Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Usha Rajaram"'
Autor:
Usha Rajaram, Khalid Al Sabti, Mumtaz Shukkur, Mohammad Al Harbi, Niran Al-Naqeeb, Niranjan Kumar, Vivek B Wani, Rima Sawaan, Seemant Raizada, Jamal Al Kandari
Publikováno v:
Clinical Ophthalmology (Auckland, N.Z.)
Clinical Ophthalmology, Vol 2013, Iss default, Pp 271-278 (2013)
Clinical Ophthalmology, Vol 2013, Iss default, Pp 271-278 (2013)
Vivek B Wani,1,2 Khalid Al Sabti,1,3 Niranjan Kumar,1 Seemant Raizada,1 Jamal Al Kandari,1 Mohammad Al Harbi,4 Rima Sawaan,5 Usha Rajaram,6 Niran Al-Naqeeb,7 Mumtaz Shukkur81Department of Ophthalmology, Al Bahar Ophthalmology Center, Kuwait city, Kuw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa0985911dd973337f499207f3c786df
http://europepmc.org/articles/PMC3569374
http://europepmc.org/articles/PMC3569374
Publikováno v:
Medical Principles and Practice. 10:145-150
Background: Neonatal septicemia (NNS) occurs frequently in neonatal intensive care units (NICU) and is often associated with high morbidity and mortality. However, information on its incidence and causative agents in Kuwait hospitals is scanty. Objec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4eb9bbbb799d33eab268f2c705c475a6
https://doi.org/10.1159/000050359
https://doi.org/10.1159/000050359
Autor:
Pia Höglund, Christer Holmberg, Juha Kere, W. Scheurlen, Hugo R. de Jonge, Markus J. Sormaala, Siru Haila, Maarten Sinaasappel, Jerzy Socha, Usha Rajaram, Hideto Yoshikawa
Publikováno v:
Human Mutation, 18, 233-242. Wiley-Liss Inc.
Congenital chloride diarrhea (CLD) is an autosomal recessive disorder characterized by defective intestinal electrolyte absorption, resulting in voluminous osmotic diarrhea with high chloride content. A variety of mutations in the solute carrier fami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c612dd62e7305ca70bbb2656083e5be1
https://pure.eur.nl/en/publications/4594c63f-e4dd-4565-90e4-3cc68ac67330
https://pure.eur.nl/en/publications/4594c63f-e4dd-4565-90e4-3cc68ac67330
Autor:
Magda H. El-Badramany, Temtamy Sa, Talaat I. Farag, Usha Rajaram, Makia J. Marafie, Sadika A. Al-Awadi
Publikováno v:
American Journal of Medical Genetics. 66:261-264
We report on the first known Bedouin family with Greig cephalopolysyndactyly syndrome (MIM 175700). The index patient and his father shared pre- and postaxial polysyndactyly, mild mental retardation, and corpus callosum dysgenesis. Their phenotypic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::883313c702c96309bc0e8daba211f56e
https://doi.org/10.1002/(sici)1096-8628(19961218)66:3<261::aid-ajmg4>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19961218)66:3<261::aid-ajmg4>3.0.co
Autor:
Usha Rajaram
Publikováno v:
Indian Journal of Medical Ethics.
In this essay I speak about the need to put the patient first when discussing the relationship between the patient and the doctor. From my own experience of having been a cancer patient, I argue that most patients appreciate and feel empowered by kno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305329c7226562743b484dcfb0d8eb10
https://doi.org/10.20529/ijme.2012.051
https://doi.org/10.20529/ijme.2012.051
Autor:
Mari Auranen, Hisham Nazer, Jerzy Socha, Juha Kere, Kataryna Popinska, Pia Höglund, Abdullah Al Sanie, Usha Rajaram, Christer Holmberg, Albert de la Chapelle, Mohammed Al-Ghanim
Publikováno v:
The American Journal of Human Genetics. (3):760-768
SummaryCongenital chloride diarrhea (CLD) is an inherited intestinal disorder caused by mutations in the down-regulated in adenoma gene. In Finland, the disease is prevalent because of a founder effect, and all but one of the CLD-associated chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d0cffddb405c3924ecea5acd9a905e