Croatian Medical Journal, Vol. 54 No. 6, 2013.

Sadržaj

Puni tekst

Why should medical editors CARE about case reports? (str. 507-509)

Hrvoje Barić, Lidija Andrijašević
Uvodnik

Estimating global and regional morbidity from acute bacterial meningitis in children: assessment of the evidence (str. 510-518)

Ivana Lukšić, Rosanda Mulić, Rachel Falconer, Mirjana Orban, Simrita Sidhu, Igor Rudan
Izvorni znanstveni članak

An estimate of asthma prevalence in Africa: a systematic analysis (str. 519-531)

Davies Adeloye, Kit Yee Chan, Igor Rudan, Harry Campbell
Izvorni znanstveni članak

Estimating the incidence of colorectal cancer in South East Asia (str. 532-540)

Inka Kokki, Angeliki Papana, Harry Campbell, Evropi Theodoratou
Izvorni znanstveni članak

Care-seeking and quality of care for outpatient sick children in rural Hebei, China: a cross-sectional study (str. 541-549)

Yanfeng Zhang, Michelle Helena van Velthoven, Li Chen, Josip Car, Ye Li, Wei Wang, Robert W. Scherpbier
Izvorni znanstveni članak

Genetic and environmental variance of renal parenchymal thickness: a twin study (str. 550-554)

David Laszlo Tarnoki, Adam Domonkos Tarnoki, Levente Littvay, Pal Bata, Viktor Berczi, Zsolt Garami, Kinga Karlinger
Izvorni znanstveni članak

Carotid atherosclerosis and right ventricular diastolic dysfunction in a sample of hypertensive Nigerian patients (str. 555-560)

Adeseye A. Akintunde, Philip B. Adebayo, Ademola A. Aremu, Oladimeji G. Opadijo
Izvorni znanstveni članak

Timing of troponin T measurements in triage of pulmonary embolism patients (str. 561-568)

Nikola Bulj, Ines Potočnjak, Mirella Sharma, Hrvoje Pintarić, Vesna Degoricija
Izvorni znanstveni članak

Post-vaccine glomerulonephritis in an infant with hereditary C2 complement deficiency: case study (str. 569-573)

Tanja Kersnik Levart
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A lethal course of hypertrophic cardiomyopathy in Noonan syndrome due to a novel germline mutation in the KRAS gene: case study (str. 574-578)

Gregor Nosan, Sara Bertok, Samo Vesel, Helger G. Yntema, Darja Paro-Panjan
Izvorni znanstveni članak

Infantile peripheral neuropathy, deafness, and proximal tubulopathy associated with a novel mutation of the RRM2B gene: case study (str. 579-584)

Vesna Stojanović, Johannes A. Mayr, Wolfgang Sperl, Nenad Barišić, Aleksandra Doronjski, Gordana Milak
Izvorni znanstveni članak

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