiple sclerosis. Our objective was to assess the relationship between serum 25(OH)D levels and thyroid...
9.
Ray D, Goswami R, Gupta N, Tomar N, Singh N, Sreenivas V
Clin Endocrinol (Oxf)
. 2008 Dec;
71(3):334-40.
PMID: 19094076
Background: Osteomalacia (OSM) and rickets are widely prevalent in developing countries especially in females. The factors associated with such predisposition are not known. Objectives: To identify nutritional, endocrine and genetic...
10.
Goswami R, Gupta N, Ray D, Singh N, Tomar N
Br J Nutr
. 2008 Feb;
100(3):526-9.
PMID: 18252022
Hypovitaminosis D is common in Asian Indians. Physicians often prescribe 1500 mug (60 000 IU) cholecalciferol per week for 8 weeks for vitamin D deficiency in India. Its efficacy to...