Works by Petchesi, Codruta

Results: 25

CURRENT DATA ABOUT THE AETIOLOGY AND TREATMENT OF INFECTIVE ENDOCARDITIS.

Published in:

Farmacia, 2022, v. 70, n. 5, p. 837, doi. 10.31925/farmacia.2022.5.8

By:

ZAHA, DANA CARMEN;
JURCA, MARIA CLAUDIA;
DAINA, CRISTIAN;
BABEȘ, VICTOR VLAD;
PETCHESI, CODRUȚA DIANA;
JURCA, ALEXANDRU DANIEL;
VESA, COSMIN;
CODREANU, IOANA CORALIA;
BABEȘ, EMILIA ELENA

Publication type:

Article

Clinical Challenges in Diagnosing Primordial Dwarfism: Insights from a MOPD II Case Study.

Published in:

Medicina (1010660X), 2024, v. 60, n. 11, p. 1906, doi. 10.3390/medicina60111906

By:

Jurca, Alexandru Daniel;
Petchesi, Codruța Diana;
Jurca, Sânziana;
Severin, Emilia;
Jurca, Aurora Alexandra;
Jurca, Claudia Maria

Publication type:

Article

Wolfram Syndrome Type I Case Report and Review—Focus on Early Diagnosis and Genetic Variants.

Published in:

Medicina (1010660X), 2024, v. 60, n. 7, p. 1064, doi. 10.3390/medicina60071064

By:

Jurca, Alexandru Daniel;
Galea-Holhos, Larisa Bianca;
Jurca, Aurora Alexandra;
Atasie, Diter;
Petchesi, Codruta Diana;
Severin, Emilia;
Jurca, Claudia Maria

Publication type:

Article

Long-term Outcome in Patients with Turner Syndrome - Retrospective Study.

Published in:

Archives of Pharmacy Practice, 2024, v. 15, n. 3, p. 54, doi. 10.51847/dfg57HvhDj

By:

Petchesi, Codruta Diana;
Iuhas, Alin Remus;
Hodisan, Ramona;
Zaha, Dana Carmen;
Jurca, Alexandru Daniel

Publication type:

Article

When Bad Luck Strikes Twice: Beckwith Wiedemann Syndrome Associated with Familial Long QT Syndrome Type I.

Published in:

2024

By:

Petchesi, Codruta Diana;
Kozma, Kinga;
Iuhas, Alin Remus;
Hodisan, Ramona;
Jurca, Alexandru Daniel

Publication type:

Case Study

Clinical-Epidemiological Study of a Cohort of 35 Patients with Craniosynostosis.

Published in:

Maedica - a Journal of Clinical Medicine, 2022, v. 17, n. 4, p. 893, doi. 10.26574/maedica.2022.17.4.893

By:

SOMOLAN, Caludia-Victoria;
PETCHESI, Codruta Diana;
JURCA, Claudia;
BEMBEA, Marius

Publication type:

Article

THE SURPRISES OF MOLECULAR TESTING IN NEUROFIBROMATOSIS TYPE 1: RARE ASSOCIATION BETWEEN TWO MUTATIONAL VARIANTS.

Published in:

Pharmacophore, 2024, v. 15, n. 2, p. 70, doi. 10.51847/QG2iHRJqUL

By:

Jurca, Aurora;
Petchesi, Codruta Diana;
Jurca, Maria Claudia;
Bembea, Dan;
Daniel Jurca, Alexandru;
Atasie, Diter

Publication type:

Article

RELATIONSHIP BETWEEN PRE-EXISTING CONDITIONS IN COVID-19 PATIENTS AND INFLAMMATION.

Published in:

Pharmacophore, 2022, v. 13, n. 4, p. 41, doi. 10.51847/VsOsr2f5dN

By:

Fritea, Luminita;
Sipponen, Maruzella;
Antonescu, Angela;
(Groza), Florina Miere;
Chirla, Razvan;
Vesa, Cosmin;
Cavalu, Simona;
Ganea, Mariana;
Horvath, Tunde;
Petchesi, Codruta;
Domuta, Maria

Publication type:

Article

THE EVOLUTION AND IMPACT OF HEMANGIOMAS OF INFANCY.

Published in:

Analele Universitatii din Oradea, Fascicula Ecotoxicologie, Zootehnie si Tehnologii în Industria Alimentara, 2018, v. 17, n. Part A, p. 149

By:

Diana, Petchesi Codruţa;
Alexandra, Iuhas Oana;
Cosmin, Vesa;
Alexandru, Jurca;
Kinga, Kozma;
Marius, Bembea

Publication type:

Article

THROMBOCYTOPENIA AND ABSENT RADIUS (TAR) SYNDROME - CASE PRESENTATION.

Published in:

2017

By:

Vesa, Cosmin Mihai;
Moisi, Mădălina;
Petchesi, Codruta;
Popa, Loredana;
Mekereş, Florica;
Bembea, Marius;
Jurca, Claudia Maria

Publication type:

Case Study

Tuberous Sclerosis Complex: New Insights into Pathogenesis and Therapeutic Breakthroughs.

Published in:

Life (2075-1729), 2025, v. 15, n. 3, p. 368, doi. 10.3390/life15030368

By:

Jurca, Aurora Alexandra;
Jurca, Alexandru Daniel;
Petchesi, Codruta Diana;
Bembea, Dan;
Jurca, Claudia Maria;
Severin, Emilia;
Jurca, Sanziana;
Vesa, Cosmin Mihai

Publication type:

Article

Cardiofaciocutaneous syndrome - a longitudinal study of a case over 33 years: case report and review of the literature.

Published in:

Romanian Journal of Morphology & Embryology, 2021, v. 62, n. 2, p. 563, doi. 10.47162/RJME.62.2.23

By:

JURCĂ, MARIA CLAUDIA;
IUHAS, OANA ALEXANDRA;
PUIU, MARIA;
CHIRIȚĂ-EMANDI, ADELA;
ANDREESCU, NICOLETA IOANA;
PETCHEŞI, CODRUȚA DIANA;
JURCĂ, ALEXANDRU DANIEL;
MAGYAR, IOAN;
JURCĂ, SÂNZIANA IULIA;
KOZMA, KINGA;
SEVERIN, EMILIA MARIA;
BEMBEA, MARIUS

Publication type:

Article

Genetics of congenital solid tumors.

Published in:

Romanian Journal of Morphology & Embryology, 2020, v. 61, n. 4, p. 1039, doi. 10.47162/RJME.61.4.06

By:

JURCĂ, MARIA CLAUDIA;
IVAŞCU, MARIUS EVELIN;
JURCĂ, AURORA ALEXANDRA;
KOZMA, KINGA;
MAGYAR, IOAN;
ŞANDOR, MIRCEA IOAN;
JURCĂ, ALEXANDRU DANIEL;
ZAHA, DANA CARMEN;
ALBU, CRISTINA-CRENGUŢA;
PANTIŞ, CARMEN;
BEMBEA, MARIUS;
PETCHEŞI, CODRUŢA DIANA

Publication type:

Article

Double autosomal trisomy with mosaicism 47,XY(+8)/ 47,XY(+21). Morphological and genetic changes of a rare case.

Published in:

Romanian Journal of Morphology & Embryology, 2018, v. 59, n. 3, p. 985

By:

JURCĂ, MARIA CLAUDIA;
BEMBEA, MARIUS;
IUHAS, OANA ALEXANDRA;
KOZMA, KINGA;
PETCHEŞI, CODRUŢA DIANA;
JURCĂ, ALEXANDRU DANIEL;
SZILÁGYI, ARIANA;
DUBĂU, DIANA LUMINIŢA;
SAVA, CRISTIAN NICOLAE;
ZAHA, DANA CARMEN;
CUC, EMILIA ALBINIŢA

Publication type:

Article

Empty sella associated with growth hormone deficiency and polydactyly.

Published in:

Romanian Journal of Morphology & Embryology, 2018, v. 59, n. 1, p. 381

By:

JURCĂ, MARIA CLAUDIA;
BEMBEA, MARIUS;
KOZMA, KINGA;
ŞANDOR, MIRCEA IOAN;
NEGREAN, RODICA ANAMARIA;
DOBJANSCHI, LUCIANA;
CUC, EMILIA ALBINIŢA;
PETCHEŞI, CODRUŢA DIANA;
JURCĂ, ALEXANDRU DANIEL

Publication type:

Article

Morphological and genetic abnormalities in a Jacobsen syndrome.

Published in:

Romanian Journal of Morphology & Embryology, 2017, v. 58, n. 4, p. 1531

By:

JURCĂ, ALEXANDRU DANIEL;
KOZMA, KINGA;
IOANA, MIHAI;
STREAȚĂ, IOANA;
PETCHEŞI, CODRUȚA DIANA;
BEMBEA, MARIUS;
JURCĂ, MARIA CLAUDIA;
CUC, EMILIA ALBINIȚA;
VESA, COSMIN MIHAI;
BUHAŞ, CAMELIA LIANA

Publication type:

Article

Anatomic variants in Dandy-Walker complex.

Published in:

Romanian Journal of Morphology & Embryology, 2017, v. 58, n. 3, p. 1051

By:

JURCĂ, MARIA CLAUDIA;
KOZMA, KINGA;
PETCHEŞI, CODRUŢA DIANA;
BEMBEA, MARIUS;
POP, OVIDIU LAUREAN;
MUŢIU, GABRIELA;
COROI, MIHAELA CRISTIANA;
JURCĂ, ALEXANDRU DANIEL;
DOBJANSCHI, LUCIANA

Publication type:

Article

A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency.

Published in:

Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2021, v. 70, n. 3, p. 186, doi. 10.37897/RJP.2021.3.4

By:

Pintilie, Sebastian Romeo;
Fodor, Adriana;
Bembea, Marius;
Petchesi, Codruța Diana;
Grad, Simona;
Damian, Laura;
Vulturar, Romana

Publication type:

Article

Bioethical aspects in type I neurofibromatosis.

Published in:

Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2021, v. 70, n. 3, p. 169, doi. 10.37897/RJP.2021.3.1

By:

Petchesi, Codruța Diana;
Ciavoi, Gabriela;
Jurca, Claudia;
Vulturar, Romana;
Bembea, Marius

Publication type:

Article

DOWN SYNDROME – LONGITUDINAL STUDY OF CLINICAL EVOLUTION AND PSYCHO-SOCIAL IMPLICATIONS.

Published in:

Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2021, v. 70, n. 2, p. 135, doi. 10.37897/RJP.2021.2.8

By:

Petchesi, Codruța Diana;
Ciavoi, Gabriela;
Feier, Florentina;
Iuhas, Oana Alexandra;
Kozma, Kinga;
Jurca, Claudia;
Bembea, Marius

Publication type:

Article

Congenital Myasthenic Syndrome-4C in a Consanguineous Romani Family: Genetic Insights and Clinical Implications.

Published in:

Diagnostics (2075-4418), 2025, v. 15, n. 3, p. 235, doi. 10.3390/diagnostics15030235

By:

Petchesi, Codruta Diana;
Jurca, Aurora Alexandra;
Jurca, Alexandru Daniel;
Dorobantu, Florica Ramona;
Iuhas, Alin Remus;
Severin, Emilia;
Jurca, Claudia Maria

Publication type:

Article

PAH Pathogenic Variants and Clinical Correlations in a Group of Hyperphenylalaninemia Patients from North-Western Romania.

Published in:

Diagnostics (2075-4418), 2023, v. 13, n. 8, p. 1483, doi. 10.3390/diagnostics13081483

By:

Iuhas, Alin;
Jurca, Claudia;
Kozma, Kinga;
Riza, Anca-Lelia;
Streață, Ioana;
Petcheși, Codruța;
Dan, Andra;
Sava, Cristian;
Balmoș, Andreea;
Marinău, Cristian;
Niulaș, Larisa;
Ioana, Mihai;
Bembea, Marius

Publication type:

Article

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

Published in:

2021

By:

Kozma, Kinga;
Bembea, Marius;
Jurca, Claudia M.;
Ioana, Mihai;
Streață, Ioana;
Şoşoi, Simona Ş.;
Pirvu, Andrei;
Petchesi, Codruța D.;
Szilágyi, Ariana;
Sava, Cristian N.;
Jurca, Alexandru;
Ujfalusi, Anikó;
Szűcs, Zsuzsanna;
Szakszon, Katalin

Publication type:

Case Study

Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways—Case Report and Literature Review.

Published in:

Genes, 2023, v. 14, n. 2, p. 433, doi. 10.3390/genes14020433

By:

Jurca, Claudia Maria;
Kozma, Kinga;
Petchesi, Codruta Diana;
Zaha, Dana Carmen;
Magyar, Ioan;
Munteanu, Mihai;
Faur, Lucian;
Jurca, Aurora;
Bembea, Dan;
Severin, Emilia;
Jurca, Alexandru Daniel

Publication type:

Article

Effects of Burosumab Treatment on Two Siblings with X-Linked Hypophosphatemia. Case Report and Literature Review.

Published in:

Genes, 2022, v. 13, n. 8, p. 1392, doi. 10.3390/genes13081392

By:

Jurca, Claudia Maria;
Iuhas, Oana;
Kozma, Kinga;
Petchesi, Codruta Diana;
Zaha, Dana Carmen;
Bembea, Marius;
Jurca, Sanziana;
Paul, Corina;
Jurca, Alexandru Daniel

Publication type:

Article