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Molecular Genetics and Metabolism Reports|January 13, 2018
Blood phenylalanine instability strongly correlates with anxiety in phenylketonuriaBozena Didycz, Miroslaw Bik-Multanowski
Journal of Inherited Metabolic Disease|September 15, 2006
LAT1 gene variants--potential factors influencing the clinical course of phenylketonuriaMiroslaw Bik-Multanowski, Jacek J Pietrzyk
Molecular Genetics and Metabolism|May 20, 2011
Blood phenylalanine clearance and BH(4)-responsiveness in classic phenylketonuriaMiroslaw Bik-Multanowski, Jacek J Pietrzyk
JIMD Reports|September 24, 2017
The Use of d2 and Benton Tests for Assessment of Attention Deficits and Visual Memory in Teenagers with PhenylketonuriaBozena Didycz, Magdalena Nitecka, Miroslaw Bik-Multanowski
Journal of Genetics|December 11, 2019
Hypermethylation of NRG1 gene correlates with the presence of heart defects in Down's syndromeArtur Dobosz, Agnieszka Grabowska, Miroslaw Bik-Multanowski
Journal of Alzheimer'S Disease : JAD|February 28, 2015
MTRNR2L12: A Candidate Blood Marker of Early Alzheimer's Disease-Like Dementia in Adults with Down SyndromeMiroslaw Bik-Multanowski, Jacek J Pietrzyk, Alina Midro
Molecular Genetics and Metabolism|November 2, 2010
Routine use of CANTAB system for detection of neuropsychological deficits in patients with PKUMiroslaw Bik-Multanowski, Jacek J Pietrzyk, Renata Mozrzymas
Molecular Genetics and Metabolism Reports|April 19, 2021
The rs113883650 variant of SLC7A5 (LAT1) gene may alter brain phenylalanine content in PKUMiroslaw Bik-Multanowski, Kinga Bik-Multanowska, Iwona Betka, et al.
BMC Pulmonary Medicine|April 22, 2020
Case report of endoprosthesis -Y implantation in severe respiratory failure in the MPSII patient; comparison with literature dataWojciech Gocyk, Janusz Warmus, Henryk Olechnowicz, et al.
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