Pulmonary candidiasis treated with 5-fluorocytosine.

Por Kohlschütter, A, Pelet, B
Publicado em 1974

NCL Disorders: Frequent Causes of Childhood Dementia

Por SCHULZ, Angela, KOHLSCHÜTTER, Alfried
Publicado em 2013

Novel Cytotoxic Vectors Based on Adeno-Associated Virus

Por Kohlschütter, Johannes, Michelfelder, Stefan, Trepel, Martin
Publicado em 2010

Abrupt withdrawal of pindolol or metoprolol after chronic therapy.

Por Szécsi, E, Kohlschütter, S, Schiess, W, Lang, E
Publicado em 1982

Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency

Por Oechsner, M, Steen, C, Sturenburg, H, Kohlschutter, A
Publicado em 1998

Influence of diagnostic categories, age, and gender on antioxidative defense and lipid peroxidation in skeletal muscle of patients with neuromuscular diseases

Por Stuerenburg, Hans-Joerg, Stangneth, Birgit, Kohlschütter, Alfried, Finckh, Barbara
Publicado em 2003

NCL diseases — clinical perspectives()

Por Schulz, Angela, Kohlschütter, Alfried, Mink, Jonathan, Simonati, Alessandro, Williams, Ruth
Publicado no Biochim Biophys Acta (2013)

Dietary fish oil blocks the microcirculatory manifestations of ischemia-reperfusion injury in striated muscle in hamsters.

Por Lehr, H A, Hübner, C, Nolte, D, Kohlschütter, A, Messmer, K
Publicado em 1991

Successful Expansion but Not Complete Restriction of Tropism of Adeno-Associated Virus by In Vivo Biopanning of Random Virus Display Peptide Libraries

Por Michelfelder, Stefan, Kohlschütter, Johannes, Skorupa, Alexandra, Pfennings, Sabrina, Müller, Oliver, Kleinschmidt, Jürgen A., Trepel, Martin
Publicado em 2009

Role of leukotrienes in leukocyte adhesion following systemic administration of oxidatively modified human low density lipoprotein in hamsters.

Por Lehr, H A, Hübner, C, Finckh, B, Angermüller, S, Nolte, D, Beisiegel, U, Kohlschütter, A, Messmer, K
Publicado em 1991

Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues.

Por Heine, Claudia, Tyynelä, Jaana, Cooper, Jonathan D, Palmer, David N, Elleder, Milan, Kohlschütter, Alfried, Braulke, Thomas
Publicado em 2003

Autophagic vacuolar myopathy is a common feature of CLN3 disease

Por Radke, Josefine, Koll, Randi, Gill, Esther, Wiese, Lars, Schulz, Angela, Kohlschütter, Alfried, Schuelke, Markus, Hagel, Christian, Stenzel, Werner, Goebel, Hans H.
Publicado no Ann Clin Transl Neurol (2018)

Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort

Por Kehrer, Christiane, Groeschel, Samuel, Kustermann-Kuhn, Birgit, Bürger, Friederike, Köhler, Wolfgang, Kohlschütter, Alfried, Bley, Annette, Steinfeld, Robert, Gieselmann, Volkmar, Krägeloh-Mann, Ingeborg
Publicado em 2014

Brain iron quantification by MRI in mitochondrial membrane protein-associated neurodegeneration under iron-chelating therapy

Por Löbel, Ulrike, Schweser, Ferdinand, Nickel, Miriam, Deistung, Andreas, Grosse, Regine, Hagel, Christian, Fiehler, Jens, Schulz, Angela, Hartig, Monika, Reichenbach, Jürgen R, Kohlschütter, Alfried, Sedlacik, Jan
Publicado no Ann Clin Transl Neurol (2014)

Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions

Por Francke, Uta, Harper, John F., Darras, Basil T., Cowan, Janet M., McCabe, Edward R. B., Kohlschütter, Alfried, Seltzer, William K., Saito, Fumiko, Goto, Jun, Harpey, Jean-Paul, Wise, Joyce E.
Publicado em 1987

Analysis of Potential Biomarkers and Modifier Genes Affecting the Clinical Course of CLN3 Disease

Por Lebrun, Anne-Hélène, Moll-Khosrawi, Parisa, Pohl, Sandra, Makrypidi, Georgia, Storch, Stephan, Kilian, Dirk, Streichert, Thomas, Otto, Benjamin, Mole, Sara E, Ullrich, Kurt, Cotman, Susan, Kohlschütter, Alfried, Braulke, Thomas, Schulz, Angela
Publicado em 2011

A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy

Por Simons, Cas, Dyment, David, Bent, Stephen J, Crawford, Joanna, D’Hooghe, Marc, Kohlschütter, Alfried, Venkateswaran, Sunita, Helman, Guy, Poll-The, Bwee-Tien, Makowski, Christine C, Ito, Yoko, Kernohan, Kristin, Hartley, Taila, Waisfisz, Quinten, Taft, Ryan J, van der Knaap, Marjo S, Wolf, Nicole I
Publicado no Brain (2017)

Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome

Por Schossig, Anna, Wolf, Nicole I., Fischer, Christine, Fischer, Maria, Stocker, Gernot, Pabinger, Stephan, Dander, Andreas, Steiner, Bernhard, Tönz, Otmar, Kotzot, Dieter, Haberlandt, Edda, Amberger, Albert, Burwinkel, Barbara, Wimmer, Katharina, Fauth, Christine, Grond-Ginsbach, Caspar, Koch, Martin J., Deichmann, Annette, von Kalle, Christof, Bartram, Claus R., Kohlschütter, Alfried, Trajanoski, Zlatko, Zschocke, Johannes
Publicado em 2012

Ataxia with Vitamin E Deficiency: Refinement of Genetic Localization and Analysis of Linkage Disequilibrium by Using New Markers in 14 Families

Por Doerflinger, Nathalie, Linder, Catherine, Ouahchi, Karim, Gyapay, Gabor, Weissenbach, Jean, Le Paslier, Denis, Rigault, Philippe, Belal, Samir, Hamida, Christiane Ben, Hentati, Faycal, Hamida, Mongi Ben, Pandolfo, Massimo, DiDonato, Stephano, Sokol, Ronald, Kayden, Herbert, Landrieu, Pierre, Durr, Alexandra, Brice, Alexis, Goutières, Françoise, Kohlschütter, Alfried, Sabouraud, Pascal, Benomar, Ali, Yahyaoui, Mohamed, Mandel, Jean-Louis, Koenig, Michel
Publicado em 1995