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SUMPh)
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IRMS - Nicolae Testemitanu SUMPh
Browsing by Author Barbova, Natalia
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Showing results 11 to 25 of 25
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Issue Date
Title
Author(s)
2016
Malabsorbția glucidelor la copil: protocol clinic naţional PCN-223
Mihu, Ion
;
Barbova, Natalia
2016
Malabsorbția lipidelor la copil: protocol clinic naţional PCN-224
Mihu, Ion
;
Barbova, Natalia
2016
Malabsorbția proteinelor la copil: protocol clinic naţional PCN-222
Mihu, Ion
;
Barbova, Natalia
2023
Malformațiile congenitale cerebrale la copiii cu accident vascular cerebral în Republica Moldova
Tihai, Olga
;
Sprîncean, Mariana
;
Racoviță, Stela
;
Barbova, Natalia
;
Revenco, Ninel
;
Hadjiu, Svetlana
2013
Oportunităţi şi perspective de diagnostic citogenetic prenatal al sindromului Down în Republica Moldova
Barbova, Natalia
;
Strătilă, Mihail
;
Sprincean, Mariana
;
Egorov, Vladimir
;
Halabudenco, Elena
;
Secrieru, Viorica
2013
Particularităţile polimorfismului clinic şi citogenetic în sindromul Turner
Sprincean, Mariana
;
Barbova, Natalia
;
Halabudenco, Elena
;
Mişina, Ana
;
Samoilenco, Tatiana
2012
Particularităţile polimorfismului clinic şi citogenetic în sindromul Turner
Sprincean, Mariana
;
Barbova, Natalia
;
Halabudenco, Elena
;
Mişina, Ana
;
Samoilenco, Tatiana
2021
Postnatal diagnosis of congenital brain malformation in children
Tihai, Olga
;
Hadjiu, Svetlana
;
Barbova, Natalia
;
Egorov, Vladimir
;
Revenco, Ninel
2021
Rare diseases in monitoring of congenital anomalies
Egorov, Vladimir
;
Barbova, Natalia
2020
Role of medico-genetic counseling and prenatal screening in diagnosis of renal urinary pathology in fetus
Sprincean, Mariana
;
Hadjiu, Svetlana
;
Halabudenco, Elena
;
Fuior, Liliana
;
Racovitsa, Stela
;
Egorov, V.
;
Barbova, Natalia
;
Neamtsu, B.M.L.
;
Neamtsu, M.L.
;
Calcii, Cornelia
;
Revenco, Ninel
2016
Rolul consultului medico-genetic în profilaxia bolilor genetice prin diagnostic citogenetic prenatal
Sprincean, Mariana
;
Barbova, Natalia
;
Uşurelu, Natalia
;
Halabudenco, Elena
;
Eţco, Ludmila
;
Secrieru, Viorica
;
Nour, Veronica
;
Sacara, Victoria
;
Stratila, M.
2014
Sindromul Klinefelter – particularităţile polimorfismului clinic şi citogenetic
Sprincean, Mariana
;
Halabudenco, Elena
;
Barbova, Natalia
;
Mişina, Ana
;
Samoilenco, Tatiana
2016
Sindromul Noonan la copil: protocol clinic naţional PCN-170
Mihu, Ion
;
Groppa, Stanislav
;
Barbova, Natalia
2013
SINDROMUL SYLVER-RUSSELL SUB ASPECT DE MALABSORBŢIE INTESTINALĂ
Mihu, Ion
;
Tighineanu, Olga
;
Barbova, Natalia
;
Clichici, Diana
2016
Sindromul Turner la copil: protocol clinic naţional PCN-171
Mihu, Ion
;
Groppa, Stanislav
;
Barbova, Natalia
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