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Jamsheer, A.
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1

Results from the Survey of Antibiotic Resistance (SOAR) 201..:

Jamsheer, A. ; Rafay, A. M. ; Daoud, Z...
Journal of Antimicrobial Chemotherapy.  71 (2016)  suppl 1 - p. i45-i61 , 2016
Link: https://doi.org/10.1093/..
 
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2

A novel nonsense mutation in CUL4B gene in three brothers w..:

Badura‐Stronka, M ; Jamsheer, A ; Materna‐Kiryluk, A...
Clinical Genetics.  77 (2010)  2 - p. 141-144 , 2010
Link: https://doi.org/10.1111/..
 
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3

A severe progressive oculodentodigital dysplasia due to com..:

Jamsheer, A ; Badura‐Stronka, M ; Sowińska, A...
Clinical Genetics.  78 (2010)  1 - p. 94-97 , 2010
Link: https://doi.org/10.1111/..
 
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4

A new sporadic case of early-onset Loeys-Dietz syndrome due..:

Jamsheer, A. ; Henggeler, C. ; Wierzba, J....
Journal of Applied Genetics.  50 (2009)  4 - p. 405-410 , 2009
Link: https://doi.org/10.1007/..
 
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5

A novelGJA1 missense mutation in a Polish child with oculod..:

Jamsheer, A. ; Wiśniewska, M. ; Szpak, A....
Journal of Applied Genetics.  50 (2009)  3 - p. 297-299 , 2009
Link: https://doi.org/10.1007/..
 
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6

The landscape of the COVID-19 pandemic in Poland emerging f..:

Mirska, Barbara ; Zenczak, Michal ; Nowis, Katarzyna...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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7

Molecular landscape of congenital vertebral malformations: ..:

Szoszkiewicz, Anna ; Bukowska-Olech, Ewelina ; Jamsheer, Aleksander
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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8

Development of a tool for predicting HNF1B mutations in chi..:

Kołbuc, Marcin ; Kołek, Mateusz F. ; Motyka, Rafał...
Pediatric Nephrology.  39 (2024)  6 - p. 1847-1858 , 2024
Link: https://doi.org/10.1007/..
 
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9

Chromatinopathies: insight in clinical aspects and underlyi..:

Bukowska-Olech, Ewelina ; Majchrzak-Celińska, Aleksandra ; Przyborska, Marta.
Journal of Applied Genetics.  , 2024
Link: https://doi.org/10.1007/..
 
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10

Evaluating the efficacy of a ketogenic diet in managing dru..:

Winczewska-Wiktor, Anna ; Braszka, Małgorzata ; Harada-Laszlo, Mia...
Epilepsy & Behavior.  150 (2024)  - p. 109535 , 2024
Link: https://doi.org/10.1016/..
 
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11

A genotype–phenotype correlation in split-hand/foot malform..:

Sowińska-Seidler, Anna ; Socha, Magdalena ; Szoszkiewicz, Anna..
Frontiers in Molecular Biosciences.  10 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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12

HOXD13-associated synpolydactyly: Extending and validating ..:

Gottschalk, Annika ; Sczakiel, Henrike L. ; Hülsemann, Wiebke...
Genetics in Medicine.  25 (2023)  11 - p. 100928 , 2023
Link: https://doi.org/10.1016/..
 
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13

Rare multiple congenital anomalies-hypotonia-seizures syndr..:

Bukowska-Olech, Ewelina ; Glista, Filip ; Dinwiddie, April..
European Journal of Medical Genetics.  66 (2023)  1 - p. 104668 , 2023
Link: https://doi.org/10.1016/..
 
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14

NGS analysis of collagen type I genes in Polish patients wi..:

Sałacińska, Kinga ; Pinkier, Iwona ; Rutkowska, Lena...
Frontiers in Endocrinology.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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15

Glycemia-Induced miRNA Changes: A Review:

Al-Mahayni, Sara ; Ali, Mohamed ; Khan, Muhammad...
International Journal of Molecular Sciences.  24 (2023)  8 - p. 7488 , 2023
Link: https://doi.org/10.3390/..
 
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