Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mohannad Abu Omar"'
Publikováno v:
Hospital Practice. 46:144-151
Acute chest syndrome (ACS) is a leading complication of sickle cell disease (SCD) with significant morbidity and mortality. ACS is the most common cause of death and the second most common cause of hospitalization in patients with SCD. Delineating th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8452d3a1ba919d2776e1d1f374b460a9
https://doi.org/10.1080/21548331.2018.1464363
https://doi.org/10.1080/21548331.2018.1464363
Autor:
Abdulraheem Qasem, Mohannad Abu Omar, Sood Kisra, Ahmad Alhariri, Aref A. Bin Abdulhak, Hassan Salameh
Publikováno v:
American Journal of Therapeutics. 23:e1110-e1115
Hemolytic uremic syndrome is the triad of nonimmune microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure. When not associated with enteric infection, it is classified as atypical hemolytic uremic syndrome (aHUS) and carries a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ec268b1ff6a77d55bec60ba28ba11eb
https://doi.org/10.1097/mjt.0000000000000133
https://doi.org/10.1097/mjt.0000000000000133
Publikováno v:
Cureus
Multiple myeloma (MM) is a common hematological malignancy that represents 1% of all cancers. MM is distinguished from other plasma cell disorders by prominent bone marrow involvement and systemic organ damage. Extramedullary plasmacytomas of the gal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc137fc7850d43c8126419219431cbc2
https://doi.org/10.7759/cureus.2688
https://doi.org/10.7759/cureus.2688
Autor:
Mohannad Abu Omar, John Foxworth
Publikováno v:
Hospital Medicine Clinics. 3:e128-e138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eacb2d4c60cf87e685112e8dfa468dd
https://doi.org/10.1016/j.ehmc.2013.09.001
https://doi.org/10.1016/j.ehmc.2013.09.001
Publikováno v:
BMJ case reports. 2016
Congenital pulmonary airway malformation (CPAM) is a rare congenital abnormality with unknown exact aetiology or clear genetic association. It is characterised by a failure of bronchial development and localised glandular overgrowth. Typically, it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fd4316d38785ac4652fd59d820007e4
https://pubmed.ncbi.nlm.nih.gov/27671988
https://pubmed.ncbi.nlm.nih.gov/27671988
Publikováno v:
American Journal of Gastroenterology. 111:S1096-S1097
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9dee0fc036abab68a18bbe9cf40c754
https://doi.org/10.14309/00000434-201610001-02271
https://doi.org/10.14309/00000434-201610001-02271
Publikováno v:
BMJ Case Reports. :bcr-2017
A 78-year-old man was referred from his primary care clinic to the emergency department due to bluish discolouration of his lips and decreased oxygen saturation on pulse oximetry. The patient was asymptomatic. Physical exam was normal except for lip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0399cc45768ea434a90cde7d5465d2f
https://doi.org/10.1136/bcr-2017-220521
https://doi.org/10.1136/bcr-2017-220521
Publikováno v:
BMJ Case Reports. :bcr2016216634
Immunocompromised patients have high risk of infections from bacteria, viruses, fungi and parasites. One of these infections is those caused by Strongyloides stercoralis Immunocompromised patients are at risk of hyperinfection syndrome which is chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d156f9413f9a348afd370e8009a21285
https://doi.org/10.1136/bcr-2016-216634
https://doi.org/10.1136/bcr-2016-216634
Publikováno v:
BMJ Case Reports. :bcr2016216771
Hamartomas are the most common benign tumours of the lung with an overall incidence of 0.025–0.32%. They are known to be amalgamation of various tissue types, originating from the embryonic mesoderm. Lung hamartomas typically involve lung parenchym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc662b0e25db3f9814e35890ed0037a8
https://doi.org/10.1136/bcr-2016-216771
https://doi.org/10.1136/bcr-2016-216771