Zobrazeno 1 - 10
of 105
pro vyhledávání: '"A Jemshad"'
Publikováno v:
Heart Views, Vol 16, Iss 3, Pp 111-113 (2015)
Candida endocarditis is an emerging infectious disease, usually involving patients with intravascular prosthetic devices, and associated with substantial morbidity and mortality. A 28-year-old primigravida at 32 weeks of gestation was admitted with l
Externí odkaz:
https://doaj.org/article/0a6a0fa5f5bb450e8a36a93a32d20deb
Publikováno v:
The Journal of Association of Chest Physicians, Vol 3, Iss 2, Pp 78-78 (2015)
Externí odkaz:
https://doaj.org/article/e0baf576e5b548a49939d9dc9d1369f0
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 29, Iss 2, Pp 470-473 (2018)
Interstitial nephritis and immune complex-mediated glomerulonephritis are the two common renal manifestations of primary Sjögren's syndrome (SS). Here, we discuss three cases of primary SS where presenting manifestation was distal renal tubular acid
Externí odkaz:
https://doaj.org/article/77b719e71a14442cb0f1b25ab8eb71ef
Publikováno v:
Indian Journal of Medical and Paediatric Oncology. 39:254-256
Disseminated malignancy can rarely present with microangiopathic hemolytic anemia and thrombocytopenia clinically similar to thrombotic thrombocytopenic purpura (TTP), but does not respond to plasma exchange. TTP carries a grave prognosis if plasma e
Publikováno v:
Indian Journal of Medical & Paediatric Oncology. Apr-Jun2018, Vol. 39 Issue 2, preceding p254-256. 3p.
Autor:
Alungal, Jemshad1 jemshadalungal@gmail.com, Abdulla, Mansoor C.1, Kunnummal, Noorudheen Kaladi2, Sivadasan, Amrutha1
Publikováno v:
International Journal of Nutrition, Pharmacology, Neurological Diseases. Jul2015, Vol. 5 Issue 3, p113-116. 4p.
Publikováno v:
Heart India, Vol 5, Iss 1, Pp 45-47 (2017)
Arrhythmogenic right ventricular dysplasia (ARVD) is a common cause of sudden cardiac death in young adults. It is a disease that has a wide spectrum of presentation. Early identification of the disorder is of paramount importance considering the fat
Publikováno v:
International Journal of Rheumatic Diseases. Dec2017, Vol. 20 Issue 12, p2168-2170. 3p.
Publikováno v:
International Journal of Rheumatic Diseases. Nov2017, Vol. 20 Issue 11, p1818-1820. 3p.
Publikováno v:
Journal of Genetics. 94:489-492
Woodhouse–Sakati syndrome (WSS, MIM: 241080), a rare autosomal recessive disorder characterized by hypogonadism, alopecia, diabetes mellitus, mental retardation and extrapyramidal manifestations, was first described in a few consanguineous Saudi fa