Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ibaad Ali"'
Autor:
Fizza Akbar, Zahraa Siddiqui, Muhammad Talha Waheed, Lubaina Ehsan, Syed Ibaad Ali, Hajra Wiquar, Azmina Tajuddin Valimohammed, Shaista Khan, Lubna Vohra, Sana Zeeshan, Yasmin Rashid, Munira Moosajee, Adnan Abdul Jabbar, Muhammad Nauman Zahir, Naila Zahid, Rufina Soomro, Najeeb Niamat Ullah, Imran Ahmad, Ghulam Haider, Uzair Ansari, Arjumand Rizvi, Arif Mehboobali, Abida Sattar, Salman Kirmani
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-19 (2022)
Abstract Background Breast cancer is the most common malignancy in women, affecting over 1.5 million women every year, which accounts for the highest number of cancer-related deaths in women globally. Hereditary breast cancer (HBC), an important subs
Externí odkaz:
https://doaj.org/article/18e7b363f9924c718f4c11e3e8f2698f
Publikováno v:
Respiratory Medicine Case Reports, Vol 31, Iss , Pp 101165- (2020)
Introduction: Whilst the use of combustible tobacco products continues to decline in the United States, the use of e-cigarettes has seen an explosive rise in recent years. In 2019 an outbreak on EVALI was seen across the country, highlighting the fac
Externí odkaz:
https://doaj.org/article/b0783e0e8ba34ce8bfebe73c44f8fb95
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 3, Pp 158-161 (2018)
We present a family with 2 members who received long-term steroid treatment for presumed classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, until molecular testing revealed nonclassic CAH, not necessarily requiring treatme
Externí odkaz:
https://doaj.org/article/8f061f5c46b04fe99c908e47a8528edd
Autor:
Saba Ahmed, Ariba Khan, Syed Ibaad Ali, Mohammad Saad, Hafsa Jawaid, Mahnoor Islam, Hanieya Saiyed, Sarosh Fatima, Aiman Khan, Maleeha A. Basham, Syeda Asfia Hussain, Maheen Akhtar, Fatima Kausar, Afshan Hussain, Kaneez Fatima
Publikováno v:
Indian Heart Journal, Vol 70, Iss 2, Pp 241-245 (2018)
Objective: A short pre-hospital delay, from the onset of symptoms to rapid initiation of reperfusion therapy, is a crucial factor in determining prognosis of myocardial infarction (MI). The purpose of this study was to evaluate symptoms and presentat
Externí odkaz:
https://doaj.org/article/fca4aa394ad1421eacdb1a395e2ef297
Publikováno v:
Encyclopedia of Evolutionary Psychological Science ISBN: 9783319169996
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a187c31d0f287e8b0fac36fce82b3be
https://doi.org/10.1007/978-3-319-19650-3_2463
https://doi.org/10.1007/978-3-319-19650-3_2463
Publikováno v:
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports, Vol 31, Iss, Pp 101165-(2020)
Respiratory Medicine Case Reports, Vol 31, Iss, Pp 101165-(2020)
Introduction Whilst the use of combustible tobacco products continues to decline in the United States, the use of e-cigarettes has seen an explosive rise in recent years. In 2019 an outbreak on EVALI was seen across the country, highlighting the fact
Autor:
Maleeha Ali Basham, Kaneez Fatima, Sarosh Fatima, Afshan Hussain, Mahnoor Islam, Hafsa Jawaid, Ariba Khan, Syeda Asfia Hussain, Aiman Khan, Hanieya Saiyed, Mohammad Saad, Saba Ahmed, Syed Ibaad Ali, Fatima Kausar, Maheen Akhtar
Publikováno v:
Indian Heart Journal, Vol 70, Iss 2, Pp 241-245 (2018)
Indian Heart Journal
Indian Heart Journal
Objective: A short pre-hospital delay, from the onset of symptoms to rapid initiation of reperfusion therapy, is a crucial factor in determining prognosis of myocardial infarction (MI). The purpose of this study was to evaluate symptoms and presentat
Autor:
Ibaad Ali, Lubaina Ehsan, Abida K. Sattar, Fizza Akbar, M. Talha Waheed, Zahraa Siddiqui, Azmina T. ValiMohammed, Salman Kirmani, Hajra Wiquar
Publikováno v:
Molecular Genetics and Metabolism. 132:S53-S54
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 68(3)
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism
We present a family with 2 members who received long-term steroid treatment for presumed classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, until molecular testing revealed nonclassic CAH, not necessarily requiring treatme