Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Hafiz Muhammad Sharjeel Arshad"'
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 5 (2017)
Median arcuate ligament syndrome is a rare disorder that is clinically characterized by the triad of postprandial abdominal pain, weight loss, and often an abdominal bruit due to compression of the celiac artery by the median arcuate ligament. Given
Externí odkaz:
https://doaj.org/article/44f5b5e1f4714c369486c85421b5762e
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 5 (2017)
Calciphylaxis can be a severe life-threatening dermatologic disease that is a known complication associated with end-stage renal disease. However, multiple non-uremic etiologies that are not yet well studied can cause calciphylaxis. We report a rare
Externí odkaz:
https://doaj.org/article/df8cf0c35c5d472da037aec357a1cf8c
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2017 (2017)
Elevated carbohydrate antigen 19-9 (CA19-9) beyond 1000 U/L occurs in nonneoplastic conditions which is causing questioning of the use of CA19-9 as a marker for screening. We report a case where a 51-year-old male with Mirrizi Syndrome (MS) presented
Externí odkaz:
https://doaj.org/article/f3fd778a41a0487b86d5de8818e175a2
Autor:
Eula Plana Tetangco MD, Natasha Shah MD, Hafiz Muhammad Sharjeel Arshad MD, Hareth Raddawi MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 4 (2016)
Liver enzyme levels are commonly obtained in the evaluation of many conditions. Elevated alanine transaminase and aspartate transaminase have traditionally been considered a “hepatocellular” pattern concerning for ischemic, viral, or toxic hepati
Externí odkaz:
https://doaj.org/article/e6a7942b3c7744b9a80aa4b02b11908a
Publikováno v:
Case Reports in Nephrology, Vol 2016 (2016)
Background. The Syndrome of Inappropriate Antidiuretic Hormone (SIADH) is considered to be the most common cause of euvolemic hyponatremia. The most common malignancy associated with SIADH is small cell lung cancer. We present a rare case of a patien
Externí odkaz:
https://doaj.org/article/578125bfad934758abe00faf7c0d93a4
Publikováno v:
Cureus.
Neurofibromatosis-1 (NF-1) is an autosomal dominant condition characterized by cutaneous pigmentation and tumour formation along nerves in the brain, skin, and other organs. Gastrointestinal stromal tumours (GIST) are rare mesenchymal tumours involvi
Autor:
Varsha Chiruvella, Jacqueline T Chan, Hafiz Muhammad Sharjeel Arshad, Ayesha Cheema, John Erikson Yap
Publikováno v:
Cureus
Congenital sucrase isomaltase deficiency (CSID) is an autosomal recessive disorder which leads to chronic intestinal malabsorption of nutrients from ingested starch and sucrose. Symptoms usually present after consumption of fruits, juices, grains, an
Autor:
Hafiz Muhammad Sharjeel Arshad, Alexis Moore, Bonnie Clark, Shreyans Doshi, Subbaramia Sridhar, Ayesha Cheema, Shreyu Umapathy, Haoran Peng
Publikováno v:
American Journal of Gastroenterology. 116:S672-S673
Publikováno v:
American Journal of Gastroenterology. 116:S1131-S1132
Autor:
Pradeep Mittal, Hafiz Muhammad Sharjeel Arshad, Ayesha Cheema, John Erikson Yap, Asad Jehangir
Publikováno v:
American Journal of Gastroenterology. 116:S671-S671