Aryan Gupta
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Explore the profile of Aryan Gupta including associated specialties, affiliations and a list of published articles.
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20
Citations
14
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Recent Articles
1.
Ahmed H, Nair S, Sache M, Das R, Gupta A, Choradia S, et al.
Eye (Lond)
. 2024 Dec;
39(3):424-435.
PMID: 39715858
Background: The lacrimal caruncle, a nodular structure located at the inner canthus, contains a variety of tissue types, leading to diverse clinical manifestations of its lesions. Caruncular lesions, though rare,...
2.
Deepika M, Srilekha A, Pavani C, Gupta A, Nazneen R, Lakshmi B
J Appl Genet
. 2024 Dec;
PMID: 39673051
Recurrent pregnancy loss (RPL) is defined as the spontaneous loss of two or more pregnancies before reaching viability. Diagnosis for couples with RPL usually involves only the female partner. However,...
3.
Bahal M, Pande V, Salunkhe S, Dua J, Mane S, Gupta A, et al.
Cureus
. 2024 Sep;
16(8):e67819.
PMID: 39323725
Background Neurodevelopmental disorders (NDDs) encompass intricate interactions among genetic, brain, cognitive, emotional, and behavioral processes. These disorders, which are influenced by hereditary and environmental factors, impair personal, social, intellectual, or...
4.
Garlapati S, Mane S, Gupte S, Mehta S, Gupta A, Avuthu O
Cureus
. 2024 Sep;
16(8):e67496.
PMID: 39310530
Klinefelter syndrome (KS; XXY syndrome) is a common chromosomal abnormality associated with various physical and developmental characteristics. It rarely presents with ambiguous genitalia, a feature more typical of disorders of...
5.
Kulkarni V, Chalipat S, Gupta A, Bhosle A, Bahal M
Cureus
. 2024 Sep;
16(8):e67041.
PMID: 39286690
There is still more to learn about the etiology of extremely uncommon developmental disorders. A heterozygous or hemizygous pathogenic variation in male-specific lethal 3 (MSL3) causes the uncommon X-linked condition...
6.
Kumar G, Verma S, Chavan S, Gupta A, Avuthu O, Mane S, et al.
Cureus
. 2024 Sep;
16(8):e66255.
PMID: 39238685
Background The etiological profile of children with bicytopenia and pancytopenia has a very wide spectrum, ranging from transient causes like infections or nutritional deficiencies to bone marrow failure syndromes. Timely...
7.
Dua J, Jadhav R, Bahal M, Mane S, Gupta A
Cureus
. 2024 Sep;
16(8):e65975.
PMID: 39221345
Peripheral arteriovenous malformations (AVMs) are rare vascular anomalies characterized by abnormal connections between arteries and veins that bypass the capillary system. This case report details a three-year-old female child who...
8.
Pande V, Bahal M, Dua J, Gupta A
Cureus
. 2024 Sep;
16(8):e65993.
PMID: 39221334
Sir Ronald Ross, a British medical doctor and researcher, is renowned for his pioneering work in malaria research. His discovery of the malaria parasite's lifecycle within mosquitoes revolutionized the understanding...
9.
Chalipat S, Talewad S, Gupta A, Bahal M, Mane S
Cureus
. 2024 Aug;
16(7):e63828.
PMID: 39099920
A class of genetically based congenital myopathies known as nemaline myopathies is defined by the development of nemaline rods within muscle fibers. We present a case involving an eight-year-old boy...
10.
Garlapati S, Venigalla N, Mane S, Dharmagadda A, Sravanthi K, Gupta A
Cureus
. 2024 Aug;
16(7):e63674.
PMID: 39092406
Background Trace elements like zinc and copper are indispensable for human growth and development, exerting significant influence on a multitude of physiological processes. Acting as pivotal components for transcription factors...