Manish Rathi

Dr. Manish Rathi

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Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2016 in Kidney International
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Journal Article
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MRManish Rathi
Manish Rathi
AGAjay Goyal
Ajay Goyal
AJAjay Jaryal
Ajay Jaryal
ASAman Sharma
Aman Sharma
PGPramod K. Gupta
Pramod K. Gupta
KGKrishan L. Gupta
Krishan L. Gupta

7 March 2008 in Nephrology Dialysis Transplantation
Verified
Journal Article
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LNL. Senthil Nayagam
L. Senthil Nayagam
AGA. Ganguli
A. Ganguli
MRManish Rathi
Manish Rathi
HKH. S. Kohli
H. S. Kohli
KGK. L. Gupta
K. L. Gupta
VJVivekanand Jha
Vivekanand Jha
Background. International guidelines have not reached a complete agreement about the optimal amount of dietary proteins in chronic kidney disease(CKD). The aim of this study was to compare, with a randomized-controlled design, the metabolic effects of two diets with different protein content (0.55 vs 0.80 g/kg/day) in patients with CKD stages 4–5.

1 July 2008 in Seminars in Nephrology
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Journal Article
Closed access
VJVivekanand Jha
Vivekanand Jha
MRManish Rathi
Manish Rathi

1 January 2012 in Indian Journal of Endocrinology and Metabolism
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Journal Article
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MRManish Rathi
Manish Rathi
RRRaja Ramachandran
Raja Ramachandran
Sexual and gonadal dysfunction/infertility are quite common in patients with chronic kidney disease. Forty percent of male and 55% of female dialysis patients do not achieve orgasm. The pathophysiology of gonadal dysfunction is multifactorial. It is usually a combination of psychological, physiological, and other comorbid factors. Erectile dysfunction in males is mainly due to arterial factors, venous leakage, psychological factors, neurogenic factors, endocrine factors, and drugs. Sexual dysfunction in females is mainly due to hormonal factors and manifests mainly as menstrual irregularities, amenorrhea, lack of vaginal lubrication, and failure to conceive. Treatment of gonadal dysfunction in chronic kidney disease is multipronged and an exact understanding of underlying pathology is essential in proper management of these patients.

5 February 2022 in Rheumatology International
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Journal Article
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APArun Prabhahar
Arun Prabhahar
GNG. S. R. S. N. K. Naidu
G. S. R. S. N. K. Naidu
PCPrabhat Chauhan
Prabhat Chauhan
ASAravind Sekar
Aravind Sekar
ASAman Sharma
Aman Sharma
RRRaja Ramachandran
Raja Ramachandran

19 August 2005 in Nephron Physiology
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Journal Article
Closed access
SBSukanta Barai
Sukanta Barai
GBG.P. Bandopadhayaya
G.P. Bandopadhayaya
CPC.D. Patel
C.D. Patel
MRManish Rathi
Manish Rathi
RKR. Kumar
R. Kumar
KGK.D. Gupta
K.D. Gupta
Background: Until now, a normal reference range for glomerular filtration rate (GFR) in adult Indian potential kidney donors has not been determined and values from a western population are being used as reference. Aim: To determine the reference range of GFR in healthy adult Indian potential kidney donors. Basic Procedures: GFR was measured in 610 (250 male, 360 female, average age 35.16 years) healthy potential kidney donors using the 99mTc-DTPA (diethylenetriamine pentaacetic acid) two-plasma sample method of Russell. Results: The mean body surface area (BSA)-normalized GFR value of a young healthy Indian adult potential kidney donor was calculated as 81.4 ± 19.4 ml/min/1.73 m2 BSA – for males it was 82.3 ± 21.3 ml/min/1.73 m2 BSA and for females 80.8 ± 18.1 ml/min/1.73 m2 BSA. There was no significant difference between derived mean GFR values in males and females with a p value of 0.37. Conclusions: The normal GFR value for the healthy Indian adult potential kidney donor appears to be much lower than the accepted value for a western population. The mean GFR value of a young healthy Indian adult potential kidney donor is 81.4 ± 19.4 ml/min/1.73 m2 BSA, which is significantly different from the normal value of 109–125 ml/min derived from a western population. These findings might be useful in deciding on a suitable kidney donor in an Indian context.