Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Rajesh Bendre"'
Publikováno v:
BioMed, Vol 4, Iss 3, Pp 268-276 (2024)
Neonatal deaths, which usually occur in the first week after delivery, account for nearly 75 percent of all deaths of children under 5 years of age. Prematurity, birth difficulties, infections, and birth defects are responsible for about 40 percent o
Externí odkaz:
https://doaj.org/article/bce76ddf30ac4bbab1491f5b190aa9e5
Autor:
Sandeep Warghade, Jyothi Britto, Reshma Haryan, Tejaswi Dalvi, Rajesh Bendre, Pratiksha Chheda, Sunmeet Matkar, Yogita Salunkhe, Milind Chanekar, Nilesh Shah
Publikováno v:
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
CONTEXT: Hemoglobinopathies constitute the world's most common genetically inherited red blood cell disorder. Screening and accurate identification of hemoglobin (Hb) variants have become increasingly important in antenatal diagnosis and prevention o
Externí odkaz:
https://doaj.org/article/ae7f33f43a934fe9aed25c811dd49911
Autor:
Milind Chanekar, Anurita Pais, Pratiksha Chheda, Rajesh Bendre, Yogita Salunkhe, Nilesh Shah, Tavisha Dama, Shailesh Pande
Publikováno v:
Molecular Diagnosis & Therapy. 22:353-359
Huntington’s disease (HD) is an autosomal-dominant neurodegenerative disorder with an average age at onset of 40 years. It is a polyglutamine (polyQ) disorder that is caused by an increase in the number of CAG repeats in the huntingtin (HTT) gene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::500b96825a2001078620555b5886518e
https://doi.org/10.1007/s40291-018-0327-y
https://doi.org/10.1007/s40291-018-0327-y
Autor:
Jyothi Britto, Nilesh Shah, Yogita Salunkhe, Tejaswi Dalvi, Milind Chanekar, Reshma Haryan, Pratiksha Chheda, Rajesh Bendre, Sandeep Warghade, Sunmeet Matkar
Publikováno v:
Journal of Laboratory Physicians
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
CONTEXT: Hemoglobinopathies constitute the world's most common genetically inherited red blood cell disorder. Screening and accurate identification of hemoglobin (Hb) variants have become increasingly important in antenatal diagnosis and prevention o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d66231a43cdeee2f579cba00c3f8116
https://doi.org/10.4103/jlp.jlp_57_17
https://doi.org/10.4103/jlp.jlp_57_17
Publikováno v:
International Journal of Advanced Research. 4:1986-1994
Natural menopause is defined by the World Health Organization (WHO) as the “permanent cessation of menstruation resulting from the loss of ovarian follicular activity,”1. The word is derived from the Greek men (month) and pausis (cessation). This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b0aafe6f9777891984aa68925239ee5
https://doi.org/10.21474/ijar01/697
https://doi.org/10.21474/ijar01/697
Publikováno v:
International Journal of Reproduction, Contraception, Obstetrics and Gynecology. :833-836
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7b758ebbeb2df77b478756aa957de70
https://doi.org/10.18203/2320-1770.ijrcog20150102
https://doi.org/10.18203/2320-1770.ijrcog20150102
Autor:
Tavisha Dama, Pratiksha Chheda, Sandeep Warghade, Rajesh Bendre, Jyothi Mathias, Sunmeet Matkar, Nilesh Shah
Publikováno v:
Journal of clinical laboratory analysis. 32(5)
Background: Determination of HLA-B27 status plays an important role as adjuvant in suspected cases for diagnosis of Ankylosing Spondilytis (AS). Objectives of this study were to evaluate (i) flow cytometry method in comparison with DNA microarray for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefe0fe76e96ba5072909c0aa29a1edb
https://pubmed.ncbi.nlm.nih.gov/29349813
https://pubmed.ncbi.nlm.nih.gov/29349813
Publikováno v:
International Journal of Clinical Case Reports.
Acardiac malformation, also known as twin reversed arterial perfusion (TRAP) sequence, is a unique complication of monochorionic twinning., occurring with a reported incidence of 1 in 35 000 deliveries. It is characterized by lack of heart developmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fc2ea7c25bf3d004a64b2f41b6f03cc
https://doi.org/10.5376/ijccr.2016.06.0006
https://doi.org/10.5376/ijccr.2016.06.0006
Publikováno v:
International Journal of Reproduction, Contraception, Obstetrics and Gynecology. :485-487
Swyer syndrome was first described by Jim Swyer in 1955. It is a form of “Pure Gonadal Dysgenesis”. The affected female has 46XY karyotype. A 17 year old unmarried girl came with complaints of primary amenorrhea, non development of breast. On exa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9230e2b0aaa89bc3b6792ffe4bacf23a
https://doi.org/10.5455/2320-1770.ijrcog20130955
https://doi.org/10.5455/2320-1770.ijrcog20130955
Publikováno v:
International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 6:2491
Background: To study indications of second stage caesarean section. To study intraoperative and postoperative complications. To review maternal and perinatal outcome.Methods: This retrospective study was conducted at a tertiary teaching Institute. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2ee8d5c9b476777b975fd9b5cd7dd9e
https://doi.org/10.18203/2320-1770.ijrcog20172337
https://doi.org/10.18203/2320-1770.ijrcog20172337