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Showing 1 to 12 of 37 entries
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[Epidemiologic technics in tuberculosis].

Viata medicala; revista de informare profesionala si stiintifica a cadrelor medii sanitare

Dumitrache S, Botezatu M, Pintilie E, Marinescu V, Floroiu C, Curcan V.
PMID: 6784327
Viata Med Rev Inf Prof Stiint Cadrelor Medii Sanit. 1981 Jan;29(1):19-20.

No abstract available.

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Dumitrache S, Botezatu M, Pintilie E, et al. Ancheta epidemiologică în tuberculoză. [Epidemiologic technics in tuberculosis]. Viata Med Rev Inf Prof Stiint Cadrelor Medii Sanit. 1981;29(1):19-20
Dumitrache, S., Botezatu, M., Pintilie, E., Marinescu, V., Floroiu, C., & Curcan, V. (1981). Ancheta epidemiologică în tuberculoză. [Epidemiologic technics in tuberculosis]. Viata medicala; revista de informare profesionala si stiintifica a cadrelor medii sanitare, 29(1), 19-20.
Dumitrache, S, et al. "Ancheta epidemiologică în tuberculoză." [Epidemiologic technics in tuberculosis]. Viata medicala; revista de informare profesionala si stiintifica a cadrelor medii sanitare vol. 29,1 (1981): 19-20.
Dumitrache S, Botezatu M, Pintilie E, Marinescu V, Floroiu C, Curcan V. Ancheta epidemiologică în tuberculoză. [Epidemiologic technics in tuberculosis]. Viata Med Rev Inf Prof Stiint Cadrelor Medii Sanit. 1981 Jan;29(1):19-20. Romanian. PMID: 6784327.
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Vibrational Spectroscopy Fingerprinting in Medicine: from Molecular to Clinical Practice.

Materials (Basel, Switzerland)

Balan V, Mihai CT, Cojocaru FD, Uritu CM, Dodi G, Botezat D, Gardikiotis I.
PMID: 31489927
Materials (Basel). 2019 Sep 06;12(18). doi: 10.3390/ma12182884.

In the last two decades, Fourier Transform Infrared (FTIR) and Raman spectroscopies turn out to be valuable tools, capable of providing fingerprint-type information on the composition and structural conformation of specific molecular species. Vibrational spectroscopy's multiple features, namely highly...

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Balan V, Mihai CT, Cojocaru FD, et al. Vibrational Spectroscopy Fingerprinting in Medicine: from Molecular to Clinical Practice. Materials (Basel). 2019;12(18)doi: 10.3390/ma12182884.
Balan, V., Mihai, C. T., Cojocaru, F. D., Uritu, C. M., Dodi, G., Botezat, D., & Gardikiotis, I. (2019). Vibrational Spectroscopy Fingerprinting in Medicine: from Molecular to Clinical Practice. Materials (Basel, Switzerland), 12(18), . https://doi.org/10.3390/ma12182884
Balan, Vera, et al. "Vibrational Spectroscopy Fingerprinting in Medicine: from Molecular to Clinical Practice." Materials (Basel, Switzerland) vol. 12,18 (2019). doi: https://doi.org/10.3390/ma12182884
Balan V, Mihai CT, Cojocaru FD, Uritu CM, Dodi G, Botezat D, Gardikiotis I. Vibrational Spectroscopy Fingerprinting in Medicine: from Molecular to Clinical Practice. Materials (Basel). 2019 Sep 06;12(18). doi: 10.3390/ma12182884. PMID: 31489927; PMCID: PMC6766044.
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Benefits and Risks of IgG Transplacental Transfer.

Diagnostics (Basel, Switzerland)

Ciobanu AM, Dumitru AE, Gica N, Botezatu R, Peltecu G, Panaitescu AM.
PMID: 32806663
Diagnostics (Basel). 2020 Aug 12;10(8). doi: 10.3390/diagnostics10080583.

Maternal passage of immunoglobulin G (IgG) is an important passive mechanism for protecting the infant while the neonatal immune system is still immature and ineffective. IgG is the only antibody class capable of crossing the histological layers of the...

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Ciobanu AM, Dumitru AE, Gica N, et al. Benefits and Risks of IgG Transplacental Transfer. Diagnostics (Basel). 2020;10(8)doi: 10.3390/diagnostics10080583.
Ciobanu, A. M., Dumitru, A. E., Gica, N., Botezatu, R., Peltecu, G., & Panaitescu, A. M. (2020). Benefits and Risks of IgG Transplacental Transfer. Diagnostics (Basel, Switzerland), 10(8), . https://doi.org/10.3390/diagnostics10080583
Ciobanu, Anca Marina, et al. "Benefits and Risks of IgG Transplacental Transfer." Diagnostics (Basel, Switzerland) vol. 10,8 (2020). doi: https://doi.org/10.3390/diagnostics10080583
Ciobanu AM, Dumitru AE, Gica N, Botezatu R, Peltecu G, Panaitescu AM. Benefits and Risks of IgG Transplacental Transfer. Diagnostics (Basel). 2020 Aug 12;10(8). doi: 10.3390/diagnostics10080583. PMID: 32806663; PMCID: PMC7459488.
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Impaired Lexical Selection and Fluency in Post-Stroke Aphasia.

Aphasiology

Botezatu MR, Mirman D.
PMID: 31598028
Aphasiology. 2019;33(6):667-688. doi: 10.1080/02687038.2018.1508637. Epub 2018 Aug 23.

BACKGROUND: Deficits in fluent language production are a hallmark of aphasia and may arise from impairments at different levels in the language system. It has been proposed that difficulty resolving lexical competition contributes to fluency deficits.AIMS: The present study...

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Botezatu MR, Mirman D. Impaired Lexical Selection and Fluency in Post-Stroke Aphasia. Aphasiology. 2018;33(6):667-688doi: 10.1080/02687038.2018.1508637.
Botezatu, M. R., & Mirman, D. (2019). Impaired Lexical Selection and Fluency in Post-Stroke Aphasia. Aphasiology, 33(6), 667-688. https://doi.org/10.1080/02687038.2018.1508637
Botezatu, Mona Roxana, and Mirman, Daniel. "Impaired Lexical Selection and Fluency in Post-Stroke Aphasia." Aphasiology vol. 33,6 (2019): 667-688. doi: https://doi.org/10.1080/02687038.2018.1508637
Botezatu MR, Mirman D. Impaired Lexical Selection and Fluency in Post-Stroke Aphasia. Aphasiology. 2019;33(6):667-688. doi: 10.1080/02687038.2018.1508637. Epub 2018 Aug 23. PMID: 31598028; PMCID: PMC6785054.
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Treatment Effects upon Prolactin and Soluble Receptor of Interleukin-2 in Psoriatic Patients.

Maedica

Botezatu D, Tovaru M, Georgescu SR, Curici A, Giurcaneanu C.
PMID: 29868137
Maedica (Bucur). 2018 Mar;13(1):25-33.

BACKGROUND: Psoriasis vulgaris is a chronic inflammatory hyper-proliferative disease of the skin, scalp, nails, and joints. It has been hypothesized that prolactin (PRL) may modulate the skin immune system and be involved in the pathogenesis of psoriasis. Psoriasis exerts...

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Botezatu D, Tovaru M, Georgescu SR, et al. Treatment Effects upon Prolactin and Soluble Receptor of Interleukin-2 in Psoriatic Patients. Maedica (Bucur). 2018;13(1):25-33
Botezatu, D., Tovaru, M., Georgescu, S. R., Curici, A., & Giurcaneanu, C. (2018). Treatment Effects upon Prolactin and Soluble Receptor of Interleukin-2 in Psoriatic Patients. Maedica, 13(1), 25-33.
Botezatu, Delia, et al. "Treatment Effects upon Prolactin and Soluble Receptor of Interleukin-2 in Psoriatic Patients." Maedica vol. 13,1 (2018): 25-33.
Botezatu D, Tovaru M, Georgescu SR, Curici A, Giurcaneanu C. Treatment Effects upon Prolactin and Soluble Receptor of Interleukin-2 in Psoriatic Patients. Maedica (Bucur). 2018 Mar;13(1):25-33. PMID: 29868137; PMCID: PMC5972783.
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Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome.

Maedica

Veduta A, Duta S, Ciobanu AM, Botezatu R, Gica N, Peltecu G, Panaitescu AM.
PMID: 34221170
Maedica (Bucur). 2021 Mar;16(1):140-144. doi: 10.26574/maedica.2020.16.1.140.

Binder syndrome and Nager syndrome are part of the spectrum of skeletal dysplasias. Although exceedingly rare, both syndromes are amenable to prenatal diagnosis because they present with features that can be detected by prenatal ultrasound. Genetic prenatal diagnosis is...

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Veduta A, Duta S, Ciobanu AM, et al. Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome. Maedica (Bucur). 2021;16(1):140-144doi: 10.26574/maedica.2020.16.1.140.
Veduta, A., Duta, S., Ciobanu, A. M., Botezatu, R., Gica, N., Peltecu, G., & Panaitescu, A. M. (2021). Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome. Maedica, 16(1), 140-144. https://doi.org/10.26574/maedica.2020.16.1.140
Veduta, Alina, et al. "Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome." Maedica vol. 16,1 (2021): 140-144. doi: https://doi.org/10.26574/maedica.2020.16.1.140
Veduta A, Duta S, Ciobanu AM, Botezatu R, Gica N, Peltecu G, Panaitescu AM. Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome. Maedica (Bucur). 2021 Mar;16(1):140-144. doi: 10.26574/maedica.2020.16.1.140. PMID: 34221170; PMCID: PMC8224714.
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Asthma in Pregnancy. Review of Current Literature and Recommendations.

Maedica

Popa M, Peltecu G, Gica N, Ciobanu AM, Botezatu R, Gica C, Steriade A, Panaitescu AM.
PMID: 34221160
Maedica (Bucur). 2021 Mar;16(1):80-87. doi: 10.26574/maedica.2020.16.1.80.

No abstract available.

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Popa M, Peltecu G, Gica N, et al. Asthma in Pregnancy. Review of Current Literature and Recommendations. Maedica (Bucur). 2021;16(1):80-87doi: 10.26574/maedica.2020.16.1.80.
Popa, M., Peltecu, G., Gica, N., Ciobanu, A. M., Botezatu, R., Gica, C., Steriade, A., & Panaitescu, A. M. (2021). Asthma in Pregnancy. Review of Current Literature and Recommendations. Maedica, 16(1), 80-87. https://doi.org/10.26574/maedica.2020.16.1.80
Popa, Maria, et al. "Asthma in Pregnancy. Review of Current Literature and Recommendations." Maedica vol. 16,1 (2021): 80-87. doi: https://doi.org/10.26574/maedica.2020.16.1.80
Popa M, Peltecu G, Gica N, Ciobanu AM, Botezatu R, Gica C, Steriade A, Panaitescu AM. Asthma in Pregnancy. Review of Current Literature and Recommendations. Maedica (Bucur). 2021 Mar;16(1):80-87. doi: 10.26574/maedica.2020.16.1.80. PMID: 34221160; PMCID: PMC8224723.
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Epigenetic approaches for cervical neoplasia screening (Review).

Experimental and therapeutic medicine

Albulescu A, Plesa A, Fudulu A, Iancu IV, Anton G, Botezatu A.
PMID: 34765022
Exp Ther Med. 2021 Dec;22(6):1481. doi: 10.3892/etm.2021.10916. Epub 2021 Oct 25.

Human papillomavirus (HPV) infection is the leading cause of cervical cancer. The Papanicolaou cytology test is the usually employed type of screening for this infection; however, its sensibility is limited. Only a small percentage of women infected with high-risk...

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Albulescu A, Plesa A, Fudulu A, et al. Epigenetic approaches for cervical neoplasia screening (Review). Exp Ther Med. 2021;22(6):1481doi: 10.3892/etm.2021.10916.
Albulescu, A., Plesa, A., Fudulu, A., Iancu, I. V., Anton, G., & Botezatu, A. (2021). Epigenetic approaches for cervical neoplasia screening (Review). Experimental and therapeutic medicine, 22(6), 1481. https://doi.org/10.3892/etm.2021.10916
Albulescu, Adrian, et al. "Epigenetic approaches for cervical neoplasia screening (Review)." Experimental and therapeutic medicine vol. 22,6 (2021): 1481. doi: https://doi.org/10.3892/etm.2021.10916
Albulescu A, Plesa A, Fudulu A, Iancu IV, Anton G, Botezatu A. Epigenetic approaches for cervical neoplasia screening (Review). Exp Ther Med. 2021 Dec;22(6):1481. doi: 10.3892/etm.2021.10916. Epub 2021 Oct 25. PMID: 34765022; PMCID: PMC8576616.
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Prenatal features of mandibulofacial dysostosis Guion-Almeida Type.

Journal of medicine and life

Dragoi V, Nedelea F, Gica N, Botezatu R, Peltecu G, Panaitescu AM.
PMID: 35027977
J Med Life. 2021 Sep-Oct;14(5):722-725. doi: 10.25122/jml-2020-0082.

Facial dysostoses are clinically and genetically heterogeneous conditions characterized by congenital craniofacial anomalies which result from abnormal development of the first two pharyngeal arches and their derivatives during embryogenesis. Mandibulofacial dysostosis Guion-Almeida type (MFDGA) is a rare and relatively...

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Dragoi V, Nedelea F, Gica N, et al. Prenatal features of mandibulofacial dysostosis Guion-Almeida Type. J Med Life. 2021;14(5):722-725doi: 10.25122/jml-2020-0082.
Dragoi, V., Nedelea, F., Gica, N., Botezatu, R., Peltecu, G., & Panaitescu, A. M. (2021). Prenatal features of mandibulofacial dysostosis Guion-Almeida Type. Journal of medicine and life, 14(5), 722-725. https://doi.org/10.25122/jml-2020-0082
Dragoi, Vlad, et al. "Prenatal features of mandibulofacial dysostosis Guion-Almeida Type." Journal of medicine and life vol. 14,5 (2021): 722-725. doi: https://doi.org/10.25122/jml-2020-0082
Dragoi V, Nedelea F, Gica N, Botezatu R, Peltecu G, Panaitescu AM. Prenatal features of mandibulofacial dysostosis Guion-Almeida Type. J Med Life. 2021 Sep-Oct;14(5):722-725. doi: 10.25122/jml-2020-0082. PMID: 35027977; PMCID: PMC8742900.
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A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation.

Diagnostics (Basel, Switzerland)

Panaitescu AM, Duta S, Gica N, Botezatu R, Nedelea F, Peltecu G, Veduta A.
PMID: 33478103
Diagnostics (Basel). 2021 Jan 19;11(1). doi: 10.3390/diagnostics11010142.

Cornelia de Lange syndrome (CDLS) is caused by pathogenic variants in genes which are structural or regulatory components of the cohesin complex. The classical Cornelia de Lange (CDLS) phenotype is characterized by distinctive facial features, growth retardation, upper limb...

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Panaitescu AM, Duta S, Gica N, et al. A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation. Diagnostics (Basel). 2021;11(1)doi: 10.3390/diagnostics11010142.
Panaitescu, A. M., Duta, S., Gica, N., Botezatu, R., Nedelea, F., Peltecu, G., & Veduta, A. (2021). A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation. Diagnostics (Basel, Switzerland), 11(1), . https://doi.org/10.3390/diagnostics11010142
Panaitescu, Anca Maria, et al. "A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation." Diagnostics (Basel, Switzerland) vol. 11,1 (2021). doi: https://doi.org/10.3390/diagnostics11010142
Panaitescu AM, Duta S, Gica N, Botezatu R, Nedelea F, Peltecu G, Veduta A. A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation. Diagnostics (Basel). 2021 Jan 19;11(1). doi: 10.3390/diagnostics11010142. PMID: 33478103; PMCID: PMC7835910.
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Severe Neonatal Anemia Due to Spontaneous Massive Fetomaternal Hemorrhage at Term: An Illustrative Case with Suspected Antenatal Diagnosis and Brief Review of Current Knowledge.

Medicina (Kaunas, Lithuania)

Gică N, Botezatu R, Demetrian M, Vayna AM, Cimpoca-Raptis BA, Ciobanu AM, Gica C, Peltecu G, Panaitescu AM.
PMID: 34946230
Medicina (Kaunas). 2021 Nov 23;57(12). doi: 10.3390/medicina57121285.

Fetomaternal hemorrhage is defined as transfer of fetal blood into placental circulation and therefore into maternal circulation during pregnancy, and represents an important contributor to intrauterine fetal demise and neonatal death. The condition is rarely diagnosed prenatally because clinical...

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Gică N, Botezatu R, Demetrian M, et al. Severe Neonatal Anemia Due to Spontaneous Massive Fetomaternal Hemorrhage at Term: An Illustrative Case with Suspected Antenatal Diagnosis and Brief Review of Current Knowledge. Medicina (Kaunas). 2021;57(12)doi: 10.3390/medicina57121285.
Gică, N., Botezatu, R., Demetrian, M., Vayna, A. M., Cimpoca-Raptis, B. A., Ciobanu, A. M., Gica, C., Peltecu, G., & Panaitescu, A. M. (2021). Severe Neonatal Anemia Due to Spontaneous Massive Fetomaternal Hemorrhage at Term: An Illustrative Case with Suspected Antenatal Diagnosis and Brief Review of Current Knowledge. Medicina (Kaunas, Lithuania), 57(12), . https://doi.org/10.3390/medicina57121285
Gică, Nicolae, et al. "Severe Neonatal Anemia Due to Spontaneous Massive Fetomaternal Hemorrhage at Term: An Illustrative Case with Suspected Antenatal Diagnosis and Brief Review of Current Knowledge." Medicina (Kaunas, Lithuania) vol. 57,12 (2021). doi: https://doi.org/10.3390/medicina57121285
Gică N, Botezatu R, Demetrian M, Vayna AM, Cimpoca-Raptis BA, Ciobanu AM, Gica C, Peltecu G, Panaitescu AM. Severe Neonatal Anemia Due to Spontaneous Massive Fetomaternal Hemorrhage at Term: An Illustrative Case with Suspected Antenatal Diagnosis and Brief Review of Current Knowledge. Medicina (Kaunas). 2021 Nov 23;57(12). doi: 10.3390/medicina57121285. PMID: 34946230.
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The association between lncRNA H19 and EZH2 expression in patients with EBV-positive laryngeal carcinoma.

Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale

Hotoboc IE, Fudulu A, Grigore R, Bertesteanu S, Huica I, Iancu IV, Botezatu A, Bleotu C, Anton G.
PMID: 34825669
Acta Otorhinolaryngol Ital. 2021 Dec;41(6):537-543. doi: 10.14639/0392-100X-N1527. Epub 2021 Nov 26.

OBJECTIVE: Laryngeal cancer is the second most common malignancy in the head and neck, with Epstein-Barr virus infection as a risk factor. Our aim is to evaluate correlations between the expression of lncRNA H19 and EBV infection in laryngeal...

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Hotoboc IE, Fudulu A, Grigore R, et al. The association between lncRNA H19 and EZH2 expression in patients with EBV-positive laryngeal carcinoma. Acta Otorhinolaryngol Ital. 2021;41(6):537-543doi: 10.14639/0392-100X-N1527.
Hotoboc, I. E., Fudulu, A., Grigore, R., Bertesteanu, S., Huica, I., Iancu, I. V., Botezatu, A., Bleotu, C., & Anton, G. (2021). The association between lncRNA H19 and EZH2 expression in patients with EBV-positive laryngeal carcinoma. Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale, 41(6), 537-543. https://doi.org/10.14639/0392-100X-N1527
Hotoboc, Irina E, et al. "The association between lncRNA H19 and EZH2 expression in patients with EBV-positive laryngeal carcinoma." Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale vol. 41,6 (2021): 537-543. doi: https://doi.org/10.14639/0392-100X-N1527
Hotoboc IE, Fudulu A, Grigore R, Bertesteanu S, Huica I, Iancu IV, Botezatu A, Bleotu C, Anton G. The association between lncRNA H19 and EZH2 expression in patients with EBV-positive laryngeal carcinoma. Acta Otorhinolaryngol Ital. 2021 Dec;41(6):537-543. doi: 10.14639/0392-100X-N1527. Epub 2021 Nov 26. PMID: 34825669.
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Showing 1 to 12 of 37 entries