Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Lavinia Postolache"'
Autor:
Stéphane Abramowicz, Philippine Delvaulx, Martina Maria Delle Fave, Pauline Le Roux, Déborah Buisseret, Lavinia Postolache
Publikováno v:
Case Reports in Ophthalmology, Vol 13, Iss 1, Pp 305-312 (2022)
A 3-year-old girl presented with recurrent exotropia following primary strabismus surgery. Careful fundus examination of the left eye revealed loss of the foveal reflex and presence of a subtle grayish mass with overlying white fluff. Optical coheren
Externí odkaz:
https://doaj.org/article/f158b7dcaa32433f930acfa74334d795
Autor:
Lavinia Postolache
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Background: Various ocular anomalies are present in the vast majority of individuals with Down syndrome; however, we know little about optic nerve abnormalities. The aim of this cross-sectional comparative study was to describe optic disc morphology
Externí odkaz:
https://doaj.org/article/256a9a014890460ab07d273d4f3ca8d3
Autor:
Anca Lavinia Postolache, Ingrith Miron, Vasile Valeriu Lupu, Ștefana Moisă, Leonard Perțea, Teodora Jescu, Cristina Rusu, Ancuța Lupu
Publikováno v:
Romanian Journal of Oral Rehabilitation, Vol 12, Iss 3, Pp 80-84 (2020)
Prader-Willi Syndrome (PWS) is a complex genetic syndrome characterized by a multitude of entities, including diminished fetal activity, obesity, severe muscular hypotonia, mental retardation, low stature, discrete cranio-facial dysmorphia, dental pr
Externí odkaz:
https://doaj.org/article/b5035237487540f49506d5884b3b8dfa
Autor:
Teodora Jescu, Ingrith Miron, Vasile Valeriu Lupu, Stefana Maria Moisa, Anca-Lavinia Postolache, Oana Tatiana Miron, Ancuta Lupu
Publikováno v:
The European Conference of Psychiatry and Mental Health "Galatia".
Polyradiculoneuritis or Guillan Barré’s Syndrome is the most common cause of acute and subacute generalized paralysis, which is likely to occur at any age. We present the case of a 17-year-old adolescent who was admitted to our clinic for swallowi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c0b735c3072d72ea4a1a3500b83547e
https://doi.org/10.35630/2022/12/psy.ro.11
https://doi.org/10.35630/2022/12/psy.ro.11
Autor:
Coralie Hemptinne, François Willermain, Casper de Jong, Lavinia Postolache, Laurence Postelmans
Publikováno v:
Ophthalmic genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e609fa55281175ba23b44df82a65877f
https://pubmed.ncbi.nlm.nih.gov/36062537
https://pubmed.ncbi.nlm.nih.gov/36062537
Publikováno v:
Ophthalmic Genetics. 41:135-145
Background: Tessellated fundus refers to a specific change in the appearance of the internal layers of the eye in which the choroidal large vessels became visible through polygonal hypopigmented ar...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0908f12390f8d6f4597bdbc88094503e
https://doi.org/10.1080/13816810.2020.1744021
https://doi.org/10.1080/13816810.2020.1744021
Autor:
Lavinia Postolache, Afshin Parsa, Paolo Simoni, Grammatina Boitsios, Khalid Ismaili, Thierry Schurmans, Anne Monier, Georges Casimir, Adelin Albert, Cameron F. Parsa
Publikováno v:
Pediatric nephrology (Berlin, Germany). 37(10)
Rare autopsy studies have described smaller kidneys as well as urinary tract anomalies in Down syndrome. This observation has never been investigated in vivo and little is known about the possible consequences upon kidney function. Here we wish to co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bfe51e978403ae55afd8c51fe5aa5bd
https://pubmed.ncbi.nlm.nih.gov/35118542
https://pubmed.ncbi.nlm.nih.gov/35118542
Publikováno v:
Eye and Brain
Eye and Brain, 13
Eye and Brain, 13
Down syndrome, caused by an extra copy of all or part of chromosome 21, is the most prevalent intellectual disability of genetic origin. Among numerous comorbidities which are part of the phenotype of individuals with Down syndrome, ocular problems a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d3c4ddbfa43592dd3a42b154637128d
https://pubmed.ncbi.nlm.nih.gov/34321946
https://pubmed.ncbi.nlm.nih.gov/34321946
Autor:
Cameron Parsa, Lavinia Postolache
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-6 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-6 (2018)
Wölfflin nodules and Brushfield spots were described essentially in light colored irides. The purpose of our study is to determine if these iris features are also present in dark irides, hidden by melanin granules of the anterior leaf of the iris. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee532fd95d6dce1dc16a032fa08e9ef2
https://pubmed.ncbi.nlm.nih.gov/30575783
https://pubmed.ncbi.nlm.nih.gov/30575783
Autor:
Petra Liskova, Bart P. Leroy, Pavlina Skalicka, Jang Hee J.H.J. Vercruyssen, Irina Balikova, Lubica Dudakova, Lavinia Postolache
Publikováno v:
Acta ophthalmologica. 96(1)
Purpose To identify the molecular genetic cause in four families of various ethnic backgrounds with cornea plana. Methods Detailed ophthalmological examination and direct sequencing of the KERA coding region in five patients of Czech and Turkish orig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3827a1eb761712464b9cd37a92d6da2e
https://pubmed.ncbi.nlm.nih.gov/28677912
https://pubmed.ncbi.nlm.nih.gov/28677912