Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Sara Mumtaz"'
Autor:
Sara Mumtaz, Atif Ali, Hajra Muhammad Sharif, Reem M. Aljowaie, Asma N. Alsaleh, Hira Khan, Muhammad Naeem, Arshad Mehmood Abbasi
Publikováno v:
Journal of King Saud University: Science, Vol 35, Iss 10, Pp 102970- (2023)
The aim of this work was to assess the effects of typical and optimal use of sunscreens in photosensitivity under UV exposure during the COVID-19 pandemic. First, a cross-sectional study was conducted among 384 participants to find out about photosen
Externí odkaz:
https://doaj.org/article/3ef293deb1734765b504ed5deacd9bce
Autor:
Hafiz Muhammad Asim Raza, Hira Jabeen, Atiq Ijaz, null Binash Afzal, Sara Mumtaz, null Hafiz Muhammad Bilal Hanif
Publikováno v:
International Health Review. 2:1-9
The disability which occurs frequently in children is known as cerebral palsy (CP). Its prevalence in Pakistan is much higher and about 2 to 3 out of every 1000 children are diagnosed with CP, which affectstheirfunctional status of life to a greater
Autor:
Kanwal Nisar, Sara Mumtaz, Sana Shamim, Miroslav Blumenberg, Sidra Younis, Farah Deeba, Sabba Mehmood, Qamar Javed
Publikováno v:
Saudi Journal of Biological Sciences, Vol 28, Iss 11, Pp 6615-6620 (2021)
Saudi Journal of Biological Sciences
Saudi Journal of Biological Sciences
Background Acne is an inflammatory condition principally affected by genetic and dietary factors. Investigation into functional polymorphisms of TNF-α gene and their association with acne vulgaris will be helpful in exploring genetic influence on sk
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 15:3527-3529
Stroke is sudden loss of neurological function. It is caused by interruption in cerebral blood flow. Objectives: To analyze the difference in the balance and postural stability score pre &post swiss ball training in stroke patients. Study Design: Ran
Publikováno v:
Life and Science. 4:11
Objective: A systematic review was conducted to evaluate recent studies performed on miRNAs as a diagnostic and therapeutic biomarker in breast cancer.Study Design: Online standard databases like PubMed, EMBASE, Web of Science and COCHRANE library we
Autor:
Nadia Gul, Alishba Mustansar, Waqas Latif, Sara Mumtaz, Talha Laique, Maham Saleem, Ahsan Javed
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 15:3063-3065
Low backache is common among urban society. It is one of the main reasons for activity limitation and absenteeism from work Purpose: To compare role of swiss ball-based core stability exercise and conventional physiotherapy among patients of non-spec
Publikováno v:
Breast Cancer: From Bench to Personalized Medicine ISBN: 9789811901966
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c6ba7b71dd8c66201ba0bbdd3d0f916
https://doi.org/10.1007/978-981-19-0197-3_9
https://doi.org/10.1007/978-981-19-0197-3_9
Autor:
Nosheen Akhtar, Uzma Azeem Awan, Rida Fatima Saeed, Asma Saleem Qazi, Sara Mumtaz, Samina Rubnawaz
Publikováno v:
Breast Cancer: From Bench to Personalized Medicine ISBN: 9789811901966
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec005dec8216fbcf31aea2a60fe4cd48
https://doi.org/10.1007/978-981-19-0197-3_14
https://doi.org/10.1007/978-981-19-0197-3_14
Autor:
Danilo Bilches Medinas, Sajid Malik, Esra Yıldız‐Bölükbaşı, Janina Borgonovo, Mirva J Saaranen, Hery Urra, Eduardo Pulgar, Muhammad Afzal, Darwin Contreras, Madison T Wright, Felipe Bodaleo, Gabriel Quiroz, Pablo Rozas, Sara Mumtaz, Rodrigo Díaz, Carlos Rozas, Felipe Cabral‐Miranda, Ricardo Piña, Vicente Valenzuela, Ozgun Uyan, Christopher Reardon, Ute Woehlbier, Robert H Brown, Miguel Sena‐Esteves, Christian Gonzalez‐Billault, Bernardo Morales, Lars Plate, Lloyd W Ruddock, Miguel L Concha, Claudio Hetz, Aslıhan Tolun
Publikováno v:
EMBO J
Recessive gene mutations underlie many developmental disorders and often lead to disabling neurological problems. Here, we report identification of a homozygous c.170G>A (p.Cys57Tyr or C57Y) mutation in the gene coding for protein disulfide isomerase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6613e8538ac476726f6e672a582c42a8
https://europepmc.org/articles/PMC8762563/
https://europepmc.org/articles/PMC8762563/
Publikováno v:
Asian Biomedicine. 13:49-60
Background Pakistan faces high incidence of congenital anomalies (CA) and hereditary anomalies due to various factors, including a high rate of consanguinity, early marriages, and predominance of extended families. There is a paucity of epidemiologic