Deepti Saxena
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Explore the profile of Deepti Saxena including associated specialties, affiliations and a list of published articles.
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33
Citations
339
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Recent Articles
1.
Aishwarya A, Agarwal A, Saxena D, Jain V, Singh A, Agarwal R
Rom J Ophthalmol
. 2025 Feb;
68(4):372-378.
PMID: 39936060
Purpose: To gain epidemiological insights by investigating the age, risk factors, and clinical features of individuals affected by the conjunctivitis outbreak. Methods: The study was conducted at various ophthalmic centers,...
2.
Yadav B, Chaudhary R, Elhence P, Phadke S, Mandal K, Saxena D, et al.
Asian J Transfus Sci
. 2024 Jan;
17(2):145-150.
PMID: 38274964
Background: One of the complications of chronic transfusions in thalassemia is the development of red cell alloimmunization. Aims: The aim of the study was to determine the frequency, specificity of...
3.
Saxena D, Tiwari A, Prasad R, Srivastav S
Eur J Med Genet
. 2023 Nov;
66(12):104888.
PMID: 37993095
Non-immune hydrops fetalis (NIHF) is abnormal accumulation of serous fluid in ≥2 interstitial spaces with no evidence of maternal red cell alloimmunization. Leaving a few treatable conditions, it is generally...
4.
Tiwari A, Srinivasan V, Phadke S, Saxena D
Clin Genet
. 2023 Oct;
105(2):226-227.
PMID: 37849383
We report the third case of FADS due to biallelic DOK7 variants, which further strengthens the association of DOK7 with this lethal phenotype and lack of genotype phenotype correlation.
5.
Saxena D, Srivastava S, Maurya R, Moirangthem A, Mandal K, Phadke S
Prenat Diagn
. 2023 Mar;
43(5):579-595.
PMID: 36964991
Objective: Genetic diseases are an important cause of neonatal and childhood mortality. For couples with a history of demise of previous children, screening for carrier status can be done by...
6.
Sait H, Srivastava S, Pandey M, Ravichandran D, Shukla A, Mandal K, et al.
Neurogenetics
. 2023 Feb;
24(2):113-127.
PMID: 36790591
Neurodegeneration with brain iron accumulation (NBIA) is an umbrella term encompassing various inherited neurological disorders characterised by abnormal iron accumulation in basal ganglia. We aimed to study the clinical, radiological...
7.
Lata I, Gupta A, Saxena D, Rekhi A, Sahu S
J Family Med Prim Care
. 2022 Dec;
11(9):5683-5685.
PMID: 36505660
Haemophilia-A is a rare, X-linked recessive inherited disease affects males and females are carrier results in prolonged bleeding after minor injuries, procedures or surgery. Spontaneous or recurrent bleeding may occur...
8.
Sait H, Srivastava S, Saxena D
Int J Gen Med
. 2022 May;
15:5133-5144.
PMID: 35637703
Epidermolysis bullosa (EB) is a group of rare genodermatoses that is characterized by skin fragility resulting from minor trauma. There are four major subtypes, namely, EB simplex, junctional EB, dystrophic...
9.
Masih S, Moirangthem A, Shambhavi A, Rai A, Mandal K, Saxena D, et al.
Eur J Med Genet
. 2022 May;
65(6):104520.
PMID: 35568357
Microcephaly is a frequent feature of neurodevelopmental disorders (NDDs). Our study presents the heterogeneous spectrum of genetic disorders in patients with microcephaly either in isolated form or in association with...
10.
Agrawal N, Verma G, Saxena D, Kabra M, Gupta N, Mandal K, et al.
Eur J Med Genet
. 2022 Feb;
65(3):104447.
PMID: 35144014
MPS II is an X linked recessive lysosomal storage disorder with multi-system involvement and marked molecular heterogeneity. In this study, we explored the clinical and molecular spectrum of 144 Indian...