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Plaseska Karanfilska, D.
324  Ergebnisse:
Personensuche X
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1

P012 Two-year neonatal screening for cystic fibrosis in Rep..:

Fustik, S. ; Anastasovska, V. ; Plaseska Karanfilska, D....
Journal of Cystic Fibrosis.  20 (2021)  - p. S42 , 2021
Link: https://doi.org/10.1016/..
 
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Frontotemporal dementia associated with SQSTM1 gene mutatio..:

Angelova, A. ; Novotni, G. ; Karanfilska, D. Plaseska...
Parkinsonism & Related Disorders.  122 (2024)  - p. 106774 , 2024
Link: https://doi.org/10.1016/..
 
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3

GNB1 mutation - A (not so) rare cause for early onset dysto..:

Novotni, G. ; Angelova, A. ; Jaceva, I....
Parkinsonism & Related Disorders.  122 (2024)  - p. 106612 , 2024
Link: https://doi.org/10.1016/..
 
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P009 The spectrum of CFTR mutations in newly diagnosed case..:

Fustik, S. ; Anastasovska, V. ; Karanfilska, D. Plaseska...
Journal of Cystic Fibrosis.  21 (2022)  - p. S63 , 2022
Link: https://doi.org/10.1016/..
 
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P016 First results from national newborn screening program ..:

Fustikj, S. ; Anastasovska, V. ; Karanfilska, D. Plaseska...
Journal of Cystic Fibrosis.  19 (2020)  - p. S59 , 2020
Link: https://doi.org/10.1016/..
 
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299 Pancreatic sufficient cystic fibrosis infants presentin..:

Fustik, S. ; Jakovska, T. ; Spirevska, L..
Journal of Cystic Fibrosis.  16 (2017)  - p. S138 , 2017
Link: https://doi.org/10.1016/..
 
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7

Comparative proteomics analysis of decidua reveals altered ..:

Davalieva, Katarina ; Terzikj, Marija ; Bozhinovski, Gjorgji...
Placenta.  154 (2024)  - p. 28-37 , 2024
Link: https://doi.org/10.1016/..
 
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8

Novel Variant ANKRD11 Gene Mutation Associated With Drug-Re..:

Babunovska, Marija ; Cepreganova Cangovska, Tatjana ; Kuzmanovski, Igor...
Pediatric Neurology.  155 (2024)  - p. 51-54 , 2024
Link: https://doi.org/10.1016/..
 
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9

Current State of Compulsory Basic and Clinical Courses in G..:

Pereza, Nina ; Terzić, Rifet ; Plaseska-Karanfilska, Dijana...
Frontiers in Genetics.  12 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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Autoimmune lymphoproliferative syndrome identified through ..:

Kocheva, Svetlana ; Gjorgijevska, Marija ; Vujovic, Marija...
Central European Journal of Immunology.  47 (2022)  2 - p. 179-182 , 2022
Link: https://doi.org/10.5114/..
 
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11

Alström Syndrome with Early Vision and Hearing Impairement:

Beqiri-Jashari, Ardiana ; Janchevska, Aleksandra ; Ahmeti, Irfan...
PRILOZI.  43 (2022)  2 - p. 159-162 , 2022
Link: https://doi.org/10.2478/..
 
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Comparative proteomics analysis of human FFPE testicular ti..:

Davalieva, Katarina ; Rusevski, Aleksandar ; Velkov, Milan...
Journal of Proteomics.  267 (2022)  - p. 104686 , 2022
Link: https://doi.org/10.1016/..
 
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13

Renal Hypouricemia 1: Rare Disorder as Common Disease in Ea..:

Stiburkova, Blanka ; Bohatá, Jana ; Pavelcová, Kateřina...
Biomedicines.  9 (2021)  11 - p. 1607 , 2021
Link: https://doi.org/10.3390/..
 
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14

Heterotopic ossifications and Charcot joints: Congenital in..:

Gucev, Zoran ; Tasic, Velibor ; Bogevska, Ivona...
European Journal of Medical Genetics.  63 (2020)  1 - p. 103613 , 2020
Link: https://doi.org/10.1016/..
 
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15

Multilevel regression modeling for aneuploidy classificatio..:

Noveski, Predrag ; Terzic, Marija ; Vujovic, Marija...
PLOS ONE.  14 (2019)  8 - p. e0221227 , 2019
Link: https://doi.org/10.1371/..
 
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