Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

135 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene.
Sutovský S, Petrovic R, Chandoga J, Turcáni P. Sutovský S, et al. J Neurol Sci. 2007 Dec 15;263(1-2):149-53. doi: 10.1016/j.jns.2007.01.082. Epub 2007 Jul 26. J Neurol Sci. 2007. PMID: 17662307
Adrenoleukodystrophy--a new mutation identified.
Vachalova I, Chandoga J, Petrovic R, Copikova-Cudrakova D, Sykora M, Traubner P. Vachalova I, et al. Bratisl Lek Listy. 2007;108(10-11):462-6. Bratisl Lek Listy. 2007. PMID: 18306728
Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia.
Konkoľová J, Petrovič R, Chandoga J, Repiský M, Zelinková H, Kršiaková J, Kolníková M, Kantarská D, Šutovský S, Böhmer D. Konkoľová J, et al. Gene. 2015 Aug 15;568(1):61-8. doi: 10.1016/j.gene.2015.05.020. Epub 2015 May 9. Gene. 2015. PMID: 25967389
A novel mutation in the PEX12 gene causing a peroxisomal biogenesis disorder.
Konkoľová J, Petrovič R, Chandoga J, Halasová E, Jungová P, Böhmer D. Konkoľová J, et al. Mol Biol Rep. 2015 Sep;42(9):1359-63. doi: 10.1007/s11033-015-3885-7. Epub 2015 Jun 21. Mol Biol Rep. 2015. PMID: 26094004
Neuropathology and biochemistry of early onset familial Alzheimer's disease caused by presenilin-1 missense mutation Thr116Asn.
Sutovsky S, Smolek T, Turcani P, Petrovic R, Brandoburova P, Jadhav S, Novak P, Attems J, Zilka N. Sutovsky S, et al. J Neural Transm (Vienna). 2018 Jun;125(6):965-976. doi: 10.1007/s00702-018-1850-z. Epub 2018 Feb 5. J Neural Transm (Vienna). 2018. PMID: 29404783
Atypical Huntington's disease with the clinical presentation of behavioural variant of frontotemporal dementia.
Sutovsky S, Smolek T, Alafuzoff I, Blaho A, Parrak V, Turcani P, Palkovic M, Petrovic R, Novak M, Zilka N. Sutovsky S, et al. J Neural Transm (Vienna). 2016 Dec;123(12):1423-1433. doi: 10.1007/s00702-016-1579-5. Epub 2016 Jun 10. J Neural Transm (Vienna). 2016. PMID: 27287334
Differing clinical presentations of two unrelated cases of X-linked adrenoleukodystrophy with identical mutation Y296C in the ABCD1 gene.
Sutovský S, Kolníková M, Petrovic R, Kollár B, Siarnik P, Chandoga J, Fischerová M, Turcáni P. Sutovský S, et al. Neuro Endocrinol Lett. 2014;35(5):411-6. Neuro Endocrinol Lett. 2014. PMID: 25275259
GAI - distinct genotype and phenotype characteristics in reported Slovak patients.
Lisyova J, Petrovic R, Jurickova K, Brennerova K, Urbanova D, Behulova D, Bzduch V, Chandoga J. Lisyova J, et al. Bratisl Lek Listy. 2016;117(11):631-638. doi: 10.4149/BLL_2016_123. Bratisl Lek Listy. 2016. PMID: 28125888
ERVW-1 gene polymorphisms related to preeclampsia.
Priscakova P, Konkolova J, Petrovic R, Lipov J, Minarik G, Bohmer D, Repiska V, Gbelcova H. Priscakova P, et al. Bratisl Lek Listy. 2016;117(6):340-4. doi: 10.4149/bll_2016_067. Bratisl Lek Listy. 2016. PMID: 27546366
135 results
Jump to page
Feedback