SPEDM

Serviços e Unidades de
Endocrinologia em Portugal
+

Este website tem o apoio da

ANO 2015 - 2º Trimestre

Duarte JV, Pereira JM, Quendera B, Raimundo M, Moreno C, Gomes L, Carrilho F, Castelo-Branco M. J
Early disrupted neurovascular coupling and changed event level hemodynamic response function in type 2 diabetes: an fMRI study.
Cereb Blood Flow Metab. 2015. Oct;35(10):1671-80. doi: 10.1038/jcbfm.2015.106. Epub 2015 Jun 10.

Sepúlveda E, Poínhos R, Constante M, Pais-Ribeiro J, Freitas P, Carvalho D.
Health-related quality of life in type 1 and type 2 diabetic patients in a Portuguese central public hospital.

Diabetes Metab Syndr Obes. 2015 Apr 29;8:219-26. doi: 10.2147/DMSO.S80472. eCollection 2015.

Marques da Silva P, Carvalho D, Nazaré J, Martins L, Aguiar C, Manso MC, Carqueja T, Polónia J.
Prevalence of microalbuminuria in hypertensive patients with or without type 2 diabetes in a Portuguese primary care setting: The RACE (micRoAlbumin sCreening survEy) study.
Rev Port Cardiol. 2015 Apr;34(4):237-46. doi: 10.1016/j.repc.2014.08.017. Epub 2015 Apr 7. English, Portuguese.

Guelho D, Grossman AB.
Emerging drugs for Cushing's disease.
Expert OpinEmerg Drugs. 2015 Sep;20(3):463-78. doi: 10.1517/14728214.2015.1047762. Epub 2015 Jun 2. PubMed PMID: 26021183.

Dusatkova P, Pfäffle R, Brown MR, Akulevich N, Arnhold IJ, Kalina MA, Kot K, Krzisnik C, Lemos MC, Malikova J, Navardauskaite R, Obermannova B, Pribilincova Z, Sallai A, Stipancic G, Verkauskiene R, Cinek O, Blum WF, Parks JS, Austerlitz F, Lebl J.
Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.
Eur J Hum Genet. 2015 Jun 10. doi: 10.1038/ejhg.2015.126. [Epub ahead of print]

Pereira MT, Lira D, Bacelar C, Oliveira JC, Carvalho AC.
Seasonal variation of haemoglobin A1c in a Portuguese adult population. Arch Endocrinol Metab. 2015 Jun;59(3):231-5. doi: 10.1590/2359-3997000000043.

Dusatkova P, Pfäffle R, Brown MR, Akulevich N, Arnhold IJ, Kalina MA, Kot K, Krzisnik C, Lemos MC, Malikova J, Navardauskaite R, Obermannova B, Pribilincova Z, Sallai A, Stipancic G, Verkauskiene R, Cinek O, Blum WF, Parks JS, Austerlitz F, Lebl J.
Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.
Eur J Hum Genet. 2016 Mar;24(3):415-20. doi: 10.1038/ejhg.2015.126. Epub 2015 Jun 10.
PMID: 26059845 [PubMed - in process]