Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Laurențiu Camil Bohîlțea"'
Autor:
Elena Evelina STOICA, Laurentiu Camil BOHILTEA, Delia-Maria Gradinaru-FOMETESCU, Monica Mihaela CIRSTOIU
Publikováno v:
Modern Medicine, Vol 31, Iss 2, Pp 187-190 (2024)
Non-invasive prenatal testing (NIPT), since its introduction in 2011, has revolutionized prenatal screening, becoming widely used globally and replacing traditional screening methods in developed countries. The accuracy of NIPT in detecting aneuploid
Externí odkaz:
https://doaj.org/article/7b4455f8b9084622a5c6775a0dd23eee
Autor:
Evelina STOICA, Laurentiu Camil BOHILTEA, Adrian DUMITRU, Catalin ALIUS, Monica Mihaela CIRSTOIU
Publikováno v:
Modern Medicine, Vol 30, Iss 4, Pp 247-351 (2023)
Primary vaginal sarcoma is an extremely rare malignant condition within the field of gynecological pathologies. We present the case of a 53-year old patient with no history of gynecological issues or associated comorbidities who presented to our clin
Externí odkaz:
https://doaj.org/article/ebae47823f4f40b5b274ae40b1e23918
Autor:
Viorica Radoi, Andrei Kozma, Vasilica Toma, Horia Lăzărescu, Radu Ursu, Agnes Katherine Lackner, Laurențiu Camil Bohîlțea, Norina Forna
Publikováno v:
Romanian Journal of Oral Rehabilitation, Vol 11, Iss 2, Pp 90-95 (2019)
Progress in genetics and molecular biology has resulted in the emergence of new concepts to explain the etiology and pathogenesis of many human disease processes including oro-dental diseases. Recent advances in molecular aspects of odontogenesis ind
Externí odkaz:
https://doaj.org/article/a105987f9bd84a04a46f9d6944db98ec
Autor:
Relu Cocoş, Beatrice Mahler, Adina Turcu-Stiolica, Alexandru Stoichiță, Andreea Ghinet, Elena-Silvia Shelby, Laurențiu Camil Bohîlțea
Publikováno v:
Viruses, Vol 14, Iss 6, p 1201 (2022)
Our study objective was to construct models using 20 routine laboratory parameters on admission to predict disease severity and mortality risk in a group of 254 hospitalized COVID-19 patients. Considering the influence of confounding factors in this
Externí odkaz:
https://doaj.org/article/e5ea0fdcc19e46dbb7392543beae1bba
Autor:
Ina-Ofelia FOCSA, Andreea TUTULAN-CUNITA, Anca PAVEL, Diana PREPELITA, Diana BRATU, Laurentiu Camil BOHILTEA, Danae STAMBOULI
Publikováno v:
Modern Medicine, Vol 29, Iss 3, Pp 187-192 (2022)
Bloom syndrome is an exceptionally rare autosomal recessive disorder characterized by a considerable genomic instability due to the defective DNA damage repair machine. It is caused by biallelic pathogenic variants in the gene encoding for one of the
Externí odkaz:
https://doaj.org/article/1dd78e45f13e416b9056a3a0a859ffea
Autor:
Viorica-Elena Rădoi, Mihaela Țurcan, Ovidiu Virgil Maioru, Andra Dan, Laurentiu Camil Bohîlțea, Elena Adriana Dumitrescu, Adelina Silvana Gheorghe, Dana Lucia Stănculeanu, Georgia Thodi, Yannis L. Loukas, Ileana-Delia Săbău
Publikováno v:
Diagnostics, Vol 13, Iss 11, p 1896 (2023)
The Homologous Recombination Deficiency (HRD) Score, determined by evaluating genomic instability through the assessment of loss of heterozygosity (LOH), telomeric allelic imbalance (TAI), and large-scale state transitions (LST), serves as a crucial
Externí odkaz:
https://doaj.org/article/0d80e79342bd413eab1fde2a20e8fcf4
Autor:
Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Radu Ursu, Agnes Katalin Lackner, Laurentiu Camil Bohiltea, Horia Lazarescu
Publikováno v:
Romanian Journal of Stomatology, Vol 65, Iss 2, Pp 97-100 (2019)
Defective enamel formation may result either from factors of environmental origin or from genetic abnormality. Such genetically determined enamel malformations have been described in patients with chromosomal anomalies and with inherited single gene
Externí odkaz:
https://doaj.org/article/27904ada8362456e92183ec672e5b106
Autor:
Relu Cocoş, Alina Şendroiu, Sorina Schipor, Laurenţiu Camil Bohîlţea, Ionuţ Şendroiu, Florina Raicu
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e98520 (2014)
Wilson's disease is an autosomal recessive disorder caused by more than 500 mutations in ATP7B gene presenting considerably clinical manifestations heterogeneity even in patients with a particular mutation. Previous findings suggested a potential rol
Externí odkaz:
https://doaj.org/article/00a70c54b0114bafb0591bb0545b4338