Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ewa Głuszkiewicz"'
Autor:
Ewa Głuszkiewicz, Paweł Sowa, Maciej Zieliński, Monika Adamczyk-Sowa, Maciej Misiołek, Wojciech Ścierski
Publikováno v:
Medicina, Vol 58, Iss 12, p 1726 (2022)
Background and objectives: Facial weakness is the most important complication of parotid gland tumor surgery. The aims of this study are as follows: (1) assessment of the prevalence of postparotidectomy facial nerve dysfunction; (2) clinical and elec
Externí odkaz:
https://doaj.org/article/bb5d9ff6a40348788012b1d37f4d5707
Publikováno v:
Child Neurology. 28:27-38
Autor:
Anna Szaflarska, Anna Gruca, Magdalena Machnikowska-Sokołowska, Katarzyna Gruszczyńska, Anna Pituch-Noworolska, Marzena Lenart, Miroslaw Bik-Multanowski, Maciej Siedlar, Marta Surman, Ewa Głuszkiewicz, Katarzyna Szewczyk, Magdalena Rutkowska-Zapała, Ilona Kopyta
Introduction In this study we describe a patient with gross deletion containing the BTK and TIMM8A genes. Mutations in these genes are responsible for X-linked agammaglobulinemia and Mohr-Tranebjaerg syndrome, respectively. X linked agammaglobulinemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dd6250e0d429c79c0c5b44b7c497d64
https://ruj.uj.edu.pl/xmlui/handle/item/117094
https://ruj.uj.edu.pl/xmlui/handle/item/117094
Autor:
Anna, Szaflarska, Magdalena, Rutkowska-Zapała, Anna, Gruca, Katarzyna, Szewczyk, Mirosław, Bik-Multanowski, Marzena, Lenart, Marta, Surman, Ilona, Kopyta, Ewa, Głuszkiewicz, Magdalena, Machnikowska-Sokołowska, Katarzyna, Gruszczyńska, Anna, Pituch-Noworolska, Maciej, Siedlar
Publikováno v:
Central-European Journal of Immunology
Introduction In this study we describe a patient with gross deletion containing the BTK and TIMM8A genes. Mutations in these genes are responsible for X-linked agammaglobulinemia and Mohr-Tranebjaerg syndrome, respectively. X linked agammaglobulinemi
Publikováno v:
Wiadomosci lekarskie (Warsaw, Poland : 1960). 65(2)
The aim of this study was to evaluate the prevalence of selected risk factors of weight deficiency in children with chronic metabolic diseases.The study group involved 160 children, from 2 months to 15 years (mean age 3.14 years), with diseases of th
[Opsoclonus-myoclonus syndrome in a 2 year old boy with prenatally diagnosed retroperitoneal tumour]
Publikováno v:
Medycyna wieku rozwojowego. 15(2)
Opsoclonus-myoclonus syndrome, also named Myoclonic Encephalopathy of Infants, Opsoclonus- Myoclonus Ataxia, Dancing Eyes - Dancing Feet Syndrome, Dancing Eyes Syndrome, Kinsbourne syndrome, is a rare, paraneoplastic or possibly post-viral chronic ne
Autor:
Ewa, Jamroz, Justyna, Paprocka, Dariusz, Adamek, Justyna, Pytel, Katarzyna, Szczechowska, Natalia, Grabska, Michalina, Malec, Ewa, Głuszkiewicz, Michał, Daab, Anatolij, Wodołażski
Publikováno v:
Folia neuropathologica. 49(1)
Increased ethylmalonic acid (EMA) in urine is a non-specific finding, and is observed in a number of inborn errors of metabolism, as well as in individuals who carry one of two common polymorphisms identified in the SCAD coding region. The authors pr
Autor:
Justyna, Paprocka, Ewa, Jamroz, Ewa, Głuszkiewicz, Andrzej, Klimczak, Ewa, Kluczewska, Elzbieta, Marszał
Publikováno v:
Wiadomosci lekarskie (Warsaw, Poland : 1960). 61(7-9)
Back pain and pain of the surrounding structures leads to significant diagnostic and therapeutic difficulties which result from a complex pathomechanism. They are the symptom of a large number of pathologic processes that may to a varying extent cont
Autor:
Justyna, Paprocka, Ewa, Jamroz, Dariusz, Adamek, Teresa J, Stradomska, Ewa, Głuszkiewicz, Urszula, Grzybowska-Chlebowczyk, Elzbieta, Marszał
Publikováno v:
Folia neuropathologica. 45(4)
Peroxisomal diseases are a heterogeneous group of genetic metabolic disorders which are caused by incorrect biogenesis of peroxisomes or a defect in activity of particular enzymes located in those organelles.D-bifunctional protein (D-BP) deficiency b
Publikováno v:
Pediatria Polska. (5):474-480
Background and aims Severe clinical course of the respiratory tract infections is very frequent in children with neurological disorders. The aim of this study was to establish the diagnostic and therapeutic procedures giving the best results in this