Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Lotz-Havla AS"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Weiss, Katharina J., Röschinger, Wulf, Blessing, Holger, Lotz-Havla, Amelie S., Schiergens, Katharina A., Maier, Esther M.
Publikováno v:
Annals of Nutrition & Metabolism, 2020 Jan 01. 76(4), 268-276.
Externí odkaz:
https://www.jstor.org/stable/48620834
Autor:
Amelie S. Lotz-Havla, Sabrina Katzdobler, Brigitte Nuscher, Katharina Weiß, Johannes Levin, Joachim Havla, Esther M. Maier
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
To pave the way for healthy aging in early treated phenylketonuria (ETPKU) patients, a better understanding of the neurological course in this population is needed, requiring easy accessible biomarkers to monitor neurological disease progression in l
Externí odkaz:
https://doaj.org/article/00476ec0bb51462ca8ad272ec72869df
Autor:
Ania C. Muntau, Alberto Burlina, François Eyskens, Peter Freisinger, Vincenzo Leuzzi, Hatice Serap Sivri, Gwendolyn Gramer, Renata Pazdírková, Maureen Cleary, Amelia S. Lotz-Havla, Paul Lane, Ignacio Alvarez, Frank Rutsch
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Background During the initial 26-week SPARK (Safety Paediatric efficAcy phaRmacokinetic with Kuvan®) study, addition of sapropterin dihydrochloride (Kuvan®; a synthetic formulation of the natural cofactor for phenylalanine hydroxylase, tet
Externí odkaz:
https://doaj.org/article/63fd4568c46247219b22665cafdc58b9
Autor:
Amelie S. Lotz-Havla, Katharina J. Weiß, Katharina A. Schiergens, Theresa Brunet, Jürgen Kohlhase, Stephanie Regenauer-Vandewiele, Esther M. Maier
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Abstract Background Cobalamin (cbl)-related remethylation disorders are a heterogeneous group of inherited disorders comprising the remethylation of homocysteine to methionine and affecting multiple organ systems, most prominently the nervous system
Externí odkaz:
https://doaj.org/article/8d5fce646f904af18efa0edc44a89bef
Autor:
Joachim Havla, Thivya Pakeerathan, Carolin Schwake, Jeffrey L. Bennett, Ingo Kleiter, Ana Felipe-Rucián, Stephanie C. Joachim, Amelie S. Lotz-Havla, Tania Kümpfel, Markus Krumbholz, Eva M. Wendel, Markus Reindl, Charlotte Thiels, Thomas Lücke, Kerstin Hellwig, Ralf Gold, Kevin Rostasy, Ilya Ayzenberg
Publikováno v:
Journal of Neuroinflammation, Vol 18, Iss 1, Pp 1-10 (2021)
Abstract Background To investigate age-related severity, patterns of retinal structural damage, and functional visual recovery in pediatric and adult cohorts of myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) optic neuritis (O
Externí odkaz:
https://doaj.org/article/e6273de0a81f4441a89f3e0d94a0bee0
Autor:
Lotz-Havla, Amelie S.1 (AUTHOR), Christmann, Tara2 (AUTHOR), Parhofer, Klaus G.3 (AUTHOR), Maier, Esther M.1 (AUTHOR), Havla, Joachim2,4 (AUTHOR) joachim.havla@med.uni-muenchen.de
Publikováno v:
Journal of Clinical Medicine. Mar2023, Vol. 12 Issue 5, p2030. 13p.
Autor:
Blankenstein, Oliver, Härtel, Christoph, Hoefele, Julia, Hoffmann, Georg F., Hörster, Friederike, Lawrenz, Burkhard, Lotz-Havla, Amelie, Maier, Esther, Sommerburg, Olaf, Speckmann, Carsten, Urschitz, Michael S.
Publikováno v:
Monatsschrift Kinderheilkunde; Nov2024, Vol. 172 Issue 11, p1001-1003, 3p
Autor:
Amelie S. Lotz-Havla, Katharina Weiß, Katharina Schiergens, Stephanie Regenauer-Vandewiele, Klaus G. Parhofer, Tara Christmann, Luise Böhm, Joachim Havla, Esther M. Maier
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
In phenylalanine hydroxylase (PAH) deficiency, an easily feasible method to access the progression of neurodegeneration is warranted to contribute to current discussions on treatment indications and targets. The objective of the present study was to
Externí odkaz:
https://doaj.org/article/dc53cab277ff4e09819fe14c49b08d4f
Autor:
Amelie S. Lotz-Havla, Mathias Woidy, Philipp Guder, Jessica Schmiesing, Ralf Erdmann, Hans R. Waterham, Ania C. Muntau, Søren W. Gersting
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Peroxisomes share metabolic pathways with other organelles and peroxisomes are embedded into key cellular processes. However, the specific function of many peroxisomal proteins remains unclear and restricted knowledge of the peroxisomal protein inter
Externí odkaz:
https://doaj.org/article/1d918e65f1b043d5b0911c91c23a0f2f