The Radial Variation of the Solar Wind Turbulence Spectra near the Kinetic Break Scale from Parker Solar Probe Measurements
Lotz, S., Nel, A. E., Wicks, R. T., Roberts, O. W., Engelbrecht, N. E., Strauss, R. D., Botha, G. J. J., Kontar, E. P., Pitňa, A., Bale, S. D.
Published in The Astrophysical journal (01.01.2023)
Published in The Astrophysical journal (01.01.2023)
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Journal Article
On the low-cycle fatigue behavior of thermo-mechanically processed high-strength aluminum alloys
Sajadifar, S.V., Scharifi, E., Wegener, T., Krochmal, M., Lotz, S., Steinhoff, K., Niendorf, T.
Published in International journal of fatigue (01.03.2022)
Published in International journal of fatigue (01.03.2022)
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Journal Article
Data driven transfer functions and transmission network parameters for GIC modelling
Heyns, M.J., Gaunt, C.T., Lotz, S.I., Cilliers, P.J.
Published in Electric power systems research (01.11.2020)
Published in Electric power systems research (01.11.2020)
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Journal Article
Fecal Carriage and Shedding Density of CTX-M Extended-Spectrum β-Lactamase-Producing Escherichia coli in Cattle, Chickens, and Pigs: Implications for Environmental Contamination and Food Production
HORTON, R. A, RANDALL, L. P, LA RAGIONE, R. M, COLDHAM, N. G, SNARY, E. L, COCKREM, H, LOTZ, S, WEARING, H, DUNCAN, D, RABIE, A, MCLAREN, I, WATSON, E
Published in Applied and Environmental Microbiology (01.06.2011)
Published in Applied and Environmental Microbiology (01.06.2011)
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Journal Article
Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples
Maier, Esther M., Mütze, Ulrike, Janzen, Nils, Steuerwald, Ulrike, Nennstiel, Uta, Odenwald, Birgit, Schuhmann, Elfriede, Lotz‐Havla, Amelie S., Weiss, Katharina J., Hammersen, Johanna, Weigel, Corina, Thimm, Eva, Grünert, Sarah C., Hennermann, Julia B., Freisinger, Peter, Krämer, Johannes, Das, Anibh M., Illsinger, Sabine, Gramer, Gwendolyn, Fang‐Hoffmann, Junmin, Garbade, Sven F., Okun, Jürgen G., Hoffmann, Georg F., Kölker, Stefan, Röschinger, Wulf
Published in Journal of inherited metabolic disease (01.11.2023)
Published in Journal of inherited metabolic disease (01.11.2023)
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Journal Article
Validating the LDi and LCi Indices in the Southern Hemisphere
Nahayo, E., Guerrero, A., Lotz, S., Cid, C., Tshisaphungo, M., Saiz, E.
Published in Space Weather (01.10.2022)
Published in Space Weather (01.10.2022)
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Journal Article
Long-term efficacy and safety of sapropterin in patients who initiated sapropterin at < 4 years of age with phenylketonuria: results of the 3-year extension of the SPARK open-label, multicentre, randomised phase IIIb trial
Muntau, Ania C, Burlina, Alberto, Eyskens, François, Freisinger, Peter, Leuzzi, Vincenzo, Sivri, Hatice Serap, Gramer, Gwendolyn, Pazdírková, Renata, Cleary, Maureen, Lotz-Havla, Amelia S, Lane, Paul, Alvarez, Ignacio, Rutsch, Frank
Published in Orphanet journal of rare diseases (03.08.2021)
Published in Orphanet journal of rare diseases (03.08.2021)
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Journal Article
Age-dependent favorable visual recovery despite significant retinal atrophy in pediatric MOGAD: how much retina do you really need to see well?
Havla, Joachim, Pakeerathan, Thivya, Schwake, Carolin, Bennett, Jeffrey L, Kleiter, Ingo, Felipe-Rucián, Ana, Joachim, Stephanie C, Lotz-Havla, Amelie S, Kümpfel, Tania, Krumbholz, Markus, Wendel, Eva M, Reindl, Markus, Thiels, Charlotte, Lücke, Thomas, Hellwig, Kerstin, Gold, Ralf, Rostasy, Kevin, Ayzenberg, Ilya
Published in Journal of neuroinflammation (29.05.2021)
Published in Journal of neuroinflammation (29.05.2021)
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Journal Article
Serum glial fibrillary acidic protein and neurofilament light chain in patients with early treated phenylketonuria
Lotz-Havla, Amelie S., Katzdobler, Sabrina, Nuscher, Brigitte, Weiß, Katharina, Levin, Johannes, Havla, Joachim, Maier, Esther M.
Published in Frontiers in neurology (29.09.2022)
Published in Frontiers in neurology (29.09.2022)
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Journal Article
iBRET Screen of the ABCD1 Peroxisomal Network and Mutation-Induced Network Perturbations
Lotz-Havla, Amelie S, Woidy, Mathias, Guder, Philipp, Friedel, Caroline C, Klingbeil, Julian M, Bulau, Ana-Maria, Schultze, Anja, Dahmen, Ilona, Noll-Puchta, Heidi, Kemp, Stephan, Erdmann, Ralf, Zimmer, Ralf, Muntau, Ania C, Gersting, Søren W
Published in Journal of proteome research (03.09.2021)
Published in Journal of proteome research (03.09.2021)
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Journal Article
Subcutaneous vitamin B12 administration using a portable infusion pump in cobalamin-related remethylation disorders: a gentle and easy to use alternative to intramuscular injections
Lotz-Havla, Amelie S, Weiß, Katharina J, Schiergens, Katharina A, Brunet, Theresa, Kohlhase, Jürgen, Regenauer-Vandewiele, Stephanie, Maier, Esther M
Published in Orphanet journal of rare diseases (12.05.2021)
Published in Orphanet journal of rare diseases (12.05.2021)
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Journal Article
Fatal pitfalls in newborn screening for mitochondrial trifunctional protein (MTP)/long-chain 3-Hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency
Lotz-Havla, Amelie S, Röschinger, Wulf, Schiergens, Katharina, Singer, Katharina, Karall, Daniela, Konstantopoulou, Vassiliki, Wortmann, Saskia B, Maier, Esther M
Published in Orphanet journal of rare diseases (20.07.2018)
Published in Orphanet journal of rare diseases (20.07.2018)
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Journal Article
Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26
Guder, Philipp, Lotz-Havla, Amelie S., Woidy, Mathias, Reiß, Dunja D., Danecka, Marta K., Schatz, Ulrich A., Becker, Marc, Ensenauer, Regina, Pagel, Philipp, Büttner, Lars, Muntau, Ania C., Gersting, Søren W.
Published in Biochimica et biophysica acta. Molecular cell research (01.03.2019)
Published in Biochimica et biophysica acta. Molecular cell research (01.03.2019)
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Journal Article
Optical Coherence Tomography to Assess Neurodegeneration in Phenylalanine Hydroxylase Deficiency
Lotz-Havla, Amelie S, Weiß, Katharina, Schiergens, Katharina, Regenauer-Vandewiele, Stephanie, Parhofer, Klaus G, Christmann, Tara, Böhm, Luise, Havla, Joachim, Maier, Esther M
Published in Frontiers in neurology (10.12.2021)
Published in Frontiers in neurology (10.12.2021)
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Journal Article
Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency
Lotz-Havla, Amelie S., Woidy, Mathias, Guder, Philipp, Schmiesing, Jessica, Erdmann, Ralf, Waterham, Hans R., Muntau, Ania C., Gersting, Søren W.
Published in Frontiers in genetics (04.11.2021)
Published in Frontiers in genetics (04.11.2021)
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Journal Article
Long-term follow-up and outcome of phenylketonuria patients on sapropterin: a retrospective study
Keil, Stefanie, Anjema, Karen, van Spronsen, Francjan J, Lambruschini, Nilo, Burlina, Alberto, Bélanger-Quintana, Amaya, Couce, Maria L, Feillet, Francois, Cerone, Roberto, Lotz-Havla, Amelie S, Muntau, Ania C, Bosch, Annet M, Meli, Concetta A P, Billette de Villemeur, Thierry, Kern, Ilse, Riva, Enrica, Giovannini, Marcello, Damaj, Lena, Leuzzi, Vincenzo, Blau, Nenad
Published in Pediatrics (Evanston) (01.06.2013)
Published in Pediatrics (Evanston) (01.06.2013)
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