361) patterns are likely to be recognized when disease surveillance methods are designed |
362) Most infectious disease surveillance methods are not well |
363) Treatment of this disease usually involves the correction of |
364) t diabetes mellitus (IDDM) is a metabolic disease usually resulting from autoimmune- |
365) iabetic patients with peripheral vascular disease were divided into two groups accor |
366) ernationally agreed criteria for Behcet's disease were the International Study Group |
367) ned in 180 patients with sickle cell (SS) disease (126 sickle homozygous and 54 sick |
368) tooth extraction, followed by periodontal disease (22.1%). |
369) literacy for preventing acute infectious disease (66.8%), literacy for preventing n |
370) uated for the presence of coronary artery disease; (7) use targeted treatment for HF |
371) nra, in patients with multiorgan Behcet's disease (BD). |
372) The etiology of Crohn's disease (CD), an autoimmune, inflammatory |
373) Camurati-Engelmann disease (CED) or progressive diaphyseal dy |
374) -month-old boy with chronic granulomatous disease (CGD) received umbilical cord bloo |
375) cipients and patients with chronic kidney disease (CKD) not on dialysis. |
376) n, diabetes mellitus, and end-stage renal disease (ESRD). |
377) The International Criteria for Behcet's Disease (ICBD) were created in 2006 to ove |
378) nd lymphadenopathy mimicking IgG4-related disease (IgG4-RD). |
379) ctors related to nonalcoholic fatty liver disease (NAFLD) among occupational populat |
380) ed both Legok 2003 H5N1 and HB1 Newcastle disease (ND) vaccine. |
381) 4-1.1) and having parents with no chronic disease (OR = 0.4, 95% CI = 0.2-0.6) sugge |
382) Peripheral artery disease (PAD) produces significant disabil |
383) body (LB) disorders, including Parkinson disease (PD), Parkinson disease dementia ( |
384) MTF) gender reassignment, pilonidal sinus disease (PSD), pseudofolliculitis barbae ( |
385) Rheumatic fever (RF) and rheumatic heart disease (RHD) are the multisystem autoimmu |
386) Transfusion associated-graft versus host disease (TA-GVHD) is a rare complication o |
387) fueled by the public phobia over mad cow disease (bovine spongiform encephalopathy |
388) dish MI patients with and without coeliac disease (equal to villous atrophy; Marsh h |
389) iated with the development of symptomatic disease (i.e., progression to HF, HF hospi |
390) ersons with chronic obstructive pulmonary disease (n = 52) following a patient educa |
391) in 36 patients with aorto-iliac occlusive disease (one patient required reinterventi |
392) cantly correlated with different stage of disease (p < 0.05). |
393) vised International Criteria for Behcet's Disease (rICBD) in Iran. |
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