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Codruta Diana Petchesi
Codruta Diana Petchesi
Faculty of Medicine and Pharmacy of Oradea/Bihor County Clinical Emergency Hospital/ CRGM
在 uoradea.ro 的电子邮件经过验证
标题
引用次数
引用次数
年份
Anatomic variants in Dandy-Walker complex
MC Jurcă, K Kozma, CŢD Petcheşi, M Bembea, OL Pop, G MuŢiu, ...
Rom J Morphol Embryol 58 (3), 1051-1055, 2017
292017
Clinical features and outcome of infective endocarditis in a university hospital in Romania
EE Babeș, DA Lucuța, CD Petcheși, AA Zaha, C Ilyes, AD Jurca, ...
Medicina 57 (2), 158, 2021
222021
Morphological and genetic abnormalities in a Jacobsen syndrome
AD Jurcă, K Kozma, M Ioana, I Streaţă, CD Petcheşi, M Bembea, ...
Rom J Morphol Embryol 58 (4), 1531-1534, 2017
162017
Double autosomal trisomy with mosaicism 47, XY (+ 8)/47, XY (+ 21). Morphological and genetic changes of a rare case
MC Jurcă, M Bembea, OA Iuhas, K Kozma, CD Petcheşi, AD Jurcă, ...
Rom J Morphol Embryol 59 (3), 985-988, 2018
112018
Empty sella associated with growth hormone deficiency and polydactyly
MC Jurcă, M Bembea, K Kozma, MI Şandor, RA Negrean, L Dobjanschi, ...
Rom J Morphol Embryol 59 (1), 381-384, 2018
102018
Cardiofaciocutaneous syndrome–a longitudinal study of a case over 33 years: case report and review of the literature
MC Jurcă, OA Iuhas, M Puiu, A Chiriţă-Emandi, NI Andreescu, ...
Romanian Journal of Morphology and Embryology 62 (2), 563, 2021
92021
Tuberous sclerosis, type II diabetes mellitus and the PI3K/AKT/mTOR signaling pathways—case report and literature review
CM Jurca, K Kozma, CD Petchesi, DC Zaha, I Magyar, M Munteanu, ...
Genes 14 (2), 433, 2023
72023
Relationship between pre-existing conditions in covid-19 patients and inflammation
L Fritea, M Sipponen, A Antonescu, FG Miere, R Chirla, C Vesa, S Cavalu, ...
Pharmacophore 13 (4-2022), 41-48, 2022
42022
CURRENT DATA ABOUT THE AETIOLOGY AND TREATMENT OF INFECTIVE ENDOCARDITIS.
DC Zaha, MC Jurca, C Daina, VV BABEȘ, CD PETCHESI, AD Jurca, ...
Farmacia 70 (5), 2022
22022
Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
K Kozma, M Bembea, CM Jurca, M Ioana, I Streață, SŞ Şoşoi, A Pirvu, ...
Genes 12 (11), 1674, 2021
22021
Effects of Burosumab Treatment on Two Siblings with X-Linked Hypophosphatemia. Case Report and Literature Review
CM Jurca, O Iuhas, K Kozma, CD Petchesi, DC Zaha, M Bembea, S Jurca, ...
Genes 13 (8), 1392, 2022
12022
Genetics of congenital solid tumors
MC Jurcă, ME Ivaşcu, AA Jurcă, K Kozma, I Magyar, MI Şandor, AD Jurcă, ...
Romanian Journal of Morphology and Embryology 61 (4), 1039, 2020
12020
Long-term Outcome in Patients with Turner Syndrome–Retrospective Study
CD Petchesi, AR Iuhas, R Hodisan, DC Zaha, AD Jurca
Archives of Pharmacy Practice¦ Volume 15 (3), 55, 2024
2024
When Bad Luck Strikes Twice: Beckwith Wiedemann Syndrome Associated with Familial Long QT Syndrome Type I
CD Petchesi, K Kozma, AR Iuhas, R Hodisan, AD Jurca
Archives of Pharmacy Practice¦ Volume 15 (3), 2024
2024
Wolfram Syndrome Type I Case Report and Review—Focus on Early Diagnosis and Genetic Variants
AD Jurca, LB Galea-Holhos, AA Jurca, D Atasie, CD Petchesi, E Severin, ...
Medicina 60 (7), 1064, 2024
2024
Genetic Diversity Based on Human Y Chromosome Analysis: A Bibliometric Review Between 2014 and 2023
R Hodișan, DC Zaha, CM Jurca, CD Petchesi, M Bembea
Cureus 16 (4), 2024
2024
The Importance of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants in NF1 Gene and CRX Gene. Case Report and Short Literature Review
A Jurca, CD Petchesi, MC Jurca, D Atasie, D Bembea, AD Jurca
Preprints, 2024
2024
The Surprises of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants
A Jurca, CD Petchesi, MC Jurca, D Bembea, AD Jurca, D Atasie
Pharmacophore 15 (2-2024), 70-78, 2024
2024
Clinical-Epidemiological Study of a Cohort of 35 Patients with Craniosynostosis
CV Somolan, CD Petchesi, C Jurca, M Bembea
Maedica 17 (4), 893, 2022
2022
Bioethical aspects in type I neurofibromatosis.
CD Petchesi, G Ciavoi, C Jurca, R Vulturar, M Bembea
Romanian Journal of Pediatrics/Revista Romana de Pediatrie 70 (3), 2021
2021
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