Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Al-Khatti A"'
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 4, Pp 751-757 (2017)
Sickle cell nephropathy is a severe complication of sickle cell disease (SCD) that has a wide range of manifestations, from asymptomatic microalbuminuria to end-stage renal disease (ESRD). The data on patients with SCD who develop ESRD are scarce. Th
Externí odkaz:
https://doaj.org/article/680589292dc64e9fa151947a016e4851
Autor:
Nasir Khalid Amra, Salwa Shaberdeen Sheikh, Basel A Abushullaih, Nafeesa A Al-Faris, Adil A Al-Khatti, Huda H Al-Sayed
Publikováno v:
Journal of Applied Hematology, Vol 7, Iss 1, Pp 17-23 (2016)
Background and Objectives: Minimal residual disease (MRD) assays for monitoring acute lymphoblastic leukemia (ALL) during treatment are defined as assays with a limit of detection of at least 0.01% leukemic blasts per mononuclear cells or total nucle
Externí odkaz:
https://doaj.org/article/1cf976696a5f49f9a98ba380d046a979
Publikováno v:
International Journal of Nephrology, Vol 2018 (2018)
Background. Proteinuria is a common feature of sickle cell nephropathy (SCN) that can progress to renal insufficiency and end stage renal disease. Microalbuminuria (MA) is the earliest manifestation of SCN and precedes the development of overt protei
Externí odkaz:
https://doaj.org/article/8958bb4bc4564ea197d554f6d103a0da
Autor:
Ahmed M Alkhunaizi, Adil A Al-Khatti
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 25, Iss 5, Pp 1038-1041 (2014)
Proteinuria is a complication of sickle cell nephropathy that can progress to renal insufficiency and end-stage renal disease. The magnitude of proteinuria among patients with sickle cell disease (SCD) has been reported with variable prevalence. The
Externí odkaz:
https://doaj.org/article/91960dcc5695417398e1f25887f070dd
Autor:
Adil A Al-Khatti, Jaffar A. Al-Tawfiq
Publikováno v:
Infection. 47:869-874
There were reports of the occurrence of TB during therapy for leukemia with possible complications. In patients with acute leukemia, therapy might be delayed or complicated by the presence of tuberculosis. We present a patient who was diagnosed with
Publikováno v:
International Journal of Nephrology. 02/27/2018, p1-6. 6p.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1988 Dec 01. 85(23), 9278-9282.
Externí odkaz:
https://www.jstor.org/stable/32932
Publikováno v:
Clinical Nephrology. 89:300-304
Dense deposit disease (DDD) is a very rare pathological finding associated with activation of the final complement pathway. DDD has been rarely found in association with multiple myeloma (MM). Here we report a patient with MM presenting with renal fa
Autor:
Adil A Al-Khatti, Ahmed M. Alkhunaizi
Publikováno v:
British Journal of Haematology. 185:959-961
Autor:
Jaffar A, Al-Tawfiq, Adil, Al-Khatti
Publikováno v:
Infection. 47(5)
There were reports of the occurrence of TB during therapy for leukemia with possible complications. In patients with acute leukemia, therapy might be delayed or complicated by the presence of tuberculosis.We present a patient who was diagnosed with a