Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ammara Bint I. Bilal"'
Autor:
Fateen Ata, Sandy Kamil Kamal Marzouk, Ammara Bint I. Bilal, Adeel Ahmed Khan, Ezzedin Ibrahim, Mohammed Taha Mahmood Almadani
Publikováno v:
IDCases, Vol 24, Iss , Pp e01103- (2021)
Salmonella Typhi (ST) is a rod-shaped gram-negative bacterium that infects humans via contaminated food or water. Humans are the only reservoirs for the bacteria. Infection usually manifests as fever, abdominal pain, and diarrhea. However, complicati
Externí odkaz:
https://doaj.org/article/6f61544be71e487e807f2cdec74f0754
Autor:
Phool Iqbal, Muhammad Murtaza, Hafiz Waqar Younis, Muhammad Abd Ur Rehman, Ammara Bint I Bilal, Sushil Niraula
Publikováno v:
Clinical Case Reports, Vol 10, Iss 1, Pp n/a-n/a (2022)
Abstract The epiploic appendages (also known as appendices epiploicae) are usually located on the anti‐mesenteric surface of the colon, extending from the caecum to the rectosigmoid, and epiploic appendagitis (EA) is the inflammation of these appen
Externí odkaz:
https://doaj.org/article/08f5fb0e642448d9b3dc14682498c4f9
Autor:
Fateen Ata, Zohaib Yousaf, Bilal N. Al Kalaji, Anas A. Ashour, Mohamad Fael, Gi Eun Kim, Ammara Bint I Bilal, Orwa Elaiwy, Akhnuwkh Jones
Publikováno v:
Qatar medical journal. 2022(4)
Back pain is a rare initial presentation of gastric cancer. Isolated back pain with red flags in middle-aged patients might indicate multiple myeloma. However, it is rarely present in advanced gastric adenocarcinoma; hence, data are limited to case r
Autor:
Fateen Ata, Saad Javed, Bassam Muthanna, Ines dakhlia, Ammara Bint I Bilal, Motwakil Musa, Mashuk Uddin, Mohamed A. Yassin
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 4, Pp 2048-2052 (2021)
Clinical Case Reports, Vol 9, Iss 4, Pp 2048-2052 (2021)
The co‐occurrence of acute hemolysis and methemoglobinemia secondary to favism in G6PD deficient individuals is rare. Identifying it promptly is of high clinical significance as treating methemoglobinemia (with methylene blue) can worsen hemolysis.
Autor:
Fateen Ata, Ammara Bint I Bilal, Omnia Tajelsir Abdalla Osman, Muhammad Awais Arif, Mawahib Elhassan, Tahir hamid, Jassim Al Suwaidi, Hassan Choudry, Galal Abushahba
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 3, Pp 1529-1533 (2021)
Clinical Case Reports, Vol 9, Iss 3, Pp 1529-1533 (2021)
This article highlights the possibility of positive outcomes associated with prolonged CPR and anoxic brain injury contesting the idea that such patients will invariably end up in a persistent vegetative state.
Autor:
Fateen Ata, Wanis H. Ibrahim, Hassan Choudry, Abdullah Shams, Abdullah Arshad, Hafiz Waqas Younas, Ammara Bint I. Bilal, Muhammad Qaiser Ikram, Shuja Tahir, Waqar W. Mogassabi, Nada Mehdi Errayes
Publikováno v:
Thrombosis research. 217
The central location, size, and instability of saddle pulmonary embolism (SPE) have raised significant concerns regarding its clinical, hemodynamic effects as well as optimal management. Pulmonary embolism (PE) guidelines barely address such concerns
Publikováno v:
Clinical Case Reports. 10
BackgroundCervical ribs are a rare and usually asymptomatic occurrence. Most are identified incidentally by Roentgenogram (X-rays). However, occasionally they can cause nerve impingements and compressive symptoms. In cervical ribs, osteomyelitis seco
Autor:
Rohit Sharma, Saad Javed, Ammara Bint I Bilal, Anand Kartha, Hammad Shabir Chaudhry, Hassan Choudry, Rubab Fatima Malik, Fateen Ata
Publikováno v:
Annals of Medicine and Surgery
Introduction Vitamin B12 (VitB12) deficiency rarely manifests with visual symptoms. Optic nerve damage in VitB12 deficiency is thought to be via degeneration. However, optic neuritis, though infrequent, has been reported secondary to VitB12 deficienc
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Whenever considering idiopathic Budd‐Chiari syndrome, consider the possibility of JAK2 mutation even if clinical parameters are within normal range.
Autor:
Fateen Ata, Zohaib Yousaf, Suresh Nalaka Menik Arachchige, Saman Rose, Awni Alshurafa, Bassam Muthanna, Ammara Bint I Bilal, Ahmed El Beltagi, Muhammad Zahid
Publikováno v:
eNeurologicalSci
eNeurologicalSci, Vol 24, Iss, Pp 100359-(2021)
eNeurologicalSci, Vol 24, Iss, Pp 100359-(2021)
Background Tolosa Hunt syndrome (THS) is a rare disease that manifests mainly as painful unilateral ophthalmoplegia. It is caused by an inflammatory process of unknown aetiology within the cavernous sinus with a rare intracranial extension. The Inter