Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Maimoona, Siddiqui"'
Autor:
Abdul Malik, Muhammad Athar Khan, Maimoona Siddiqui, Bushra Ammad Taimuri, Syed Tariq Ali Adnan, Kamal Ahmed, Aisha Athar, Nishat Waqas
Publikováno v:
Khyber Medical University Journal, Vol 16, Iss 3, Pp 225-30 (2024)
OBJECTIVE: To evaluate acute stroke care services in Sindh province of Pakistan. METHODS: This cross-sectional descriptive study, conducted from January to May 2024, assessed stroke care services in hospitals across Sindh, Pakistan. The study inclu
Externí odkaz:
https://doaj.org/article/0471eb3a8b51407daa6c23152efd9c39
Autor:
Memoona Rasheed, Valeed Khan, Ricardo Harripaul, Maimoona Siddiqui, Madiha Amin Malik, Zahid Ullah, Muhammad Zahid, John B. Vincent, Muhammad Ansar
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-12 (2021)
Abstract Background Intellectual disability (ID) is a phenotypically and genetically heterogeneous disorder. Methods In this study, genome wide SNP microarray and whole exome sequencing are used for the variant identification in eight Pakistani famil
Externí odkaz:
https://doaj.org/article/895309951fb34a2eb4c3272e7450a373
Autor:
Neha Siddiqui, Rahy Farooq, Shoab Saadat, Maimoona Siddiqui, Zain Ahmad Javed, Arooj Fatimah Shah, Salman Mansoor
Publikováno v:
Journal of the Pakistan Medical Association (2020)
Abstract Objectives: To assess the burden of sleep disorders in the elderly, and the effects of various co-morbidities linked with sleep disorders. Method: The longitudinal cross-sectional study was conducted in different outpatient departments
Externí odkaz:
https://doaj.org/article/036b564eb73c48ad9bb21897b3645ffb
Autor:
null Sadaf Majid, null Waseem Tariq Malik, null Asfandyar Khan Niazi, null Ehsan Ul Haq, null Hina Yusuf, null Raja Farhat Shoaib, null Maimoona Siddiqui
Publikováno v:
Pakistan Journal of Neurological Sciences. 17
Background and objective: Cerebral venous sinus thrombosis (CVST) is a rare cause of stroke and may lead to the development of raised intracranial pressure due to edema, infarct or bleed. These patients may require decompressive hemicraniectomy to re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ec6b1df32a77451924f1ed9389e42ef
https://doi.org/10.56310/pjns.v17i04.164
https://doi.org/10.56310/pjns.v17i04.164
Autor:
Arooj Fatimah Shah, Rahy Farooq, Zain Ahmad Javed, Neha Siddiqui, Salman Mansoor, Shoab Saadat, Maimoona Siddiqui
Publikováno v:
Journal of the Pakistan Medical Association. :1-14
Objectives: To assess the burden of sleep disorders in the elderly, and the effects of various co-morbidities linked with sleep disorders. Method: The longitudinal cross-sectional study was conducted in different outpatient departments at a tertiary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d75b529d0920fc82c00ce57bf330a2a0
https://doi.org/10.47391/jpma.296
https://doi.org/10.47391/jpma.296
Autor:
Asfandyar Khan Niazi, Somair Ul Haq Lodhi, Sadaf Majid, Omair Ul Haq Lodhi, Maimoona Siddiqui
Publikováno v:
Proc (Bayl Univ Med Cent)
In stroke patients, a high neutrophil-to-lymphocyte ratio (NLR) has been associated with poor functional outcome at 3 months, higher mortality, and a higher hemorrhagic transformation. We assessed the role of NLR in patients with acute ischemic strok
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cf35b1d5aa787741da399ca485de9d0
https://pubmed.ncbi.nlm.nih.gov/34732981
https://pubmed.ncbi.nlm.nih.gov/34732981
Autor:
Muhammad Ikram Ullah, Tahir N. Khan, Maimoona Siddiqui, Gaurav V. Harlalka, Erica E. Davis, Talia Akram, Zaineb Akram, Chunyu Liu, Muhammad Jameel, Arsalan Ahmad, Kamal Khan, Sarmad Mehmood, Barry A. Chioza, Muhammad Jawad Hassan, Humayoon Shafique Satti, Raees Khan, Emma A. Baple, Andrew H. Crosby, Shahid Mahmood Baig, Belqees Yawar Faiz, Feng Zhang
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 188(2)
Autosomal recessive limb-girdle muscular dystrophy-1 (LGMDR1) is an autosomal recessive disorder characterized by progressive weakness of the proximal limb and girdle muscles. Biallelic mutations in CAPN3 are reported frequently to cause LGMDR1. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8396234000a7691c505bb9260affcc45
https://pubmed.ncbi.nlm.nih.gov/34697879
https://pubmed.ncbi.nlm.nih.gov/34697879
Autor:
Maimoona Siddiqui, Muhammad Jawad Noon, Nadia Mehboob, Rabel Khalid, Salman Mansoor, Hamza Hassan Khan
Publikováno v:
Annals of Global Health, Vol 82, Iss 5, Pp 768-769 (2016)
Externí odkaz:
https://doaj.org/article/3cd055b617bb4909ae2d1e02c9b4d2d6
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 33(2)
Stroke is a worldwide disease with high morbidity. Various scales are used to measure the severity and outcome of stroke. National Institute of Health Stroke Scale (NIHSS) is a quantifiable scale used to assess stroke severity. However, it is biased
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cfcbd88429469739e4111a584ae0b025
https://pubmed.ncbi.nlm.nih.gov/34137544
https://pubmed.ncbi.nlm.nih.gov/34137544
Autor:
Muhammad Zahid, John B. Vincent, Ricardo Harripaul, Maimoona Siddiqui, Valeed Khan, Zahid Ullah, Madiha Amin Malik, Memoona Rasheed, Muhammad Ansar
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-12 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-12 (2021)
Background Intellectual disability (ID) is a phenotypically and genetically heterogeneous disorder. Methods In this study, genome wide SNP microarray and whole exome sequencing are used for the variant identification in eight Pakistani families with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66fa0ae4ba8acf57169d823cae6e90f4
https://pubmed.ncbi.nlm.nih.gov/34452636
https://pubmed.ncbi.nlm.nih.gov/34452636