Sumana Chatterjee
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Explore the profile of Sumana Chatterjee including associated specialties, affiliations and a list of published articles.
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21
Citations
113
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Recent Articles
1.
Chatterjee S, Gupta J, Srinivas S, Rao S
Indian J Ophthalmol
. 2024 Dec;
73(1):10-18.
PMID: 39723850
Demodexblepharitis (DB) has become one of the common differential diagnoses in patients presenting with red eyes in daily clinics. In this review article, we have incorporated a detailed discussion about...
2.
Ganguly P, Bhunia J, Das K, Ghosh A, Chatterjee S, Chatterjee D, et al.
Indian J Ophthalmol
. 2023 Apr;
71(4):1561-1565.
PMID: 37026302
Purpose: In cases of eyelid malignancies requiring full thickness excisional biopsy followed by reconstruction of the created defect, the Meibomian glands are lost. Post-operative varying degrees of dry eye disease...
3.
Iyer G, Srinivasan B, Agarwal S, Chatterjee S, Swarup R, Srinivas P
Indian J Ophthalmol
. 2023 Apr;
71(4):1407-1412.
PMID: 37026273
Dry Eye Module (DEM), a software application, was developed to facilitate the streamlining of dry eye evaluation and documentation, to unify diagnostic jargon, and to analyze data input to generate...
4.
Cottrell E, Maharaj A, Williams J, Chatterjee S, Cirillo G, Del Giudice E, et al.
J Clin Endocrinol Metab
. 2021 Aug;
PMID: 34453441
Context: Severe forms of growth hormone insensitivity (GHI) are characterized by extreme short stature, dysmorphism, and metabolic anomalies. Objective: This work aims to identify the genetic cause of growth failure...
5.
Cottrell E, Maharaj A, Williams J, Chatterjee S, Cirillo G, Del Giudice E, et al.
J Clin Endocrinol Metab
. 2021 Jul;
PMID: 34318893
Context: Severe forms of Growth Hormone Insensitivity (GHI) are characterized by extreme short stature, dysmorphism and metabolic anomalies. Objective: Identification of the genetic cause of growth failure in 3 'classical'...
6.
Andrews A, Maharaj A, Cottrell E, Chatterjee S, Shah P, Denvir L, et al.
J Clin Endocrinol Metab
. 2021 Jun;
106(11):e4716-e4733.
PMID: 34136918
Context: Growth hormone insensitivity (GHI) in children is characterized by short stature, functional insulin-like growth factor (IGF)-I deficiency, and normal or elevated serum growth hormone (GH) concentrations. The clinical and...
7.
Cottrell E, Cabrera C, Ishida M, Chatterjee S, Greening J, Wright N, et al.
Eur J Endocrinol
. 2020 Oct;
183(6):581-595.
PMID: 33055295
Objective: Copy number variation (CNV) has been associated with idiopathic short stature, small for gestational age and Silver-Russell syndrome (SRS). It has not been extensively investigated in growth hormone insensitivity...
8.
Chatterjee S, Iyer G, Srinivasan B, Agarwal S, Kuila J
Indian J Ophthalmol
. 2020 Mar;
68(4):642-644.
PMID: 32174590
No abstract available.
9.
GHR gene transcript heterogeneity may explain phenotypic variability in GHR pseudoexon (6Ψ) patients
Chatterjee S, Cottrell E, Rose S, Mushtaq T, Maharaj A, Williams J, et al.
Endocr Connect
. 2020 Feb;
PMID: 32061156
Objectives: The homozygous GH receptor (GHR) pseudoexon (6Ψ) mutation leads to growth hormone insensitivity (GHI) with clinical and biochemical heterogeneity. We investigated whether transcript heterogeneity (6Ψ-GHR to WT-GHR transcript ratio)...
10.
Biswas P, Chatterjee S, Batra S, Ginodia A, Biswas P
Indian J Ophthalmol
. 2019 Sep;
67(10):1742-1744.
PMID: 31546549
An 84-year-old gentleman underwent uneventful femtolaser-assisted cataract surgery (FLACS) with an arcuate keratotomy (AK) in the left eye. On the 18 post-operative day, a corneal infiltrate developed involving the AK....