Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Debasish Patro"'
Autor:
Radhakrishna Telagareddy, Padala Ravi Kumar, Sudhi Ranjan Pattanaik, Deepak Kumar Dash, Debasish Patro, Bijay K Sahoo, Mahija Sahu
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 1, Pp 91-97 (2024)
Introduction: Studies investigating the alterations of serum irisin and its change with metformin therapy in patients with polycystic ovary syndrome (PCOS) are conflicting. Our aim is to study serum irisin in PCOS patients and the change of irisin le
Externí odkaz:
https://doaj.org/article/c1861097741e42a4aed524779c4b9083
Autor:
Bijay K. Sahoo, Padala Ravi Kumar, Sudhi Ranjan Pattanaik, Deepak Kumar Dash, Debasish Patro, Radhakrishna Telagareddy
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 2, Pp 153-159 (2023)
Introduction: This study aimed to distinguish isolated hypogonadotropic hypogonadism (IHH) from constitutional delay in growth and puberty (CDGP) by various hormonal tests in both sexes. Methods: Boys with testicular volume (TV)
Externí odkaz:
https://doaj.org/article/3a29b21a12f743f9bacc8e432bd0c97d
Autor:
Swayamsidha Mangaraj, MBBS, MD, DM, Debasish Patro, MBBS, MD, Arun Kumar Choudhury, MBBS, MD, DM, Anoj Kumar Baliarsinha, MBBS, MD, DM
Publikováno v:
AACE Clinical Case Reports, Vol 5, Iss 5, Pp e302-e306 (2019)
ABSTRACT: Objective: Acromegaly is a classic endocrine disorder caused by a growth hormone (GH)–secreting pituitary adenoma in an overwhelming majority of patients. The diagnosis may be delayed by several years due to the slow growing and insidious
Externí odkaz:
https://doaj.org/article/4532580b43444e41a58d27cf2e1bff6c
Autor:
Purna Chandra Dash, Debasish Patro
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 7, Pp MC19-MC22 (2014)
Background: Aetiological diagnosis for meningitis remains a challenge and often a thorough Cerebrospinal fluid (CSF) examination may not give a precise diagnosis as at times CSF findings may simulate meningitis like picture as in carcinomatous me
Externí odkaz:
https://doaj.org/article/9b8898ceebef43c7b9b9a2a0889864d6
Autor:
M. Aruna, Padala Ravi Kumar, Deepak Kumar Dash, Debasish Patro, T. Radhakrishna, Manas Ranjan Kundu, Sudhi Ranjan Pattanaik
Publikováno v:
International Journal of Diabetes in Developing Countries.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dbe5782c63ce637ffdb3aa02081bc7a
https://doi.org/10.1007/s13410-023-01199-z
https://doi.org/10.1007/s13410-023-01199-z
Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 4, Iss 91, Pp 5461-5464 (2017)
BACKGROUND Amenorrhea refers to the absence of menstrual periods and may result from a number of different conditions. The normal menstrual cycle involves complex interactions between the hypothalamic pituitary axis, the ovaries and the outflow tract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be822f0729fb38fcc1be7e19f0406a6e
https://doi.org/10.18410/jebmh/2017/1091
https://doi.org/10.18410/jebmh/2017/1091
Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 4, Iss 87, Pp 5090-5094 (2017)
BACKGROUND Disorders of Sex Development (DSD), formerly described as intersex conditions, are a conglomerate of rare disorders defined as discrepancy of chromosomal, gonadal or anatomic sex. There are limited data on the incidence of DSD with an over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c6c91520ff71923d05c4cf30045a61b
Publikováno v:
AACE Clinical Case Reports, Vol 5, Iss 5, Pp e302-e306 (2019)
Objective: Acromegaly is a classic endocrine disorder caused by a growth hormone (GH)–secreting pituitary adenoma in an overwhelming majority of patients. The diagnosis may be delayed by several years due to the slow growing and insidious nature of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3ff5bf2e2ab4ecbee603bbf753a47c9
http://www.sciencedirect.com/science/article/pii/S2376060520300821
http://www.sciencedirect.com/science/article/pii/S2376060520300821
Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 4, Iss 83, Pp 4921-4923 (2017)
Turner syndrome occurs in one out of every 2500-3000 live female births and the diagnosis is usually based on the clinical presentation. It is a genetic condition in which a female does not have the usual pair of two X chromosomes. Deletions of propo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50940f25554d6013702d52877a754d14
https://doi.org/10.18410/jebmh/2017/981
https://doi.org/10.18410/jebmh/2017/981
Autor:
Debasish Patro, Mamata Singh, Swayamsidha Mangaraj, Arun Kumar Choudhury, Anoj Kumar Baliarsinha
Publikováno v:
Clinical Cases in Mineral and Bone Metabolism. 14:258
Spondylocarpotarsal synostosis is a very rare skeletal disorder characterized by vertebral malsegmentation defects. Apart from severe vertebral defects, the disease is associated with carpal and tarsal synostosis which is quite characteristic for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74055396cd89e60f49056fbd0f588ccc
https://doi.org/10.11138/ccmbm/2017.14.2.258
https://doi.org/10.11138/ccmbm/2017.14.2.258