[HTML][HTML] Disseminated systemic Nocardia farcinica infection complicating alefacept and infliximab therapy in a patient with severe psoriasis

JA Al-Tawfiq, AA Al-Khatti - International Journal of Infectious Diseases, 2010 - Elsevier
Nocardiosis is a cause of significant morbidity and mortality in the immunocompromised host,
and is an infrequent complication of tumor necrosis factor alpha (TNF-α) blockers in …

Additive effect of sirolimus and hydroxycarbamide on fetal haemoglobin level in kidney transplant patients with sickle cell disease.

AA AlKhatti, AM Alkhunaizi - British Journal of Haematology, 2019 - search.ebscohost.com
The presents a case study of two patients who have sickle cell disease (SCD) and who
were treated with sirolimus as part of their post-kidney transplantation immunosuppressive …

[PDF][PDF] Are we underestimating the leukemogenic risk of hydroxyurea

AH Al-Jam a, IA Al-Dabbous, AA Al-Khatti… - Saudi medical journal, 2002 - Citeseer
Case Report. The patient was a 25-year-old Saudi Arabian woman suffering from SCD with
frequent vaso-occlusive crises. She had more than 6 episodes per year requiring hospital …

Listeria monocytogenes brain abscess in a patient with multiple myeloma

AA Al-Khatti, JA Al-Tawfiq - The Journal of Infection in Developing Countries, 2010 - jidc.org
Listeria monocytogenes is an uncommon cause of illness in the general population.
Meningoencephalitis is the most common central nervous system (CNS) manifestation of listeriosis. …

Stimulation of fetal hemoglobin synthesis by erythropoietin in baboons

A Al-Khatti, RW Veith… - … England Journal of …, 1987 - Mass Medical Soc
Stimulating the production of fetal hemoglobin may benefit patients with sickle cell anemia
by inhibiting sickling. We gave pulsed treatments with high doses of recombinant human …

End-stage renal disease in patients with sickle cell disease

AM Alkhunaizi, AA Al-Khatti, SH Al-Mueilo… - Saudi Journal of …, 2017 - journals.lww.com
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 (…

Fetal hemoglobin in acute and chronic states of erythroid expansion

CA Blau, P Constantoulakis, A Al-Khatti, E Spadaccino… - 1993 - ashpublications.org
Physiologic principles underlying the differences in fetal hemoglobin (HbF) induction between
acute and chronic states of erythroid expansion are poorly understood. Whereas abrupt …

Induction of fetal hemoglobin by cell-cycle-specific drugs and recombinant erythropoietin

…, R Veith, A Al-Khatti… - Journal of Pediatric …, 1990 - journals.lww.com
During the last several years, studies in humans and experimental animals have identified
several compounds that induce fetal hemoglobin in the adult. These include: cell-cycle-…

[HTML][HTML] Prevalence of microalbuminuria in adult patients with sickle cell disease in Eastern Saudi Arabia

AM Alkhunaizi, AA Al-Khatti… - International Journal of …, 2018 - hindawi.com
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 …

Proteinuria in patients with sickle cell disease

AM Alkhunaizi, AA Al-Khatti - Saudi Journal of Kidney Diseases …, 2014 - journals.lww.com
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 …