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1.
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.
Am J Hum Genet
; 109(12): 2270-2282, 2022 12 01.
Article
in English
| MEDLINE | ID: mdl-36368327
2.
Age of natural menopause onset in BRCA1/2 carriers - systematic review and meta-analysis.
Prz Menopauzalny
; 19(4): 171-173, 2020 Dec.
Article
in English
| MEDLINE | ID: mdl-33488327
3.
Association between C3435T polymorphism of MDR1 gene and the incidence of drug-resistant epilepsy in the population of Polish children.
Behav Brain Funct
; 12(1): 21, 2016 Jul 08.
Article
in English
| MEDLINE | ID: mdl-27391700
4.
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.
Brain Sci
; 14(3)2024 Mar 13.
Article
in English
| MEDLINE | ID: mdl-38539661
5.
The Clinical and Epidemiological Profile of Paediatric-Onset Multiple Sclerosis in Poland.
J Clin Med
; 11(24)2022 Dec 17.
Article
in English
| MEDLINE | ID: mdl-36556109
6.
Pediatric-onset multiple sclerosis in Poland: A registry-based retrospective cohort study.
Mult Scler Relat Disord
; 57: 103344, 2022 Jan.
Article
in English
| MEDLINE | ID: mdl-35158453
7.
No evidence for change in expression of TBC1D1 and TBC1D4 genes in cultured human adipocytes stimulated by myokines and adipokines.
Adipocyte
; 10(1): 153-159, 2021 12.
Article
in English
| MEDLINE | ID: mdl-33769190
8.
An Increase in Alpha Band Frequency in Resting State EEG after Electrical Stimulation of the Ear in Tinnitus Patients-A Pilot Study.
Front Neurosci
; 10: 453, 2016.
Article
in English
| MEDLINE | ID: mdl-27766069
9.
Friedreich ataxia is not only a GAA repeats expansion disorder: implications for molecular testing and counselling.
J Appl Genet
; 57(3): 349-55, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-26906906
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