Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tillmann Wallborn"'
Autor:
Mario Hönemann, Stephanie Thiem, Sandra Bergs, Tom Berthold, Christian Propach, Manuela Siekmeyer, Armin Frille, Tillmann Wallborn, Melanie Maier, Corinna Pietsch
Publikováno v:
Viruses, Vol 15, Iss 4, p 877 (2023)
Following the extensive non-pharmaceutical interventions (NPIs) and behavioral changes in the wake of the SARS-CoV-2 pandemic, an interseasonal rise in respiratory syncytial virus (RSV) cases was observed in Germany in 2021. The aim of this study was
Externí odkaz:
https://doaj.org/article/a237b83563cd4069a98f8aba7ff70890
Autor:
Lea Maria Merz, Florian Buerger, Niels Ziegelasch, Martin Zenker, Ilse Wieland, Tobias Lipek, Tillmann Wallborn, Nicolas Terliesner, Freerk Prenzel, Manuela Siekmeyer, Katalin Dittrich
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Epidermal nevus syndromes encompass a highly heterogeneous group of systemic disorders, characterized by epidermal nevi, and a spectrum of neuromuscular, ocular, and bone abnormalities. Cutaneous-skeletal hypophosphatemia syndrome (CSHS) constitutes
Externí odkaz:
https://doaj.org/article/219374aca3734a2791dc9d90aa316406
Autor:
Eva Müller, Desiree Dunstheimer, Jürgen Klammt, Daniela Friebe, Wieland Kiess, Jürgen Kratzsch, Tassilo Kruis, Sandy Laue, Roland Pfäffle, Tillmann Wallborn, Peter H Heidemann
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e38220 (2012)
Intrauterine and postnatal longitudinal growth is controlled by a strong genetic component that regulates a complex network of endocrine factors integrating them with cellular proliferation, differentiation and apoptotic processes in target tissues,
Externí odkaz:
https://doaj.org/article/b1058d4c285b425c95fc2b8bc19b0cb2
Autor:
Michael Thamm, Katalin Dittrich, Jürgen Kratzsch, Mandy Vogel, Wieland Kiess, Antje Kneuer, Tillmann Wallborn
Publikováno v:
European Journal of Nutrition
Purpose Iodine deficiency in childhood and adolescence may lead to later thyroid dysfunction, stunted growth and cognitive impairment. The World Health Organization (WHO) has issued recommended age-dependent urine iodine concentration targets, but a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56b6f66dbc31b30c69a0445453c6b630
http://europepmc.org/articles/PMC7867514
http://europepmc.org/articles/PMC7867514
Autor:
Desiree Dunstheimer, Tassilo Kruis, Tillmann Wallborn, Peter H. Heidemann, Jürgen Klammt, D Friebe, Roland Pfäffle, Wieland Kiess, Jürgen Kratzsch, S. Laue, Eva Müller
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 5, p e38220 (2012)
PLoS ONE, Vol 7, Iss 5, p e38220 (2012)
Intrauterine and postnatal longitudinal growth is controlled by a strong genetic component that regulates a complex network of endocrine factors integrating them with cellular proliferation, differentiation and apoptotic processes in target tissues,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34db49749f6f961fe42cf6a1a697157e
http://europepmc.org/articles/PMC3365032
http://europepmc.org/articles/PMC3365032
Autor:
Tillmann Wallborn, Rasha Odeh, Eva Müller, Tassilo Kruis, Roland Pfäffle, Wieland Kiess, Jürgen Klammt, Marina Schlicke, Juergen Kratzsch
Publikováno v:
Hormone research in paediatrics. 76
Mutations of numerous genes encoding proteins that affect multiple pathways responsible for regulation of cell proliferation can cause growth disturbances in humans. Genes such as HESX1, PROP1, PIT1/POU1F1 and GLI2 have been shown to cause pituitary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6192519c221ed66510c6416165eb4f
https://pubmed.ncbi.nlm.nih.gov/21912148
https://pubmed.ncbi.nlm.nih.gov/21912148
Autor:
Tassilo Kruis, Wieland Kiess, Marina Schlicke, Jürgen Klammt, Eva Müller, Roland Pfäffle, Jürgen Kratzsch, Stefan Wüller, Hildegard Schmitz-Van de Leur, Tillmann Wallborn, Gabriele Schmidt
Publikováno v:
The Journal of clinical endocrinology and metabolism. 95(5)
Background: Mutations in the IGF-I receptor (IGF1R) gene can be responsible for intrauterine and postnatal growth disorders. Objective: Here we report on a novel mutation in the IGF1R gene in a female patient. The aim of our study was to analyze the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40dd16133d0b529ad9584d83597f0f5d
https://pubmed.ncbi.nlm.nih.gov/20357178
https://pubmed.ncbi.nlm.nih.gov/20357178
Autor:
Marina Schlicke, Wieland Kiess, Roland Pfäffle, Jürgen Kratzsch, Eva Müller, Tillmann Wallborn, Jürgen Klammt, Rasha Odeh, Antje Körner, Assimina Galli-Tsinopoulou, Tassilo Kruis
Publikováno v:
Endocrinology. 151:840-841
IGF-I receptor (IGF1R) plays an essential role in human intrauterine and postnatal development. Few heterozygous mutations in IGF1R leading to IGF-I resistance and intrauterine and postnatal growth retardation have been described to date.The clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7373e777856e75a00d566cf14a1b0eae
https://doi.org/10.1210/endo.151.2.9996
https://doi.org/10.1210/endo.151.2.9996
Autor:
Satz Mengensatzproduktion, Jan M. Wit, Druck Reinhardt Druck Basel, Tassilo Kruis, John Chaplin, Marina Schlicke, Christopher J. H. Kelnar, Roland Pfäffle, Emanuela Peschiaroli, Stefano Cianfarani, Annalisa Deodati, Sandro Loche, Paul Czernichow, Wieland Kiess, Jürgen Klammt, Peter Fibiger Bang, Isabelle Durand-Zaleski, Meinolf Noeker, Leo Dunkel, Anders Lindberg, L.B. Johnston Rohrbasser, Tillmann Wallborn, Rasha Odeh, Anita C. S. Hokken-Koelega, Markus Perola, E. E. Müller, Jovanna Dahlgren, Monika Bullinger, Michael B. Ranke, Juergen Kratzsch, David B. Allen, David E. Sandberg, Steven D. Chernausek
Publikováno v:
Hormone Research in Paediatrics. 76:60-60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edba5a166b97475aae7786141d1fcee5
https://doi.org/10.1159/000330130
https://doi.org/10.1159/000330130