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Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|
May 20, 2017
A novel method for measuring subcutaneous adipose tissue using ultrasound in children - interobserver consistency
Adela ChiriŢă-Emandi, Maria Camelia Papa, Liliana Abrudan, et al.
Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|
February 9, 2017
-759C÷T polymorphism of the HTR2C gene is not correlated with atypical antipsychotics-induced weight gain, among Romanian psychotic patients
Raluca Claudia Grădinaru, Nicoleta Ioana Andreescu, Laura Alexandra Nussbaum, et al.
Molecules (Basel, Switzerland)
|
January 24, 2019
Development and Validation of a LC⁻MS/MS-Based Assay for Quantification of Free and Total Omega 3 and 6 Fatty Acids from Human Plasma
Vlad Serafim, Diana-Andreea Tiugan, Nicoleta Andreescu, et al.
Frontiers in Pediatrics
|
July 25, 2019
A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation-Case Report With Literature Review
Adela Chirita Emandi, Andreea Iulia Dobrescu, Gabriela Doros, et al.
Recent Patents on Nanotechnology
|
August 10, 2016
Nanocarriers as Tools in Delivering Active Compounds for Immune System Related Pathologies
Codruta Soica, Dorina Coricovac, Cristina Dehelean, et al.
International Journal of Nanomedicine
|
June 14, 2019
Synthesis and preliminary characterization of polyurethane nanoparticles with ginger extract as a possible cardiovascular protector
Florin Borcan, Adela Chirita-Emandi, Nicoleta Ioana Andreescu, et al.
International Journal of Molecular Sciences
|
January 10, 2026
The <i>CTDP1</i> Founder Variant in CCFDN: Insights into Pathogenesis, Phenotypic Spectrum and Therapeutic Approaches
Iulia Maria Sabau, Alexandra Chera, Victor Gabriel Ungureanu, et al.
Journal of Medical Genetics
|
August 27, 2020
Biallelic variants in <i>BRCA1</i> gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
Adela Chirita-Emandi, Nicoleta Andreescu, Cristina Popa, et al.
Gene
|
September 4, 2015
Comparative molecular approaches in Prader-Willi syndrome diagnosis
Anca Botezatu, Maria Puiu, Natalia Cucu, et al.
Frontiers in Genetics
|
April 25, 2022
Case Report: Novel Biallelic Variants in <i>DNAJC21</i> Causing an Inherited Bone Marrow Failure Spectrum Phenotype: An Odyssey to Diagnosis
Adela Chirita-Emandi, Carmen-Angela-Maria Petrescu, Cristian G Zimbru, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 87) with videos related to
Sort By:
Page
of 9
Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|
May 20, 2017
A novel method for measuring subcutaneous adipose tissue using ultrasound in children - interobserver consistency
Adela ChiriŢă-Emandi, Maria Camelia Papa, Liliana Abrudan, et al.
Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|
February 9, 2017
-759C÷T polymorphism of the HTR2C gene is not correlated with atypical antipsychotics-induced weight gain, among Romanian psychotic patients
Raluca Claudia Grădinaru, Nicoleta Ioana Andreescu, Laura Alexandra Nussbaum, et al.
Molecules (Basel, Switzerland)
|
January 24, 2019
Development and Validation of a LC⁻MS/MS-Based Assay for Quantification of Free and Total Omega 3 and 6 Fatty Acids from Human Plasma
Vlad Serafim, Diana-Andreea Tiugan, Nicoleta Andreescu, et al.
Frontiers in Pediatrics
|
July 25, 2019
A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation-Case Report With Literature Review
Adela Chirita Emandi, Andreea Iulia Dobrescu, Gabriela Doros, et al.
Recent Patents on Nanotechnology
|
August 10, 2016
Nanocarriers as Tools in Delivering Active Compounds for Immune System Related Pathologies
Codruta Soica, Dorina Coricovac, Cristina Dehelean, et al.
International Journal of Nanomedicine
|
June 14, 2019
Synthesis and preliminary characterization of polyurethane nanoparticles with ginger extract as a possible cardiovascular protector
Florin Borcan, Adela Chirita-Emandi, Nicoleta Ioana Andreescu, et al.
International Journal of Molecular Sciences
|
January 10, 2026
The <i>CTDP1</i> Founder Variant in CCFDN: Insights into Pathogenesis, Phenotypic Spectrum and Therapeutic Approaches
Iulia Maria Sabau, Alexandra Chera, Victor Gabriel Ungureanu, et al.
Journal of Medical Genetics
|
August 27, 2020
Biallelic variants in <i>BRCA1</i> gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
Adela Chirita-Emandi, Nicoleta Andreescu, Cristina Popa, et al.
Gene
|
September 4, 2015
Comparative molecular approaches in Prader-Willi syndrome diagnosis
Anca Botezatu, Maria Puiu, Natalia Cucu, et al.
Frontiers in Genetics
|
April 25, 2022
Case Report: Novel Biallelic Variants in <i>DNAJC21</i> Causing an Inherited Bone Marrow Failure Spectrum Phenotype: An Odyssey to Diagnosis
Adela Chirita-Emandi, Carmen-Angela-Maria Petrescu, Cristian G Zimbru, et al.
Page
of 9