Sarah Catharina Grünert (S C Grünert, Sarah C Grünert)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 37

Top Venues

JIMD reports

Genes

Orphanet journal of rare diseases

Annals of clinical and translational neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Ruben J Overduin, Sarah Catharina Grünert, Martine T P Besouw, Mathieu S Bolhuis, Joost Groen, Andrea B Schreuder, Mathias Woidy, Simona Murko, René Santer, Terry G J Derks
Repurposing SGLT2 inhibitors: Treatment of renal proximal tubulopathy in Fanconi-Bickel syndrome with empagliflozin. Journal of inherited metabolic disease (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology (2024)
Maren Thiel, Sven F Garbade, Stefanie Rosenbaum-Fabian, Ute Spiekerkoetter, Sarah Catharina Grünert
Psychosocial issues and coping strategies in families affected by long-chain fatty acid oxidation disorders. JIMD reports 65 (1) (2023)
Maren Thiel, Sven F Garbade, Stefanie Rosenbaum-Fabian, Ute Spiekerkoetter, Sarah Catharina Grünert
Psychosocial issues and coping strategies in families affected by long-chain fatty acid oxidation disorders. JIMD reports 65 (1) (2023)
Sarah Catharina Grünert, Athanasia Ziagaki, André Heinen, Anke Schumann, Sara Tucci, Ute Spiekerkoetter, Miriam Schmidts
Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum. Genes 14 (7) (2023)
Sarah Catharina Grünert, Annieke Venema, Jamas LaFreniere, Blair Schneider, Enrique Contreras, Saskia B Wortmann, Terry G J Derks
Patient-reported outcomes on empagliflozin treatment in glycogen storage disease type Ib: An international questionnaire study. JIMD reports 64 (3) (2023)
Sarah Catharina Grünert, Annieke Venema, Jamas LaFreniere, Blair Schneider, Enrique Contreras, Saskia B Wortmann, Terry G J Derks
Patient-reported outcomes on empagliflozin treatment in glycogen storage disease type Ib: An international questionnaire study. JIMD reports 64 (3) (2023)
Maria Veiga-da-Cunha, Saskia B Wortmann, Sarah Catharina Grünert, Emile Van Schaftingen
Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors. Diagnostics (Basel, Switzerland) 13 (10) (2023)
Sarah Catharina Grünert, Anke Schumann, Ute Spiekerkoetter
Severe loss of appetite and refusal to eat as severe side effect of glycerol phenylbutyrate. JIMD reports 63 (6) (2022)
Aida Corrillero Bravo, Maria Nieves Ligero Aguilera, Nahuel R Marziali, Lennart Moritz, Victoria Wingert, Katharina Klotz, Anke Schumann, Sarah Catharina Grünert, Ute Spiekerkoetter, Urs Berger, Ann-Kathrin Lederer, Roman Huber, Luciana Hannibal
Analysis of S-Adenosylmethionine and S-Adenosylhomocysteine: Method Optimisation and Profiling in Healthy Adults upon Short-Term Dietary Intervention. Metabolites 12 (5) (2022)
Sarah Catharina Grünert, Jörn Oliver Sass
Correction to: 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces. Orphanet journal of rare diseases 17 (1) (2022)
Vanessa Hübner, Luciana Hannibal, Nils Janzen, Sarah Catharina Grünert, Peter Freisinger
Methionine Adenosyltransferase I/III Deficiency Detected by Newborn Screening. Genes 13 (7) (2022)
Sarah Catharina Grünert, Matthias Eckenweiler, Ute Spiekerkoetter
Reversible sensory neuropathy in mitochondrial trifunctional protein deficiency. JIMD reports 63 (3) (2022)
Sarah Catharina Grünert, Stefanie Rosenbaum-Fabian, Anke Schumann, Anne-Christine Selbitz, Waltraut Merz, Andrea Gieselmann, Ute Spiekerkoetter
Two successful pregnancies and first use of empagliflozin during pregnancy in glycogen storage disease type Ib. JIMD reports 63 (4) (2022)
Terry G J Derks, David F Rodriguez-Buritica, Ayesha Ahmad, Foekje de Boer, Maria-Luz Couce, Sarah Catharina Grünert, Philippe Labrune, Nerea López Maldonado, Carolina Fischinger Moura de Souza, Rebecca Riba-Wolman, Alessandro Rossi, Heather Saavedra, Rupal Naik Gupta, Vassili Valayannopoulos, John Mitchell
Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs. Nutrients 13 (11) (2021)
Sarah Catharina Grünert, Uta Matysiak, Franka Hodde, Gunda Ruzaike, Ekkehart Lausch, Anke Schumann, Natascha van der Werf-Grohmann, Ute Spiekerkoetter, Miriam Schmidts
Isolated Hypomethylation of IGF2 Associated with Severe Hypoglycemia Responsive to Growth Hormone Treatment. Diagnostics (Basel, Switzerland) 11 (5) (2021)
Ulrike Teufel-Schäfer, Christian Huhn, Sabine Müller, Christoph Müller, Sarah Catharina Grünert
Severe allergic contact dermatitis to two different continuous glucose monitoring devices in a patient with glycogen storage disease type 9b. Pediatric dermatology 38 (5) (2021)
Sarah Catharina Grünert, Matthias Eckenweiler, Dorothea Haas, Martin Lindner, Konstantinos Tsiakas, René Santer, Sara Tucci, Ute Spiekerkoetter
The spectrum of peripheral neuropathy in disorders of the mitochondrial trifunctional protein. Journal of inherited metabolic disease 44 (4) (2021)
Sarah Catharina Grünert, Anke Schumann, Federico Baronio, Konstantinos Tsiakas, Simona Murko, Ute Spiekerkoetter, René Santer
Evidence for a Genotype-Phenotype Correlation in Patients with Pathogenic GLUT2 (SLC2A2) Variants. Genes 12 (11) (2021)
Khaled Ibrahim Alatibi, Stefan Tholen, Zeinab Wehbe, Judith Hagenbuchner, Daniela Karall, Michael J Ausserlechner, Oliver Schilling, Sarah Catharina Grünert, Jerry Vockley, Sara Tucci
Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders. International journal of molecular sciences 22 (19) (2021)
Sarah Catharina Grünert, Luciana Hannibal, Ute Spiekerkoetter
The Phenotypic and Genetic Spectrum of Glycogen Storage Disease Type VI. Genes 12 (8) (2021)
Khaled Ibrahim Alatibi, Judith Hagenbuchner, Zeinab Wehbe, Daniela Karall, Michael J Ausserlechner, Jerry Vockley, Ute Spiekerkoetter, Sarah Catharina Grünert, Sara Tucci
Different Lipid Signature in Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders. Cells 10 (5) (2021)
Sarah Catharina Grünert, Luciana Hannibal, Anke Schumann, Stefanie Rosenbaum-Fabian, Stefanie Beck-Wödl, Tobias B Haack, Mona Grimmel, Miriam Bertrand, Ute Spiekerkoetter
Identification and Characterization of a Novel Splice Site Mutation Associated with Glycogen Storage Disease Type VI in Two Unrelated Turkish Families. Diagnostics (Basel, Switzerland) 11 (3) (2021)
Julia Kopp, Cristina Has, Alrun Hotz, Sarah Catharina Grünert, Judith Fischer
Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome. Genes 12 (8) (2021)
Isabel Schüle, Urs Berger, Uta Matysiak, Gunda Ruzaike, Brigitte Stiller, Martin Pohl, Ute Spiekerkoetter, Ekkehart Lausch, Sarah Catharina Grünert, Miriam Schmidts
A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome. Genes 12 (6) (2021)
Sven F Garbade, Viviane Ederer, Peter Burgard, Udo Wendel, Ute Spiekerkoetter, Dorothea Haas, Sarah Catharina Grünert
Impact of glycogen storage disease type I on adult daily life: a survey. Orphanet journal of rare diseases 16 (1) (2021)
Sarah Catharina Grünert, Jörn Oliver Sass
3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces. Orphanet journal of rare diseases 15 (1) (2020)
Sarah Catharina Grünert, Jörn Oliver Sass
2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways. Orphanet journal of rare diseases 15 (1) (2020)
Sarah Catharina Grünert, Roland Elling, Bärbel Maag, Saskia B Wortmann, Terry G J Derks, Luciana Hannibal, Anke Schumann, Stefanie Rosenbaum-Fabian, Ute Spiekerkoetter
Improved inflammatory bowel disease, wound healing and normal oxidative burst under treatment with empagliflozin in glycogen storage disease type Ib. Orphanet journal of rare diseases 15 (1) (2020)
Sarah Catharina Grünert, A Schumann, P Freisinger, S Rosenbaum-Fabian, M Schmidts, A J Mueller, S Beck-Wödl, T B Haack, H Schneider, H Fuchs, U Teufel, G Gramer, L Hannibal, U Spiekerkoetter
Citrin deficiency mimicking mitochondrial depletion syndrome. BMC pediatrics 20 (1) (2020)
Julia Hinkel, Johannes Schmitt, Michael Wurm, Stefanie Rosenbaum-Fabian, Karl Otfried Schwab, Donald W Jacobsen, Ute Spiekerkoetter, Sergey N Fedosov, Luciana Hannibal, Sarah Catharina Grünert
Elevated Plasma Vitamin B12 in Patients with Hepatic Glycogen Storage Diseases. Journal of clinical medicine 9 (8) (2020)
Sarah Catharina Grünert, Stefanie Rosenbaum-Fabian, Luciana Hannibal, Anke Schumann, Ute Spiekerkötter
Three successful pregnancies in a patient with glycogen storage disease type 0. JIMD reports 57 (1) (2020)
Sarah Catharina Grünert, Thorsten Marquardt, Ekkehart Lausch, Hans Fuchs, Christian Thiel, Martin Sutter, Anke Schumann, Luciana Hannibal, Ute Spiekerkoetter
Unsuccessful intravenous D-mannose treatment in PMM2-CDG. Orphanet journal of rare diseases 14 (1) (2019)

Sarah Catharina Grünert.css-eqlu8i{font-size:small;padding-left:4px;} (S C Grünert, Sarah C Grünert)

Publication Activity (10 Years)

Top Topics

Top Venues

Sarah Catharina Grünert (S C Grünert, Sarah C Grünert)