Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Tahir Masood, Ahmad"'
Autor:
Ghazanfar Ali, Sikander Ali Khan, Muhammad Tariq, Habib ur Rehman, Tahir Masood Ahmad, Shehzad Ahmed Abbasi
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 74, Iss 2 (2024)
Objective: To investigate the relationship between the severity of hand injury with anxiety and depression. Study design: Cross-sectional study Place and Duration of Study: Departments of Psychiatry and Plastic Surgery, Combined Military Hospital
Externí odkaz:
https://doaj.org/article/98fd8da7814e4068b6cf93866badd22d
Autor:
Tahir Masood Ahmad
Publikováno v:
Journal of the College of Physicians and Surgeons Pakistan. 29:401-402
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03950d16fd47658ccb749b4ea3a9a3c7
https://doi.org/10.29271/jcpsp.2019.05.401
https://doi.org/10.29271/jcpsp.2019.05.401
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 26(2)
Fibrodysplasia Ossificans Progressiva (FOP) is a rare autosomal dominant disorder characterized by postnatal progressive heterotopic ossification of connective tissue and congenital malformation of big toes. We report a 3-year male toddler with clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbcdc9e5984da5e97aff8c1d25736957
https://pubmed.ncbi.nlm.nih.gov/26876407
https://pubmed.ncbi.nlm.nih.gov/26876407
Autor:
Samia, Naz, Asma, Mushtaq, Saira, Rehman, Attia, Bari, Amnah, Maqsud, Muhammad Zeeshan, Khan, Tahir Masood, Ahmad
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 23(6)
To determine the spectrum of clinical presentation, laboratory parameters and drug therapy in patients with Juvenile Rheumatoid Arthritis (JRA).Case series.The Children's Hospital and The Institute of Child Health, Lahore, from October 2008 to Octobe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c25c12a501fd95c85fe38131ee20a801
https://pubmed.ncbi.nlm.nih.gov/23763801
https://pubmed.ncbi.nlm.nih.gov/23763801
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 22(4)
The majority of individuals with joint hypermobility remain asymptomatic. However, those associated with Benign Joint Hypermobility Syndrome (BJHS), develop a number of systemic manifestations. Our objective was to determine the relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66b975cce79ca07bf0c24bb47f91282f
https://pubmed.ncbi.nlm.nih.gov/22455285
https://pubmed.ncbi.nlm.nih.gov/22455285
Autor:
Muhammad Haroon, Hamid, Muhammad Akbar, Malik, Jawad, Masood, Ahmed, Zia, Tahir Masood, Ahmad
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 22(3)
To determine the frequency of Ventilator-Associated Pneumonia (VAP) and to identify the associated factors, causative organisms and outcome of VAP in children admitted to ICU.Cross-sectional, observational study.Medical ICU (MICU) of the Children's H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a167032f27b6ad5ffd03f6c843226409
https://pubmed.ncbi.nlm.nih.gov/22414355
https://pubmed.ncbi.nlm.nih.gov/22414355
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 60(8)
To compare the performance of paediatric medicine residents following a regular 6 hour and an extended 24 hour call and their own insight into their performance following each duty.The study was conducted at The Children's Hospital, Lahore, from Sept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70ef1fa4750b308bd81355e6022d4049
https://pubmed.ncbi.nlm.nih.gov/20726195
https://pubmed.ncbi.nlm.nih.gov/20726195
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 21(10)
Poland-Mobius syndrome is a combination of two rare congenital syndromes characterized by congenital facial weakness, loss of abduction of eyes, limb defects, and absence or hypoplasia of the pectoral muscles. A patient with features of both the Mobi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e233c72bc2ae95dcd2902e8f18d8521f
https://pubmed.ncbi.nlm.nih.gov/22015131
https://pubmed.ncbi.nlm.nih.gov/22015131
Autor:
Rabia, Abbas, Sahar, Waqar, Tahir Masood, Ahmad, Khawaja Ahmad, Irfan Waheed, Tipu, Sultan, Ahmad Usaid, Qureshi
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 21(7)
Roberts syndrome is a genetically determined rare birth defect causing, skeletal deformities, particularly symmetrical limb reduction and craniofacial anomalies. For any child with limb and craniofacial bony malformations, this syndrome should be con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0a68f269bee931c379fbdc10139631b
https://pubmed.ncbi.nlm.nih.gov/21777535
https://pubmed.ncbi.nlm.nih.gov/21777535
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 20(9)
Johanson Blizzard syndrome (JBS) is a rare multi-system disorder characterized by congenital aplasia or hypoplasia of alae nasi, exocrine pancreatic insufficiency, hypothyroidism, deafness, growth retardation, varying degree of mental retardation, al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::344d10ba9157adee472e03a0f4c6c536
https://pubmed.ncbi.nlm.nih.gov/20810061
https://pubmed.ncbi.nlm.nih.gov/20810061