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Articles from Nr. 3(September)/2014
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A glance on recent progresses in diagnosis and treatment of primary immunodeficiencies |
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Peter J. Späth |
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The importance of genetic testing in adolescent-onset steroid-resistant nephrotic syndrome - Case report |
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Zsuzsanna Gáll, Éva Kiss, Kálmán Tory, Attila Fintha, Carmen Duicu |
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Hypouricemia - the simple key towards diagnosis in a case of purine nucleoside phosphorylase deficiency, a rare and severe disease |
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Alexis-Virgil Cochino, Jean-Louis Pérignon, Mihaela Bătăneanț, Mihai Craiu, Ioan Gherghina, Margit Șerban |
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A case of fatal acute intermittent porphyria: laboratory diagnosis and pathogenesis considerations |
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Rodica Bălaşa, Smaranda Maier, Anca Moţăţăianu, Zoltan Bajko, Otilia Moldovan, Erzsébet Benedek |
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Optimisation of the quantitative analysis of inflammatory cell infiltrates in breast cancer |
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Anca-Raluca Vrânceanu, Cristina Claudia Tărniceriu, Daniela Jitaru, Cristina Terinte, Florin Zugun-Eloae, Eugen Carasevici |
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Genotype-phenotype correlations in patients treated with acenocoumarol |
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Florentina Claudia Militaru, Ștefan Cristian Vesa, Sorin Crișan, Valentin Militaru, Adrian Pavel Trifa, Anca Dana Buzoianu |
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7. |
Parathyroidectomy in the treatment of secondary hyperparathyroidism. Clinical and laboratory outcomes |
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Radu Mircea Neagoe, Daniela Tatiana Sala, Ionela Pașcanu, Septimiu Voidăzan, Radu Moldovanu |
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The neuroendocrine markers assay and the glycemia profile in patients with neuroendocrine tumors under octreotide therapy: a 2 years study |
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Cătălina Poiană, Diana Păun, Mara Carsote |
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Determination of the phosphorylated neurofilament subunit NF-H (pNF-H) in cerebro-spinal fluid as biomarker in acute traumatic spinal cord injuries |
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Didona Ungureanu, Ștefan Mircea Iencean, Cristina Dimitriu, Andrei Ștefan Iencean, Alexandru Tascu |
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10. |
Detection of the genetically modified organisms from food products |
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Manuela Curticăpean, Augustin Curticăpean |
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11. |
Letter to the editor - Report from a rare diseases event in Târgu Mureş, Romania |
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Peter J. Späth |
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