Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Krystyna, Kanigowska"'
Publikováno v:
International Ophthalmology
Purpose To evaluate choroidal thickness (CTh) in children with chronic heart failure (CHF) secondary to dilated cardiomyopathy (DCM) using spectral domain optical coherence tomography (SD-OCT) and to compare their values to those of healthy children.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac0ff36a94c14d6772bb0808881653df
http://europepmc.org/articles/PMC8172512
http://europepmc.org/articles/PMC8172512
Publikováno v:
Klinika Oczna. 123:166-172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecf4cebe5f57bdcaab35091daac0bbf7
https://doi.org/10.5114/ko.2021.111817
https://doi.org/10.5114/ko.2021.111817
Autor:
Klaudia Rakusiewicz, Wojciech Hautz, Marlena Młynek, Joanna Jędrzejczak-Młodziejewska, Agnieszka Czeszyk, Krystyna Kanigowska, Małgorzata Danowska, Marta Wyszyńska, Anna Rogowska, Dorota Wicher
Publikováno v:
Open Medicine
Open Medicine, Vol 16, Iss 1, Pp 156-160 (2021)
Open Medicine, Vol 16, Iss 1, Pp 156-160 (2021)
Background Cohen syndrome (Q87.8;ORPHA:193; OMIM#216550) is an autosomal recessive inherited genetic disorder caused by mutation in the VPS13B/COH1 gene. It is characterized by variable clinical symptoms such as deformity of the head, face, hands and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20c61581280da5893bc4770f1b99f63a
http://europepmc.org/articles/PMC7819545
http://europepmc.org/articles/PMC7819545
Autor:
Klaudia Rakusiewicz, Krystyna Kanigowska, Agnieszka Czeszyk, Małgorzata Danowska, Anna Rogowska, Wojciech Hautz, Marta Wyszyńska, Joanna Jędrzejczak-Młodziejewska
Publikováno v:
Klinika Oczna. 122:117-120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aab103b93cf93d66b189a82c7606f3d3
https://doi.org/10.5114/ko.2020.97521
https://doi.org/10.5114/ko.2020.97521
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 12
Journal of Clinical Medicine, Vol 10, Iss 2659, p 2659 (2021)
Volume 10
Issue 12
Journal of Clinical Medicine, Vol 10, Iss 2659, p 2659 (2021)
(1) Introduction: The aim of this study is to assess retinal vessel density (VD) in the superficial capillary plexus layer (SP) and deep capillary plexus layer (DP) in children with chronic heart failure (CHF) in the course of dilated cardiomyopathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94b84509f7dd438e8bc6cd0a6930e1c5
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 9
Journal of Clinical Medicine, Vol 9, Iss 2882, p 2882 (2020)
Volume 9
Issue 9
Journal of Clinical Medicine, Vol 9, Iss 2882, p 2882 (2020)
Purpose: To assess ganglion cell complex (GCC) thickness in children with chronic heart failure (CHF) due to dilated cardiomyopathy (DCM) using optical coherence tomography (OCT). Methods: Sixty eyes of 30 patients with chronic heart failure (CHF) du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa4f0bbe70eac1427668d0d2ea840d47
http://europepmc.org/articles/PMC7563704
http://europepmc.org/articles/PMC7563704
Publikováno v:
Klinika Oczna. 2019:29-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df87cfffd80885d7afa09c5795de9751
https://doi.org/10.5114/ko.2019.85213
https://doi.org/10.5114/ko.2019.85213
Publikováno v:
Klinika oczna. 113(7-9)
The purpose of the article is to present the clinical abnormalities of Patau's syndrome (trisomy13).Examination was performed on 18 months old girl with trisomy13 in which we noted characteristic malformations in ocular system. The patient underwent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06b37617df610ebb9525a8e320c5fb5d
https://pubmed.ncbi.nlm.nih.gov/22256570
https://pubmed.ncbi.nlm.nih.gov/22256570
Autor:
Mirosława, Grałek, Krystyna H, Chrzanowska, Krystyna, Kanigowska, Beata, Kocyła-Karczmarewicz
Publikováno v:
Klinika oczna. 113(4-6)
Nijmegen Breakage Syndrome (NBS) is a genomic instability disease caused by inherited mutations in the NBN/NBS1 gene. The clinical symptoms of NBS are: primary microcephaly, characteristic facial appearance, recurring respiratory tract infections cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::80ea5f50cbc99b9c52eabaf5bb23f7f6
https://pubmed.ncbi.nlm.nih.gov/21913446
https://pubmed.ncbi.nlm.nih.gov/21913446
Publikováno v:
Klinika oczna. 113(1-3)
The study included 31 eyes in 31 children in age between 4 and 12 years. One - point suture fixation of PC IOL to the sclera was performed primary, because of partial loss of the posterior capsule support. Poly-propylene suture 10-0 was used for IOL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ad62824ab875743805f9883da30f79a
https://pubmed.ncbi.nlm.nih.gov/21853944
https://pubmed.ncbi.nlm.nih.gov/21853944