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Zmyslowska, Agnieszka
63  results:
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1

Bartter[StQuote]s syndrome as a forgotten cause of polyhydr..:

Malarska, Maria ; Moczulska, Hanna ; Pachniak, Paulina...
European Journal of Obstetrics & Gynecology and Reproductive Biology.  293 (2024)  - p. 58 , 2024
Link: https://doi.org/10.1016/..
 
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2

Screening for Rare Mitochondrial Genome Variants Reveals a ..:

Płoszaj, Tomasz ; Skoczylas, Sebastian ; Gadzalska, Karolina...
International Journal of Molecular Sciences.  25 (2024)  4 - p. 2438 , 2024
Link: https://doi.org/10.3390/..
 
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3

Serum metabolomics identified specific lipid compounds whic..:

Jeziorny, Krzysztof ; Pietrowska, Karolina ; Sieminska, Julia...
Frontiers in Molecular Biosciences.  10 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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4

Searching for Effective Methods of Diagnosing Nervous Syste..:

Waszczykowska, Arleta ; Jeziorny, Krzysztof ; Barańska, Dobromiła...
Genes.  14 (2023)  9 - p. 1784 , 2023
Link: https://doi.org/10.3390/..
 
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5

Proteomic and Transcriptomic Landscapes of Alström and Bard..:

Smyczynska, Urszula ; Stanczak, Marcin ; Kuljanin, Miljan...
Genes.  13 (2022)  12 - p. 2370 , 2022
Link: https://doi.org/10.3390/..
 
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6

Association of circulating miRNAS in patients with Alstrőm ..:

Zmyslowska, Agnieszka ; Smyczynska, Urszula ; Stanczak, Marcin...
Frontiers in Endocrinology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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7

Incomplete phenotypic presentation in a girl with rare Rabs..:

Chrzanowska, Joanna ; Skarul, Jagoda ; Zubkiewicz-Kucharska, Agnieszka..
Acta Diabetologica.  60 (2022)  3 - p. 449-453 , 2022
Link: https://doi.org/10.1007/..
 
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8

Identification of bone metabolism disorders in patients wit..:

Jeziorny, Krzysztof ; Zmyslowska-Polakowska, Ewa ; Wyka, Krystyna...
Bone Reports.  17 (2022)  - p. 101600 , 2022
Link: https://doi.org/10.1016/..
 
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9

Reduced Corneal Sensitivity With Neuronal Degeneration is a..:

Waszczykowska, Arleta ; Zmysłowska, Agnieszka ; Bartosiewicz, Krzysztof...
American Journal of Ophthalmology.  236 (2022)  - p. 63-68 , 2022
Link: https://doi.org/10.1016/..
 
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10

Multiomic analysis on human cell model of wolfram syndrome ..:

Zmyslowska, Agnieszka ; Kuljanin, Miljan ; Malachowska, Beata...
Cell Communication and Signaling.  19 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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11

Screening for extremely rare pathogenic variants of monogen..:

Płoszaj, Tomasz ; Antosik, Karolina ; Jakiel, Paulina..
Endocrine.  73 (2021)  3 - p. 752-757 , 2021
Link: https://doi.org/10.1007/..
 
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12

Next-Generation Sequencing in the Diagnosis of Patients wit..:

Jeziorny, Krzysztof ; Antosik, Karolina ; Jakiel, Paulina...
Genes.  11 (2020)  11 - p. 1283 , 2020
Link: https://doi.org/10.3390/..
 
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13

Multiple Retinal Anomalies in Wfs1-Deficient Mice:

Waszczykowska, Arleta ; Zmysłowska, Agnieszka ; Braun, Marcin...
Diagnostics.  10 (2020)  9 - p. 607 , 2020
Link: https://doi.org/10.3390/..
 
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14

A cross‐sectional study of patients referred forHNF1B‐MODY ..:

Sztromwasser, Paweł ; Michalak, Arkadiusz ; Małachowska, Beata...
Pediatric Diabetes.  21 (2020)  3 - p. 422-430 , 2020
Link: https://doi.org/10.1111/..
 
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15

Corneal Abnormalities Are Novel Clinical Feature in Wolfram..:

Waszczykowska, Arleta ; Zmysłowska, Agnieszka ; Braun, Marcin...
American Journal of Ophthalmology.  217 (2020)  - p. 140-151 , 2020
Link: https://doi.org/10.1016/..
 
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