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Year | Number of Results |
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2020 | 2 |
2021 | 3 |
2022 | 1 |
2024 | 0 |
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Page 1
Primitive Reflex Activity in Relation to Motor Skills in Healthy Preschool Children.
Brain Sci. 2021 Jul 23;11(8):967. doi: 10.3390/brainsci11080967.
Brain Sci. 2021.
PMID: 34439585
Free PMC article.
FINCA syndrome-Defining neurobehavioral phenotype in survivors into late childhood.
Badura-Stronka M, Śmigiel R, Rutkowska K, Szymańska K, Hirschfeld AS, Monkiewicz M, Kosińska J, Wolańska E, Rydzanicz M, Latos-Bieleńska A, Płoski R.
Badura-Stronka M, et al. Among authors: wolanska e.
Mol Genet Genomic Med. 2022 Apr;10(4):e1899. doi: 10.1002/mgg3.1899. Epub 2022 Mar 7.
Mol Genet Genomic Med. 2022.
PMID: 35255187
Free PMC article.
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Primitive Reflex Activity in Relation to the Sensory Profile in Healthy Preschool Children.
Pecuch A, Gieysztor E, Telenga M, Wolańska E, Kowal M, Paprocka-Borowicz M.
Pecuch A, et al. Among authors: wolanska e.
Int J Environ Res Public Health. 2020 Nov 6;17(21):8210. doi: 10.3390/ijerph17218210.
Int J Environ Res Public Health. 2020.
PMID: 33172138
Free PMC article.
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A Child's Perception of Their Developmental Difficulties in Relation to Their Adult Assessment. Analysis of the INPP Questionnaire.
Demiy A, Kalemba A, Lorent M, Pecuch A, Wolańska E, Telenga M, Gieysztor EZ.
Demiy A, et al. Among authors: wolanska e.
J Pers Med. 2020 Oct 5;10(4):156. doi: 10.3390/jpm10040156.
J Pers Med. 2020.
PMID: 33027926
Free PMC article.
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Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 Gene.
Klaniewska M, Jedrzejowska M, Rydzanicz M, Paprocka J, Biela M, Wolanska E, Pollak A, Debek E, Sasiadek M, Ploski R, Gos M, Smigiel R.
Klaniewska M, et al. Among authors: wolanska e.
Front Genet. 2021 Apr 28;12:620752. doi: 10.3389/fgene.2021.620752. eCollection 2021.
Front Genet. 2021.
PMID: 33995476
Free PMC article.
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The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes.
Wolańska E, Pollak A, Rydzanicz M, Pesz K, Kłaniewska M, Rozensztrauch A, Skiba P, Stawiński P, Płoski R, Śmigiel R.
Wolańska E, et al.
Genes (Basel). 2021 Feb 27;12(3):350. doi: 10.3390/genes12030350.
Genes (Basel). 2021.
PMID: 33673493
Free PMC article.
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