Search Results - Hennermann, Julia

Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening by Gramer, Gwendolyn, Hoffmann, Georg F., Hennermann, Julia B.

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Eight-Year Follow-Up of Neuropsychiatric Symptoms and Brain Structural Changes in Fabry Disease by Lelieveld, Irene M., Böttcher, Anna, Hennermann, Julia B., Beck, Michael, Fellgiebel, Andreas

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Vertical saccadic palsy and foveal retinal thinning in Niemann-Pick disease type C by Hopf, Susanne, Hennermann, Julia B., Schuster, Alexander K., Pfeiffer, Norbert, Pitz, Susanne

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Retinal thinning in phenylketonuria and Gaucher disease type 3 by Hopf, Susanne, Schuster, Alexander K., Hennermann, Julia B., Pfeiffer, Norbert, Pitz, Susanne

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Saccadic reaction time and ocular findings in phenylketonuria by Hopf, Susanne, Nowak, Caroline, Hennermann, Julia B., Schmidtmann, Irene, Pfeiffer, Norbert, Pitz, Susanne

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Retinal and optic nerve degeneration in α-mannosidosis by Matlach, Juliane, Zindel, Thea, Amraoui, Yasmina, Arash-Kaps, Laila, Hennermann, Julia B., Pitz, Susanne

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The cardiovascular phenotype of adult patients with phenylketonuria by Azabdaftari, Aline, van der Giet, Markus, Schuchardt, Mirjam, Hennermann, Julia B., Plöckinger, Ursula, Querfeld, Uwe

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A comprehensive monocentric ophthalmic study with Gaucher disease type 3 patients: vitreoretinal lesions, retinal atrophy and characterization of abnormal saccades by Hopf, Susanne, Pfeiffer, Norbert, Liesenfeld, Matthias, Mengel, Karl-Eugen, Hennermann, Julia B., Schmidtmann, Irene, Pitz, Susanne

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Mortality in patients with alpha-mannosidosis: a review of patients’ data and the literature by Hennermann, Julia B., Raebel, Eva M., Donà, Francesca, Jacquemont, Marie-Line, Cefalo, Graziella, Ballabeni, Andrea, Malm, Dag

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Cerebellar atrophy on top of motor neuron compromise as indicator of late-onset GM2 gangliosidosis by Hölzer, Hans Thomas, Boschann, Felix, Hennermann, Julia B., Hahn, Gabriele, Hermann, Andreas, von der Hagen, Maja, Tüngler, Victoria

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Heart and Cardiovascular Involvement in Patients with Mucopolysaccharidosis Type IVA (Morquio-A Syndrome) by Kampmann, Christoph, Abu-Tair, Tariq, Gökce, Seyfullah, Lampe, Christina, Reinke, Jörg, Mengel, Eugen, Hennermann, Julia B., Wiethoff, Christiane M.

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Analysis of Renal and Cardiac Outcomes in Male Participants in the Fabry Outcome Survey Starting Agalsidase Alfa Enzyme Replacement Therapy Before and After 18 Years of Age by Parini, Rossella, Pintos-Morell, Guillem, Hennermann, Julia B, Hsu, Ting-Rong, Karabul, Nesrin, Kalampoki, Vasiliki, Gurevich, Andrey, Ramaswami, Uma

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Growth charts for patients with Sanfilippo syndrome (Mucopolysaccharidosis type III) by Muschol, Nicole M., Pape, Daniel, Kossow, Kai, Ullrich, Kurt, Arash-Kaps, Laila, Hennermann, Julia B., Stücker, Ralf, Breyer, Sandra R.

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Predictors of growth patterns in children with mucopolysaccharidosis I after haematopoietic stem cell transplantation by Maier, Stefanie, Zivicnjak, Miroslav, Grigull, Lorenz, Hennermann, Julia B., Aries, Charlotte, Maecker‐Kolhoff, Britta, Sauer, Martin, Das, Anibh M., Beier, Rita

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Extent, impact, and predictors of diagnostic delay in Pompe disease: A combined survey approach to unveil the diagnostic odyssey by Lagler, Florian B., Moder, Angelika, Rohrbach, Marianne, Hennermann, Julia, Mengel, Eugen, Gökce, Seyfullah, Hundsberger, Thomas, Rösler, Kai M., Karabul, Nesrin, Huemer, Martina

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The SPARKLE registry: protocol for an international prospective cohort study in patients with alpha-mannosidosis by Hennermann, Julia B., Guffon, Nathalie, Cattaneo, Federica, Ceravolo, Ferdinando, Borgwardt, Line, Lund, Allan M., Gil-Campos, Mercedes, Tylki-Szymanska, Anna, Muschol, Nicole M.

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Axonopathy and Reduction of Membrane Resistance: Key Features in a New Murine Model of Human G(M1)-Gangliosidosis by Eikelberg, Deborah, Lehmbecker, Annika, Brogden, Graham, Tongtako, Witchaya, Hahn, Kerstin, Habierski, Andre, Hennermann, Julia B., Naim, Hassan Y., Felmy, Felix, Baumgärtner, Wolfgang, Gerhauser, Ingo

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Use of the Bruininks-Oseretsky test of motor proficiency (BOT-2) to assess efficacy of velmanase alfa as enzyme therapy for alpha-mannosidosis by Phillips, Dawn, Hennermann, Julia B., Tylki-Szymanska, Anna, Borgwardt, Line, Gil-Campos, Mercedes, Guffon, Nathalie, Amraoui, Yasmina, Geraci, Silvia, Ardigò, Diego, Cattaneo, Federica, Lund, Allan M.

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Identification and Affinity Determination of Protein-Antibody and Protein-Aptamer Epitopes by Biosensor-Mass Spectrometry Combination † by Lupu, Loredana-Mirela, Wiegand, Pascal, Holdschick, Daria, Mihoc, Delia, Maeser, Stefan, Rawer, Stephan, Völklein, Friedemann, Malek, Ebrahim, Barka, Frederik, Knauer, Sascha, Uth, Christina, Hennermann, Julia, Kleinekofort, Wolfgang, Hahn, Andreas, Barka, Günes, Przybylski, Michael

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Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease by Lenders, Malte, Hennermann, Julia B., Kurschat, Christine, Rolfs, Arndt, Canaan-Kühl, Sima, Sommer, Claudia, Üçeyler, Nurcan, Kampmann, Christoph, Karabul, Nesrin, Giese, Anne-Katrin, Duning, Thomas, Stypmann, Jörg, Krämer, Johannes, Weidemann, Frank, Brand, Stefan-Martin, Wanner, Christoph, Brand, Eva

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