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of 3
pro vyhledávání: '"Claudiu Gabriel, Socoliuc"'
Autor:
Claudiu Gabriel Socoliuc, Alexandra Oprisan, Amelia Dobrescu, Emilia Manole, Alexandra Eugenia Bastian
Publikováno v:
Romanian Journal of Neurology, Vol 20, Iss 2, Pp 264-270 (2021)
Objectives. Dysferlinopathies are a group of rare genetic myopathies characterized by muscle weakness and atrophy with four distinct clinical phenotypes: Miyoshi myopathy, limb girdle muscular dystrophy type 2B, distal myopathy with anterior tibial o
Externí odkaz:
https://doaj.org/article/f1630390a8f24a52a024b6aa45acb31d
Autor:
Elena Florentina MARINGICA, Oana Elisabeta MORARI, Claudiu Gabriel SOCOLIUC, Alexandra Eugenia BASTIAN, Bogdan Ovidiu POPESCU
Publikováno v:
Modern Medicine, Vol 27, Iss 1, Pp 47-53 (2020)
Introduction: Myotonic dystrophy (DM) type 1 is a genetic disorder, caused by a trinucleotide CTG repeat expansion in the DMPK gene on chromosome 19. The skeletal muscle is the most severely affected organ, patients clinically presenting weakness and
Externí odkaz:
https://doaj.org/article/ff139b837ec94229b2214a6d8a4bd721
Autor:
Stana, Păunică, Sabina Andrada, Zurac, Anca Silvia, Dumitriu, Ştefana, Popa, Claudiu Gabriel, Socoliuc, Marina Cristina, Giurgiu
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 63(1)
Periodontal pathology is often represented by increases in gingival volume, with pronounced inflammatory phenomena. These manifestations require a more accurate diagnosis and knowledge of the etiopathogenic factors involved. The periodontal treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f11b4a06c0fb15d9f5debb82e5425ef8
https://pubmed.ncbi.nlm.nih.gov/36074692
https://pubmed.ncbi.nlm.nih.gov/36074692